CA2744893A1 - Aryl carbonyl derivatives as glucokinase activators - Google Patents

Aryl carbonyl derivatives as glucokinase activators Download PDF

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CA2744893A1
CA2744893A1 CA2744893A CA2744893A CA2744893A1 CA 2744893 A1 CA2744893 A1 CA 2744893A1 CA 2744893 A CA2744893 A CA 2744893A CA 2744893 A CA2744893 A CA 2744893A CA 2744893 A1 CA2744893 A1 CA 2744893A1
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compound according
alkyl
alkylene
aryl
treatment
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Dharma Rao Polisetti
Janos Tibor Kodra
Paw Bloch
Maria Carmen Valcarce-Lopez
Niels Blume
Mustafa Guzel
Kalpathy Chidambareswaran Santhosh
Adnan M. M. Mjalli
Robert Carl Andrews
Govindan Subramanian
Michael Ankersen
Per Vedso
Anthony Murray
Lone Jeppesen
Jesper Lau
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Novo Nordisk AS
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Novo Nordisk AS
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    • C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/72—Nitrogen atoms
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Abstract

This invention relates to aryl carbonyl derivatives of the general formula (I), (see formula I) which are activators of glucokinase which may be useful for the management, treatment, control, or adjunct treatment of diseases, where increasing glucokinase activity is beneficial.

Description

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ARYL CARBONYL DERIVATIVES AS GLUCOKINASE ACTIVATORS
FIELD OF THE INVENTION
This invention relates to compounds which are activators of glucokinase (GK), which may be useful for the management, treatment, control, or adjunct treatment of diseases, where increasing glucokinase activity is beneficial.
BACKGROUND OF THE INVENTION
Diabetes is characterised by an impaired glucose metabolism manifesting itself among other things by. an elevated blood glucose level in the diabetic patients. Underlying defects lead to a classification of diabetes Into two. major groups: Type I
diabetes, or insulin demanding diabetes mellitus (IDDM), which arises when patients lack $-cells producing insulin in their pancreatic glands, and type 2 diabetes, or non-insulin dependent diabetes mellitus (NIDDM), which ocurs Inpatients with an impaired fl-cell function besides a range of other abnormalities.
Type I diabetic patients are currently treated with insulin, while the majority of type 2 diabetic patients are treated either with sulphonylureas that stimulate fl-cell function or with agents that enhance the tissue sensitivity of the patients towards insulin or with insulin.
Among the agents applied to enhance tissue sensitivity towards insulin metformin is a representative example.
Even though sulphonylureas are widely used in the treatment of. NIDDM this therapy is, In most instances, not satisfactory: In a large number of NIDDM patients suiphonylureas do not suffice to normalise blood sugar levels and the patients are, therefore, at high risk for acquiring diabetic complications. Also, many patients gradually lose the ability to respond to treatment with suiphonylureas and are thus gradually forced into insulin treatment. This shift of patients from oral hypoglycaemic agents to insulin therapy is usually ascribed to exhaustion of the fl-cells In NIDDM patients.
In normal subjects as well as in diabetic subjects, the liver produces glucose In order to avoid hypoglycaemia. This glucose production is derived either from the release of glucose from glycogen stores or from gluconeogenesis, which is a de novo intracellular synthesis of glucose. In type 2 diabetes, however, the regulation of hepatic glucose output Is poorly controlled and is increased, and may be doubled after an overnight fast. Moreover, in these patients there exists a strong correlation between the Increased fasting plasma glucose levels and the rate of hepatic glucose production. Similarly, hepatic glucose production will be increased in type I diabetes, if the disease is not properly controlled by insulin treatment.
Since existing forms of therapy of diabetes does not lead to sufficient glycaemic control and therefore are unsatisfactory, there is a great demand for novel therapeutic approaches.
Atherosclerosis, a disease of the arteries, is recognized to be the leading cause of death in the United States and Western Europe. The pathological sequence leading to atherosclerosis and oclusive heart disease Is well known. The earliest stage In this sequence is the formation of "fatty streaks" in the carotid, coronary and cerebral arteries and in the aorta. These lesions are yellow in colour due to the presence of lipid deposits found principally within smooth-muscle cells and in macrophages of the intima layer of the arteries and aorta. Further, it is postulated that most of the cholesterol found within the fatty streaks, in turn, give rise to development of the "fibrous plaque". which consists of accumulated intimal smooth muscle cells laden with lipid and surrounded by extra-cellular lipid, collagen, elastin and proteoglycans. The cells plus matrix form a fibrous cap that covers a deeper deposit of cell debris and more extracellular lipid. The lipid is primarily free and esterifled cholesterol. The fibrous plaque forms slowly, and is likely in time to become calcified and necrotic, advancing to the "complicated lesion" which accounts for the arterial occlusion and tendency toward mural thrombosis and arterial muscle spasm that characterize advanced atherosclerosis.
Epidemiological evidence has firmly established hyperlipidemia as a primary risk factor in causing cardiovascular disease (CVD) due to atherosclerosis. In recent years, leaders of the medical profession have placed renewed emphasis on lowering plasma cholesterol levels, and low density lipoprotein cholesterol In particular, as an essential step in prevention of CVD. The upper limits of "normal" are now known to be significantly lower than heretofore appreciated. As a result, large segments of Western populations are now realized to be at particular high risk. Independent risk factors Include glucose intolerance, left ventricular hypertrophy, hypertension, and being of the male sex_ Cardiovascular disease is especially prevalent among diabetic subjects, at least in part because. of the existence of multiple independent risk factors in this population. Successful treatment of hyperlipidemia in the general population, and in diabetic subjects in particular, is therefore of exceptional medical importance.
Hypertension (or high blood pressure) is a condition, which oars in the human population as a secondary symptom to various other disorders such as renal artery stenosis, pheochromocytoma, or endocrine disorders. However, hypertension is also evidenced in many patients in whom the causative agent or disorder is unknown. While such "essential"
hypertension is often associated with disorders such as obesity, diabetes, and hypertriglyceridemia, the relationship between these disorders has not been elucidated..
Additionally, many patients display the symptoms of high blood pressure in the complete absence of any other signs of disease or disorder.
It is known that hypertension can directly lead to heart failure, renal failure, and stroke (brain haemorrhaging). These conditions are capable of causing short-term death in a patient. Hypertension can also contribute to the development of atherosclerosis and coronary disease. These conditions gradually weaken a patient and can lead to long-term death.
The exact cause of essential hypertension is. unknown, though a number of factors are believed to contribute to the onset of the disease. Among such factors are stress, uncontrolled emotions, unregulated hormone release (the renin, angiotensin aldosterone system), excessive salt and water due to kidney malfunction, wall thickening and hypertrophy of the vasculature resulting in constricted blood vessels and genetic factors..
The treatment of essential hypertension has been undertaken bearing the foregoing factors in mind. Thus a broad range of beta-blockers, vasoconstrictors, angiotensin converting enzyme inhibitors and the like have been developed and marketed as antihypertensives. The treatment of hypertension utilizing these compounds has proven beneficial in the prevention of short-interval deaths such as heart failure, renal failure, and brain haemorrhaging. However, the development of atherosclerosis or heart disease due to hypertension over a long period of time remains a problem. This implies that although high blood pressure is being reduced, the underlying cause of essential hypertension is not responding to this treatment.
Hypertension has been associated with elevated blood insulin levels, a condition known as hyperinsulinemia. Insulin, a peptide hormone whose primary actions are to promote glucose utilization, protein synthesis and the formation and storage of neutral lipids, also acts to promote vascular cell growth and increase renal sodium retention, among other things. These latter functions can be accomplished without affecting glucose levels and are known causes of hypertension. Peripheral vasculature growth, for example, can cause constriction of peripheral capillaries, while sodium retention increases blood volume. Thus, the lowering of insulin levels in hyperinsulinemics can prevent abnormal vascular growth and renal sodium retention caused by high insulin levels and thereby alleviates hypertension.
Cardiac hypertrophy is a significant risk factor in the development of sudden death, myocardial infarction, and congestive heart failure. Theses cardiac events are due, at least in part, to increased susceptibility to myocardial injury after ischernia and reperfusion, which can ocur in out-patient as well as perioperative settings. There is an unmet medical need to prevent or minimize adverse myocardial perioperative outcomes, particularly perioperative myocardial infarction. Both non-cardiac and cardiac surgery are associated with substantial risks for myocardial infarction or death. Some 7 million patients undergoing non-cardiac surgery are considered to be at risk, with incidences of perioperative death and serious cardiac complications as high as 20-25% in some series. In addition, of the 400,000 patients undergoing coronary by-pass surgery annually, perioperative myocardial infarction is estimated to ocur in 5% and death in 1-2%. There is currently no drug therapy in this area, which reduces damage to cardiac tissue from perioperative myocardial ischemia or enhances cardiac resistance to ischemic episodes. Such a therapy is anticipated to be life-saving and reduce hospitalizations,. enhance quality of life and reduce overall health care costs of high risk patients.
Obesity is a well-known risk factor for the development of many very common diseases such as atherosclerosis, hypertension, and diabetes. The incidence of obese people and thereby also these diseases is increasing throughout the entire industrialised world. Except for exercise, diet and food restriction no convincing pharmacological treatment for reducing body weight effectively and acceptably currently exist. However, due to its indirect but important effect as a risk factor in mortal and common diseases it will be important to find treatment for obesity and/or means of appetite regulation.
The term obesity implies an excess of adipose tissue. In this context obesity is best viewed as any degree of excess adiposity that imparts a health risk. The cut off between normal and obese individuals can only. be approximated, but the health risk imparted by the obesity is probably a continuum with increasing adiposity. The Framingham study demonstrated that a 20% excess over desirable weight dearly imparted a health risk (Mann GV N.Engl.J.Med 291:226, 1974). In the United States a National Institutes of Health consensus panel on obesity agreed that a 20% increase in relative weight or a body mass index (BMI = body weight in kilograms divided by the square of the height in meters) above the 85th percentile for young adults constitutes a health risk. By the use of these criteria 20 to 30 percent of adult men and 30 to 40 percent of adult women in the United States are obese. (NIH, Ann Intern Med 103:147, 1985).
Even mild obesity increases the risk for premature death, diabetes, hypertension, atherosclerosis, gallbladder disease, and certain types of cancer. In the industrialised western world the prevalence of obesity has increased significantly in the past few decades.
Because of the high prevalence of obesity and its health consequences, its prevention and treatment should be a high public health priority.

When energy intake exceeds expenditure, the excess calories are stored In adipose tissue, and if this net positive balance is prolonged, obesity results, i.e.
there are two components to weight balance, and an abnormality on either side (intake or expenditure) can lead to obesity.
5 The regulation of eating behaviour is incompletely understood. To some extent appetite is controlled by discrete areas in the hypothalamus: a feeding centre in the ventrolateral nucleus of the hypothalamus (VLH) and a satiety centre in the ventromedial hypothalamus (VMH). The cerebral cortex receives positive signals from the feeding centre that stimulate eating, and the satiety centre modulates this process by sending inhibitory Impulses to the feeding centre. Several regulatory processes may influence these hypothalamic centres. The satiety centre may be activated by the increases in plasma glucose and/or insulin that follow a meal. Meal-induced gastric distension is another possible inhibitory factor. Additionally the hypothalamic centres are sensitive to catecholamines, and beta-adrenergic stimulation inhibits eating behaviour. Ultimately, the cerebral cortex controls eating behaviour, and impulses- from the feeding centre to the cerebral cortex are only. one input. Psychological, social, and genetic factors also influence food intake.
At present a variety of techniques are available to effect Initial weight loss.
Unfortunately, initial weight loss is not an optimal therapeutic goal. Rather, the problem Is that most obese patients eventually regain- their weight. An effective means to establish and/or sustain weight loss is the major challenge in the treatment of obesity today..
WO 00/58293, WO 01/44216, WO/0183465, WO/0183478, WO/0185706, WO
01/85707, and W002/08209, to Hoffman-La Roche, discloses compounds as glucokinase activators.

SUMMARY OF THE INVENTION
This invention provides amide derivatives of the general formula (I), as described below, as activators of glucokinase. The compounds of the present invention are useful as activators of glucokinase and thus are useful for the management, treatment, control and adjunct treatment of diseases where increasing the activity of glucokinase is beneficial. Such diseases include type I diabetes and type II diabetes. The present invention provides compounds as described below, pharmaceutical compositions comprising the compounds, their use for increasing the activity of glucokinase, their use in preparation of a medicament for treating said diseases and conditions and the use of compounds or pharmaceutical preparations of the present invention for treating said diseases and conditions as well as methods for treating said diseases and conditions, which methods comprise administering to a subject in need thereof an effective amount of a compound according to the present invention.
The present invention also provides glucokinase activators, for instance of the general formula (I). which are glucose sensitive glucokinase activators, that is, glucokinase activators, the activity of which decreases with increasing glucose concentrations.
The present invention also provides glucokinase activators, for instance of the general formula (I), which are liver specific glucokinase activators, that is, glucokinase activators which increase glucose utilization in the liver (i.e. increase glycogen deposition).
without inducing any increase in insulin secretion in response to glucose.
The present invention provides the use of a compound or a pharmaceutical preparation according to the present invention for treatment of metabolic disorders.
The present invention provides the use of a compound or a pharmaceutical preparation according to the present invention for blood glucose lowering.
The present invention. provides the use of a compound or a pharmaceutical preparation according to the present invention for prevention of hyperglycemia.
The present invention provides the use of a compound or a pharmaceutical preparation according to the present invention for treatment of impaired glucose tolerance IGT.
The present invention provides the use of a compound or a pharmaceutical preparation according to the present invention for treatment of Syndrome X.
The present invention provides the use of a compound or a pharmaceutical preparation according to the present invention for the treatment of impaired fasting-glucose (IFG).
The present invention provides the use of a compound or a pharmaceutical preparation according to the present invention for treatment of type 2 diabetes.
The present invention provides the use of a compound or a pharmaceutical preparation according to the present invention for treatment of type 1.
diabetes.
The present Invention provides the use of a compound or a pharmaceutical preparation according to the present invention for delaying the progression of impaired glucose tolerance (IGT) to type 2 diabetes.
The present invention provides the use of a compound or a pharmaceutical preparation according to the present invention for delaying the progression of non-insulin requiring type 2 diabetes to insulin requiring type 2 diabetes.
The present invention provides the use of a compound or a pharmaceutical preparation according to the present invention for treatment of dyslipidemia or hyper-lipidemia.
The present invention provides the use of a compound or a pharmaceutical preparation according to the present invention for treatment of hypertension.
The present invention provides the use of a compound or a pharmaceutical preparation according to the present invention for the treatment of obesity.
The present invention provides the use of a compound or a pharmaceutical preparation according to the present invention for lowering of food intake The present invention provides the use of a compound. or a pharmaceutical preparation according to the present invention for appetite regulation.
The present invention provides the use of a compound or a pharmaceutical preparation according to the present invention for regulating feeding behaviour.
The present invention provides the use of a compound or a pharmaceutical preparation according to the present invention for enhancing the secretion of enteroincretins, such as GLP-1.
The present invention provides the use of a compound or a pharmaceutical' preparation according to the present invention for the adjuvant treatment of type 1 diabetes for preventing the onset of diabetic complications.
The present invention provides the use of a compound or a pharmaceutical preparation according to the present Invention for increasing the number and/or the size of beta cells in a mammalian subject The present invention provides the use of a compound or a pharmaceutical preparation according to the present invention for treatment of beta cell degeneration, in . particular apoptosis of beta cells.
The present invention provides the use of a compound or a pharmaceutical preparation according to the present invention for treatment of functional dyspepsia, in particular irritable bowel syndrome.
The present invention provides the use of a compound according to the present invention for the preparation of a medicament for treatment of metabolic disorders.
The present invention provides the use of a compound according to the present invention for the preparation of a medicament for blood glucose lowering.
The present invention provides the use of a compound according to the present invention for the preparation of a medicament for the treatment of hyperglycemia.
The present invention provides the use of a compound according to the present invention for the preparation of a medicament for the treatment of IGT.
The present invention provides the use of a compound according to the present invention for the preparation of a medicament for the treatment of Syndrome X.
The present invention provides the use of a compound according to the present invention for the preparation of a medicament for the treatment of impaired fasting glucose (IFG).
The present invention provides the use of a compound according to the present invention for the preparation of a medicament for the treatment of type 2 diabetes.
The present invention provides the use of a compound according to the present invention for the preparation of a medicament for the treatment of type 1 diabetes.
The present invention provides the use of a compound according to the present invention for the preparation of a medicament for delaying the progression of impaired-glucose tolerance (IGT) to type 2 diabetes.
The present invention provides the use of a compound according to the present invention for the preparation of a medicament for delaying the progression of non-insulin requiring type 2 diabetes to insulin requiring type 2 diabetes.
The present invention provides the use of a compound according to the present invention for the preparation of a medicament for the treatment of dyslipidemia.
The present invention provides. the use. of a compound according to the present invention for the preparation of a medicament for the treatment of hyperlipidemia.
The present invention provides the use of a compound according to the present invention for the preparation of a medicament for the treatment of hypertension.
The present invention provides the use of a compound according to the present invention for the preparation of a medicament for lowering of food intake.
The present invention provides the use of a compound according to the present invention for the preparation of a medicament for appetite regulation.
The present invention provides the use of a compound according to the present invention for the preparation of a medicament for the treatment of obesity.
The present invention provides the use of a compound according to the present invention for the preparation of a medicament for regulating feeding behaviour.
The present invention provides the use of a compound according to the present invention for the preparation of a medicament for enhancing the secretion of enteroincretins, such as GLP-1.
The present invention provides the use of a compound according to the present invention for the preparation of a medicament for the adjuvant treatment of type 1 diabetes for preventing the onset of diabetic complications.
The present invention provides the use of a compound according to the present invention for the preparation of a medicament for increasing the number and/or the size of beta cells in a mammalian subject.
The present invention provides the use of a compound according to the present invention for the preparation of a medicament for treatment of beta cell degeneration, in particular apoptosis of beta cells.
The present invention provides the use of a compound according to the present invention for the preparation of a medicament for treatment of functional dyspepsia, in particular irritable bowel syndrome.
The present invention provides a method of preventing hypoglycaemia comprising administration of a liver-specific glucokinas activator.
The present invention provides the use of a liver-specific glucokinas activator for the preparation of a medicament for the prevention of hypoglycaemia.
The present invention provides a compound of Formula (la) G ~L1 L3-N`

R25 Formula (la) wherein R25 is selected from the group consisting of F, Cl, Br and methyl;
L1 is a bond, -D-C1_6-alkylene-E-, -0-, -S-, -S(O)-, -S(O)2-, -C(O)-, -N(R11)-, or -C(=N-OR12);
D is a direct bond or -0-;
E is a direct bond or -0-;
R11 is hydrogen;
R12 is hydrogen;
G1 is C1_6-alkyl, C2_6-alkenyl, C2_6-alkynyl, C3_10-cycloalkyl or C3_10-heterocyclyl, optionally substituted with one or more substituents selected from the group consisting of -CN, -CF3, -OCF3, -OR18, -NR18R19, C3_10-cycloalkyl and C1_6-alkyl;
R18 and R19, independently of each other, are hydrogen or C1.6-alkyl;
L2 is -N-R20-;

9a L3 is -C(O)-;
R' is hydrogen;
R20 is hydrogen;
G2 is S

R43 is -C1_6-alkylene-C(O)OR54;
R54 is hydrogen, methyl, ethyl, propyl, butyl, isopropyl, isobutyl, sec-butyl, tert-butyl, 3-pentyl, 2-pentyl, or 3-methyl-butyl;
or a pharmaceutically acceptable salt thereof or solvate of any of the foregoing.
Other embodiments and aspects are as defined below and by the appended claims.

Definitions In the structural formulas given herein and throughout the present specification, the following terms have the indicated meaning:
The term "optionally substituted" as used herein means that the group in question is either unsubstituted or substituted with one or more of the substituents specified. When the group in question are substituted with more than one substituent the substituent may be the same or different.
The term "adjacent" as used herein regards the relative positions of two atoms or variables, these two atoms or variables sharing a bond or one variable preceding or succeeding the other in a variable specification. By way of example, "atom A
adjacent to atom B" means that the two atoms A and B share a bond.
The term "halogen" or "halo" means fluorine, chlorine, bromine or iodine.
The term "perhalomethyl" means trifluoromethyl, trichloromethyl, tribromomethyl, or triiodomethyl.

The use of prefixes of this structure: Cx_y-alkyl, C,_yalkenyl, Cx_y-alkynyl, Cx y-cycloalyl or C.,y-cycloalkyl-C,galkenyl- designates radical of the designated type. having from x to y carbon atoms.
The term "alkyl" as used herein, alone or in combination, refers to a straight or 5 branched chain saturated monovalent hydrocarbon radical having from one to ten carbon atoms, for example C14-alkyl or C1s-alkyl. Typical C1s-alkyl groups and C1.6-alkyl groups include, but are not limited to e.g. methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl, n-pentyl, 2-methylbutyl, 3-methylbutyl, 4-methylpentyl, neopentyl, n-pentyl, n-hexyl, 1,2-dimethylpropyl, 2.2-dimethylpropyl, 1,2,2-trimethylpropyl and the like.
10 The term "C1$-alkyl" as used herein also includes secondary Cis-alkyl and tertiary C,,s-alkyl.
The term "C,s-alkyl" as used herein also includes secondary Cis-alkyl and tertiary Cos-alkyl.
The term "alkylene" as used herein, alone or in combination, refers to a straight or branched chain saturated divalent hydrocarbon radical having from one to ten carbon atoms;
for example C1s-alkylene. or C1$-alkylene. Examples of "alkylene" as used herein include, but are not limited to, methylene, ethylene, and the like.
The term " alkenyl" as used herein, alone or in combination, refers to a straight or branched. chain monovalent hydrocarbon radical containing from two to ten carbon atoms and at least one carbon-carbon double bond, for example C2.8-alkenyl or Cgs-alkenyl. Typical C2.8-alkenyl groups and Cgs-alkenyl groups include, but are not limited to, vinyl, 1-propenyl, 2-propenyl, iso-propenyl, 1,3-butadienyl, 1-butenyl, 2-butenyl, 3-butenyl, 2-methyl-l-propenyl, 1-pentenyl, 2-pentenyl, 3-pentenyl, 4-pentenyl, 3-methyl-2-butenyl, 1-hexenyl, 2-hexenyl, 3-hexenyl,. 2,4-hexadienyl, 5-hexenyl. and the like.
The term "alkenylene" as used herein, alone. or in combination, refers to a straight or branched chain divalent hydrocarbon radical having from two to ten carbon atoms and at least one carbon-carbon double bond, for example C2.8-alkenylene or Cgs-alkenylene.
Typical C24-alkenylene groups and C2$-alkenylene groups include, but are not limited to, ethene-1,2-diyl, propene-1,3-diyl, methylene-1,1-diyl,. and the like.
The term "alkynyl" as used herein alone or in combination, refers to a straight or branched monovalent hydrocarbon radical containing from two to ten carbon atoms and at least one triple carbon-carbon bond, for example Cgs-alkynyl or C26-alkynyl.
Typical C2.8-alkynyl groups and Cgs-alkynyl groups include, but are not limited to, ethynyl, 1-propynyl, 2-propynyl, 1-butynyl, 2-butynyl, 3-butynyl, 1-pentynyl, 2-pentynyl, 3-pentynyl, 4-pentynyl, 1-hexynyl, 2-hexynyl, 3-hexynyl, 5-hexynyl, 2,4-hexadiynyl and the like.
The term "alkynylene" as used herein alone or in combination, refers to a straight or branched chain divalent hydrocarbon radical having from two to ten carbon atoms and at least one carbon-carbon triple bond, for example C2 -alkynylene or C2$-alkynylene. Typical C24-alkynylene groups and C24-alkynylene groups include, but are not limited to, ethyne-1,2-diyl, propyne-1,3-diyl, and the like.
The term "cycloalkyl" as used herein, alone or in combination, refers to a non-aromatic monovalent hydrocarbon radical having from three to twelve carbon atoms, and optionally with one or more degrees of unsaturation, for example C"-cycloalkyl. Such a ring may be optionally fused to one or more benzene rings or to one or more of other cydoalkyl ring(s). Typical C3.a-cycloalkyl groups include, but are not limited to, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cyclohexenyl,. cycloheptyl, cycloheptenyl, cydooctyl and the like.
The term "cycloalkylene" as used herein, alone or in combination, refers to a non-aromatic carbocyclic divalent hydrocarbon radical having from three to twelve carbon atoms and optionally possessing one or more degrees of unsaturation, for example C3a-cydoalkyl-ene. Such a ring may be optionally fused to one or more benzene rings or to one or more of other cycloalkyl ring(s). Typical C34-cycloalkylene groups include, but are not limited to, cyclopropyl-1,1-diyl, cyclopropyl-1,2-diyl, cydobutyl-1,2-diyl, cydopentyl-1,3-diyl, cyclohexyl-1,4-diyl, cycloheptyl-1,4-diyl, or cydooctyl-1,5-diyl, and the like.
The term "heterocyclic" or the term "heterocyclyl" as used herein, alone or in combination, refers to a three to twelve membered heterocyclic ring having one or more degrees of unsaturation containing one or more heteroatomic substitutions selected from S, SO, SO2, 0, or N, for example Cie-heterocyclyl. Such a ring may be optionally fused to one or more of another "heterocyclic" ring(s) or cycloalkyl ring(s). Typical C34-heterocyclyl groups include, but are not limited to, tetrahydrofuran, 1,4-dioxane,.1,3-dioxane, pipeadne, pyrrolidine,'morpholine, piperazine, and the like.
The term "heterocyclylene" as used herein, alone or in combination, refers to a three to twelve-membered heterocyclic ring diradical optionally having one or more degrees of unsaturation containing one or more heteroatoms selected from S, SO, SO2, 0, or N. Such a ring may be optionally fused to one or more benzene rings or to one or more of another "heterocyclic" rings or cycloalkyl rings. Examples of "heterocydylene"
include, but are not limited to, tetrahydrofuran-2,5-diyl, morpholine-2,3-diyl, pyran-2,4-diyl, 1,4-dioxane-2,3-diyl, 1,3-dioxane-2,4-diyl, piperadne-2,4-dlyl, piperadne-1,4-diyl, pyrrolidine-1,3-diyl, morpholine-2,4-diyl, piperazine-1,4-dyil, and the like.
The term "alkoxy" as used herein, alone or in combination, refers to the monovalent radical RaO-, where Ra is alkyl as defined above, for example C14-alkyl giving C1$-alkoxy.
Typical C1.a-alkoxy groups include, but are not limited to, methoxy, ethoxy, n-propoxy, isopropoxy, butoxy, sec-butoxy, tert-butoxy, pentoxy, isopentoxy, hexoxy, isohexoxy and the like.
The term "alkylthio" as used herein, alone or in combination, refers to a straight or branched monovalent radical comprising an alkyl group as described above linked through a divalent sulphur atom having its free valence bond from the sulphur atom, for example C,.B-alkylthio. Typical C,$-alkylthio groups include, but are not limited to, methylthio, ethylthio, propylthlo, butytthio, pentylthio, hexylthio and the like.
The term "alkoxycarbonyl" as used herein refers to the monovalent radical ReOC(O)-, where R is alkyl as described above, for example C14-alkoxycarbonyl. Typical C1.e-alkoxycarbonyl groups include, but are not limited to, methoxycarbonyl, ethoxycarbonyl, propoxycarbonyl, isopropoxycarbonyl, n-butoxycarbonyl, sec-butoxycarbonyl, tertbutoxycarbonyl, 3-methylbutoxycarbonyl, n-hexoxycarbonyl and the like..
The term "carbamoyl" as used herein refers to NH2C(O)-.
The term "aryl" as used herein refers to a carbocyclic aromatic ring radical or to a aromatic ring system radical. Aryl is also intended to include the partially hydrogenated derivatives of the carbocyclic systems.
The term "heteroaryl", as used herein, alone or in combination, refers to an aromatic ring radical with for instance 5 to 7 member atoms, or to a aromatic ring system radical with for instance from 7 to 18 member atoms, containing one or more heteroatoms selected from nitrogen, oxygen. or sulfur heteroatoms, wherein N-oxides and sulfur monoxides and. sulfur dioxides are permissible heteroaromatic substitutions; such as e.g. furanyl, thienyl, thiophenyl, pyrrolyl, imidazolyl, pyrazolyl, triazolyl, tetrazolyl, thiazolyl, oxazolyl, isoxazolyl, oxadiazolyl, thiadiazolyl, isothiazolyl, pyridinyl, pyridazinyl, pyrazinyl, pyrimidinyl, quinolinyl, isoquinoltnyl, benzofuranyl, benzothiophenyl, indolyl, and indazolyl, and the like. Heteroaryl is .25 also Intended to include the partially hydrogenated derivatives of the heterocyclic systems enumerated below.
Examples of "aryl" and "heteroaryl" includes, but are not limited to phenyl, biphenyl, indene, fluorene, naphthyl (1 -naphthyl, 2-naphthyl). anthracene (1-anthracenyl, 2-anthracenyl, 3-anthracenyl), thiophene (2-thienyl, 3-thienyl), furyl (2-furyl, 3-furyl), indolyl, oxadiazolyl, Isoxazolyl, thiadiazolyl, oxatazolyl, thiatriazolyl, quinazolin, fluorenyl, xanthenyl, isoindanyl, benzhydryl, acridinyl, thiazolyl, pyrrolyl (1-pyrrolyl, 2-pyrrolyl, 3-pyrrolyl), pyrazolyl (1-pyrazolyl, 3-pyrazolyl, 4-pyrazolyl, 5-pyrazolyl), imidazolyl (1-Imidazolyl, 2-imidazolyl, 4-imidazolyl, 5-imidazolyl), triazolyl (1,2,3-triazol-1 yl, 1,2,3-triazol-4-yl 1,2,3-triazol-5-yl,1,2,4-triazol-3-yl,1,2,4-triazol-5-yl), oxazolyl (2-oxazolyl, 4-oxazolyl, 5-oxazolyl), isooxazolyl (isooxazo-3-yl, isooxazo-4-yl, isooxaz-5-yl), isothiazolyl (isothiazo-3-yl, isothiazo- -yl, isothiaz-5-yl) thiazolyl (2-thiazolyl, 4-thiazolyl, 5-thiazolyl), pyridyl (2-pyridyl, 3-pyridyl, 4-pyridyl), pyrimidinyl (2-pyrimidinyl, 4-pyrimidinyl, 5-pyrimidinyl, 6-pyrimidinyl), pyrazinyl, pyridazinyl (3- pyridazinyl, 4-pyridazinyl, 5-pyridazinyl), quinolyl (2-quinolyl, 3-quinolyl, 4-quinolyl, 5-quinolyl, 6-quinolyl, 7-quinolyl, 8-quinolyl), isoquinolyl (1-isoquinolyl, 3-isoquinolyl, 4-isoquinolyl, 5-isoquinolyl, 6-isoquinolyl, 7-isoquinolyl, 8-isoquinolyl), benzo[b]furanyl (2-benzo[b]furanyl, 3-benzo[b]furanyl, 4-benzo[b]furanyl, 5-benzo[b]furanyl, 6-benzo[b]furanyl, 7-benzo[b]furanyl), 2,3-dihydro-benzo[b]furanyl (2-(2,3-dihydro-benzo[b]furanyl), 3-(2,3-dihydro-benzo[b]furanyl), 4-(2,3-dihydro-benzo[b]furanyl), 5-(2,3-dihydro-benzo[b]furanyl), 6-(2,3-dihydro-benzo[b]furanyl), 7-(2,3-dihydro-benzo[b]furanyl)), benzo[b]thiophenyl (benzo[bjthiophen-2-yl, benzo[b]thiophen-3-yl, benzo[b]thiophen-4-yl, benzo[b]thiophen-5-yl, benzo[b]thiophen-6-yl, benzo[b]thiophen-7-yl), 2,3-dihydro-benzo[b]thiophenyl (2,3-dihydro-benzo[b]thiophen-2-yl, 2,3-dihydro-benzo[b]thlophen-3-yl,. 2,3-dihydro-benzo[b]thiophen-4-yl.
2,3-dihydro-benzo[b]thiophen-5-yl, 2,3-dihydro-benzo[bjthiophen-6-yl, 2,3-dihydro- benzo[b]thiophen-7-yl), indolyl (1-indolyl, 2-indolyl, 3-indolyl, 4-indolyl, 5-indolyl, 6-indolyl, 7-indolyl), indazole (1-indazolyl, 3-indazolyl, 4-indazolyl,. 5-indazolyl, 6-indazolyl, 7-indazolyl), benzimidazolyl (1-benzimidazolyl, 2-benzimidazolyl, 4-benzimidazolyl, 5-benzimidazolyl, 6-benzimidazolyl, 7-benzimidazolyl, 8-benzimidazolyl), benzoxazolyl (2-benzoxazolyl, 3-benzoxazolyl, 4-benzoxazolyl, 5-benzoxazolyl, 6-benzoxazolyl, 7-benzoxazolyl), benzothiazolyl (2-benzothiazolyl, 4-benzothiazolyl, 5-benzothiazolyl, 6-benzothiazolyl, 7-benzothiazolyl), carbazolyl (1-carbazolyl, 2-carbazolyl, 3-carbazolyl, 4-carbazolyl), 5H-dibenz[b,f]azepine (5H-dibenz[b,t]azepin-1-yl, 5H-dibenz[b,f]azepine-2-yl, 5H-dibenz[b,f]azepine-3-yl, 5H-dibenz[b,f]azepine-4-yl, 5H-dibenz[b,f]azepine-5-yl), 10,11-dihydro-5H-dibenz[b,f]azepine (10,11-dihydro-5H-dibenz[b,f]azepine-1-yl, 10,11-dihydro-5H-dibenz[b,fjazepine-2-yl, 10,11-dihydro-5H-dibenz[b,fjazepine-3-yl, 10,11-dlhydro-5H-dibenz[b,fjazepine-4-yl, 10,11-dihydro-5H-dibenz[b,fjazepine-5-yl), benzo[1,3]dioxole (2-benzo[1,3]dioxole, 4-benzo[1,3]dioxole, 5-benzo[1,3]dioxole, 6-benzo[1,3]dioxole, 7-benzo[1,3]dioxole), purinyl, and tetrazolyl (5-tetrazolyl, N-tetrazolyl).
The present invention also relates to partly or fully saturated analogues of the ring systems mentioned above.
When two such terms are used in combination, such as in aryl-alkyl-, heteroaryl-alkyl-, cydoalkyl-C1$-alkyl- and the like, it is to be understood that the first mentioned radical is a substituent on the latter mentioned radical, where the point of substitution is on the latter of the radicals, for example aryl-alkyl- :

cycloalkyl-alkyl- : , and O>\
aryl-alkoxy- :
The term "arylene", as used herein, alone or in combination, refers to carbocyclic aromatic ring diradical or to a aromatic ring system diradical. Examples of "arylene" include, but 'are not limited to, benzene-1,4-diyl, naphthalene-1,8-diyl, and the like.
The term "arylene"
alone or in combination also include other divalent radicals of the monovalent radicals mentioned in the definition of aryl.
The term "heteroarylene", as used herein,. alone or in combination, refers to a five to seven membered aromatic ring diradical, or to a aromatic ring system diradical, containing one or more heteroatoms selected from nitrogen, oxygen, or sulfur heteroatoms, wherein N-oxides and sulfur monoxides and sulfur dioxides are permissible heteroaromatic substitutions. Examples of. "heteroarylene" used herein are furan-2,5-diyl, thiophene-2,4-diyl, 1,3,4-oxadiazole-2,5-diyl, 1,3,4-thiadiazole-2,5-diyl, 1,3-thiazole-2,4-diyl, 1,3-thiazole-2,5-diyl, pyridine-2,4-diyl, pyridine-2,3-diyl, pyridine-2,5-diyl, pyrimidine-2,4-diyt, quinoline-2,3-diyl, and the like. The term "heteroarylene" alone or in combination also indude other divalent radicals of the monovalent radicals mentioned in the definition of heteroaryl.
As used herein, the term "fused cycloalkylaryl" refers to a cycloalkyl group fused to an aryl group, the two having two atoms in common, and wherein the aryl group is the point of substitution. Examples of "fused cydoalkylaryl" used herein indude 5-indanyl, 5,6,7,8-tetrahydro-2-naphthyl, and the like.

As used herein, the term "fused cycloalkylarylene" refers to a fused cycloalkylaryl, wherein the aryl group is divalent. Examples include Nz~

and the like.
As used herein, the term "fused arylcydoalkyl" refers to an aryl group fused to a 5 cycloalkyl group, the two having two atoms in common, and wherein the cycloalkyl group is the point of substitution Examples of "fused arylcycloalkyl" used herein include.1-indanyl, 2-indanyl, 1-(1,2,3,4-tetrahydronaphthyl), and the like.
As used herein, the term "fused arylcycloalkylene" refers to a fused arylcycloalkyl, 10 wherein the cycloalkyl group is divalent. Examples include and the like.
As used herein, the term "fused heterocyclylaryl" refers. to a heterocyclyl group fused to an aryl group, the two having two atoms in common, and wherein the aryl group is the point of substitution. Examples of "fused heterocydylaryl" used herein include 3,4-15 methylenedioxy-l-phenyl, N /
and the like As used herein, the term "fused heterocydylarylene" refers to a fused heterocydylaryl, wherein the aryl group is divalent. Examples include '~ , and the like.
As used herein, the term "fused arylheterocyclyl" refers to an aryl group fused to a heterocyclyl group, the two having two atoms in common, and wherein the heterocyclyl group is the point of substitution. Examples of" fused aryiheterocyclyl" used herein include 2-(1,3-benzodioxolyl), N , and the like.
As used herein, the term "fused arylheterocyclylene" refers to a fused aryiheterocyclyl, wherein the heterocydyl group is divalent. Examples include N , and the like.
As used herein, the term "fused cycloalkyiheteroaryl" refers to a cycloalkyl group fused to a heteroaryl group, the two having two atoms in common, and wherein the heteroaryl group is the point of substitution. Examples of "fused cycloalkyiheteroaryl" used herein include 5-aza-6-indanyl, =N-4,5,6,7-tetrahydro-benzothiazole-2-yi, N, S
5,6-dihydro-4 H-cyclopentatiazole-2-yl, aN
S
and the like.
As used herein, the term "fused heteroaryicydoalkylene" refers to a fused heteroarylcycloalkyl, wherein the cycloalkyl group is divalent. Examples include (N--and the like.
As used herein, the term "fused heterocyclylheteroaryl" refers to a heterocyclyl group fused to a heteroaryl group, the two having two atoms in common, and wherein the heteroaryl group. is the point of substitution. Examples of "fused heterocyclyiheteroaryi" used herein include 1,2,3,4-tetrahydro-beta-carbolin-8-yi, I \
N
N and the like.
As used herein, the term "fused heterocydylheteroarylene" refers to a fused heterocyclylheteroaryt, wherein the heteroaryl group is divalent. Examples include N
N
and the like.
As used herein, the term "fused heteroarylheterocydyl" refers to a heteroaryl group fused to a heterocyclyl group, the two having two atoms in common, and wherein the heterocyclyl group is the point of substitution. Examples of "fused heteroarylheterocyclyl"
used herein include 5-aza-2,3-dihydrobenzofuran-2-yl, N~ l N and the like.
As used herein, the term "fused heteroarylheterocyclylene" refers to a fused heteroarylheterocyclyl, wherein the heterocyclyl group is divalent. Examples include N~ I
N
and the like.
The term "alkylsulfanyl", as. used herein, refers to the group R8S-, where Re is alkyl as described above.
The term "alkylsulfenyl", as used herein, refers to the group R8S(O)-, where Re is alkyl as described above.
The term "alkylsulfonyl", as used herein, refers to the group RaSOr, where Ra is alkyl as described above.
The term "acyl", as used herein, refers to the group R8C(O)-, where Ra is alkyl, alkenyl, alkynyl, cycloalkyl, cydoalkenyl, or heterocydyl as described above.
The term "amyl", as used herein, refers to the group R8C(O)-, where Ra is aryl as described above.
The term "heteroaroyl", as used herein, refers to the group RaC(O)-, where RR
is heteroaryl as described above.
The term "aryloxycarbonyl", as used herein, refers to the group Ra-O-C(O)-, where Ra is aryl as described above.
The term "acyloxy", as used herein, refers to the group RaC(O)O-, where Ra is alkyl, alkenyl, alkynyl,. cycloalkyl, cydoalkenyl, or heterocyclyl as described above.
The term "aryloxy", as used herein refers to the group Ra-O-, where Ra is aryl as described above.
The term "aroyloxy", as used herein, refers to the group ReC(O)O-, where Ra is aryl as described above.
The term "heteroaroyloxy", as used herein, refers to the group R'C(O)O-, where Ra is heteroaryl as described above.
Whenever the terms "alkyl", "cydoalkyl", "aryl", "heteroaryl" or the like or either of their prefix roots appear in a name of a substituent (e.g. arylalkoxyaryloxy) they shall be interpreted as including those limitations given above for "alkyl" and "aryl".
As used herein, the term "oxo" shall refer to the substituent =0.
As used herein, the term "mercapto" shall refer to the substituent -SH.
As used herein, the term "carboxy" shall refer to the substituent -COOH.
As used herein, the term "cyan" shall refer to the substituent -CN.
As used herein, the term "aminosulfonyl" shall refer to the substituent -S02NH2.
As used herein, the term "sulfanyl" shall refer to the substituent -5-.
As used herein, the term "sulfenyr shall refer to the substituent -S(O}.
As used herein, the term "sulfonyl" shall refer to the substituent -S(O)2-.
As used herein, the term "direct bond", where part of a structural variable specification, refers to the direct joining of the substituents flanking (preceding and succeeding) the variable taken as a 'direct bond".
The term "lower", as used herein, refers to an group having between one and six carbons, and may be indicated with the. prefix C,,-e-. Lower alkyl may thus be indicated as C1.g-alkyl, while lower alkylene may be indicated as C24-alkylene.
A radical such as Cx.y-cycloalkyl-Cwalkenyl shall designate that the radical's point of attachment is in part of the radical mentioned last.
As used herein, the term "optionally" means that the subsequently described event(s) may or may not ocur, and includes both event(s) which ocur and events that do not ocur.
As used herein, the term 'substituted" refers to substitution with the named substituent or substituents, multiple degrees of substitution being allowed unless otherwise stated.
As used herein, the terms "contain' or "containing" can refer to in-line substitutions at any position along the above defined alkyl, alkenyl, alkynyl or cycloalkyl substituents with one or more of any of 0, S, SO, SO2, N, or N-alkyl, including, for example, -CH2-0-CH2-, CH2-S02-CHz-, -CH2-NH-CH3 and so forth.
Certain of the above defined terms may ocur more than once in the structural formulae, and upon such ocurrence. each term shall be defined independently of the other.
As used herein, the term "solvate" is a complex of variable stoichiometry formed by a solute (in this invention, a compound of formula (I)) and a solvent. Such solvents for the purpose of the present invention may not interfere with the biological activity of the solute.
Solvents may be, by way of example, water, ethanol, or acetic acid.
As used herein, the term "biohydrolyzable ester" is an ester of a drug substance (in this invention, a compound of formula (I) ) which either a) does not interfere with the biological activity of the parent substance but confers on that substance advantageous properties in vivo such as duration of action, onset of action, and the like, or b) is biologically inactive but is readily converted in vivo by the subject to the biologically active principle. The advantage is that, for example, the biohydrolyzable ester is orally absorbed from the gut and is transformed to (I) in plasma. Many examples of such are known in the art and include by way of example lower alkyl esters (e.g., C1.4), lower acyloxyalkyl esters, lower alkoxyacyloxyalkyl esters, alkoxyacyloxy esters, alkyl acylamino alkyl esters, and choline esters.
5 As used herein, the term "biohydrolyzable amide" is an amide of a drug substance (in this invention, a compound of general formula (1)) which either a) does not Interfere with the biological activity of the parent substance but confers on that substance advantageous properties in vivo such as duration of action, onset of action, and the like, orb) is biologically inactive but is readily converted in vivo by the subject to the biologically active principle. The 10 advantage is that, for example, the biohydrolyzable amide is orally absorbed from the-gut and is transformed to (I) in plasma. Many examples of such are known in the art and include by way of example lower alkyl amides, a-amino acid amides. alkoxyacyl amides, and alkylaminoalkylcarbonyl amides.
As used herein, the term "prodrug" includes biohydrolyzable amides and 15 biohydrolyzable esters and also encompasses a) compounds in which the biohydrolyzable functionality in such a prodrug is encompassed in the compound of formula (1) and b) compounds which may be oxidized or reduced biologically at a given functional group to yield drug substances of formula (I). Examples of these functional groups include, but are not limited to, 1,4-dihydropyridine, N-alkylcarbonyl-1,4-dihydropyridine, 1,4-cyclohexadlene, tart 20 butyl, and the like.
The term "pharmacologically effective amount" or shall mean that amount of a drug or pharmaceutical agent that will elicit the biological or medical response of a tissue, animal or human that Is being sought by a researcher or clinician. This amount can be a therapeutically effective amount. The term "therapeutically effective amount"
shall mean that amount of a drug or pharmaceutical agent that will elicit the therapeutic response of an animal or human that is being sought.
The term "treatment" and "treating" as used herein means the management and care of a patient for the purpose of combating a disease, disorder or condition. The term is intended to include the full spectrum of treatments for a given disorder from which the patient is suffering, such as the delaying of the progression of the disease, disorder or condition, the alleviation or relief of symptoms and complications, the prevention of the disease and/or the cure or elimination of the disease, disorder or condition. The patient to be treated is preferably a mammal, in particular a human being.
The term "human insulin" as used herein refers to naturally produced insulin or recombinantly produced insulin. Recombinant human insulin may be produced in any suitable host cell, for example the host cells may be bacterial, fungal (including yeast), insect, animal or plant cells.
The expression "insulin derivative" as used herein (and related expressions) refers to human insulin or an analogue thereof in which at least one organic substituent is bound to one or more of the amino acids.
By "analogue of human insulin" as used herein (and related expressions) is meant human insulin in which one or more amino acids have been deleted and/or replaced by other amino acids, including non-codeable amino acids, or human insulin comprising additional amino acids, i.e. more than 51 amino acids, such that the resulting analogue possesses insulin activity.

DETAILED DESCRIPTION OF THE INVENTION

Glucokinase (GK) plays an essential role in blood glucose homeostasis. GK
catalyses glucose phosphorylation, and is the rate-limiting reaction for glycolysis in hepatocytes and pancreatic 0-cells. In liver GK determine the rates of both glucose uptake and glycogen synthesis, and it is also thought to be essential for the regulation of various glucose-responsive genes (Girard, J.et al., Annu Rev Nutr 17, 325-352 (1997)).
In the fl-cells, GK determines glucose utilization and thus is necessary for glucose-stimulated insulin secretion. GK is also. expressed in a population of neurones in the hypothalamus where it might be involved in feeding behaviour, and in the gut where it might contribute to the secretion of enteroincretins.
GK has two main distinctive characteristics: its expression, which is limited to tissues that require glucose-sensing (mainly liver and pancreatic-cells), and its So.5for glucose, which is much higher (8-12 mM) than that of the other members of the hexokinase family. Due to these kinetic characteristics, changes in serum glucose levels are paralleled by changes in glucose metabolism in liver which in turn regulate the balance between hepatic glucose output and glucose consumption.
Activators of glucokinase may thus be useful for treating diseases where increasing the activity of glucokinase is beneficial. Thus, there is a need for agents which activate glucokinase-and increase glucokinase enzymatic activity. Such agents would be useful for the treatment of type I diabetes and type II diabetes.
Activators of glucokinase may also play a role in sensing low glucose levels and generating neurohumoral responses to hypoglycemia and may thus be useful for treating those patients with type 1 diabetes, which have a higher tendency to suffer from hypoglycemia.
Type I diabetes mellitus is a complex disease characterized by an elevated blood glucose concentration and polyuria. Secondary to the persistent elevation in blood glucose, patients develop devastating complications such as retinopathy, nephropathy, neuropathy, and cardiovascular disease. A major goal to improve the diabetic phenotype is to reduce fasting and postprandial hyperglycemia and, thus, avoid or delay the onset of diabetic complications. The Diabetes Control and Complications Trial has indicated that tight glycemic control through administration of daily multiple insulin injections delays the onset of complications. However, such intensive therapy is associated with an increase in body weight and higher risk for development of hypoglycaemic events. Alternative treatments to achieve glucose control without these side effects are, therefore, being developed. The combination of GK overexpression in the liver and subcutaneous insulin injections provides better glycemic control in type I diabetic animals than treatment with insulin alone (Morral, N., et al. Human Gene Therapy L3,1561-1570 (2002)). Moreover, overexpression of hepatic GK can compensate, in part, for the metabolic disorders developed by insulin receptor-deficient mice (Jackerott, M. et al. Diabetologia 45,1292-1297 (2002)).
The present invention also relates to the use of a GK activator for the combined treatment of diabetes and obesity. GK, the GK regulatory protein and the KATP
channel are expressed in neurones of the hypothalamus, a region of the brain that is important in the regulation of energy balance and the control of food intake. These neurones have been shown to express orectic and anorectic neuropeptides and have been assumed to be the glucose-sensing neurones within the hypothalamus that are either inhibited or excited by changes in ambient glucose concentrations (Mobbs, C. V. et al, American Journal of Physiology, Endocrinology. & Metabolism 281, E649-54 (2001)). The ability of these neurones to sense changes in glucose levels is defective in a variety of.
genetic and experimentally induced models of obesity (Spanswick, D. et al, Nature Neuroscience 3, 757-8 (2000), Levin, B. E. et al, Brain Research 808, 317-9 (1998)).
Intracerebroventricular (icv) infusion of glucose analogues, which are competitive inhibitors of glucokinase, stimulate food intake in lean rats (Kurata, K. et al, Metabolism: Clinical & Experimental 38 46-51 (1989)). In contrast, icv infusion of glucose suppresses feeding (Kurata, K.et al, Physiology & Behavior 37, 615-20 (1986)). Small molecule activators of GK may thus decrease food intake and weight gain through central effects on GK. Therefore, GK activators may be of therapeutic use in treating eating disorders, including obesity, in addition to diabetes.
The hypothalamic effects will be additive or synergistic to the effects of the same compounds acting in the liver and/or pancreas in normalising glucose homeostasis, for the treatment of type 2 diabetes.
Thus the GK/GK regulatory protein system can be described as a potential target of benefit in both diabetes and obesity.
The amplitude of glucose-induce insulin release is highly dependent on the action of the gastrointestinal hormones GLP-1 (glucogen-like peptide 1) and GIP. Unlike sulfonylureas, which stimulate insulin release at low as well as high glucose levels, the action of GLP-1 on #-cells is glucose dependent (Gromada, J. et al., PflOgers Arch 435, 583-594 (1998)). GLP-1 receptor agonist and drugs that slow the degradation of active GLP-1 are -therefore under development as a novel treatments for type 2 diabetes. An alternative strategy would be to enhance endogenous GLP-1 levels. Of potential interest is the possibility that the release of GLP-1 and GIP might be regulated by glucokinase-expressing endocrine cells (Jetton, T.L. et al., J. Biol.. Chem. 269, 3641-3654 (1994)) and glucose-responsive neurons (Liu, M. et al., J. Neuroses. 19, 10305-10317 (1999)). It has been reported that the release of GIP by intestinal K -cells; is directly controlled by glucose (Kieffer, T.J. et al., Am J Physiol 267, E489-E496 (1994)), and GLP-1 secretion from GLUTag cells is triggered by glucose through a mechanism similar to that found In fl-cells for insulin secretion (Reimann, F. et al, Diabetes 51, 2757-2763 (2002)). Small molecule activators of glucokinase may thus be used. to increase GLP-1 and. /or GIP secretion and thus for treatment, modulation, inhibition, decreasion, reduction, arrest or prevention of beta cell degeneration, such as necrosis or apoptosis of fl-cells.
In a first embodiment, the present invention provides compounds of the general formula (I).
G' Al L2 R1 ~3 LN

G

(I) wherein A' is selected from the group consisting of arylene, heteroarylene, fused cycloalkylarylene, fused heterocyclylarylene, fused cydoalkylheteroarylene,. or fused heterocydyiheteroarylene;
optionally substituted with one or more substitutents R23, R24, R25, R28,. and R27,. wherein R23, R24, R25, R28, and R27 independently of each other are selected from the group consisting of halogen, -C(O)OR2, -CN, -CF3, -OCF3, -NO2, -OR2, -NR2R3, C1$-alkyl-Z-, C2$-alkenyl-Z-, C2-6-alkynyl-Z-, cycloalkyl-Z-, heterocyclyl-Z-, aryl-Z-, heteroaryl-Z-, aryl-C14-alkylene-Z-, heteroaryl-C14-alkylene-Z-, heterocyclyl-Cl.B-alkylene-Z-, cydoalkyl-C1$-alkylene-Z-, N(R4R5}C1$-alkylene-Z-, Re-W'-Z-, W -W'-N(W)-Z-, R8-N(R4)-Z, and Re-W'-C1$-alkyIene-Z-, wherein R2 and. R3 independently of each other are hydrogen, C1.8-alkyl, aryl-C1$-alkylene-, heteroaryl-C14-alkylene-, C1.8-alkyl-arylene-, C1$-alkyl-heteroarylene-, heteroaryl, or aryl;
or R2 and R3, when attached to the same nitrogen atom, together with said nitrogen atom may form a 3 to 8 membered heterocyclic ring optionally containing one or two further heteroatoms selected from nitrogen, oxygen and sulfur, and optionally containing one or two double bonds;
Z and W' independently of each other are a direct bond, -0-, -N(R7)-, -S-, -SO2-, -C(O)N(R7)-, -N(R7)C(O)-, -N(R7)CON(R8)-, -N(R7)SOr, -SO2N(R7)-, -C(O)-O-, -N(R7)SO2N(Re}, or -O-C(O)-, wherein R7 and R8 in each individual case independently of each other are hydrogen or alkyl; and R4, R5, and Re independently of each other are selected from the group consisting of hydrogen, aryl, alkyl, heteroaryl-alkylene-, and aryl-alkylene-;

or R4 and R5 may be taken together to form a ring having the formula -(CH2),-Q-(CH2)k-. bonded to the nitrogen atom to which R4 and R5 are attached, wherein 5 j and k independently of each other is 1, 2, 3, or 4; and Q is a direct bond, -CH2-, -0-,. -S-, -S(02)-, -C(O)-, -C(O)NH-, NHC(Oy, -NHC(O)NH-, -NHSO2-, -S02NH-, -C(O}O-, -O-C(0}, -NHSO2NH-, OyR9 0yOR9 02?,R9 02S.N(H)R! 02S-N-R9 -N- -N- -N- -N- -N-O\/NHR9 O,N-R9 i e N- -N- or -N-10 wherein R9 and R10 independently of each other are selected from the group consisting of hydrogen, aryl, alkyl, and aryl-alkylene-;
L' is -D-alkylene-E-, -D-alkenylene-E-, -D-alkynylene-E-, -D-cycloalkylene-E-,.
15 -D-heterocyclylene-E-,. -0-, -S-, -S(O)-, -S(0)2-, -C(O)-, -N(R")-, or -C(=N-OR12)_,. wherein D and E independently of each other are a direct bond, -0- or -S-;
R" is selected from hydrogen, alkyl, aryl, carbamoyl, aryl-alkylene-, heteroaryl-alkylene-, alkyl-O-C(O)-, aryl-alkylene-O-C(O)-, heteroaryl-alkylene-0-C(O)-, alkyl-NH-C(O)-, aryl-alkylene-NH-C(O}, 20 heteroaryi-alkylene-NH-C(0)-, alkyl-SO2-, aryl-alkylene-S02-, heteroaryl-alkylene-S02-, aryl-SO2-, heteroaryl-SOr, alkyl-NH-SO2-, aryl-alkylene-NH-S02-, heteroaryl-alkylene-NH-S02-, alkyl-C(O)-, aryl-alkylene-C(O)-, heteroaryi-alkylene-C(O)-, alkyl-Y-, aryl-Y-, heteroaryl-Y-, aryl-alkylene-Y-, heteroaryl-alkylene-Y-, N(R13)(R14)alkylene-Y-, and 25 R15-W2-alkylene-Y-, wherein Y and W2 independently of each other are a direct bond, -CH2-, -SO2-, -N(H)CO-, -N(H)SO2-, or. .0-C(0};
R13 and R14 independently of each other are selected from hydrogen, aryl, heteroaryl, C1$-alkyl, C1.5-alkoxy, aryl-C1$-alkylene-, heteroaryl-C14-alkylene-, aryl-C14-alkoxy-, heteroaryl-C1 -alkoxy-, C14-alkyl-arylene-, C1$-alkyl-heteroarylene-, C,$-alkoxy-heteroarylene-, or C1.6-alkoxy-arylene-;
or R13 and R14 may be taken together to form a ring having the formula -(CH2)o-X-(CH2)p bonded to the nitrogen atom to which R13 and R14 are.
attached, wherein o and p are independently of each other are 1, 2,. 3,. or 4; and X is a direct bond, -CH2-, -0-, -S-, -S(02)-, -C(O)-, -CON(H)-, -NHC(0)-, -NHCON(H}, -NHSOr, -SO2N(H)-, -C(O)O-, -0-C(O)-, -NHSO2NH-, 0 yR16 OyOR's 0R 1e zIl -N- -N- , -N-0 'N(H)R's 02S N_R16 zT I
-N- -N-O,NHR18 O)N-R's i 1s -N- -N- or -N-wherein R1 and R17 are selected from hydrogen, aryl, heteroaryl, C14-alkyl, C1.6-alkoxy, aryl-C14-alkylene-,.
heteroaryl-C1.6-alkylene-, Cs-alkyl-arylene-, C1õg-alkyl-heteroarylene-, C,$-alkoxy-arylene-, C1$-alkoxy-heteroarylene-, heteroarylaryl-C1$-alkoxy-, or aryl-C1 -alkoxy-; and R15 is selected. from the group consisting of aryl, heteroaryl, cycloalkyl, heterocyclyl, alkyl, heteroaryl-alkylene-, or aryl-alkylene-; and R 12 is selected from hydrogen, aryl, heteroaryl, alkyl, aryl-alkylene-, heteroaryl-alkylene-, alkyl-arylene-, alkyl-heteroarylene-, alkoxy-heteroarylene-, or alkoxy-arylene-;
G' is alkyl, alkenyl, alkynyl, cycloalkyl or heterocydyl, optionally substituted with one or more substituents selected from the group consisting of -CN, -CF3, -OCF3, -ORt8, -NR18R19, C3.,o-cydoalkyl and C14-alkyl, wherein R18 and R19 independently of each other are hydrogen, C1.6-alkyl, heteroaryl-C14-alkylene-, aryl-C1.6-alkylene-, C1.6-alkyl-arylene-, C1.6-alkyl-heteroarylene-, heteroaryl, or aryl;.
or Rt8. and R19, when attached to the same nitrogen atom, together with the said nitrogen atom may form a 3 to 8 membered heterocyclic ring optionally containing one or two further heteroatoms selected from nitrogen, oxygen and sulfur, and optionally containing one or two double bonds;
or G' is aryl, heteroaryl, fused cycloalkylheteroaryl, fused heterocyclylaryl, or fused cydoalkylaryl, optionally substituted with one or more substituents R40, R41, and R42;
L2 is a direct bond, alkylene, alkenylene, alkynylene, -N(R20)-, -alkylene-N(RZ0)-, -alkenylene-N(R20)-, -alkynylene-N(R20)-, wherein RZ0 is hydrogen, or R20 is alkyl, alkenyl, alkynyl, cydoalkyl W3-, heterocydyl-W3-, aryl-W3-, heteroaryl-W3-, optionally substituted with one or more substituents R30, R3, and R32, wherein W3 is alkylene or a direct bond;
wherein L' and L2 are attached to adjacent atoms in A1;
L3 is -C(O)-, or -S(O)2-;
R' is hydrogen, or R' is alkyl, alkenyl, alkynyl. cycloalkyl-W4-, heterocydyl-W4-, aryl-W4-,. or heteroaryl-W4-, optionally substituted with one or more substituents e, R34, and R35, wherein W4 is alkylene or a direct bond;
G2 is heteroaryl, fused heterocyclyiheteroaryl, or fused cycloalkylheteroaryl, optionally substituted with one or more substituents R43, R44, and R45.
wherein said heteroaryl group posesses a nitrogen atom adjacent to the atom joining said heteroaryl group to -N(R')-;
or a group of the formula ,AG3 0 or wherein G3 and G5 independently of each other are alkyl, alkenyl, alkynyl, cycloalkyl-R22-, heterocydyl-W2-, aryl-R2-, heteroaryl-R22-, optionally substituted with one or more substituents R46, R47, and R48, wherein R22 Is alkylene or a direct bond; and R21 is hydrogen, alkyl, alkenyl,. alkynyl,. cycloalkyl-W5, or heterocydyl-W5, optionally substituted with one. or more. substituents R30,. R37, and e, or R21 is aryl-W5-, or heteroaryl-W5-, optionally substituted with one or more substituents R40, R50, and R51, wherein W5 is alkylene or a direct bond;
wherein R30, R31, R32, R33, e. R35, R38, R37, and e independently of each other are selected from -CHF2, -CF3, -OCF3, -OCHF2. -OCH2CF3, -OCF2CHF2, -S(O)2CF3, -SCF3, -OR52, -NR52R5', -SR52, -NRS2S(0)2R53, -S(O)2NR52R53, -S(O)NR52Rb3, -S(O)R52, -S(0)2R52, -C(O)NR52R53, -OC(O)NR82R53, -NR52C(O)R53, -CH2C(O)NR52R53, -OCH2C(O)NR52Rb3, -CH2OR52, -CH2NR52R53, -OC(O)R52, -C(O)R52and -C(O)OR52; or C2.e-alkenyl and C24-alkynyl, which may optionally be substituted with one or more substituents selected from -CN, -CF3,. -OCF3, -OR52. -NR52R53 and C14-alkyl, or C3.1o-cycloalkyl, C44-cycloalkenyl, heterocydyl, C3.10-cydoalkyl-C14-alkylene-, C3.1o-cycloalkyl-Ct.ralkoxy-, C3.10-cycloalkyloxy, C3.10-.10-C14-alkylthio-, C3.10-cydoalkylthio, C,._1o-cydoalkyl-C24-alkenyIene-, C3,0-cydoalkyl-C2 raikynylene-, C44-cycloalkenyl-C14-alkylene-, C4$-cydoalkenyl-C24-alkenylene-, C,$-cydoalkenyl-C2 e-alkynylene-, heterocyclyl-C14-alkylene-, heterocydyl-Cz.-alkenylene-, heterocyclyl-C2$-alkynylene-, aryl, aryloxy, aryloxycarbonyl, aroyl, aryl-C1.6-alkoxy-, aryl-C1.e-alkylene-, aryl-C24-alkenylene-, aryl-C2--alkynylene-, heteroaryl, heteroaryl-C14-alkylene-, heteroaryl-C24-alkenylene- and heteroaryl-C2$-alkynylene-, of which the aryl and heteroaryl moieties optionally may be substituted with one or more substituents selected from halogen, -C(O)OR52, -CN, -CF3. -OCF3, -NO2, -OR52, -NR52R53 and C1.$-alkyl, wherein R52 and R53 independently of each other are hydrogen, C14-alkyl, aryl-C1$-alkylene-heteroaryl-C1.-alkylene- heteroaryl. or aryl;
or R52 and e, when attached to the some nitrogen atom, together with the said nitrogen atom may form a 3 to 8 membered heterocyclic ring optionally containing one or two further heteroatoms selected from nitrogen, oxygen and sulfur, and optionally containing one or two double bonds;
R40, R41, R42, R49, R44, R45, R46, R47, R'S, R40, R50 and R61 independently of each other are halogen, -CN, -NO2, C1.6-alkyl, -CHF2, -CF3, -OCF3, -OCHF2, -OCH2CF3, -OCF2CHF2, -S(O)2CF3i -SCF3, -0RS`, -NR54e, -SRTM, -NR54S(O)2RSS, -S(O)2NR54R55, -S(O)NR64R55, -S(O)R54, -S(O)2R54, -C(O)NR54R5, -0C(O)NR4R55, -NRMC(O)RS', -CI2C(O)NRMR55, -CH2C(O)OR54, -0CH2C(0)NR54R55, _CH2OR54, -CH2NR50R5S, -OC(O)R54, -C(O)R54and.
-C(O)OR54; or C2-6-alkenyl and C2-0-alkynyl, which may optionally be substituted with one or more substituents selected from -CN, -CF3, -OCF3, -OR54, -NR54R55 and C1.4-alkyl;
C3.10-cycloalkyl, C44-cycloalkenyl, heterocyclyl, C3.10-cycloalkyl-C,4-alkylene-, CC.to-cycloalkyl-C14-alkoxy-, C3.10-cycloalkyloxy, Cs.,o-cydoalkyl-Ci alkylthio-, C3_10-cydoalkylthlo, C3.1o-CYdoalkyl-C24-alkenylene-, C3.10-cydoalkyl-C2$-alkynylene-, C"-cydoalkenyl-C14-alkylene-, C44-cycloalkenyl-C2$-alkenylene-, C44-cydoalkenyl-C2.$-alkynylene-, heterocydyl-Cl.o-alkylene-, heterocydyl-C2.e-alkenylene-, heterocydyl-C2.s-alkynylene-; or aryl, aryloxy, aryloxycarbonyi, aroyl. aryl-C14-alkoxy-, aryl-C,.6-alkylene-, aryl-C24-alkenylene-, aryl-C2.6-alkynylene-, heteroaryi, heteroaryl-C14-alkylene-, -heteroaryl-C2.8-alkenylene- and heteroaryl-C2.8-alkynylene-, of which the aryl and heteroaryl moieties optionally may be substituted with one or more substituents selected from halogen, -C(O)OR54, -CN, -CF3r -OCF3i -NO2, -OR54, -NR54R55 or C1$-alkyl, wherein R54 and e independently of each other are hydrogen, C1.4-alkyl, C14-alkyl-arylene-, C1.e-alkyl-heteroarylene-, aryl-C,$-alkylene-, heteroaryl-C14-alkylene-, heteroaryl, or aryl;
or R54 and R55 independently of each other are hydrogen or -(CHFe3)õ-(CHR84), Z, wherein uis.lor2;
v is 0, 1 or 2;
R3 and RM independently of each other are hydrogen, C,.o-alkyl, C14-alkyl-arylene- aryl, hydroxy, hydroxyalkyl, amino, or aminoalkyl;

Z is hydrogen, -0-R85, -C(O)O-RO5, -CONeRB , alkylamino, or dialkylamino, wherein R S and R88 independently of each other is hydrogen or C1.8-alkyl;
or 5 Z is a five or six membered ring wherein at least one ring atom is nitrogen and the remaining ring. atoms are either carbon or oxygen;
or R54 and R55, when attached to the same nitrogen atom, together with the said nitrogen atom may form a 3 to 8 membered heterocyclic ring. optionally containing 10 one or two further heteroatoms selected from nitrogen, oxygen and sulfur, and.
optionally containing one, or two double bonds, and optionally substituted with one or more Cta-alkyl groups;.
or a pharmaceutically acceptable salt,. solvate, or prodrug thereof.
Other embodiments of the present invention are dear from the following list of 15 embodiments.
Embodiment 2: A compound according to embodiment 1, wherein A' is arylene or heteroarylene, optionally substituted with one or more substitutents R23, R24, R25, R28, and RZ7, wherein R23, R24, e, R, and R27 independently of each other are selected from the group 20 consisting of halogen, -C(O)OR2, -CN, -CF3, -OCF3, -NO2, -OR2, -NR2R3, C,4-alkyl-Z-, C2.8-alkenyl-Z-, C2.8-alkynyl-Z-, cycloalkyl-Z-, heterocyclyl-Z-,. aryl-Z-, heteroaryl-Z-, aryl-C,.6-alkylene-Z , heteroaryl-C,$-alkylene-Z-, heterocydyl-C1$-alkylene-Z-, cydoalkyl-C14-alkylene-Z-, N(R4R5)-C1.8-alkylene-Z-, R -W'-Z-, R -W'-N(R4)-Z-, R -25 N(R4)-Z, and R -WesC,$-alkylene-Z-, wherein R2, R3, R4, R5, R , Z, and W' are as defined for embodiment 1.
Embodiment 3: A compound according to embodiment 2, wherein A' is C .10-arylene or Cato-heteroarylene, optionally substituted with one or more substitutents e, R24, e, R28, and R27, wherein 30 R23, R24, R25, RZB, and R27 independently of each other are selected from the group consisting of halogen, -C(O)OR2, -CN, -CF3, -OCF3, -NO2, -OR2, -NR2R3. C14alkyl-Z , C24-alkenyl-Z-, C2.8-alkynyl-Z-, cycloalkyl-Z-, heterocyclyl-Z-, aryl-Z-, heteroaryl-Z-, aryl-C1.e-alkylene-Z , heteroaryl-C14-alkylene-Z-, heterocydyl-C1. alkylene-Z-, cycloalkyl-C14-alkylene-Z-, N(R4R5)-C14-alkylene-Z-, Re W'-Z-, Re W'-N(R4)-Z-, R -N(R4)-Z, and R6-W'-C1_g-alkylene-Z-, wherein R2, R3, R4, R5, R ,. Z, and W' are as defined for embodiment 1.
Embodiment 4: A compound according to any of embodiments 1 to 3, wherein R23, R24, R25, R2 , and R27 independently of each other are selected from the group consisting of halogen, -C(O)OR2, -CN, -CF3, -OCF3, -NO2, -OR2, -NR2R3, C1$-alkyl-Z-, cycloalkyl-Z-, heterocyclyl-Z-, aryl-Z-, or heteroaryl-Z-, N(R4R5)-C14-alkylene-Z-, RB-W'-Z-, RB-W'-N(R4)-Z-, R6-N(R4)-Z, and Re-W'-C1.8-alkylene-Z-, wherein R2, R3, R4, R5, Re, Z, and W1 are as defined for embodiment 1.
Embodiment 5: A compound according to any of embodiments 1 to 4, wherein R4, R5,. and R independently of each other are selected from the group consisting of hydrogen, aryl, alkyl, heteroaryl-alkylene-,. and aryl-alkylene-.
Embodiment 6: A compound according to embodiment 5, wherein 15. R4, R5, and Rs independently of each other are hydrogen or alkyl.
Embodiment 7: A compound according to embodiment 6, wherein R4, R5, and R are hydrogen.
Embodiment 8: A compound according to any of embodiments 1 to 4, wherein R4 and R5 is taken together to form a ring having the. formula -(CH2),-Q-(CH2)k-bonded to the nitrogen atom to which R4 and R5 are attached, wherein j and k independently of each other is 1, 2, 3, or 4;
Q is a direct bond, -CH2-, -0-, -S-, -S(02}, -C(0)-, -C(O)NH-, -NHC(O)-, NHC(O)NH-, -NHSO2-, -S02NH-, -C(O}0-, -0-C(O)-, -NHSO2NH-, 0 Y R9 0YOR9 02S~R9 02SN(H)R p21 -N- . -N- -N- -N- -N-O,NHRs O)N-Re i 9 N- -N- or -N-wherein R and R10 independently of each other are selected from the group consisting of hydrogen, aryl, alkyl, and arylalkyl-.
Embodiment 9: A compound according to embodiment 8, wherein Q Is a direct bond, -CH2-, -0-, -S-, -S(02) , -C(O) -, -C(O)NH-, -NHC(O) , -NHC(O)NH-, -NHSO2-, -SO2NH-, -C(O)-O-, -0-C(O)-, -NHSO2NH-, Rio OyR9 0\/OR9 O4/R9 02f N(H)R9 02f N-R9 `~
-N- -N- -N- -N- --N-R'o a O\/NHR9 0YN-R9 i - - -N- or -N-wherein R9 and R10 independently of each other are hydrogen or alkyl.
Embodiment 10: A compound according to embodiment 9, wherein Q is a direct bond, -CH2-, -0-, -S-, -S(02)-, -C(0)-, -C(O)NH-, -NHC(O)-, -NHC(0)NH-, -NHSOr, -SO2NH-, -C(O)-O-, -0-C(O)-, -NHSO2NH-, 0 Y H 0YOH 041A 02S,NH2 -N- -N- -N- -N-0 Y NHz -N- or -N-Embodiment 11: A compound according to embodiment 10, wherein Q is a direct bond.
Embodiment 12: A compound according to any of embodiments I to 11, wherein W' is a direct bond, -0-, -NH-, -5-, -SO2-, -C(O)NH-, -NHC(O)-, -N(H)CON(H)-, N(H)SO2-, -SO2N(H)-, -C(O)-O-, -N(H)SO2N(H)-, or -0-C(O)-.
Embodiment 13: A compound according to embodiment 12, wherein W' is a direct bond, -0-,.
-S-, or -SO2-.
Embodiment 14: A compound according to embodiment 13, wherein W1 is a direct bond.
Embodiment 15: A compound according to embodiment 4, wherein at least one of R23, R24, e, R2, and R27 is halogen, -C(O)OR2, -CN, -CF3, -OCF3, -NO2, -OR2, -NR2R3, C1$-alkyi-Z-, cydoalkyi-Z-, heterocydyl-Z-, aryl-Z-, or heteroaryl-Z-, wherein R2, R3, and Z are as defined for embodiment 1.
Embodiment 16: A compound according to embodiment 15, wherein at least one of e, R24, R25, 0, and R27 is halogen, -C(0)OR2, -CN, -CF3, -OCF3, -NO2, -OR2, -NR2R3, C1$-alkyl-Z-, C_-cydoaIkyl-Z-, C3.10-heterocyciyl-Z-, 03.10-aryl-Z-, or C3_t0-heteroaryl-Z-, wherein R2, R3, and Z are as defined for embodiment 1.
Embodiment 17: A compound according to embodiment 16, wherein at least one of R23, R24, R25, e, and e is halogen, -C(O)OR2, -CN, -NO2, -OR2, -NR2R3, C14-alkyl-Z-, 03.10-cycloalkyl-Z-,. C3.10-heterocydyl-Z-, C3.10-aryl-Z-, or C3.10-heteroaryl-Z-, wherein R2, R3, and Z are as defined for embodiment 1.
Embodiment 18: A compound. according to embodiment 17,. wherein at least one of R23, R24, R25, R20, and R27 is halogen, -C(O)OR2, -CN, -NO2, -OR2, or -NR2R3, wherein W. R3, and Z are as defined for embodiment 1.
Embodiment 19: A compound according to any of embodiments 1 to 18, wherein R2 and R3 independently of each other are hydrogen, C1.8-alkyl, aryl-C14-alkylene-, heteroaryl-C14-alkylene-, C1$-alkyl-arylene-, C1$-alkyl-heteroarylene-, heteroaryl, or aryl.
Embodiment 20: A compound according to embodiment 19, wherein R2 and R3 independently of each other, are hydrogen,. C14-alkyl, aryl-Cl.e-alkylene-or aryl.
Embodiment 21: A compound according to embodiment 20, wherein R2 is hydrogen or C14-alkyl.
Embodiment 22: A compound according to embodiment 21, wherein R2 is hydrogen.
Embodiment 23: A compound according to any of embodiments 1 to 22, wherein R3 is hydrogen or C14-alkyl.
Embodiment 24: A compound according to embodiment 23, wherein R3 is hydrogen.
Embodiment 25: A compound according to any of embodiments I to 15, wherein R2 and R3, when attached to the same nitrogen atom, together with said nitrogen atom may form a 3 to 8 membered heterocyclic ring optionally containing one or two further heteroatoms selected from nitrogen, oxygen and sulfur, and optionally containing one or two double bonds.
Embodiment 26: A compound according to any of embodiments 1 to 25, wherein Z is a direct bond, -0-, -NH-, -S-, -SO2-, -C(O)NH-, -NHC(O)-, -N(H)CON(H)-, -N(H)SO2-, -SO2N(H)-, -C(O)-O-, -N(H)SO2N(H)-, or -O-C(O)-.
Embodiment 27: A compound according to embodiment 26, wherein Z is a direct bond, -0-, -S-, or -SO2-.
Embodiment 28: A compound according to embodiment 27, wherein Z is a direct bond.
Embodiment 29: A compound according to embodiment 2, wherein A' is R , wherein R23, R24, e, and R28, independently of each other, are hydrogen or as defined for embodiment 1.
Embodiment 30: A compound according to embodiment 29, wherein R23, R24, R25, and R28 independently of each other are selected from the group consisting of halogen, -C(O)OR2, -CN, -CF3i -OCF3, -NO2, -OR2, -NR2R3, C,$-alkyl-Z-, cycloalkyl-Z-, heterocydyl-Z-, aryl-Z-, or heteroaryl-Z-, N(R4R5)-C1$-alkylene-Z-, R -W'-Z-, R -W'-N(R4)-Z-, R -N(R4}Z, and R -W'-C1. -alkylene-Z-, wherein R2, R3, R4, Z, and W1 are as defined for embodiment 1.
Embodiment 31: A compound according to embodiment 29 or 30, wherein R4, R5, and R independently of each other are selected from the group consisting of hydrogen, aryl, alkyl, heteroaryl-alkylene-, and aryl-alkylene-.
Embodiment 32: A compound according to embodiment 31,. wherein R4, R5, and R independently of. each other are hydrogen or alkyl..
Embodiment 33: A compound according to embodiment 32, wherein R4, R5, and R are hydrogen.
Embodiment 34: A compound according to embodiment 29 or 30, wherein R4 and R5 is taken together to form a ring having the formula -(CH2),-Q-(CH2)k-bonded to the nitrogen atom to which R4 and R5 are attached, wherein j and k independently of each other is 1, 2, 3, or 4;
Q is a direct bond, -CH2-, -0-, -S-, -S(02}, -C(O)-, -C(O)NH-, -NHC(O)-, -NHC(O)NH-, -NHSO2-, -S02NH-, -C(O)-0-, -O-C(O)-, -NHSO2NH-, O\ /R OyOR9 Oz(' 02~'N(H)R Oj.N-R9 `~
-N- -N- -N- -N-. -N-O\ /NHR9 O,N-R9 i s -N- -N- or -N-wherein R9 and R10 independently of each other are selected from the group. consisting of hydrogen, aryl, alkyl, and arylalkyl-.
5 Embodiment 35: A compound according to embodiment 34, wherein Q is a direct bond, -CH2-, -0-, -S-, -S(02)-, -C(O)-,. -C(O)NH-, -NHC(O)-, -NHC(O)NH-, -NHSOr, -SO2NH-, -C(0)-0-, -0-C(O}, -NHSO2NH-, Rto O\ /R9 O\/OR9 ? _1 ,N(H)R9 'N-R9 ~" 0Y OR! OZC OzC
-N- -N- -N- -N- -N-R1o O\/NHR9 O,N-R9 R19 -N- -.N- or -N-wherein 10 R9 and R10 independently of each other are hydrogen or alkyl.
Embodiment 36: A compound according to embodiment 35, wherein Q is a direct bond, -CHz-, -0-, -S-, -S(02}, -C(O)-, -C(O)NH-, -NHC(O)-.
-NHC(O)NH-, -NHSO2-, -S02NH-, -C(O)-0-,. -0-C(O}, -NHSO2NH-, H
02S,NH2 0 Y H 0YOH Oz( -N- , -N- . -N- -N-0`\ /NH2 -N- , or -N-15 Embodiment 37: A compound according to embodiment 36, wherein Q is a direct bond.
Embodiment.38: A compound according to any of embodiments 29 to 37, wherein W1 is a direct bond, -0-, -NH-, -S-, -SO2-, -C(O)NH-, -NHC(O}, -N(H)CON(H)-, -N(H)S02-, -SO2N(H}, -C(O)-O-, -N(H)SO2N(H)-, or -O-C(O)-.

Embodiment 39: A compound according to embodiment 38, wherein W' is a direct bond, -0-, -S-, or -SO2-.
Embodiment 40: A compound according to embodiment 39, wherein W1 is a direct bond.
Embodiment 41: A compound according to embodiment 29, wherein at least one of e, R24, R25, and R25 is halogen, -C(O)OR2, -CN, -CF3, -OCF3, -N02, -OR2, -NR2R 3, C14-alkyl-Z-, cycloalkyl-Z-, heterocyclyl-Z-, aryl-Z-, or heteroaryl-Z-, wherein R2, R3, and Z are as defined for embodiment 29.
10. Embodiment 42: A compound according to embodiment 41, wherein at least one of R23, R24, R25, and RZ5 is halogen, -C(O)OR2, -CN, -CF3, -OCF3, -NO2, -OR2, -NR2R3, C1$-alkyl-Z-, C3.10-cycloalkyl-Z-, C310-heterocydyl-Z-, C3.10-aryl-Z-,. or C3.10-heteroaryl-Z-, wherein R2, R3, and Z are as defined for embodiment 29.
Embodiment 43: A compound according to embodiment 42, wherein at least one of R23, R24, R25, and RZ5 is halogen, -C(O)ORZ, -CN, -NO2, -OR2, -NR2R3, C1.g-alkyl-Z-, C3.10-cycloalkyl-Z-, C3.70-heterocydyl-Z-, C3-t0-aryl-Z-, or C3.10-heteroaryl-Z-, wherein R2, R3, and Z are as defined for embodiment 29.
Embodiment 44: A compound according to any of embodiments 29 to 43, wherein Z is a direct bond, -0-, -NH-, -S-, -SO2-, -C(O)NH-, -NHC(O)-, -N(H)CON(H)-, -N(H)SO2-, -SO2N(H)-, -C(O)-O-, -N(H)SO2N(H)-, or -0-C(O)-.
Embodiment 45: A compound according to embodiment 44, wherein Z is a direct bond, -0-, -S-, or -SO2-.
Embodiment 46: A compound according to embodiment 45, wherein Z is a direct bond.
Embodiment 47: A compound according to embodiment 43, wherein at least one of e, R24, R25, and e is halogen, -C(O)OR2, -CN, -NO2, -OR2, -NR2R3, or C1$-alkyl, wherein R2, and R3 are as defined for embodiment 29.
Embodiment 48: A compound according to any of embodiments 29 to 47, wherein R2 and R3 independently of each other are hydrogen, C1$-alkyl, aryl-C14-alkylene-, heteroaryl-C14-alkylene-, C1.8-alkyl-arylene-, C1.8-alkyl-heteroarylene-, heteroaryl, or aryl.
Embodiment 49: A compound according to embodiment 48, wherein R2 and R3 independently of each other, are hydrogen, C14-alkyl, aryl-C14-alkylene-or aryl.
Embodiment 50: A compound according to embodiment 49, wherein R2 is hydrogen or C,.e-alkyl.
Embodiment 51: A compound according to embodiment 50, wherein R2 is hydrogen.
Embodiment 52: A compound according to any of embodiments 29 to 51, wherein R3 is hydrogen or C,$-alkyl.
Embodiment 53: A compound according to embodiment 52, wherein R3 is hydrogen.
Embodiment 54: A compound according to any of embodiments 29 to 41, wherein R2 and R3, when attached to the same nitrogen atom, together with said nitrogen atom may form a 3 to 8 membered heterocyclic ring optionally containing one or two further heteroatoms selected from nitrogen, oxygen and sulfur, and optionally containing one or two double bonds.
Embodiment 55: A compound according to any of embodiments 29 to 46, wherein . at least one of R23, R24, R25, and R28 are hydrogen.
Embodiment 56: A compound according to embodiment 55, wherein at least two of e, R24, R25, and e are hydrogen.
Embodiment 57. A compound according to claim 56, wherein R23 and Rte are hydrogen.
Embodiment 58: A compound according to embodiment 56 or claim 57, wherein at least three of R23, R24, R25, and e are hydrogen.
Embodiment 59: A compound according to any of embodiments 29 to 58, wherein R24 or R25 is halogen.
Embodiment 60: A compound according to embodiment 59, wherein R24 or R25 is fluoro.
Embodiment 61: A compound according to any of embodiments 29 to 58, wherein R24 or R25 Is C1.6-alkyl.
Embodiment 62: A compound according to embodiment 59, wherein R24 or R25 is methyl.
Embodiment 63: A compound according to any of embodiments 29 to 58, wherein R24 is hydrogen.
Embodiment 64: A compound according to any of embodiments 29 to 63, wherein R?8 is hydrogen.
Embodiment 65: A compound according to embodiment 29, wherein R23, R24, e, and R2B are hydrogen.

Embodiment 66: A compound according to any of embodiments 1 to 65, wherein L' is -D-alkylene-E-, -0-, -S-, -S(O)-, -S(O)r, -C(O)-, -N(R"}, or -C(=N-OR12), wherein D, E, R" and R12 are as defined for embodiment 1.
Embodiment 67: A compound according to embodiment 66, wherein L' is -D-alkylene-E-, -0-, -C(O)-, -N(R")-, or-C(=N-OR12}, wherein D, E,. R11 and R12 are as defined for embodiment 1.
Embodiment 68: A compound according to embodiment 66, wherein L' is -0-.
Embodiment 69: A compound according to embodiment 66, wherein L' is -5-.
Embodiment 70: A compound according to embodiment 66, wherein L' is -C(O)-.
Embodiment 71: A compound according to any of embodiments 1 to 67, wherein D is a direct bond or -0-;
E is a direct bond or -0-; and R" and R 12 are as defined for embodiment 1.
Embodiment 72: A compound according to embodiment 71, wherein D is a direct bond.
Embodiment 73: A compound according to embodiment 71, wherein D is -0-.
Embodiment 74: A compound according to any of embodiments 71 to 73, wherein E is a direct bond..
Embodiment 75: A compound according to any of embodiments 71 to 73, wherein E is -0-.
Embodiment 76: A compound according to any of embodiments 1 to 75, wherein R" is selected from hydrogen, alkyl, aryl, car amoyl, aryl-alkylene-, alkyl-NH-C(O)-, aryl-alkylene-NH-C(O)-, alkyl-SOr, aryl-alkylene-SOZ-, aryl-SO2-, SO2-, alkyl-C(O)-, aryl-alkylene-C(O)-, N(Rt3)(R14)_alkylene-Y-, and R15 W2 alkylene-Y , wherein Y and W2 independently of each other are a direct bond, -CH2-, -SO2-, N(H)CO-. -N(H)SOr, or -0-C(O)-;
R13 and R14 independently of each other are selected from hydrogen, aryl, C1$-alkyl, or aryl-Cl.6-alkylene-;
or R 13 and R14 may be taken together to form a ring having the formula -(CH2)o X-(CH2)p- bonded to the nitrogen atom to which R13 and R14 are attached, wherein o and p are independently of each other are 1, 2, 3, or 4; and X is a direct bond, -CH2-, -0-, -S-, -S(02)-, -C(O)-, -CON(H)-, -NHC(O), -NHCON(H}, -NHSO2-, -S02N(H)-, -C(O)-O-, -0-C(O)-, -NHSO2NH-, z -N- -N- ' -N-18 1e 027 N(H)R 02S,N-R
-N- -N-O`/NHRte O`\/N-R18 - I -N- or -N-- , wherein R16 and R" are selected from hydrogen, aryl, heteroaryl, C1.0-alkyl, C1.6-alkoxy, aryl-C1.6-alkylene-, heteroaryl-C,$-alkylene-, C,$-alkyl-arylene-, C,$-alkyl-heteroarylene-, C1. alkoxy-arylene-, C,.6-alkoxy-heteroarylene-, heteroarylaryi-C,4-alkoxy-, or aryl-C,4-alkoxy-; and R15 is selected from the group consisting of aryl, heteroaryl, cycloalkyl, heterocyclyl, alkyl, or aryl-alkylene-.
Embodiment 77: A compound according to embodiment 76, wherein R" is selected from hydrogen, alkyl, aryl, carbamoyl, aryl-alkylene-, alkyl-NH-C(O}, aryl-alkylene-NH-C(O}, alkyl-S02-, aryl-alkylene-SO2-, aryl-S02-, SO2-, alkyl-C(0)-, aryl-alkylene-C(O}, N(R13)(R74)-alkylene-Y-, and R15-W2-alkylene-Y-, wherein Y and W2 independently of each other are a direct bond, -CH2-, -SO2--, -N(H)CO-, -N(H)SO2-, or -0-C(O};
R13 and R74 independently of each other are selected from hydrogen, aryl, C1.e-alkyl, or aryl-C,$-alkylene-;

or R13 and R14 may be taken together to form a ring having the formula -(CHs); X-(CH2)P bonded to the nitrogen atom to which R13 and R 14 are attached, wherein 5 o and p are independently of each other are 1, 2, 3, or 4; and X is a direct bond, -CH2-, -0-, -S-, -S(02)-, -C(O}, -CONCH)-, NHC(O), -NHCON(H)-, -NHSO2-, -S02N(H)-, -C(O}O-, -0-C(O)-, -NHSO2NH-, CR
0YR16 0YOR18 02?

-N- -N- -N-0 S'N(H)R 0 N_R
-N- -N-R'7 O\ /NHRt6 0 N-R18 i - N- or 10 wherein R16 and R17 are hydrogen; and R15 is selected from the group consisting of aryl, heteroaryl,. cycloalkyl, heterocyclyl, alkyl, or aryl-alkylene-.
Embodiment 78: A compound according to embodiment 77, wherein 15 R" is selected from hydrogen, alkyl,. aryl, carbamoyl, aryl-alkylene-, alkyl-NH-C(O)-, aryl-alkylene-NH-C(O}, alkyl-S02-, aryl-alkylene-S02-, aryl-S02-, SO2-, alkyl-C(O)-, aryl-alkylene-C(0)-, N(Rt3)(R14)-alkylene-Y-, and R15-W2-alkylene-Y-, wherein Y and W2 independently of each other are a direct bond, -CH2-, -SO2-, -N(H)CO-, -N(H)SO2-, or-0-C(O};
20 R73 and R14 independently of each other are selected from hydrogen, aryl, C1. -alkyl, or aryl-C1$-alkylene-;
or R13 and R14 may be taken together to form a ring having the formula -(CH2)6-X-(CH2)p bonded to the nitrogen atom to which R13 and R14 are 25 attached, wherein o and p are independently of each other are 1, 2, 3, or 4;
X is a direct bond; and R15 is selected from the group consisting of aryl, heteroaryl, cycloalkyl, heterocyclyl, alkyl, or aryl-alkylene-.
Embodiment 79: A compound according to embodiment 78, wherein R" is selected from hydrogen, alkyl, aryl, carbamoyl, aryl-alkylene-, alkyl-NH-C(O)-, aryl-alkylene-NH-C(O)-, alkyl-SOZ-, aryl-alkylene-SOr, aryl-SOZ-, SO2-, alkyl-C(O)-, aryl-alkylene-C(O)-, N(R13)(R14)-alkylene-Y-, and Rt5-W2-alkylene-Y-, wherein Y and W2 independently of each other are a direct bond, -CH2-, -SOz-, -N(H)CO-, -N(H)SO2-, or -O-C(O)-;
R13 and R'4 independently of each other are selected from hydrogen, aryl, C1.6-alkyl, or aryl-Cl.B-alkylene-; and R15 is selected from the group consisting of aryl, heteroaryl, cycloalkyl, heterocydyi, alkyl, or aryl-alkylene-.
Embodiment 80: A compound according to embodiment 79, wherein R" is selected from hydrogen, alkyl, aryl, carbamoyl,. aryl-alkylene-, alkyl-NH-C(O)-, aryl-alkylene-NH-C(O)-, alkyl-SO2-, aryl-alkylene-SO2, aryl-SO2-, SO2-, alkyl-C(O)-, aryl-alkylene-C(O)-, N(R13)(R14)-alkylene-Y , and Rt5-W2-alkylene-Y-, wherein Y and W2 independently of each other are a direct bond, -CH2-, -SO2-, -N(H)CO-, -N(H)SO2-, or -O-C(O)-;
R13 and R'4 are hydrogen; and R15 is selected from the group consisting of aryl, heteroaryl, cycloalkyt, heterocyclyl, alkyl, or aryl-alkylene-.
Embodiment 81: A compound according to embodiment 80, wherein R" Is selected from hydrogen, alkyl, aryl, carbamoyl, aryl-alkylene-, alkyl-NH-C(O)-, aryl-alkylene-NH-C(O)-, alkyl-SO2, aryl-alkylene-SO2-, aryl-SOz-, SOX-, alkyl-C(O)-.
aryl-alkylene-C(O)-, N(Rt3}(R14)-alkylene-Y-, and R15-W2 alkylene-Y , wherein Y is a direct bond;
W2 is a direct bond, -CHr, -SO2-, -N(H)CO-, -N(H)SOr, or -O-C(O)-;
R13 and R14 are hydrogen; and R15 is selected from the group consisting of aryl, heteroaryl, cycloalkyl, heterocyclyl, alkyl, or aryl-alkylene-.
Embodiment 82: A compound according to embodiment 80, wherein R" is selected from hydrogen, alkyl, aryl, carbamoyl, aryl-alkylene-, alkyl-NH-C(O)-, aryl-alkylene-NH-C(O)-, alkyl-SOr, aryl-alkylene-SOr, aryl-SO2-, SO2-, alkyl-C(O)-, aryl-alkylene-C(O)-, N(R13)(R14)-alkylene-Y , and R15-W2-alkylene-Y-, wherein Y is a direct bond, -CHr, -SO2-, -N(H)CO-, -N(H)SOZ-, or -0-C(0)-;
W2 is a direct bond;
R13 and R14 are hydrogen; and.
R15 is selected from the group consisting of aryl, heteroaryl, cydoalkyl, heterocyclyl, alkyl, or aryl-alkylene-.
Embodiment 83: A compound according to any of embodiments 80 to 82, wherein R" is selected from hydrogen, alkyl, aryl, carbamoyl, aryl-alkylene-, alkyl-NH-C(0}, aryl-alkylene-NH-C(O)-, alkyl-SO2, aryl-alkylene-SO2, aryl-SO2, SO2-, alkyl-C(O)-, aryl-alkylene-C(O)-, NHralkylene-, and R'5-alkylene-, wherein R15 is selected from the group consisting of aryl, heteroaryl, cycloalkyl, heterocydyl, alkyl, or aryl-alkylene-.
Embodiment 84: A compound according to embodiment 83, wherein R" is selected from hydrogen, alkyl, aryl, carbamoyl, aryl-alkylene-, alkyl-NH-C(0)-, aryl-alkylene-NH-C(O)-, alkyl-SO2, aryl-alkyleneSO2-, aryl-SO2, SOr, alkyl-C(O)-, aryl-alkylene-C(O)-, and NH2-alkylene-.
Embodiment 85: A compound according to embodiment 84, wherein R" is hydrogen or alkyl.
Embodiment 86: A compound according to embodiment 85, wherein R" is hydrogen.
Embodiment 87: A compound according to any of embodiments 1 to 86, wherein R12 is hydrogen or alkyl.
Embodiment 88: A compound according to embodiment 87,. wherein R1Z is hydrogen.
Embodiment 89: A compound according to any of embodiments I to 88, wherein G' is alkyl, alkenyl, alkynyl, cydoalkyl or heterocyclyl, optionally substituted with one or more substituents selected from the group consisting of -CN, -CF3, -OCF3, -OR'8.
-NR18R19, C3.10-cydoaikyl and C1.6-alkyl, wherein R18 and R19 are as defined for embodiment 1.
Embodiment 90: A compound according to embodiment 89, wherein G' is alkyl, alkenyl, alkynyl, cydoalkyl or heterocyclyl, optionally substituted with one or more substituents selected from the group consisting of -CN, -CF3i -OCF3, -OR1 , -NR18R19 and C14-alkyl, wherein R18 and R19 are as defined for embodiment 1.
Embodiment 91: A compound according to embodiment 89, wherein G' is C148-alkyl, C24-alkenyl, C24-alkynyl, C3.,o-cydoalkyl or C3.,o-heterocydyt, optionally substituted with one or more substituents selected from the group consisting of -CN, -CF3. -OCF3, -OR18, -NR18R'9, C3_,0-cydoalkyl and C,4-alkyl, wherein R18 and R'9 are as defined for embodiment 1.
Embodiment 92: A compound according to embodiment 90 or embodiment 91, wherein G' is C,$-alkyl, Cam-alkenyl, C2$-alkynyl, C3.,0-cydoalkyl or C3.,o-heterocyclyl, optionally substituted with one.or more substituents selected from the group consisting of -CN, -CF3, -OCF3, -OR18, -NR1BR1e and C,4-alkyl, wherein Rt8 and R19 are as defined for embodiment 1.
Embodiment 93: A compound according to any of embodiments 89. to 92, wherein R1B and R19, independently of each other, are hydrogen,. C,$-alkyl, heteroaryl-C14-alkylene-, aryl-C,.8-alkylene-, C1.e-alkyl-arylene-, C,.e-alkyl-heteroarylene-, heteroaryl. or aryl.
Embodiment 94: A compound, according to embodiment 93, wherein R18 and R19, independently of each other, are hydrogen, C1.6-alkyl, C3.,0-heteroaryl-C,$-alkylene-, C3.1o-aryl-C14-alkylene-, C,.8-alkyl-C3.10-arylene-, C1.B-alkyl-C3.,0-heteroarylene-, C3.,o-heteroaryl, or C3.,o-aryl.
Embodiment 95: A compound according to embodiment 94, wherein R18 and R19, independently of each other, are hydrogen or C,.e-alkyl.
Embodiment 96: A compound according to embodiment 95, wherein R18 is hydrogen.
Embodiment 97: A compound according to embodiment 95 or 96, wherein R19 is hydrogen.
Embodiment 98: A compound according to embodiment 90 or embodiment 92, wherein R'8 and R19, when attached to the same nitrogen atom, together with the said nitrogen atom forms a 3 to 8 membered heterocyclic ring optionally containing one or two further heteroatoms selected from nitrogen, oxygen and sulfur, and optionally containing one or two double bonds.
Embodiment 99: A compound according to any of embodiments 1 to 88, wherein G' is alkyl or cycloalkyl, optionally substituted with one or more substituents selected from the group consisting of -CN, -CF3, -OCF3, -OR18, -NR18R19 and C,-0-alkyl, or G' is aryl optionally substituted with one or more substituents R40, R41, and R42, wherein R18, R'9, R40, R41, and R42 are as defined for embodiment 1.
Embodiment 100: A compound according to embodiment 99, wherein G' is C1.a-alkyl or C3.10-cydoalkyl, optionally substituted with one or more substituents selected from the group consisting of -CN, -CF3, -OCF3, -OR18, -NR18R19 and C1.8-alkyl, or G' is C3.10-aryl optionally substituted with one or more substituents R40, R41, and R42, wherein Rt8, R19, R4D, R41, and e are as defined for embodiment 1.
Embodiment 101: A compound according to embodiment 99 or embodiment 100, wherein R18 and Rf8, independently of each other, are hydrogen, C1$-alkyl, heteroaryl-C/.B-alkylene-, aryl-C/.B-alkylene-, Ct8-alkyl-arylene-, C1.8-alkyl-heteroarylene-, heteroaryl, or aryl.
Embodiment 102: A compound according to embodiment 101, wherein R18 and R19, independently of each other, are hydrogen, C14-alkyl, C3.1o-heteroaryl-C1.B-alkylene-, C3.10-aryl-C14-alkylene-, C1$-alkyl-C3.10-arylene-, C1$-alkyl-C3.10-heteroarylene-, C310-heteroaryl, or C310-aryl.
Embodiment 103: A compound according to embodiment 102, wherein R18 and R'9, independently of each other, are hydrogen or C1.6-alkyl.
Embodiment 104: A compound according to embodiment 103, wherein R1 is hydrogen.
Embodiment 105: A compound according to embodiment 103 or 104, wherein R19 is hydrogen.
Embodiment 106: A compound according to embodiment 99 or embodiment 100, wherein R1 and Rt9, when attached to the same nitrogen atom, together with the said nitrogen atom forms a 3 to 8 membered heterocyclic ring optionally containing one or two further heteroatoms selected from nitrogen, oxygen and sulfur, and optionally containing one or two double bonds.
Embodiment 107: A compound according to any of embodiments 99 to 106, wherein R40, R41, and R42 independently of each other are halogen, -CN, -NO2, C1$-alkyl,. -CHF2, -CF3, -OR54, -NRs`R56, -SRM, -NeS(O)2Rb5, -S(O)2NR54e, -S(O)NR84R55, -S(O)R", -S(O)2R54, -C(O)NR$4R , -OC(O)NR84R86, -NR54C(O)e, -CH2C(O)NR54e, -CH2C(O)OR", -0CH2C(O)NR5''Rli5, -CH2OR54, -CH2NRs'R5 i, and -C(O)ORS`; or C24-alkenyl and CZ$-alkynyl, which may optionally be substituted with one or more substituents selected from -CN, -CF3, -OCF3, -OR54, -NR54R and C,4-alkyl, wherein R54 and R55 independently of each other are hydrogen, C1.4-alkyl, 5 C,.B-alkyl-arylene-, C,$-alkyl-heteroary-lene-, aryl-C,4-alkylene-, heteroaryl-C1.s-alkylene-, heteroaryl, or aryl;
or R54 and e, when attached to the same nitrogen atom, together with the said nitrogen atom may form a 3 to 8 membered heterocyclic ring optionally 10 containing one. or two further heteroatoms selected from nitrogen, oxygen and sulfur, and optionally containing one or two double bonds.
Embodiment 108: A compound according to embodiment 107, wherein R54 and R55 independently of each other are hydrogen, or C,4-alkyl, C,.o-alkyl-C3.10-arylene-, C14-alkyl-C3.10-heteroarylene-, 0310-aryl-C,4-alkylene-, 15 C3.10-heteroaryl-C,$-alkylene-, C3.10-heteroaryl, or C3.,o-aryl.
Embodiment 109: A compound according to embodiment 108, wherein RM and e independently of each other are hydrogen or C,$-alkyl.
Embodiment 110: A compound according to embodiment 109, wherein RM is hydrogen.
20 Embodiment 111: A compound according to embodiment 109 or embodiment 110, wherein R is hydrogen..
Embodiment 112: A compound according to any of embodiments I to 88, wherein G' is aryl or heteroaryl, optionally substituted with one or more substituents R40, R41, and R42, wherein 25 R40, R41, and R02 are as defined for embodiment 1.
Embodiment 113: A compound according to embodiment 112, wherein G' is C3_,0-aryl or C3.,o-heteroaryl, optionally substituted with one or more substituents R4O, R41, and R42, wherein R40, R41, and R42 are as defined for embodiment 1..
30 Embodiment 114: A compound according to embodiment 112, wherein G' is aryl, optionally substituted with one or more substituents R40, R41, and R42, wherein R40, R41, and R42 are as defined for embodiment 1.
Embodiment 115: A compound according to embodiment 114, wherein G' is C310-aryl, optionally substituted with one or more substituents R40, R41, and R42, wherein R40, R41, and R42 are as defined for embodiment 1.
Embodiment 116: A compound according to any of embodiments 112 to 115,.
wherein R40, R41, and R42 independently of each other are halogen, -CN, -NO2, C1$-alkyl, -CHF2, -CF3, -OR50, -NR54R55, -SR 54, -NRb4S(O)2R55, -S(O)2NR54R55, -S(O)NR4R55, S(O)R54, -S(O)2R54, -C(O)NR54R66, -OC(O)NR54R55, -NR54C(O)R56, -CH2C(O)NR54R55, -CH2C(O)OR54, -OCH2C(O)NR54R55, -CH2OR54, -CH2NR54R55, and -C(O)OR54; or C2.8-alkenyl and C2$-alkynyl, which may. optionally be substituted with one or more substituents selected from -CN, -CF3, -OCF3, -OR 54, -NR54R55 and C1.g-alkyl;
wherein R54 and RS5 independently of each other are. hydrogen, C14-alkyl, C1.e-alkyl-arylene-, C1.5-alkyl-heteroarylene-, aryl-C14-alkylene-, heteroaryl-C,$-alkylene-, heteroaryl, or aryl;
or e and e, when attached to the same nitrogen atom, together with the said nitrogen atom may form a 3 to 8 membered heterocyclic ring optionally containing one or two further heteroatoms selected from nitrogen, oxygen and sulfur, and optionally containing one or two double bonds.
Embodiment 117: A compound according to embodiment 116, wherein, e and e independently of each other are hydrogen, or C1.8-alkyl, C1.e-alkyl-C3.10-arylene-, C,.-alkyl-C3_70-heteroarylene-, C3_,0-aryl-C,$-alkylene-, C3.,0-heteroaryl-C14-alkylene-, 03.10-heteroaryl, or C3.10-aryl.
Embodiment 118: A compound according to embodiment 117, wherein R54 and e independently of each other are hydrogen or C1.8-alkyl.
Embodiment 119: A compound according to embodiment 118, wherein Rb4 is hydrogen.
Embodiment 120: A compound according to embodiment 118 or embodiment 119, wherein R65 is hydrogen.
Embodiment 121: A compound according to embodiment 114, wherein G1 is Rss , wherein e, R57, R. RS , and RHO, independently of each other, are hydrogen or halogen, -CN, -NO2, C1$-alkyl, -CHF2, -CF3, -OCF3, -OCHF2, -OCH2CF3, -OCF2CHF2, -S(O)2CF3, -SCF3, -OR81, -NRW'R 2, -SR61, -NR81S(0)2R 2, -S(0)2NR 'R 2, -S(O)NR 'R 2, -S(O)R81, -S(O)2RH', -C(O)NR 1R62, OC(O)NR lR 2, -NR 'C(O)R82, -CH2C(O)NR 1R 2, -CH2C(O)OR 1, -OCH2C(O)NR67R62, -CH2OR81, -CH2NR 1R 2, -OC(O)R81, -C(O)R81 and -C(O)OR '; or C2.4-alkenyl and C2.6-alkynyl, which may optionally be substituted with one or more substituents selected from -CN. -CF3,. -OCF3, -ORB', -NR81R82 and C14-alkyl;
C3.10-cycloaikyl, C"-cycloalkenyl, heterocyclyl, C3.10-cycloalkyl-Cl.6-alkylene-, C3.10-cydo-alkyl-C1$-alkoxy-, C3.10-cycloalkyloxy, C3.10-cydoalkyl-C14-alkylthio-,. C..1o-cydoalkylthio, C3.10-cycloalkyl-C2$-alkenylene-,. C3.10-cydoalkyl-C2$-alkynylene-, C44-cycloalke-nyl-C14-alkylene-,. C44-cydoalkenyl-C2$-alkenylene-, C44-cycloalkenyl-C2.8-alkynylene-,.
heterocydyl-C1$-alkylene-, heterocycly-C2. -alkenylene-, heterocydy-C2.8-alkynylene-; or aryl, aryloxy, aryloxycarbonyl, aroyl, aryl-C1.8-alkoxy-, aryl-C1$-alkylene-, aryl-C2.e-alkenylene-, aryl-C2$-alkynylene-, heteroaryl, heteroaryl-C1$-alkylene-, heteroaryl-C2$-alkenylene- and heteroaryl-C24-alkynylene-, of which the aryl and heteroaryl moieties optionally may be substituted with one or more substituents selected from halogen, -C(O)OR81, -CN, -CF3, -OCF3, -NO2, -OR 1, -NR81R 2 or C1. -alkyl, wherein R81 and R 2 independently of each other are hydrogen, C14-alkyl, C16-alkyl-aryyene-, C1$-alkyl-heteroarylene-, aryl-Cl.6-alkylene-, heteroaryl-C14-alkylene-, heteroaryl, or aryl;
or R61 and R62, when attached to the same nitrogen atom, together with the said nitrogen atom may form a 3 to 8 membered heterocyclic ring optionally containing one or two further heteroatoms selected from nitrogen, oxygen and sulfur, and optionally containing one or two double bonds.
Embodiment 122: A compound according to embodiment 121, wherein RSB, R57, e, R69, and e Independently of each other are halogen, -CN, -NO2, C14-alkyl, -CHF2, -CF3, -OR87, -NR 'R 2, -SR ', -NR
1S(O)2R82, -S(O)2NR6'R82, _S(O)NRB1R 2, -S(O)R81, -S(O)2R61, -C(O)NR81R 2, -OC(O)NR61RB2, -NR87C(0)R62, -CH2C(0)NR61R82, -CH2C(O)ORe1, -OCH2C(O)NR61RB2, -CH20R81, -CH2NR81R82, and -C(O)OR81; or C24-alkenyl and C2..-alkynyl, which may optionally be substituted with one or more substituents selected from -CN, -CF3, -OCF3, -OR81, -NR81R82 and C14-alkyl, wherein RB1 and R82 independently of each other are hydrogen, C1$-alkyl, C14-alkyl-arylene-, C1.6-alkyl-heteroarylene-, aryl-Cl B-aikyiene-, heteroaryl-Cl.B-alkylene-, heteroaryl, or aryl;
or R81 and R62, when attached to the same nitrogen atom, together with the said nitrogen atom may form a 3 to 8 membered heterocyclic ring optionally containing one or two further heteroatoms selected from nitrogen, oxygen and sulfur, and optionally containing one or two double bonds.
Embodiment 123: A compound according to embodiment 121 or embodiment 122, wherein R24 or e is -OR81.
Embodiment 124: A compound according to embodiment 122, wherein R81 and R82 independently of each other are hydrogen, or C1.3-alkyl, C14-alkyl-03.10-aryyene-, C14-alkyl-C3.10-heteroarylene-, C3_10-aryl-C1$-alkylene-, C3.10-heteroaryl-C1$-alkylene-, C3.10-heteroaryl, or C3.10-aryl.
Embodiment 125: A compound according to embodiment 124, wherein R81 and R82 independently of each other are hydrogen or C1.6-alkyl.
Embodiment 126: A compound according to embodiment 125, wherein R81 is hydrogen.
Embodiment 127: A compound according to embodiment 125 or embodiment 126;
wherein R62 is hydrogen.
Embodiment 128: A compound according to any of embodiments 121 to 127, wherein at least one of 0, R57, R58, R59, and R80 are hydrogen.
Embodiment 129: A compound according to embodiment 128, wherein at least two of e, R24, R25, and. R28 are hydrogen.
Embodiment 130: A compound according to embodiment 129, wherein at least three of e, R24, R25, and R28 are hydrogen.
Embodiment 131: A compound according to any of embodiments 1 to 130, wherein I-2 is a direct bond, C1$-alkylene, C2$-alkenylene, C2$-alkynylene, -N-RZ0-, -C1$-alkytene-N(RZ0)-, -C24-alkenylene-N(R2D)-, or -C24-alkynylene-N(RZ0}-, wherein R20 Is as defined for embodiment 1.

Embodiment 132: A compound according to any of embodiments 1 to 127, wherein L2 is -N-R20-, -alkylene-N(R20)-, -alkenylene-N(R20)-, or -alkynylene-N(RZ0)-, wherein R20 is as defined for embodiment 1.
Embodiment 133: A compound according to embodiment 131 or embodiment 132, wherein L2 Is -N-R20-, -C,. -alkylene-N(R2 )-, -C2$-alkenylene-N(R20)-, or -C24-alkynylene-N(RZ0)-, wherein R20 is as defined for embodiment 1.
Embodiment 134: A compound according to embodiment 133, wherein L2 is -N-R20-, wherein R2 is as defined for embodiment 1.
Embodiment 135: A compound according to embodiment 131, wherein L2 is a direct bond.
Embodiment 136:. A compound according to any of embodiments 1 to 134, wherein R20 Is hydrogen, or RZ0 is C14-alkyl, C24-alkenyl,. C2.$-alkynyl, C3.t0-cycloalkyl-W3-, C3.t0-hetenxyclyl-W3-, C3,10-aryl-W3, or C4.10-heteroaryl-W3-, optionally substituted with one or more. substituents R30, R31, and R32, wherein W3, R30, R31, and R32 are as defined for embodiment 1.
Embodiment 137: A compound according to embodiment 136, wherein W3 is alkylene.
Embodiment 138: A compound according to embodiment 137, wherein W3 is C2$-alkylene.
Embodiment 139: A compound according to embodiment 136, wherein W3 is a direct bond.
Embodiment 140: A compound according to any of embodiment;-1 to 134, wherein R20 is hydrogen, alkyl, alkenyl, or alkynyl, optionally substituted with one or more substituents R30, R31, and R32, wherein R30, R31, and R32 are as defined for embodiment 1.
Embodiment 141: A compound according to any of embodiments 136 to 140, wherein R20 is hydrogen, or e is C1--alkyl, C14-alkenyl, or C14-alkynyl, optionally substituted with one or more substituents R30, R", and RS2, wherein R30, R31, and R32 are as defined for embodiment 1.
Embodiment 142: A compound according to any of embodiments 1 to 141, wherein R30, R31, and R32 independently of each other are selected from -CHF2r -CF3, -OCF3, -OCHF2, -OCH2CF3i -OCF2CHF2, -S(O)2CF3, -SCF3, -OR 12 , -NR R53, -SRO, -NR S(O)2R , -S(O)2NR R53, -S(0)NR-'12e, -S(O)R52, -S(O)2RR, -C(O)NR 52 R0, -OC(O)NR52R53, _NR2C(O)R3, -CH2C(O)NR52R53, -OCH2C(O)NR52R53, -CH2OR52, 5 -CH2NR52R53, -OC(O)R52, -C(O)R52 and -C(O)OR52, wherein R52 and R53 are as defined for embodiment 1.
Embodiment 143: A compound according to embodiment 142, wherein R52 and 0, when attached to the same nitrogen atom, together with the said nitrogen atom may form a 3 to 8 membered heterocyclic ring optionally containing 10 one or two further heteroatoms selected from nitrogen, oxygen and sulfur, and optionally containing one or two double. bonds.
Embodiment 144: A compound according to any of embodiments 1 to 142, wherein RS2 and e independently of each other are hydrogen, C14-alkyl,. aryl-C, B-alkylene-heteroaryl-C1.8-alkylene- heteroaryl, or aryl.
15 Embodiment 145: A compound according to embodiment 144, wherein e and e independently of each other are hydrogen, C1.6-alkyl, aryl-Cl.B-alkylene-or aryl.
Embodiment 146: A compound according to embodiment 145, wherein R52 and e independently of each other are hydrogen or C1$-alkyl.
20 Embodiment 147: A compound according to embodiment 146, wherein R52 is hydrogen.
Embodiment 148: A compound according to embodiment 146 or embodiment 147, wherein R53 is hydrogen.
Embodiment 149: A compound according to embodiment 141, wherein 25 R20 is hydrogen.
Embodiment 150: A compound according to any of embodiments 1. to 149, wherein L3 is -C(O)-.
Embodiment 151: A compound according to any of embodiments I to 150, wherein R1 is hydrogen, or 30 R1 is C1.8-alkyl, C2.6-alkenyl, C24-alkynyl, C3.10-cycloalkyl-W4-, C3.10-heterocyclyl-W4-, C3.t0-aryl-W4-, or C4.10-heteroaryl-W4-, optionally substituted with one or more substituents R33, R34, and R35, wherein W4, R33, R34, and R35 are as defined for embodiment 1.
Embodiment 152: A compound according to embodiment 151, wherein 35 W4 is alkylene.

Embodiment 153: A compound according to embodiment 152, wherein W4 is C2.a-alkylene.
Embodiment 154: A compound according to embodiment 151, wherein W4 is a direct bond.
Embodiment 155: A compound according to any of embodiments 1 to 150, wherein R' is hydrogen, alkyl, alkenyl, or alkynyl, optionally substituted with one or more substituents R33, R34, and R35, wherein R33, R34, and R35 are as defined for embodiment 1.
Embodiment 156: A compound according to any of embodiments 151 to 155, wherein R' is hydrogen, C1.6-alkyl, C2$-alkenyl, or C24-alkynyl, optionally substituted with one or more substituents R33,. R34, and R35, wherein R33, e, and e are as defined for embodiment 1.
Embodiment 157: A compound according to embodiment 156, wherein R' is hydrogen or C,$-alkyl optionally substituted with one or more substituents R33, R34, and e, wherein R33, R34, and e are as defined for embodiment 1.
Embodiment 158: A compound according to any of embodiments 1 to 157, wherein R33, R30, and e independently of each other are selected from -CHF2, -CF3, -OCF3, -OCHF2, -OCH2CF3, -OCF2CHF2, -S(O)2CF3, -SCF3, -OR52, -NR52R , -SR52, -NRSZS(O)2R53, -S(0)2NR52R53, -S(O)NR52R53, -S(O)R52, -S(O)2R52, -C(O)NR52R53, -OC(O)NR52R, _NR52C(O)R53, -CH2C(O)NRSZR53, -OCH2C(O)NR52R53, -CH2OR52, -CH2NR52R53, -OC(O)R52, -C(O)W2 and -C(O)OR52, wherein R52 and R53 are as defined for embodiment 1.
Embodiment 159: A compound according to embodiment 157, wherein R52 and e, when attached to the same nitrogen atom,. together with the said nitrogen atom may form a 3 to 8 membered heterocyclic ring. optionally containing one or two further heteroatoms selected from nitrogen, oxygen and sulfur, and optionally containing one or two double bonds.
Embodiment 160: A compound according to embodiment 157, wherein R52 and e independently of each other are hydrogen, C14-alkyl, aryl-C1.6-alkylene-heteroaryl-C,-e-alkylene- heteroaryl, or aryl.
Embodiment 161: A compound according to embodiment 160, wherein R52 and e independently of each other are hydrogen, C,a-alkyl, aryl-C,$-alkylene-or aryl.
Embodiment 162: A compound according to embodiment 161, wherein R52 and R53 independently of each other are hydrogen or C1.8-alkyl.
Embodiment 163: A compound according to embodiment 162, wherein e is hydrogen.
Embodiment 164: A compound according to embodiment 162 or embodiment 163, wherein R53 is hydrogen.
Embodiment 165: A compound according to embodiment 157, wherein R' is hydrogen.
Embodiment 166: A compound according to any of embodiments 1 to 165, wherein G2 is heteroaryl, fused heterocydylheteroaryl, or fused cydoalkyiheteroaryl, optionally substituted with one or more substituents R43, R44, and R45, wherein said heteroaryl group posesses a nitrogen atom adjacent to the atom joining G2with -N(R')-, and wherein e, R44, and e are as defined for embodiment 1.
Embodiment 167: A compound according to embodiment 166, wherein G2 is heteroaryl optionally substituted with one or more substituents R43, R44, and R45, wherein said heteroaryl group posesses a nitrogen atom adjacent to the atom joining G2With -N(R')-, and wherein R43, R44,.. and R45 are as defined for embodiment 1.
Embodiment 168: A compound according to embodiment 167, wherein 20. G2 is furanyl, thienyl, thiophenyl, pyrrolyl, imidazolyl, pyrazolyl, triazolyl, tetrazolyl, thiazolyl, oxazolyl, isoxazolyl, oxadiazolyi, thiadiazolyl, isothiazolyl, pyridinyl, pyridazinyl, pyrazinyl, pyrimidinyl, quinolinyl, isoquinolinyl, benzofuranyl, benzothiophenyl, indolyl, or. indazolyl, optionally substituted with one or more substituents R43, R44, and R45, wherein R43, R44, and R45 are as defined for embodiment 1.
Embodiment 169: A compound according to any of embodiments I to 168, wherein R43, R44, and R45 independently of each other are selected from halogen, -CN, -NO2, C,$-alkyl, -CHF2, -CF3, -OCF3, -OCHF2, -OCH2CF3, -OCF2CHF2, -S(O)2CF3, -SCF3, -0R54, -NR54R55, -SR54, -NR54S(O)2R55,.
-S(0)2NR54R55, -S(O)NR54R55, -S(O)IV, -S(O)2RM, -C(O)NR54R65, -OC(O)NRS4R55, -NR54C(O)R56, -CI2C(0)NR54R5s, -CH2C(O)OR54, -OCH2C(O)NR51R5, -CH20R54, CH2NR54R55, -0C(O)R54, -C(O)R54 and -C(O)OR54, wherein R' and Fe are as defined for embodiment 1.
Embodiment 170: A compound. according to embodiment 169, wherein Rs' and e, when attached to the same nitrogen atom, together with the said nitrogen atom may form a 3 to 8 membered heterocyclic ring optionally containing one or two further heteroatoms selected from nitrogen, oxygen and sulfur, and optionally containing one or two double bonds, and optionally substituted with one or more C14-alkyl groups..
Embodiment 171: A compound according to embodiment 170, wherein e and R65, when attached to the same nitrogen atom, together with the said nitrogen atom may form a 3 to 8 membered heterocyclic ring optionally containing one or two further heteroatoms selected from nitrogen, oxygen and sulfur, and optionally containing one or two double. bonds.
Embodiment 172: A compound according to embodiment 169, wherein R54 and e independently of each other are hydrogen, C14-alkyl, aryl-C14-alkylene-or aryl.
Embodiment 173: A compound according to embodiment 172, wherein R54 and e independently of each other are hydrogen, C14-alkyl, C3.10-aryl-C1$-alkylene- or C3.1o-aryl.
Embodiment 174: A compound according to embodiment 173, wherein R54 and e independently of each other are hydrogen or C1$-alkyl.
Embodiment 175: A compound according to embodiment 174, wherein R54 is hydrogen.
Embodiment 176: A compound according to embodiment 174 or embodiment 175;
wherein e is hydrogen.
Embodiment 177: A compound according to embodiment 169, wherein R54 and R65 independently of each other are hydrogen or -(CHe),-(CHR84)W-Z, wherein u is 1 or 2;
v is 0, 1 or 2;
e and R84 independently of each other are hydrogen, C1.8-alkyl, C1-a-alkyl-03.10-arylene- C3.1o-aryl, hydroxy, hydroxy-C1.S-alkyl. amino, or amino-C14-alkyl;
Z is hydrogen. -C-O-R65, -C(O)O-R85, -CONR65R66, C14-alkylamino, or di(C1.8-alkyl)-amino, wherein R~ and R8 independently of each other is hydrogen or C14-alkyl;
or Z is a five or six membered ring wherein at least one ring atom is nitrogen and the remaining ring atoms are either carbon or oxygen.
Embodiment 178: A compound according to embodiment 177, wherein u is 1; and vis0,or1.
Embodiment 179: A compound according to embodiment 177 or embodiment 178, wherein e and R64 independently of. each other are hydrogen, C14-alkyl, hydroxy, hydroxy-C,$-alkyl, amino, or amino-C,.e-alkyl.
Embodiment 180: A compound according to any of embodiments 177 to 179, wherein Z is -C-O-R55, or -C(O)O-e, wherein R65 and e independently of each other is hydrogen or C14-alkyl.
Embodiment 181: A compound according to any of embodiments 177 to 179, wherein Z is a five or six membered ring where at least one ring atom is nitrogen and the remaining ring atoms are either carbon or oxygen.
Embodiment 182: A compound according to embodiment 181, wherein Z is a five or six membered ring. wherein at least one ring atom is nitrogen, one ring atom is oxygen and the remaining ring atoms are carbon.
Embodiment 183: A compound according to embodiment 181, wherein Z is a five or six membered ring wherein at least one ring atom is nitrogen, and the remaining ring atoms are carbon.
Embodiment 184: A compound according to any of embodiments 181 to 183, wherein Z is a five or six membered ring. wherein one ring atom is nitrogen.
Embodiment 185: A compound according to any of embodiments 181 to 184, wherein is a nitrogen atom is the point of attachment of the Z group to the -(CHR63)õ-(CHR4v group.
Embodiment 186: A compound according to any of embodiments 177 to 185, wherein R55 is hydrogen.
Embodiment 187: A compound according to any of embodiments 166 to 169, wherein G2 is substituted with a substituent R'3, wherein R43 is halogen, -CN, -NO2, C1--alkyl, -CHF2, -CF3, -OCF3, -OCHF2, -OCH2CF3, -OCF2CHF2, -S(O)2CF3, -SCF3, -OR54, -NR54R55, -SR54, -NR54S(O)2R55, -S(O)2NR54R55, -S(O)NR54R55, -S(O)R54, -S(O)2R54, -C(O)NeR55, -OC(O)NR54R55, -NR54C(O)R55, -CH2C(O)NR54R55, -CH2C(O)OR54, -OCH2C(O)NR54R55, -CH2OR54, -CI2NRS4R55, -OC(O)R54, -C(O)R5' or -C(O)OR54, wherein R54 and R55 are as defined for embodiment 1.
Embodiment 188: A compound according to embodiment 187, wherein e and e, when attached to the same nitrogen atom, together with the said nitrogen atom may form a 3 to 8 membered heterocyclic ring optionally containing 5 one or two further heteroatoms selected from nitrogen, oxygen and sulfur, and optionally containing one or two double bonds, and optionally substituted with one or' more C1$-alkyl groups.
Embodiment 189: A compound according to embodiment 188, wherein R6a and e, when attached to the same nitrogen atom, together with the said 10 nitrogen atom may form a 3 to 8 membered heterocyclic ring optionally containing one or two further heteroatoms selected from nitrogen, oxygen and sulfur, and optionally containing one or two double bonds.
Embodiment 190: A compound according. to embodiment 187, wherein RM and R55 independently of each other are hydrogen, C1.g-alkyl, aryl-C1$-alkylene-15 or aryl.
Embodiment 191: A compound according to embodiment 190, wherein R5' and R55 independently of each other are hydrogen, C1.6-alkyl, C--jo,aryl-Cj.o-aIkylene- or C3-lo-aryl.
Embodiment 192: A compound according to embodiment 191, wherein 20 R54 and R!5 independently of each other are hydrogen or C1.6-alkyl.
Embodiment 193: A compound according to embodiment 192, wherein R54 is hydrogen.
Embodiment 194: A compound according to embodiment 192 or embodiment 193, wherein R55 is hydrogen.
25 Embodiment 195: A compound according to embodiment 187, wherein Rs` and R55 independently of each other are hydrogen or -(CHR3 O ),-(CHR ')r-Z, wherein u is 1 or 2;
v is 0, 1 or 2;
30 R6s and R80 independently of each other are hydrogen, C1$-alkyl, C1.6-alkyl-C3.10-arylene- C3.10-aryl, hydroxy, hydroxy-C14-alkyl, amino, or amino-C1$-alkyl;
Z is hydrogen, -C-O-R65, -C(O)O-RB5, -CONR65R60, C1$-alkylamino, or di(C,4-alkyl)-amino, wherein 35 R65 and R66 independently of each other is hydrogen or C1$-alkyl;

or Z is a five or six membered ring wherein at least one ring atom is nitrogen and the remaining ring atoms are either carbon or oxygen.
Embodiment 196: A compound according to embodiment 195, wherein u is 1; and vis0,or1.
Embodiment 197: A compound according to embodiment 195 or embodiment 196, wherein e and Rd4 independently of each other are hydrogen, C1.6-alkyl, hydroxy, hydroxy-C1. -alkyl, amino, or amino-C14-alkyl.
Embodiment 198: A compound according to any of embodiments 195 to 197, wherein Z is -C-O-R5, or -C(O)O-Res, wherein R85 and R6 independently of each other is hydrogen or C,a-alkyl.
Embodiment 199: A compound according to any of embodiments 195 to 197, wherein Z is a five or six membered ring where. at least one ring atom is nitrogen and the remaining ring atoms are either carbon or oxygen.
Embodiment 200: A compound. according to. embodiment 199, wherein Z Is a five or six membered ring wherein at least one ring atom is nitrogen, one ring atom is oxygen and the remaining ring atoms are carbon.
Embodiment 201: A compound according to embodiment 199, wherein Z is a five or six membered ring wherein at least one ring atom is nitrogen, and the remaining ring atoms are carbon.
Embodiment 202: A compound according to any of embodiments 199 to 201, wherein Z is a five or six membered ring wherein one ring atom Is nitrogen.
Embodiment 203: A compound according to any of embodiments 199 to 202, wherein a nitrogen atom is the point of attachment of the Z group to the -(CHR83)õ-(CHR64),r group.
Embodiment 204: A compound according to any of embodiments 195 to 203, wherein e is hydrogen.
Embodiment 205: A compound according to embodiment 187, wherein R43 is -CH2C(O)ORb4, wherein R54 is as defined for embodiment 1.
Embodiment 206: A compound according to embodiment 205, wherein R54 is hydrogen, C14-alkyl, aryl-Cl.6-alkylene- or aryl.
Embodiment 207: A compound according to embodiment 206, wherein R54 is hydrogen, C,.8-alkyl, C3.10-aryl-C,$-alkylene- or C3.10-aryl.

Embodiment 208: A compound according to embodiment 207, wherein e is hydrogen or C1.g-alkyl.
Embodiment 209: A compound according to embodiment 208, wherein R5` is hydrogen.
Embodiment 210: A compound according to any of embodiments 187 to 209, wherein R43 is attached to the atom adjacent to the nitrogen atom adjacent to to the atom joining G2with -N(R')-.
Embodiment 211: A compound according to any of embodiments 166 to 210, wherein G2 is N,N / N;
S

R R or R R , wherein R43, R4'', and independently of each other are hydrogen or as defined for embodiment 1..
Embodiment 212: A compound according to embodiment 211, wherein G2 is R44 R~ R44 or , wherein R', R44, and R45 independently of each other are hydrogen or as defined for embodiment 1.
Embodiment 213: A compound according to embodiment 211 or embodiment 212, wherein R'3, R,`, and RR Independently of each other are selected from hydrogen, halogen, -CN, -NO2, C1.g-alkyl, -CHF2, -CF3, -OCF3, -OCHF2, -OCH2CF3, OCF2CHF2i -S(O)2CF3, -SCF3, -ORS`, -Nee, -SRS`, -NR5`S(O)2R'5, -S(0)2NRb`R", -S(O)NRMe, -S(O)RM, -S(O)2Ru, -C(O)NRMRM, -0C(O)NRMR6, -NR54C(O)R6, -CH2C(O)NR5'R53, -CH2C(O)OR5`, -OCH2C(O)NR6`R5, -CH2Oe, -CH2NeR", -OC(O)R5`, -C(O)RD` and -C(O)ORS`, wherein R6` and R55 are as defined for embodiment 1.
Embodiment 214: A compound according to embodiment 213, wherein R 3 Is halogen, -CN, -NO2, C14-alkyl, -CHF2, -CF3, -OCF3, -OCHF2, -OCH2CF3, -OCF2CHF2, -S(O)2CF3r -SCF3, -OR5'', -NeR5', -SRS`, -NeS(O)2R", -S(0)2NR54R55, -S(0)NR54R55, -S(O)R54, -S(O)2R54, -C(O)NR54R55, -OC(O)NR54R55, -NR54C(O)R55, -CH2C(O)NR54R55, -CH2C(O)OR50, -0CH2C(O)NR4R 5, -CH2OR54, -CH2NR54R55, -OC(0)R54, -C(O)R54 or -C(O)Oe, wherein R54 and R55 are as defined for embodiment 1.
Embodiment 215: A compound according to embodiment 213 or 214, wherein R43 is -C(O)OR54, -CH2C(O)OR54, -C(O)NR4R55, or -CH2C(O)NR54R55, wherein R54 and R55 are as defined for embodiment 1.
Embodiment 216: A compound according to embodiment 214 or 215, wherein e is alkyl or hydrogen.
Embodiment 217: A compound according to embodiment 216, whereinR44 is C,$-alkyl or hydrogen.
Embodiment 218: A compound according to embodiment 217, wherein R44 is hydrogen.
Embodiment 219: A compound according to. embodiment 213, wherein R40 is halogen, -CN, -NO2, C,.g-alkyl, -CHF2, -CF3, -OCF3, -OCHF2, -OCH2CF3, -OCF2CHF2, -S(O)2CF3, -SCF3i -OR54, -NRs`R55, -SR54, -NR54S(O)2R55, -S(0)2NR54R55, -S(O)NR54R55, -S(O)R54, -S(O)2R54, -C(O)NR54R55, -OC(O)NR54R55, -NR54C(O)R55, -CH2C(O)NR54R55, -CH2C(O)OR54, -OCH2C(O)NR54R5', -CH2OR54, -CH2NR54R55, -OC(0)R54, -C(0)R54 or-C(0)OR54, wherein R54 and e are as defined for embodiment 1..
Embodiment 220: A compound according to embodiment 213 or embodiment 219, wherein R44 is -C(O)0R54, -CH2C(O)OR54, -C(0)NR54R55, or -CH2C(0)NR54R55, wherein R54 and e are as defined for embodiment 1.
Embodiment 221: A compound according to embodiment 219 or 220, wherein R43 is alkyl or hydrogen.
Embodiment 222: A compound according to embodiment 221, wherein R43 is C,$-alkyl or hydrogen.
Embodiment 223: A compound according to embodiment 222, wherein R43 is hydrogen.
Embodiment 224: A compound according to any of embodiments 211 to 223, wherein R45 is hydrogen.
Embodiment 225: A compound according to any of embodiments 211 to 224, wherein e and e, when attached to the same nitrogen atom, together with the said nitrogen atom may form a 3 to 8 membered heterocyclic ring optionally containing one or two further heteroatoms selected from nitrogen, oxygen and sulfur, and optionally containing one or two double bonds, and optionally substituted with one or more C1.e-alkyl groups.
Embodiment 226: A compound according to embodiment 225, wherein RM and R55, when attached to the same nitrogen atom, together with the said nitrogen atom may form a 3 to 8 membered heterocyclic ring optionally containing one or two further heteroatoms selected from nitrogen, oxygen and sulfur, and optionally containing one or two double bonds.
Embodiment 227: A compound according to any of. embodiments 211 to 224, wherein R54 and e independently of each other are hydrogen, C1. -alkyl, aryl-C,.ralkylene-or aryl.
Embodiment 228: A compound according to any of embodiments 211 to 224, wherein R54 and R55 independently of each other are hydrogen, C,.B-alkyl, aryl-C,$-alkylene-or aryl.
Embodiment 229: A compound according to embodiment 228, wherein R54 and R' independently of each other are hydrogen or C,$-alkyl.
Embodiment 230: A compound according to embodiment 229, wherein e is hydrogen.
Embodiment 231: A compound according to any of embodiments 211 to 230, wherein R55 is hydrogen.
Embodiment 232: A compound according to any of embodiments 211 to 224, wherein R54 and R55 independently of each other are hydrogen or -(CHR63)õ (CHR64WZ, wherein u is 1 or 2;
v is 0, 1 or 2;
e and e independently of each other are hydrogen, C1.B-alkyl, C,$-alkyl-03.10-arylene- C310-aryl, hydroxy,, hydroxy-C1.8-alkyl, amino, or amino-C1 -alkyl;
Z is hydrogen, -C-O-RS', -C(O)O-R85, -CONRS iRO6, C1.4-alkyiamino, or di(C,4-alkyl)-amino, wherein R85 and r independently of each other is hydrogen or C14-alkyl;
or Z is a five or six membered ring wherein at least one ring atom is nitrogen and the remaining ring atoms are either carbon or oxygen.
Embodiment 233: A compound according to embodiment 232, wherein u is 1; and vis0,or1.
Embodiment 234: A compound according to embodiment 232 or embodiment 233, wherein Rea and RB'' independently of each other are hydrogen, C,.g-alkyl, hydroxy, hydroxy-C,$-alkyl, amino, or amino-C1 -alkyl.
5 Embodiment 235: A compound according to any of embodiments 232 to 234, wherein Z is -C-O-R5, or -C(0)0-R , wherein e and R68 independently of each other is hydrogen or C14-alkyl.
Embodiment 236: A compound according to any of embodiments 232 to 234, wherein Z is a five or six membered ring where at least one ring atom is nitrogen and the 10 remaining ring atoms are either carbon or oxygen..
Embodiment 237: A compound according to embodiment 236, wherein Z is a five or six membered ring wherein at least one ring atom is nitrogen, one ring atom is oxygen and the remaining ring atoms are carbon.
Embodiment 238: A compound according to embodiment 236, wherein 15 Z is a five or six membered ring wherein at least one ring atom is nitrogen, and the remaining ring atoms are carbon.
Embodiment 239: A compound according to any of embodiments 236 to 238, wherein Z is a five or six membered ring wherein one ring atom is nitrogen.
Embodiment 240: A compound according to any of embodiments 236 to 239, wherein 20 a nitrogen atom is the point of attachment of the Z group to the -(CHR83)õ(CHR64)õ-group.
Embodiment 241: A compound according to any of embodiments 195 to 240, wherein R is hydrogen.
Embodiment 242: A compound according to embodiment 213, wherein 25 R44 is hydrogen.
Embodiment 243: A compound according to embodiment 213 or embodiment 242, wherein R43 is hydrogen.
Embodiment 244: A compound according to embodiment 242 or embodiment 243, wherein e is hydrogen.
30 Embodiment 245: A compound according to embodiment 1, which is, N-(2-phenoxyphenyl)-N'-(thiazol-2-yl)urea, N-[2-(2,3-dimethoxyphenoxy)-5-fluorophenyl]-N'-(thizol-2-yi)sulfamide, 1-(2-phenoxyphenyl)-5-(thiazol-2-yl)biuret, 2-[(a(2-phenoxyanilino)sulfonyl]amino]carbonyl)amino]thiazole, 35 N-(2-phenylsulfanylphenyl)-N'-(thiazol-2-yl)urea, N-(2-phenylsulfonylphenyl)-N'-(thiazol-2-yl)urea, N-(2-benzylphenyl)-N'-(thiazol-2-yl)urea, N-(2-benzoylphenyl)-N'-(thiazol-2-yl)urea, N-[2-(phenylamino)phenyl]-N'-(thiazol-2-yl)urea, N-[2-fluoro-6-(4-methoxyphenoxy)benzyl]-N'-(thiazol-2-yl)urea, N-(2-benzyloxyphenyl)-N'-(thiazol-2-yl)urea, N-[2-(2,3,4-trimethoxybenzyloxy)phenyl]-N'-(thiazol-2-yl)urea, N-(2-ethoxyphenyl}N'-(thiazol-2-yl)urea, N-(2-phenoxyphenyl)-N'-(pyridin-2-yl)urea, N-(2-phenoxyphenyl)-N'-((4-methoxycarbonylmethyl)thiazol-2-yi]urea, N-methyl-N-(2-phenoxyphenyl)-N'-(thiazol-2-yl)urea, N-isopropyl-N-(2-phenoxyphenyl)-N'-(thiazol-2-yl)urea, N-[2-(4-methoxyphenoxy)phenyi}N'-(thiazol-2-yl)urea, N-[2-(4-fluorophenoxy)phenyl-N'-(thiazol-2-yl)urea, N-[2-(4-chlorophenoxy)phenyq-N'-(thiazol-2-yl)urea, N-[2-(4-cyanophenoxy)phenyl]-N'-thiazolylurea, N-[2-(4-methoxycarbonylphenoxy)phenyl]-N'-(thiazol-2-yl)urea, N-[2-(4-isopropylphenoxy)phenyq-N'-(thiazol-2-yl)urea, N-[2-(3,4-dicuorophenoxy)phenyl]-N'-(thiazol-2-yl)urea, N-[2-(3,4-dichlorophenoxy)phenyl]-N'-(thiazol-2-yl)urea, N-[2-(4-chloro-3-methylphenoxy)phenyl]-N'-(thiazol-2-yl)urea, N-[2-(3,4-dimethoxyphenoxy)phenyl]-N'-(thiazol-2-yl)urea, N-[2-(3,4-methylenedioxyphenoxy)phenyl]-N'-(thiazol-2-yi)urea, N-[2-(2,4-dichlorophenoxy)phenyf -N'-(thiazol-2-yl)urea, N-[2-(2,4-difluorophenoxy)phenyl]-N'-(thiazol-2-yl)urea, N42-(4-fluoro-2-methoxyphenoxy)phenyq-N'-(thiazol-2-yl)urea, N-[2-(4-metho)cy-2-methoxycarbonylphenoxy)phenyl]-N'-(thiazol-2-yl)urea, N-[2-(3-methoxyphenoxy)phenyl]-N'-(thiazol-2-yl)urea, N-12-(3-fluorophenoxy)phenylj-N'-(thiazol-2-yl)urea, N-[2-(3-trifluoromethylphenoxy)phenyl]-N'-(thiazol-2-yl)urea, N-[2-(2-methylphenoxy)phenyl]-N'-(thiazol-2-yl)urea, N-[2-(2-methoxyphenoxy)phenyq-N'-(thiazol-2-yl)urea, N-[2-(2-isopropoxyphenoxy)phenyq-N'-(thiazol-2-yl)urea, N-[2-(2-fluorophenoxy)phenyq-N'-(thiazol-2-yl)urea, N-[2-(2-methylsulfanylphenoxy)phenyl]-N'-(thiazol-2-yl)urea, N-[2-(2-methylsulfonylphenoxy)phenyl]-N'-thiazolylurea, N-[2-(2-trifluoromethylphenoxy)phenyl]-N'-(thiazol-2-yl)urea, N-[2-(2,6-dimethoxyphenoxy)phenyl]-N'-(thiazol-2-yl)urea, N-[2-(2,6-dicuorophenoxy)phenyl]-N'-(thiazol-2-yl)urea, N-[2-(2-fluoro-6-methoxyphenoxy)phenyl]-N'-(thiazol-2-yl)urea, N-[2-(2-methoxy-6-methoxycarbonylphenoxy)phenyl]-N'-(thiazol-2-yl)urea, N-[(3-methoxy-2-methoxycarbonylphenoxy)phenyl]-N'-(thiazol-2-yl)urea, N-[2-(2,3-dimethoxyphenoxy)phenyl]-N'-(thiazol-2-yl)urea,.
N-[2-(2,3,4-tichlorophenoxy)phenyl]-N'-(thiazol-2-yl)urea, N-[2-(2,4,6-trifluorophenoxy)phenyl]-N'-(thiazol-2-yl)urea, N-[2-(2,4-dichloronaphth-1-oxy)phenyl]-N'-(thiazol-2-yl)urea, N-[2-(2-methoxyphenoxy)-5-(methylsulfonyl)phenyl]-N'-(thiazol-2-yl)urea, N-[5-cyano-2-(2-methoxyphenoxy)phenyl]-N'-(thiazol-2-yl)urea, N-[5-fluoro-2-(2-methylsulfanylphenoxy)phenyq-N'-thiazolylurea, N-[5-fluoro-2-(2-fluoro-6-methoxyphenoxy)phenyl]-N'-(thiazol-2-yl)urea, N-[2-(2,3-dimethoxyphenoxy)-5-fluorophenyl]-N'(thiazol-2-yl)urea, N-[2-(3,4-difluorophenoxy)-5-fluorophenyl]-N'-(thiazol-2-yl)urea, N-[5-fluoro-2-(4-fluorophenoxy)phenyl]-N'-(thiazol-2-yl)urea, N-[2-(2,4-dichlorophenoxy)-5-fluorophenyq-N'-(thiazol-2-yl)urea, N-[5-fluoro-2-(4-methoxyphenoxy)phenyl]-N'-(thiazol-2-yl)urea, N-[5-fluoro-2-(2-methoxyphenoxy)phenyl]-N'-(thiazol-2-yl)urea, N-[5-fluoro-2-(2-trifluoromethylphenoxy)phenyl]-N'-(thiazol-2-yl)urea, N-[5-fluoro-2-(naphth-2-oxy)phenyq-N'-(thiazol-2-yl)urea, N-[2-(2,3-dimethoxyphenoxy)-6-fluorophenyq-N'-(thiazol-2-yl)urea, N-[2-(4-fluoro-2-methoxyphenoxy)phenyl]-N'-(thiazol-2-yl)urea, N-[2-(2,3-dimethoxyphenoxy)- 4-fluorophenyl]-N'-(thiazol-2-yl)urea, N-[4-fluoro-2-(2-fluoro-6-methoxyphenoxy)phenyl-N'-(thiazol-2-yl)urea, N-[2-(2-fluoro-6-methoxyphenoxy)-4-methoxyphenyl]-N'-(thiazol-2-yl)urea, N-[3-fluoro-2-(2-fluoro-6-methoxyphenoxy)phenyq-N'-(thiazol-2-yl)urea, N-[2-(2,3-dimethoxyphenoxy)-5-methoxyphenylj-N'-thiazol-2-ylurea, N-[2-(2,3-dimethoxyphenoxy)-4-methylphenyl]-N'-(thiazol-2-yl)urea, N-[2-(2,3-dimethoxyphenoxy)-3-methylphenyi]-N'-(thiazol-2-yl)urea, N-[2-(2-chlorophenoxy)-5-chlorophenylj-N'-(thiazol-2-yl)urea, N-[5-chloro-2-(4-chloro-3-methylphenoxy)phenyl]-N'-(thiazol-2-yl)urea, N-[2-(4-chlorophenoxy)-5-(trifluoromethyl)phenyl]-N'-(thiazol-2-yl)urea, N-[4,5-difluoro-2-(2,3-dimethoxyphenoxy)phenyl]-N'-(thiazol-2-yl)urea, N-[4,5-dichloro-2-(2,3-d imethoxyphenoxy)phenyl]-N'-(thiazol-2-yl)urea, N-[5-chloro-2-(2,3-dimethoxyphenoxy)-4-dimethylaminophenyl]-N'-(thiazol-2-yl)urea, N-[5-chloro-2-(2,3-dimethoxyphenoxy)-4-(4-morpholino)phenyl]-N'-(thiazol-2-yl)urea, N-[2-(2,4-difluorophenoxy)pyridin-3-yI-N'-(thiazol-2-yl)urea, N-[2-(2-fluorophenoxy)pyridin-3-yl]-N'-[thiazol-2-yl]urea, N-[2-(2-methoxyphenoxy)pyridin-3-yl]-N'-(thiazol-2-yl)urea, N-[2-(2,3-dimethoxyphenoxy)pyridin-3-yl]-N-(thiazol-2-yl)urea, N-[4-chloro-2-(2-chlorobenzoyl)phenyl]-N'-(thiazol-2-yl)urea, N-[4-chloro-2-(2-fluorobenzoyl)phenyl]-N'-(thiazol-2-yl)urea, N-[2-(2,4-difluorophenylsulfanyl)phenyl]-N'-(thiazol-2-yl)urea, 1-[2-(2-fluorophenylsulfanyl)phenyl]-3-(thiazol-2-yl)urea, N-[2-(2-chloro-4-fluorophenylsulfanyl)phenyl]-N'-(thiazoi-2-yl)urea, N-[2-(2,3-dichlorophenylsulfanyl)phenyl]-N'-(thiazol-2-yl)urea, N-[2-(3,5-dimethylphenylsulfanyl)phenyl]-N'-(thiazol-2-yl)urea, N-[2-(2-methoxycarbonylphenylsulfanyl)phenyl]-N'-(thiazol-2-yl)urea,.
N-[2-(2-methoxyphenylsulfanyl)phenyl]-N'-(thiazol-2-yl)urea, N-[2-(2-pyridinylsulfanyl)phenyl]-N'-(thiazol-2-yl)urea, N-(2-propyloxyphenyl)-N'-(thiazol-2-yi)urea, N-(2-butyloxyphenyl)-N'-(thiazol-2-yl)urea, N-(2-(cyclopentyloxyphenyl}N'-(thiazol-2-yl)urea, N-(2-isopropoxyphenyl)-N'-(thiazol-2-yl)urea, N-[2-(2-methylpropoxy)phenyl]-N'-(thiazol-2-yl)urea, N-[2-(cyclopentylmethoxy)pheny]YN'-(thiazol-2-yl)urea, N-[2-(3-pentoxy)phenyl]-N'-(thiazol-2-yl)urea, N-[2-(2-pentoxy)phenyl]-N'-(thiazol-2-yl)urea, N-[2-(2-methoxyethoxy)phenyl]-N'-(thiazol-2-yl)urea, (2-[3-(2-benzylphenyl)ureido]thiazol-4-yl)acetic acid.
(2-[3-(2-benzoyl-4-chlorophenyl)ureido]thiazol-4-yl)acetic acid, (2-[3-(2-(2-methytphenoxy)phenyl)ureido]thiazol-4-yl)acetic acid, (2-[3-(2-(4-methoxyphenoxy)-5-(trifluoromethyl)phenyl)ureido]thiazol-4-yl)acetic acid, {2-[3-(2-phenoxyphenyl)ureido]thiazol-4-y}acetic acid, 2-{3-[5-fluoro-2-(2-fluoro-6-methoxyphenoxy)phenyl]ureido}thiazole-4-carboxylic acid, 2-(3-[2-(2,3-dimethoxyphenoxy)-5-fluorophenyljureido}thiazole-4-carboxylic acid ethyl ester, (2-{3-[2-(2,3-dimethoxyphenoxy)-5-fluorophenyl]ureido)thiazol-4-yl)acetic acid ethyl ester, (2-{3-[5-fluoro-2-(2-fluoro-6-methoxyphenoxy)phenyl]ureido)thiazol-4-yl)acetic acid, 2-{3-[2-(2,3-dimethoxyphenoxy)-5-fluorophenyl]ureido}thiazole-4-carboxylic acid, (2-(3-[2-(2,3-dimethoxyphenoxy)-5-fluorophenyqureido}thiazol-4-yl)acetic add, 2-{3-[5-fluoro-2-(2-fluoro-6-methoxyphenoxy)phenyl]ureido}-4-methylthiazole-5-carboxylic acid ethyl ester, 2-(3-[5-fluoro-2-(2-fluoro-6-methoxyphenoxy)phenyl]ureido)-4-methylthiazole-5-carboxylic acid, N-ethyl-2-(2-{3-[5-fluoro-2-(2-fluoro-6-methoxyphenoxy)phenyqureido}thiazol-4-yl)acetamide, 2-(2-(3-(5-fluoro-2-(2-fluoro-6-methoxyphenoxy)phenyl]ureido)thiazol-4-yl)-N-(2-methoxy-ethyl)acetamide, 2-(2-{3-[5-fluoro-2-(2-fluoro-6-methoxyphenoxy)phenyl]ureldo}thiazol-4-yl)-N-(2-morpholin-4-ylethyl)acetamide, [2-(2-{3-[5-fluoro-2-(2-fluoro-6-methoxyphenoxy)phenyl]ureido}thiazol-4-yl)acetylamino]acetic acid methyl ester, 2-(3-[2-(2,3-dimethoxyphenoxy)-5-fluorophenyl]ureido}thiazole-4-carboxylic acid (2-methoxyethyl)amide, [2-(2-{3-[5-fluoro-2-(2-fluoro-6-methoxyphenoxy)phenyl]ureido}thiazol-4-yl)acetylamino]acetic add, 2-{3-[2-(2,3-dimethoxyphenoxy)-5-fluorophenyl]ureido}thiazole-4-carboxylic acid ethylamide, [(2-{3-[2-(2,3-dimethoxyphenoxy)-5-fluorophenyl]ureido)thiazole-4-carbonyl)aminojacetic acid methyl ester, (5-{3-[5-fluoro-2-(2 fluoro-6-methoxyphenoxy)phenyl]ureido)-[1,3,4]thiadiazol-2-yl)acetic acid ethyl ester, [(2-{3-[2-(2,3-dimethoxyphenoxyj-5-fluorophenyl]ureido}thiazole-4-carbonyl)amino]acetic acid, (5-{3-[5-fluoro-2-(2-fluoro-6-methoxyphenoxy)phenyl]ureido}-[1,3,4]thiadiazol-2-yl)acetic acid, 5-{3-[2-(2,3-dimethoxyphenoxy)-5-fluorophenyl]ureido}-(1,3,4]thiadiazole-2-carboxylic acid ethyl ester, (5-{3-[2-(2,3-dimethoxyphenoxy)-5-fluorophenyl]ureido}-[1,3,4]thiadiazol-2-yl) acetic acid ethyl ester, 3-[2-(2-(3-[2-(2,3-dimethoxyphenoxy)-5-fluorophenyqureido}thiazol-4-yl)acetylamino]propionic acid methyl ester, 2-(2-(3-[2-(2,3-dimethoxyphenoxy)-5-fluorophenyljureido}thiazol-4-yl}N-(2-morpholin-4-ylethyl)acetamide, [(2-{3-[5-fluoro-2-(2-fluoro-6-methoxyphenoxy)phenyl]ureido}thiazole-4-carbonyl)amino]acetic acid methyl ester, 3-[2-(2-{3-[2-(2,3-dimethoxyphenoxy)-5-fluorophenyl]ureido}thiazol-4-yl)acetylamino]propionic acid, 5 [(2-(3{5-fluoro-2-(2 fluoro-6-methoxyphenoxy)phenyl]ureido)thiazole-4-carbonyl)amino]acetic acid, (R) 3-[(2-{3-[5-fluoro-2-(2-fluoro-6-methoxyphenoxy)phenyl]ureido}thiazole-4-carbonyl)amino]-2-hydroxy-propionic acid, 2-[(2-{3-[5-fluoro-2-(2-fluoro-6-methoxyphenoxy)phenyl]ureido}thiazole-4-carbonyl)aminoj-3-10 hydroxy-propionic acid, 1-(2-cyclopentanecarbonyl-4-methylphenyl)-3-thiazol-2-yl-urea, 1-(2-isobutyryl-4-methylphenyl)-3-thiazol-2-yl-urea, 1-[5-fluoro-2-(3-methylbutyryl)phenyl]-3-thiazol-2-yl-urea, 1 -[5-methyl-2-(3-methylbutyryl)phenyl]-3-thiazol-2-yl-urea, 15. [3-cydopentanecarbonyl-4-(3-thiazol-2-yl-ureido)phenyljacetic add ethyl ester, [3-cydopentanecarbonyl-4-(3-thiazol-2-yt-ureido)phenyl]acetic acid, 2-[3-cyclopentanecarbonyl-4-(3-thiazol-2-yl-ureido)phenyl]-N-methylacetamide, {2-[3-(2-cydopentanecarbonyl-4-methyl-phenyl)ureido]-thiazol-4-yl}-acetic add ethyl ester, {2-[3-(2-cydopentanecarbonyl-4-methyl-phenyl)-ureido]-thiazol-4-yl}acetic acid, 20 {3-cyclopentanecarbonyl-4-{3-(4-ethoxycarbonylmethylthiazol-2-yl)-ureido}phenyl}acetic acid ethyl ester, 1-(2-cydopentanecarbonyl-4-methyl-phenyl)-3-(5-methanesulfonyl-thiazol-2-yl)-urea, 2-[3-(2-cydopentanecarbonyl-4-methylphenyl)-ureido]-thiazole-4-carboxylic add ethyl ester, 2-[3-(2-cyclopentanecarbonyl-4-methylphenyl)-ureido]-thiazole-4-carboxylic acid, 25 2-[3-(2-cyclopentanecarbonyl-4-methylphenyl}ureido]-thiazole-4-carboxamide, 2-{2-[3-(2-cydopentanecarbonyl-4-methylphenyl)-ureido]-thiazot-4-y1}-acetamide.
2-{2-(3-(2-cydopentanecarbonyl-4-methyiphenyl)-ureido]-thiazol-4-yl}-N-methyl-acetamide, 4-(2-{2-[3-(2-cyclopentanecarbonyl-4-methylphenyl)-ureido]-thiazol-4-yl}acetyl)-1-methyl-piperazinium chloride, 30 1-[4-methyl-2-(2-methylpropoxy)phenyl]-3-thiazol-2-yl-urea, {2-[3-(4-methyl-2-[2-methylpropoxy]phenyl)-ureido]-thiazol-4-yl}-acetic acid, or (2-[3-(4-methyl-2-[2-methylpropoxy]phenyl}-ureido]-thiazol-4 yl)-N-methyl-acetamide.
Embodiment 246: A compound according to any of embodiments I to 245, which compound is an activator of glucokinase, when tested in the Glucokinase Activation Assay (I) disclosed 35 herein at a glucose concentration of 2 mM.

Embodiment 247: A compound according to any of embodiments 1 to 246, which compound is an activator of glucokinase, when tested in the Glucokinase Activation Assay (I) disclosed herein at a glucose concentration of from 10 to 15 mM.
Embodiment 248: A compound according to any of embodiments 1 to 247, which compound, at a concentration of 30 NM, Is capable of providing an at least 1.5, such as at least 1.7, for instance at least 2.0 fold activation of glucokinase In the Glucokinase Activation Assay (1) disclosed herein at a glucose concentration. of 2 mM.
Embodiment 249: A compound according to any of embodiments 1 to 248, which compound, at a concentration of 30 NM, is capable of providing an at least 1.5, such as at least 1.7, for instance at least 2.0 fold activation of glucokinase in the Glucokinase Activation Assay (I) disclosed herein at a glucose concentration of from 10 to 15 mM.
Embodiment 250: A compound according to any of embodiments I to 249, which at a concentration of 5 NM is capable of providing an at least 1.5, such as at least 1.7, for instance at least 2.0 fold activation of glucokinase in the Glucokinase Activation Assay (t) disclosed herein at a glucose concentration of 2 mM.
Embodiment 251: A compound according to any of embodiments I to 250, which at a concentration of 5 IN is capable of providing an at least 1.5, such as at least 1.7, for instance at least 2.0 fold activation of glucokinase in the Glucokinase Activation Assay (1) disclosed herein at a glucose concentration of from 10 to 15 mM.
Embodiment 252: A glucose kinase activator compound defined as a compound which at a compound concentration of at or below 30 pM at a glucose concentration of 2 mM
In the Glucokinase Activation Assay (I) disclosed herein gives 1.5 - fold higher glucokinase activity than measured at a glucose concentration of 2 mM in the Glucokinase Activation Assay (I) without compound, where the increase in glucokinase activity provided by the compound increases with decreasing concentrations of glucose.
Embodiment 253: A compound according to any of embodiments 1 to 251, which compound provides an increase in glucokinase activity, where the increase in glucokinase activity provided by the compound increases with decreasing concentrations of glucose.
Embodiment 254: A compound according to embodiment 252 or embodiment 253, which provides an increase in glucokinase activity in Glucokinase Activation Assay (I) disclosed herein at a glucose concentration of 5 mM, which increase is significantly higher than the increase in glucokinase activity provided by the compound in Glucokinase Activation Assay (I) disclosed herein at a glucose concentration of 15 mM.
Embodiment 255: A compound according to any of embodiments 252 to 254, which at a compound concentration of 10 pM provides an increase in glucokinase activity in Glucokinase Activation Assay (I) disclosed herein at a glucose concentration of 5 mM, which increase is significantly higher than the increase in glucokinase activity provided by the compound at a compound concentration of 10 pM in Glucokinase Activation Assay (I) disclosed herein at a glucose concentration of 15 mM.
Embodiment 256: A compound according to any of embodiments 252 to 255, which at a compound concentration of 10 pM provides an increase in glucokinase activity in Glucokinase Activation Assay (l) disclosed herein at a glucose concentration of 5 mM, which increase is at least 1.1 fold higher,. such as at least 1.2 fold higher, for instance at least 1.3 fold higher. such as at least 1.4 fold higher, for instance 1.5 fold higher, such as at least 1.6 fold higher, for instance at least 1.7 fold higher, such as at least 1.8 fold higher, for instance at least 1.9 fold higher, such as at least 2.0 fold higher than the increase in glucokinase activity provided by the compound at a compound concentration of 10 pM in Glucokinase Activation Assay (I) disclosed herein at a glucose concentration of 15 mM.
Embodiment 257: A glucose kinase activator compound defined as a compound which at a compound concentration of at or below 30 pM at a glucose concentration of 2 mM
in the Glucokinase Activation Assay (I) disclosed herein gives 1.5 - fold higher glucokinase activity than measured at,a glucose concentration of 2 mM in the Glucokinase Activation Assay (I) without compound, which glucose kinase activator compound increases glucose utilization in the liver without inducing any increase in insulin secretion in response to glucose.
Embodiment 258: A glucose kinase activator compound defined as a compound which at a compound concentration of at or below 30 pM at a glucose concentration of 2 mM
in the Glucokinase Activation Assay (I) disclosed herein gives 1.5 - fold higher glucokinase activity than measured at a glucose concentration of 2 mM in the Glucokinase Activation Assay (I) without compound, which glucokinase. activator compound shows a significantly higher activity in isolated hepatocytes compared to the activity of the glucokinase compound in Ins-1 cells.
Embodiment 259: A compound according to any of embodiments I to 256, which compound increases glucose utilization in the liver without inducing any increase in insulin secretion in response to glucose.
Embodiment 260: A compound according to any of embodiments 1 to 256, which compound shows a significantly higher activity in isolated hepatocytes compared to the activity of the compound in Ins-1 cells.
Embodiment 261: A compound according to any of embodiments 257 to 260, which compound shows a significantly higher activity in isolated hepatocytes measured as described in the Glucokinase Activity Assay (II) compared to the activity of the compound in Ins-1 cells measured as described in the Glucokinase Activity Assay (III).
Embodiment 262: A compound according to embodiment 261, which compound shows an activity in isolated hepatocytes measured as described in the Glucokinase Activity Assay (1I) which activity Is at least 1.1 fold higher, such as at least 1.2 fold higher, for instance at least 1.3 fold higher, such as at least 1.4 fold higher, for instance. 1.5 fold higher, such as at least 1.6 fold higher, for instance at least 1.7 fold higher, such as at least 1.8 fold higher, for instance at least 1.9 fold higher, such as at least 2.0 fold higher, for instance at least a 3.0 fold higher, such as at least a 4.0 fold higher, for instance at least 5.0 fold higher, such as at .10 least 10 fold higher than the activity of the compound in Ins-1 cells measured as described in the Glucokinase Activity Assay (III).
Embodiment 263: A compound according to embodiment 261, which compound shows no activity in the Ins-1 cells measured as described in the Glucokinase. Activity Assay (III).
Embodiment 264: A compound according to any one of embodiments 1 to 263, which is an agent useful for the treatment of an indication selected from the group consisting of hyperglycemia, IGT, insulin resistance syndrome, syndrome X, type 2 diabetes, type 1 diabetes, dyslipidemia, hypertension, and obesity.
Embodiment 265: A compound according to any one of embodiments 1 to 264 for use as a medicament..
Embodiment 266: A compound according to any one of embodiments I to 264 for treatment of hyperglycemia, for treatment of IGT, for treatment of Syndrome X, for treatment of type 2 diabetes, for treatment of type 1 diabetes, for treatment of dyslipidemia, for treatment of hyperlipidemia, for treatment of hypertension, for treatment of obesity, for lowering of food intake, for appetite regulation, for regulating feeding behaviour, or for enhancing the secretion of enteroincretins, such as GLP-1.

In a further aspect the invention provides in an Embodiment Al a compound of the general formula (I) G' L' L2 R' G

(I) A' is selected from the group consisting of arylene, heteroarylene, fused cydoalkylarylene, fused heterocydylarylene, fused cycloalkyiheteroarylene, or fused heterocyclylheteroarylene;
optionally substituted with one or more substitutents R23, RZ4, R25, R28, and R27, wherein R23, R24, R25, R26, and e independently of each other are selected from the group consisting of halogen, -C(O)OR2, -C(O)R2, -CN, -CF3, -OCF3, -NO2, -OR2, -NR2R3, C14-alkyl-Z-, C2.8-alkenyl-Z-, C2$-alkynyl-Z-, aryl-Cl,g-alkylene-Z-, heteroaryl-C,$-alkylene-Z-, heterocydyl-C,4-alkylene-Z-, cydoalkyl-C1.6-alkylene-Z-, N(R4R5)-C,$-alkylene-Z-, R -W'-Z-, Re-W'-C,$-alkylene-Z-, Re-W'-C,$-arylene-Z-, R -W'-heteroarylene-Z-, Re-W'-heterocydylene-Z-, R -W'-N(R4)-Z-, Re-N(W)-Z, RB-W'-C14-alkylene-Z-, heterocydyl-Z-C,e-alkylene-, heterocyclyl-C,.e-alkylene Z-C,$-alkylene-, C310-cycloalkyl-Z-C,.g-alkylene-, C3.,o-cycoalkyl-C,4-alkylene-Z-C,.S-alkylene-, C310-cycloalkyl-arylene-Z-, heterocyclyl-arylene-Z-, C3,0-cycloalkyl-heteroarylene-Z-, heterocydyl-heteroarylene-Z-, aryl-C3,0-cydoalkylene-Z-, aryl-heterocydylene-Z-, heteroaryl-C310-cycloalkylene-Z-, heteroaryl-heterocydylene-Z-, hetenxydyl-C3.,a-cydoalkylene-Z-, aryi-heteroarylene-Z , heteroaryl-arylene-Z-, aryl-arylene-Z-, heteroaryl-heteroarylene-Z-, wherein any mono- or divalent C1.6-alkyl, C~-,a-cycloalkyl, heterocyclyl, aryl or heteroaryl moiety can optionally be substituted with one or more substituents independently selected from R2, and wherein R2 and R3 independently of each other are hydrogen, halogen, hydroxy, -CN, -CF3, -OCF3, -NO2, -C(O)OH, -NH2, C,.6-alkyl, C14-alkoxy, aryloxy, Re-Z-, aryl-C,$-alkylene-, heteroaryl-C,.6-alkylene-, C,$-alkyl-arylene-, C,4-alkyl-heteroarylene-, heteroaryl, or aryl;
or R2 and R3, when attached to the same nitrogen atom, together with said nitrogen atom may form a 3 to 8 membered heterocyclic ring optionally containing one or two further heteroatoms selected from nitrogen, oxygen and sulfur, and optionally containing one or two double bonds;

Z and W' independently of each other are a direct bond, -0-, -N(R7)-, -N(R')C(R'R )-, -S-, -SO2-, -C(O)N(R')-, -N(R7)C(O)-, -N(R7)C(O)C(R'Re}, -N(R7)CON(R8)-, -N(R7)SO2-, -S02N(R')-, -C(O)-, -C(O)-O-, -N(R7)S02N(R )-, or -O-C(O)-, wherein 10 R7 and R8 in each individual case independently of each other are hydrogen or C1e-alkyl; and R4, R5, and R independently of each other are selected from the group consisting of hydrogen, cyano, halogen, aryl, heteroaryl, heteroaryl-C,. -alkylene-, aryl-alkylene-, C3.1 -cycloalkyl, heterocydy optionally substituted with one or more 15 C14-alkyl, or C1. -alkyl optionally substituted with halogen, -S(O)2CH3 or COOH;
or R4 and R5 may be taken together to form a ring having the formula -(CH2)rQ-(CH2)k-bonded to the nitrogen atom to which R4 and R5 are attached, wherein j and k Independently of each other is 1, 2, 3, or 4; and 20 Q is a direct bond, -CH2-, -0-, -S-, -S(02)-, -C(O)-, -C(O)NH-, -NHC(O)-, -NHC(O)NH-, -NHSO2-, -SO2NH-, -C(O)-O-, -0-C(O)-, -NHSO2NH-, 0YR0 OyOR OZIiR9 .N(H)Rs 02fN-R9 `r S 02?' -N- , -N- -N- -N- -N-OyNHR9 OyN-R9 i 9 - I -N- or -N-wherein 25 R9 and R10 independently of each other are selected from the group consisting of hydrogen, aryl, C1$-alkyl, and aryl-alkylene-;

L1 is a bond, -D-C1. -alkylene-E-, -D- C2--alkenylene-E-, -D- C2$-alkynylene-E-, 30 -D-cycioalkylene-E-, -D-heterocydylene-E-, -0-, -S-, -S(O)-, -S(O)z-.

-C(O)-, -N(R")-, or-C(=N-OR12)-, wherein D and E independently of each other are a direct bond, -0- or -S-;
R" is selected from hydrogen, C,$-alkyl, aryl, carbamoyl, aryl-C14-alkylene-, heteroaryl-C1.e-alkylene-, C,.6-alkyl-O-C(O)-, aryl-C148-alkylene-O-C(O)-, heteroaryl-C,_e-alkylene-O-C(O)-, C,$-alkyl-NH-C(O)-, aryl-C,$-alkylene-NH-C(O)-, heteroaryl-C14-alkylene-NH-C(O)-, C14-alkyl-SOr, aryl-C,$-alkylene-SO2-, heteroaryl-C,_e-alkylene-SO2-, aryl-SOZ-, heteroaryl-SO2-, C,$-alkyl-NH-SOr, aryl-C,4-alkylene-NH-SOr, heteroaryl-C14-alkylene-NH-SOr, C1$-alkyl-C(O)-, aryl-C1.g-alkylene-C(O)-, heteroaryl-C,.e-alkylene-C(0)-, C,$-alkyl-Y-, aryl-Y-, heteroaryl-Y , aryl-C,.-alkylene-Y-, heteroaryl-C14-alkylene-Y-, N(R13)(R14)-C,4-alkylene-Y-, and R15-W2-C,.e-alkylene-Y-, wherein Y and W2 independently of each other are a direct bond, -CHr, -SOr, N(H)CO-, -N(H)SOr, or -0-C(O)-;
R 13 and R14 Independently of each other are selected from hydrogen, aryl, heteroaryl, C14-alkyl, C,.e-alkoxy, aryl-C14-alkylene-, heteroaryl-C14-alkylene-, aryl-C,$-alkoxy-, heteroaryl-C11-alkoxy-, C,.g-alkyl-arylene-, C1.e-alkyl-heteroarylene-, C14-alkoxy-heteroarylene-, or C1.4-alkoxy-arylene-;
or R13 and R14 may be taken together to form a ring having the formula -(CH2)o X-(CH2)p- bonded to the nitrogen atom to which R13 and R14 are attached, wherein o and p are independently of each other are 1, 2, 3, or 4; and X is a direct bond, -CHr, -0-, -S-, -S(O2) , -C(O)-, -CON(H}, -NHC(O) , -NHCON(H), -NHSOr, -SO2N(H}, -C(O)-O-, -O-C(O), -NHSO2NH-, to 0YR1e 0 yOR16 027 ,R -N- -N- . -N-O2S,N(H)R18 02fN-R18 -N- -N-if R
18 1e OONHR76 O`Y /N-R ' or -N-wherein R18 and R'7 are selected from hydrogen, aryl, heteroaryl, C14-alkyl, C1$-alkoxy, aryl-C1$-alkylene-, heteroaryl-C1$-alkylene-, C14-alkyl-arylene-, C14-alkyl-heteroarylene-, C1.8-alkoxy-arylene-, C1.s-alkoxy-heteroarylene-, heteroarylaryl-C14-alkoxy-, or aryl-C1.e-alkoxy-; and R15 is selected from the group consisting of aryl, heteroaryl, cycloalkyl, heterocydyl, C14-alkyl, heteroaryl-C1.6-alkylene-, or aryl-Cl.6-alkylene-; and R12 is selected from hydrogen, aryl, heteroaryl, C1.e-alkyl, aryl-C1$-alkylene-, heteroaryl-C1 -alkylene-, C14-alkyl-arylene-, C1$-alkyl-heteroarylene-, C1.8-alkoxy-heteroarylene-, or C1.4-alkoxy-arylene-;
G' is C1.4-alkyl, C3.10-cydoalkyl, C~.10-cydoalkyl-Cl-0-alkylene-, C28-alkenyl, or CZ-0-alkynyl, all of which may optionally be substituted with one or more substituents independently selected from the group consisting of -CN, -CF3r -OCF3, -OR18, -NR18R19, C3.10-cydoalkyl and C1.8-alkyl, wherein R18 and R19 independently of each other are hydrogen, C14-alkyl, heteroaryl-C1$-alkylene-, aryl-C1$-alkylene-, C1$-alkyl-arylene-, C14-alkyl-heteroarylene-, heteroaryl, or aryl;
or R7B and R19, when attached to the same nitrogen atom, together with the said nitrogen atom may form a 3 to 8 membered heterocyclic ring optionally containing one or two further heteroatoms selected from nitrogen, oxygen and sulfur, and optionally containing one or two double bonds;

or G' is aryl, heteroaryl, heterocyclyl, fused cycloalkylheteroaryl, fused heterocyclylaryl, fused arylheterocyclyl, or fused cycloalkylaryl, all of which may optionally be substituted with one or more substituents selected from R40, R41, and R42;
L2 is.a direct bond, C1.6-alkylene, C2.8-alkenylene, C2.g-alkynylene, -N(R20)-, -C1.6-alkylene-N(R20)-, -C2$-alkenylene-N(R20)-, -C2.s-alkynylene-N(R20)-, wherein R20 is hydrogen, or RZ0 is C1.8-alkyl, C2.8-alkenyl, C24-alkynyl, cycoalkyl-W3-, heterocydyl-W3-, aryl-W3-, heteroaryl-W3-, optionally substituted with one or more substituents R30, R31, and R32, wherein W3 is C1.8-alkylene or a direct bond;
wherein L' and L2 are attached to adjacent atoms in A';
L3 is -C(O)-, -C(O)-C(O)-, -C(O)CH2C(O)- or -S(O)r;
R' is hydrogen, or R' is C14-alkyl, C2.8-alkenyl, C2-,-alkynyl, cycloalkyl W4-, heterocyclyl-W4-, aryl-W4-, or heteroaryl-W4-, -optionally substituted with one or more substituents R33, R34, and R35, wherein W4 is C1$-alkylene or a direct bond;
G2 is heteroaryl, fused heterocyclylheteroaryl, or fused cycloalkyiheteroaryl, optionally substituted with one or more substituents R43, R44, and R45, wherein said heteroaryl group posesses a nitrogen atom adjacent to the atom joining said heteroaryl group to -N(R')-;
or a group of the formula O

R or wherein G3 and G5 independently of each other are C1.6-alkyl, C2$-alkenyl, C2-6-alkynyl, cycloalkyl-R22-, heterocydyl-R22-, aryl-R22-, heteroaryl-R22-, optionally substituted with one or more substituents R46, R47, and R48, wherein R22 is alkylene or a direct bond; and R21 is hydrogen, C1.6-alkyl, C2-g-alkenyl, C24-alkynyl, cycloalkyl-W5-, or heterocyclyl-W5-=
optionally substituted with one or more substituents e, R37, and e, or R21 is aryl-W5-, or heteroaryl-W5-, optionally substituted with one or more substituents R49, R50, and R51, wherein W5 is C1.3-alkylene or a direct bond;
wherein R30, R31, R32, R, R34, R, R38, R37, and R38 independently of each other are selected from -CHF2, -CF3, -OCF3, -OCHF2, -OCH2CF3, -OCF2CHF2, -S(O)2CF3, -SCF3, -OR52, -NR52Rb3, -SR52, -NR52S(O)2R53, -S(O)2NR52R53, -S(O)NR52R53, -S(O)R52, -S(O)2R62, -C(O)NR52R53, -0C(O)NR52R53, -NR52C(O)R53, -CH2C(O)NR52R53, -OCH2C(O)NR52R53, -CH2OR52, -CH2NR52R53, -OC(O)R52, -C(O)R52 and -C(O)OR52; or C2.6-alkenyi and C2$-alkynyl, which may optionally be substituted with one or more substituents selected from -CN, -CF3, -OCF3, -OR52, -NR52Rb3 and C14-alkyl; or C3 10-cydoalkyl, C44-cycloalkenyl, heterocyclyl, C3.10-cydoalkyl-C,$-alkylene-, C3.10-cydoalkyl-C16-alkoxy-, C310-cycloalkyloxy, C310-cycloalkyl-C,$-alkylthio-, C3.10-cydoalkylthio, C3.10-cydoalkyl-C2$-alkenylene-, C310-cydoalkyl-C2.e-alkynylene-, C4.8-cydoalkenyl-Cl.B-alkylene-, C44-cycloalkenyl-C2$-alkenylene-, C"-cydoalkenyl-C2$-alkynylene-, heterocydy-C1.6-alkylene-, heterocydyl-C24-alkenylene-, heterocyclyl-C2.e-alkynylene-, aryl, aryloxy, aryloxycarbonyl, aroyl, aryl-C1$-alkoxy-, aryl-C,.6-alkylene-, aryl-C24-alkenylene-, aryl-C2.g-alkynylene-, heteroaryl, heteroaryl-Cl.6-alkylene-, heteroaryl-C2-6-alkenylene- and heteroaryl-C2-0-alkynylene-, of which the aryl and heteroaryl. moieties optionally may be substituted with one or more substituents selected from halogen, -C(O)OR52, -CN, -CF3, -OCF3, -NO2, -OR52, -NR52R53 and C1.6-alkyl, wherein R52 and R53 independently of each other are hydrogen, C14-alkyl, aryl-C14-alkylene-A heteroaryl-Cl-e-alkylene- heteroaryl, or aryl;
or R52 and R. when attached to the same nitrogen atom, together with the said nitrogen atom may form a 3 to 8 membered heterocyclic ring optionally containing one or two further heteroatoms selected from nitrogen, oxygen and sulfur, and optionally containing one or two double bonds;
R40, R41, R42, R43, R44, R45, R4B, R47, R, R49, e and R51 independently of each other are -CN, -NO2, -S(O)2CF3, -SCF3, -0R64, -NRMR55, -SR54, -NR54S(O)2R66, -S(O)2NR54R65, -S(O)NR64R66, -S(O)R54, -S(O)2R54, -C(O)NR54R55, -0C(O)NR54R55, -NR54C(O)R55, halogen, -S-C14-alkylene-OR54, -S(O)2-C16-alkylene-OR54, -C14-alkylene-S-R54, -C14-alkylene-S(O)R54, -C14-alkylene-S(O)2R54, -C14-alkylene-N(R54)S(O)2R55, -N(R54)S(O)2R55, -C1.6-alkylene-CN, -C,4-alkylene-C(O)NR54e, -C,$-aikylene-N(e)C(O)R, -N(Rs')C(O)e, -C,.a-alkylene-N(R54)C(O)NR R56, -C,.$-alkylene-NHC(=NR54)NR55e, -C,$-alkylene-N(R'4)C(O)OR55, -N(R54)C(O)OR 5, C,$-alkylene-C(O)Oe.
-C,.4-alkylene-N(R54)S(O)2R55, -OCH2C(O)ISle 5, -O(CH2),.3OR54, -C,$-alkylene-O-R54, 5 -C,.-alkylene-C(O)RM, -C,.B-alkylene-NR54R55, -C(=NR54)-O-R55, -C(=N(ORM))C(O)Oe, -C(=N(OR54))C(O)R55, -C,$-alkylene-C(=N(Oe))C(O)R55, -C, B-alkylene=N-O-RM, -C,4-alkylene-N(RS4)S(O)2NR55R50, -N(R4)S(OhNR55R38, -N(e)S(O)2NR58R58,-OC(O)R54, -C,4-alkylene-C(O)N(RM)S(O)2R55. -C(O)N(RM)S(O)2e, -C,.e-alkylene-C(R)=N-Oe, -NHC(=NR54)NR55R58, -C, e-alkylene-NHC(=NRM)NR54R55, -C,$-alkylene-N=C(N(R54e))2, 10. N=C(N(R5 Rb5))2, -C(O)RM and -C(O)OR54; or C,4-alkyl, C24-alkenyl and C2$-alkynyl, each of which may optionally be substituted with one or more substituents independently selected from halogen, e, -CN, -CF3, -OCF3, -0R51, -C(O)OR5', -NR54RS5 and C,-e-alkyl; or C3.,o-cydoalkyl, C*a-cycloalkenyl, heterocyclyl, C3.,a-cydoalkyl-C,$-alkylene-, 15 C3.,o-cycloalkyl-C,$-alkoxy-, C3.,o-cycloalkyloxy, C3.,o-cydoalkyl-C,$-alkylthio-, C3.,o-cycloalkyithio, C3.,o-cycloalkyl-C2.ralkenylene-, C3.,o-cydoalkyl-C24-alkynylene-, C44-cycloalkenyl-C,.e-alkylene-, C44-cydoalkenyl-C2$-alkenylene-, C"-cydoalkenyl-C24-alkynylene-, heterocydyl-C,$-alkylene-, heterocydyl-C2$-alkenylene-, heterocyclyl-C2$-alkynylene- of which the heterocydyl moieties optionally may be substituted 20 with one or more substituents independently selected from R'o; or aryl, aryloxy, aryloxycarbonyl, amyl, aryl-C1.6-alkoxy-, aryl-C,$-alkylene-, aryl-C2.g-alkenylene-, aryl-C2$-alkynylene-, heteroaryl, heteroaryl-C14-aikylene-, heteroaryl-S-C,.6-alkylene-, heteroaryl-C2.8-alkenylene- and heteroaryl-C2.s-alkynylene-, of which the aryl and heteroaryl moieties optionally may be substituted with one or more substituents selected 25 from halogen, -C(O)OR54, -CN, -CF3, -0CF3, -NO2, -0R54, -NR54Rss or C14-alkyl, wherein R54. R55 and R55 independently of each other are hydrogen, C,.0-alkyl; Si(C,$-alkyl}, C,.e-alkyl-arylene-, C,4-alkyl-heteroarylene-, aryl-C,.$-alkylene-, heteroaryl-C14-alkylene-, heterocyclyl, heterocydyl-C,4-alkylene-, heteroaryl, or aryl, each of which is optionally substituted with one or more substituents independently 30 selected from R";
or R54 and RS5 independently of each other are hydrogen or -(CHR'2),-(CHR73~-W8, wherein uis0,1or2;
35 v is 0, 1 or 2;

R72 and R73 independently of each other are hydrogen, C1.8-alkyl, C1.8-alkyl-arylene- aryl, hydroxy, hydroxyalkyl, -C(O)O-R75, amino, or aminoalkyl;
We is hydrogen, -O-R75, -C(O)O-R75, -C(O)-R76, -CONR75R78, -NR 75R78, NHCH2C(O)R75, -NHC(O)R75, -NHC(O)OR75, -S(O)2R75, -NHS(O)2R75, alkylamino, or dialkylamino, or We is a five or six membered ring wherein at least one ring atom is nitrogen and the remaining ring atoms are either carbon or oxygen or optionally substituted with C14-alkyl, -C(0)0-R75, -(CH2)13C(O)O-R75, =0;
or We is phathalimido or heterocyclyl.
or.
R$4 and e, when attached to the same nitrogen atom, together with the said nitrogen atom may form a 3 to 8 membered heterocyclic ring optionally containing one or two further heteroatoms selected from nitrogen, oxygen and sulfur, and optionally containing one or two double bonds, and optionally substituted with one or more C14-alkyl groups;
R7 is =0, -C(O)CH3,, -S(O)2CH3r -CF3, -C(O)O-R75, -(CH2)13C(O)O-R75 or C1.6-alkyl;
R77 is =0, C1.8-alkyl, cydoalkyl, -C(O)O-R76, -(CH2)14C(0)O-R75, -(CH2)13NR75R76, -OH or amino;
R75 and R78 independently of each other is hydrogen, halogen, -OH, -CF3, or C1$-alkyl optionally substituted with -NH2;

or a pharmaceutically acceptable salt, solvate, or prodrug thereof Embodiment A2. A compound according to embodiment Al. wherein A' is arylene or heteroarylene, optionally substituted with one or more substitutents e, R24, R25, R26, and R27, wherein R23, R24, e, e, and R27 independently of each other are selected from the group consisting of halogen, -C(O)OR2, -CN, -CF3, -OCF3, -NO2, -OR2, -NR2R3, C13-alkyl-Z-, C2$-alkenyl Z-, C24-alkynyl-Z-, cydoalkyl-Z-, heterocydyl-Z-, aryl-Z-, heteroaryl-Z-, aryl-Cl.B-alkylene-Z-, heteroaryl-C1.e-alkylene-Z-, heterocydyl-C14-alkylene-Z-, cycloalkyl-C,. -alkylene-Z-, N(R`R5}C,-0-alkylene-Z-, Re W'-Z-, Re W'-N(R4}Z-, W
N(R4)-Z, and R -W'-C,$-alkylene-Z-, wherein R2, R3, R4, R5, R , Z, and W1 are as defined in embodiment Al.
Embodiment A3. A compound according to embodiment A2, wherein A' is C .,o-arylene or C4.10-heteroarylene, optionally substituted with one or more substitutents R23, R24, e. R26, and R27, wherein R23, R24, R2S, R26, and R27 Independently of each other are selected from the group consisting of halogen, -C(O)OR2, -CN, -CF3. -OCF3, -NO2, -OR2, -NR2R3, Cl,,ralkyl-Z-, C2$-alkenyl-Z-, C2. -alkynyl-Z-, cycloalkyl-Z-, heterocyclyl-Z-, aryl-Z-, heteroaryl-Z-, aryl-C,. -alkylene-Z-, heteroaryl-C14-alkylene-Z-, heterocyclyl-C,$-alkylene-Z-, cycloalkyl-C,.3-alkylene-Z-, N(R4R5}C,4-alkylene-Z-, Re-W'-Z-, R W'-N(R4)-Z-, R -N(R4)-Z, and R -W'-C,-0-alkylene-Z-, wherein R2, R3, R4, R5, R , Z, and W' are as defined in embodiment Al.
Embodiment A4. A compound according to embodiment A3 wherein A' is phenylene optionally substituted with one or more substitutents e, R.
R2, R, and R27, wherein Rea, R24, R25, R2 , and R21 Independently of each other are selected from the group consisting of halogen, -C(O)OR2, -CN, -CF3, -OCF3, -NO2, -OR2, -NR2R3, C,$-alkyl-Z-, C2$-alkenyl-Z-, C2$-alkynyl-Z-, cycloalkyl-Z-, heterocyclyl-Z-, aryl-Z-, heteroaryl-Z-, aryl-C,.6-alkylene-Z-. heteroaryl-C14-alkylene-Z-, heterocyclyI-C14-alkylene-Z-, cydoatkyl-C,.0-alkylene-Z-, N(R4R)C14-alkytene-Z-, R -W'-Z-, R -W'-N(R4)-Z-, R
-N(R4)-Z, and R -W'-C,$-alkylene-Z-, wherein W. R3, W. R5, R , Z. and W' are as defined In embodiment Al.

Embodiment A5. A compound according to embodiment A4 of the formula (Ia) G

L' L2 R' LN 2 Formula (la) G

wherein L', G', L2, L3, R', G2 and e are as defined in embodiment Al.
Embodiment A6. A compound according to embodiment A4 of the formula (Ib) G' L' L2 R' 24 / \L3 N Formula (lb) wherein L', G', L2, L3, R', G2 and R24 are as defined in embodiment Al.

Embodiment AT A compound according to any one of the embodiments Al to A6, wherein R23, R24, R25, R28, and R27 independently of each other are selected from the group consisting of 10 halogen, -C(O)OR2, -CN, -CF3, -OCF3, -NO2, -OR2, -NR2R3, C,. -alkyl-Z-, cycloalkyl-Z-, heterocydyl-Z-, aryl-Z-, or heteroaryl-Z-, N(R4R5)-Cj4-alkylene-Z-, R -W'-Z-, R -W'-N(R4}Z-, R -N(R4)-Z, and R -W'-C,. -alkylene-Z-, wherein R2, R3, R4, R5, R , Z, and W1 are as defined in embodiment Al.
Embodiment A8. A compound according to embodiment A7 wherein 15 R23, R24, R, R28, and R27 independently of each other are selected from the group consisting of halogen, -CN, -CF3, -OR2, -NR2R3, C,$-alkyl-Z-, cycloalkyl-Z-, heterocyclyl-Z-, aryl-Z-, or heteroaryl-Z-, R -W'-Z-, RB W'-N(R4)-Z-, R -N(R4}Z, and R -W'-C,. -alkylene-Z-, wherein 20 R2, R3, R4, R5, R , Z. and W1 are as defined in embodiment Al.
Embodiment A9. a compound according to embodiment A8 wherein R23, R24, R25, R28, and R27 independently of each other are selected from the group consisting of halogen, -OR2, -NR2R3, C1.6-alkyl-Z-, RB-W'-Z-, and Re-W'-C1.6-alkylene-Z-, wherein R2, W. R4, R5, Re, Z, and W' are as defined in embodiment Al.
Embodiment A10. A compound according to embodiment A9 wherein 0, R24, e, e, and R27 independently of each other are selected from the group consisting of F. Cl, Br, and methyl.

Embodiment Al 1. A compound according to any one of the embodiments Al to Al 0, wherein R4, R5, and Re independently of each other are selected from the group consisting of hydrogen, aryl, C1. -alkyl, heteroaryl-C1.B-alkylene-, and aryl-Cl.B-alkylene-.

Embodiment Al 2. A compound according to embodiment All, wherein R4, R5, and Re independently of each other are hydrogen or C1$-alkyl.
Embodiment Al 3. A compound according to embodiment A12, wherein R4, R5, and Re are hydrogen.

Embodiment A14. A compound according to any one of the embodiments Al to A9, wherein R4 and R5 is taken together to form a ring having the formula -(CH2);-Q-(CH2)k-bonded to the nitrogen atom to which R4 and R5 are attached, wherein j and k independently of each other is 1, 2. 3, or 4;
Q is a direct bond, -CH2-, -0-, -S-, -S(02)-, -C(O)-, -C(O)NH-, -NHC(O)-, -NHC(O)NH-, -NHSOZ-, -SO2NH-, -C(O)-0-, -O-C(O)-, -NHSO2NH-, O R9 0 OR9 04 ""R O2~ .N(H)R 9 02`g .N-R9 2~
-N- -N-- -N- -N-ONHR9 0 N-R9 r N -N- or -N-wherein R9 and R10 independently of each other are selected from the group consisting of hydrogen, aryl, C1.e-alkyl, and aryl-Cl.B-alkyl-.
Embodiment Al 5. A compound according to embodiment A14, wherein Q is a direct bond, -CHr, -0-, -S-, -S(02}, -C(O)-, -C(O)NH-, -NHC(O}, -NHC(O)NH-, -NHSOr, -SO2NH-, -C(O)-0-, -0-C(O}, -NHSO2NH-, 0 R9 0\/OR9 O S~Re Oz?, N(H)R9 04'N-R
`~ 21 -N- = -N- -N- -N- -N-O yNHR9 O`\ A -R9 i 9 N- -`N~- or -N-wherein 5 R and R10 independently of each other are hydrogen or Q1.6-alkyl.
Embodiment Al 6. A compound according to embodiment Al 5, wherein Q is a direct bond, -CH2-, -0-, -5-, -S(02)-. -C(O)-, C(O)NH-, -NHC(O)-, -NHC(O)NH-, -NHSOr, -SO2NH-, -C(O}O-, -O-C(O}, -NHSO2NH-, 0 Y H 0YOH OZ(H OZ?'NH2 -N- -N- -N- -N-OYNHZ

-N- , or -N-10 Embodiment A17. A compound according to embodiment A16, wherein Q is a direct bond.
Embodiment Al 8. A compound according to any one of the embodiments Al to Al 7, wherein W1 is a direct bond, -0-, -C(O)-, -NH-, -S-, -SO2-, -C(O)NH-, -NHC(O)-, -N(H)CON(H}, -N(H)SO2, -S02N(H)-, -C(O)-O-, -N(H)SO2N(H)-, or -O-C(O}.

Embodiment Al 9. A compound according to embodiment Al 8, wherein 15 W1 is a direct bond, -0-, -C(O}, -SO2-, -C(O)NH-, -NHC(O)-, -N(H)SO2, -C(O)-O-, or-O-C(O)-.

Embodiment A20. A compound according to embodiment Al 9, wherein W' is a direct bond or -C(O)-0-.

Embodiment A21. A compound according to embodiment A20, wherein W1 is a direct bond.
Embodiment A22. A compound according to embodiment A7, wherein at least one of R23, R24, R2, 0, and R27 is halogen, -C(O)OR2, -CN, -CF3, -OCF3, -NO2, -OR2, -NR2R3, C,.8-alkyl-Z-, cycloalkyl-Z-, heterocyciyl-Z-, aryl-Z-, or heteroaryl-Z-, wherein R2, R3, and Z are as defined in embodiment Al.
Embodiment A23. A compound according to embodiment A22, wherein at least one of R23, R24, R25, R26, and R27 is halogen, -C(O)OR2, -CN, -CF3, -OCF3, -NO2, -OR2, -NR2R3, C,.6-alkyl-Z-, C3.,o-cycloalkyl-Z-, C3.,o-heterocyclyl-Z-, C3_,o-aryl-Z-, or C3.10-heteroaryl-Z-, wherein R2, R3, and Z are as defined in embodiment Al.
Embodiment A24. A compound according to embodiment A23, wherein at least one of R23, R24, R2s,.R26, and R27 is. halogen, -C(O)OR2, -CN, -NO2, -OR2, -NR2R3, C,.6-alkyl Z-, C3.10-cydoalkyl-Z-, C3.,o-heterocyclyl-Z-, C3-lo-aryl-Z-, or C3.,o-heteroaryl Z-, wherein R2, R3, and Z are as defined in embodiment Al.
Embodiment A25. A compound according to embodiment A24, wherein at least one of R, R24, R25, R26, and Rv Is F, Cl, Br, or methyl.
Embodiment A26. A compound according to embodiment A24, wherein at least one of e, R24, Res, R, and R27 is halogen, -C(O)OR2, -CN, -NO2, -OR2, or -NR2R3, wherein R2, R3, and Z are as defined in embodiment Al.

Embodiment A27. A compound according to any one of the embodiments Al to A26, wherein R2 and R3 independently of each other are hydrogen, C1.0-alkyl, aryl-C,$-alkylene-, heteroaryl-C1.3-alkylene-, C,.g-alkyl-arylene-, C,$-alkyl-heteroarylene-, heteroaryl, or aryl.

Embodiment A28. A compound according to embodiment A27, wherein R2 and R3 independently of each other, are hydrogen, C14-alkyl, aryl-C,$-alkylene-or aryl.

Embodiment A29. A compound according to embodiment A28, wherein R2 is hydrogen or C1.6-alkyl.

Embodiment A30. A compound according to embodiment A29, wherein R2 is hydrogen.

Embodiment A31. A compound according to any one of the embodiments Al to A30, wherein R3 is hydrogen or C,$-alkyl.

Embodiment A32. A compound according to embodiment A31, wherein R3 is hydrogen.

Embodiment A33. A compound according to any one of the embodiments Al to A22, wherein R2 and R3, when attached to the same nitrogen atom, together with said nitrogen atom may form a 3 to 8 membered heterocyclic ring optionally containing one or two further heteroatoms selected from nitrogen, oxygen and sulfur, and optionally containing one or two double bonds.

Embodiment A34. A compound according to any one of the embodiments Al to A33, wherein Z is a direct bond, -0-, -NH-, -NHCH2-, -S-, -SO-, -C(O)NH-, -NHC(O)-, -N(H)CON(H)-, -N(CH3)CONH-, -N(H)SOr, -SO2N(H)-, -C(O)-O-, -N(H)SO2N(H)-, or -O-C(0)-.

Embodiment A35. A compound according to embodiment A34, wherein Z is a direct bond, -0-, -S-, -SO2-, -C(O)NH-, -NHC(O)-, -N(H)SO2, -C(O)-0-, -N(H)SO2N(H)-, or -0-C(O}.

Embodiment A36. A compound according to embodiment A35, wherein Z is a direct bond, -NHC(O}, or -NHS(0)2-.

Embodiment A37. A compound according to embodiment A2, wherein A' is 2s R wherein e, R24, 0, and R28, independently of each other, are hydrogen or as defined in embodiment Al.

Embodiment A38. A compound according to embodiment A37, wherein R23, R24, e, and RZ8 independently of each other are selected from the group consisting of halogen, -C(0)OR2, -CN, -CF3, -OCF3, -NO2, -0R2, -NR2R3, C,$-alkyl-Z-, cycloalkyl-Z-, heterocydyl-Z-, aryl-Z-, or heteroaryl-Z-, N(R4Rs)-C1.6-alkylene-Z-, Re-W'-Z-, Re-W'-N(W)-Z-, Re-N(W)-Z-, and R -W'-C,$-alkylene-Z-, wherein R2, R3, R4, R5, R , Z, and W1 are as defined in embodiment Al.
Embodiment A39. A compound according to embodiment A37 or A38, wherein R4, R5, and R independently of each other are selected from the group consisting of hydrogen, aryl, C14-alkyl, heteroaryl-C1.a-alkylene-, and aryl-C,4-alkylene-.
Embodiment A40. A compound according to embodiment A39, wherein R4, R5, and R independently of each other are hydrogen or C14-alkyl.
Embodiment A41. A compound according to embodiment A40, wherein R4, R5, and R are hydrogen.

Embodiment A42. A compound according to embodiment A37 or A38, wherein R4 and R5 is taken together to form a ring having the formula -(CH2)j-Q-(CH2)k-bonded to the nitrogen atom to which R4 and R5 are attached, wherein j and k independently of each other Is 1, 2, 3, or 4;
Q is a direct bond, -CH2-, -0-, -5-, -S(02)-, -C(O)-, -C(O)NH-, -NHC(O)-, -NHC(O)NH-, -NHSO2-, -SO2NH-, -C(O)-O-, -0-C(O)-, -NHSO2NH-, 0yR9 O,OR9 0 /R9 02I .N(H)R9 ON-R9 zI S2~
-N- -N- -N- -N- -N-R1o 0,,NHR9 0YN-R9 R19 -N-. - or -N-wherein R9 and R10 independently of each other are selected from the group consisting of hydrogen, aryl, C14-alkyl, and arylalkyl-.
Embodiment A43. A compound according to embodiment A42, wherein Q is a direct bond, -CH2-, -0-, -S-, -S(02}, -C(O)-, -C(O)NH-, -NHC(O)-, -NHC(O)NH-, -NHSO2-, -SO2NH-, -C(O}O-, -0-C(O), -NHSO2NH-, RI io 9 iR9 02.N(H)R9 OzN,N-R9 -W- -N- -N- -N- --R1o OyNHR9 0YN-R9 R, -N- -N- or -N-wherein R9 and R10 independently of each other are hydrogen or alkyl.
Embodiment A44. A compound according to embodiment A43, wherein Q is a direct bond, -CH2-, -0-, -S-, -S(02) , -C(O), -C(O)NH-, -NHC(O)-, -NHC(O)NH-, -NHSOz-, -SO2NH-, -C(O)-0-, -0-C(O}, -NHSO2NH-, OyH OyOH O2SI OH O2T NH2 -N- I - , -N- -N-III

-N- or -N-Embodiment A45. A compound according to embodiment A44, wherein Q is a direct bond.

Embodiment A46. A compound according to any one of the embodiments A37 to A45, wherein W1 is a direct bond, -0-, -C(O)-, -NH-, -5-, SO2, --C(O)NH-, -NHC(O)-, -N(H)CON(H)-, -N(H)SO2-, -SO2N(H)-, -C(O)-O-, -N(H)SO2N(H)-, or -O-C(O)-.

Embodiment A47. A compound according to embodiment A46 wherein W1 is a direct bond, -0-, -C(O)-, -SO2-, -C(O)NH-, -NHC(O)-, -N(H)SOr, -C(O)-O-, or-O-C(0)-.

Embodiment A48. A compound according to embodiment A47, wherein 10 W' is a direct bond, or-C(O)-O-.

Embodiment A49. A compound according to embodiment A48, wherein W' is a direct bond.

Embodiment A50. A compound according to embodiment A37, wherein at least one of R23, R24, R25, and R2 is halogen, -C(O)OR2, -CN, -CF3, -OCF3, -NO2, 15 -OR2, -NR2R3, C14-alkyl-Z-, cycloalkyl-Z-, heterocydyl-Z-, aryl-Z-, or heteroaryl-Z-, wherein R2, R3, and Z are as defined in embodiment A37.
Embodiment A51. A compound according to embodiment A50, wherein at least one of R23, R24, R25, and R28 is halogen, -C(O)OR2, -CN, -CF3, -OCF3, -NO2, 20 -OR2, -NR2R3, C1$-alkyl-Z-, C310-cydoalkyl-Z-, C3_1o-heterocydyl-Z-, r,3.10-aryl-Z-, or C3.10-heteroaryl-Z-, wherein W. R3, and Z are as defined in embodiment A37.
Embodiment A52. A compound according to embodiment A51, wherein at least one of R23, R24, R25, and R25 is halogen, -C(O)OR2, -CN, -NO2, -OR2, 25 -NR2R3, C1$-alkyl-Z-, C31o-cycloalkyl-Z-, C3.10-heterocyclyi-Z-, C3.10-aryl-Z-, or C3.10-heteroaryl-Z-, wherein R2, R3, and Z are as defined in embodiment A37.

Embodiment A53. A compound according to any one of the embodiments A37 to A52, wherein Z is a direct bond, -0-, -NH-, -NHCHr, -S-, -SOr, -C(O)NH-1 -NHC(O)-, -N(H)CON(H)-, -N(CH3)CON(H)-, -N(H)SO2-, -S02N(H)-, -C(O)-O-,. N(H)SO2N(H)-, or-O-C(O)-.

Embodiment A54. A compound according to embodiment A53, wherein Z is a direct bond, -0-, -S-, -SO2-, -C(O)NH-, -NHC(O)-, -N(H)SOr, -C(O)-O-, -N(H)SO2N(H)-, or -O-C(0)-.

Embodiment A55. A compound according to embodiment A54, wherein Z is a direct bond, -NHC(O)-, or -NHS(O)2.

Embodiment A56. A compound according to embodiment A52, wherein at least one of R23, R24, R25, and R2 is halogen, -C(O)OR2, -CN, -NO2, -0R2, NR2R9, or C1.B-alkyl, wherein R2, and R3 are as defined in embodiment A37.

Embodiment A57. A compound according to any one of the embodiments A37 to A56, wherein R2 and R3 independently of each other are hydrogen, C1.6-alkyl, aryl-C,$-alkylene-, heteroaryl-C14-alkylene-, C,$-alkyl-arylene-, C1$-alkyl-heteroarylene-, heteroaryl, or aryl.

Embodiment A58. A compound according to embodiment A57, wherein R2 and R3 independently of each other, are hydrogen, C1.e-alkyl, aryl-C14-alkylene-or aryl.

Embodiment A59. A compound according to embodiment A58, wherein R2 is hydrogen or C14-alkyl.

Embodiment A60. A compound according to embodiment A59, wherein R2 is hydrogen.

Embodiment A61. A compound according to any one of the embodiments A37 to A60, wherein R3 is hydrogen or C,$-alkyl.

Embodiment A62. A compound according to embodiment A61, wherein R3 is hydrogen.

Embodiment A63. A compound according to any one of the embodiments A37 to A50, wherein R2 and R3, when attached to the same nitrogen atom, together with said nitrogen atom may form a 3 to 8 membered heterocyclic ring optionally containing one or two further heteroatoms selected from nitrogen, oxygen and sulfur, and optionally containing one or two double bonds.

Embodiment A64. A compound according to any one of the embodiments A37 to A55, wherein at least one of R23, R24, R, and e are hydrogen.
Embodiment A65. A compound according to embodiment A64, wherein at least two of R23, R24, e, and RZ8 are hydrogen.

Embodiment A66. A compound according to embodiment A65, wherein RZ3 and e are hydrogen.

Embodiment A67. A compound according to embodiment A65 or embodiment A66, wherein at least three of R23, R24, R25, and R28 are hydrogen.

Embodiment A68. A compound according to any one of the embodiments A37 to A67, wherein R24 or R25 is halogen.

69. A compound according to embodiment A68, wherein R24 or e is fluoro.
Embodiment A70. A compound according to any one of the embodiments A37 to A67, wherein R24 or e is C1.g-alkyl.

Embodiment A71. A compound according to embodiment A68, wherein R24 or e is methyl.
Embodiment A72. A compound according to any one of the embodiments A37 to A67, wherein R24 is hydrogen.

Embodiment A73. A compound according to any one of the embodiments A37 to A72, wherein R25 is hydrogen.

Embodiment A74. A compound according to embodiment A37, wherein R2, R24, e, and e are hydrogen.

Embodiment A75. A compound according to any one of the embodiments Al to A74, wherein L' is a bond, -D-alkylene-E-, -0-, -S-, -S(O)-, -S(O)2-, -C(O)-, -N(R"}, or -C(=N-OR12), wherein D. E, R" and R72 are as defined in embodiment Al.
Embodiment A76. A compound according to embodiment A75, wherein L' is a bond, -D-alkylene-E-, -0-, -C(O)-, -N(R")-, or -C(=N-OR12)-, wherein D, E, R" and R12 are as defined in embodiment Al.

Embodiment A77. A compound according to embodiment A75, wherein L' is -0-.

Embodiment A78. A compound according to embodiment A75, wherein L' is -S-.

Embodiment A79. A compound according to embodiment A75, wherein L' is a bond.

80. A compound according to embodiment A75, wherein L' is -C(O)-.

Embodiment A81. A compound according to any one of the embodiments Al to A76, wherein D is a direct bond or -0-;
E is a direct bond or -0-; and R" and R'2 are as defined in embodiment Al.

Embodiment A82. A compound according to embodiment A81, wherein D is a direct bond.

Embodiment A83. A compound according to embodiment A81, wherein D is -0-.

Embodiment A84. A compound according to any one of the embodiments A81 to A83, wherein E is a direct bond.

Embodiment A85. A compound according to any one of the embodiments A81 to A83, wherein E is -0-.

Embodiment A86. A compound according to any one of the embodiments Al to A85, wherein R" is selected from hydrogen, C1$-alkyl, aryl, carbamoyl, aryl-C1$-alkylene-, C1.6-alkyl-NH-C(O)-, aryl-C1 -alkylene-NH-C(O)-, Ci.e-alkyl-S02-, aryl-C,.e-alkylene-SO2-, aryl-SOr, SO2-, C1$-alkyl-C(O)-, aryl-C1$-alkylene-C(O)-, N(R13)(R74)-C14-alkylene-Y-, and R15-W2-C14-alkylene-Y-, wherein Y and W2 independently of each other are a direct bond, -CH2-, -SO2-, -N(H)CO-, -N(H)SOr, or -0-C(O)-;
R 13 and R14 independently of each other are selected from hydrogen, aryl, C1$-alkyl, or aryl-C1$-alkylene-;
or R13 and R14 may be taken together to form a ring having the formula -(CH2)6-X-(CH2)p- bonded to the nitrogen atom to which R13 and R14 are attached, wherein o and p are independently of each other are 1, 2, 3, or 4; and X is a direct bond, -CH2-, -0-, -S-, -S(02)-, -C(O)-, -CON(H)-, -NHC(O)-, -NHCON(H)-, -NHSOr. -S02N(H)-. -C(O)-O-, -0-C(O) -, -NHSO2NH-, 0YR16 0 /OR16 0 ~/R

-N- -N- -N-N(H)R76 N-R
025" 025"
-N- -N-OyNHR16 0YN-Rt6 RI'6 -N- -N- or wherein R18 and R" are selected from hydrogen, aryl, heteroaryl, C1.6-alkyl, C1$-alkoxy, aryl-C14-alkylene-, 5 heteroaryl-C,.6-alkylene-, C1.6-alkyl-arylene-, C1.6-alkyl-heteroarylene-, C1$-alkoxy-arylene-, C1.6-alkoxy-heteroarylene-, heteroarylaryl-C1$-alkoxy-, or aryl-C1.6-alkoxy-; and R15 is selected from the group consisting of aryl, heteroaryl, cycloalkyl, heterocyclyl, 10 C1-6-alkyl, or aryl-C1.6-alkylene-.

Embodiment A87. A compound according to embodiment A86, wherein R" is selected from hydrogen, C14-alkyl, aryl, carbamoyl, aryl-C1$-alkylene-, C1$-alkyl-NH-C(0)-, aryl-C1$-alkylene-NH-C(O)-, C14-alkyl-SO2-, aryl-Cl.6-alkylene-S02-, aryl-S02-, 502-, C1.g-alkyl-C(O)-, aryl-C,4-alkylene-C(O}, 15 N(Rt3)(R14)-C1.6-alkylene-Y-, and R15-W2-C14-alkylene-Y-, wherein Y and W2 independently of each other are a direct bond, -CH2-, -SO2-, -N(H)CO-, -N(H)SO2-, or -O-C(0)-;
R13 and R14 independently of each other are selected from hydrogen, aryl, C1.6-alkyl, or aryl-Cl.6-alkylene-;
20 or R13 and R 14 may be taken together to form a ring having the formula -(CH2)0-X-(CH2)P bonded to the nitrogen atom to which R13 and R14 are attached, wherein o and p are independently of each other are 1, 2, 3, or 4; and X is a direct bond, -CH2-, -0-, -S-, -S(02) , -C(O) -, -CON(H)-, -NHC(O)-, -NHCON(H~, -NHSOZ-, -S02N(H) , -C(O}O-, -O-C(O)-, -NHSO2NH-, ~/R1e OyR1e OyOR18 O z -N- -N- -N-Rt7 0 'N(H)R1e O S'N_R16 2~ z~
-N- -N.-OyNHR18 0` /N-R1e r N- -N- or -N-wherein We and R" are hydrogen; and R15 is selected from the group consisting of aryl, heteroaryl, cydoalkyl, heterocyclyl, C1$-alkyl. or aryl-C,.B-alkylene-.

Embodiment A88. A compound according to embodiment A87, wherein R" is selected from hydrogen, C1.e-alkyl, aryl, carbamoyl, aryl-Cl.6-alkylene-, C1.e-alkyl-NH-C(O)-, aryl-C1$-alkylene-NH-C(O)-, C1.$-alkyl-SO2, aryl-Cl.a-alkylene-SOr, aryl-SOr, SO2-, C,$-alkyl-C(0)-, aryl-C1.6-alkylene-C(O)-, N(R13)(R14)C1$-alkylene-Y , and R15-W2-C,.e-alkylene-Y , wherein Y and W2 independently of each other are a direct bond, -CHI-, -SO2-, -N(H)CO-, -N(H)SO2-, or -O-C(O)-;
R13 and R" independently of each other are selected from hydrogen, aryl, C1.6-alkyl, or aryl-C1$-alkylene-;
or R13 and R" may be taken together to form a ring having the formula -(CH2)o X-(CHI)P- bonded to the nitrogen atom to which R13 and R" are attached, wherein o and p are independently of each other are 1, 2, 3, or 4;
X is a direct bond; and R15 is selected from the group consisting of aryl, heteroaryl, cycloalkyl, heterocycyl, C1$-alkyl, or aryl-C1$-alkylene-.

Embodiment A89. A compound according to embodiment A88, wherein R" is selected from hydrogen, C18-alkyl, aryl, carbamoyl, aryl-C,.6-alkylene-.
C1$-alkyl-NH-C(O)-, aryl-C1$-alkylene-NH-C(O)-, C14-alkyl-SO2-, aryl-C1.6-alkylene-SO2-, aryl-SOZ-, SO2-, C14-alkyl-C(Oy, aryl-C,$-alkylene-C(0)-, N(R13)(R14)-C14-alkylene-Y-, and R15-W2-C14-alkylene-Y-, wherein Y and W2 Independently of each other are a direct bond, -CH2-, -SO2-, -N(H)CO-, -N(H)SOZ-, or -O-C(O)-;
R 13 and R" independently of each other are selected from hydrogen, aryl, C1$-alkyl, or aryl-C1.g-alkylene-; and R15 is selected from the group consisting of aryl, heteroaryl, cycloalkyl, heterocyclyl, C1$-alkyl, or aryl-C1.8-alkylene-.

Embodiment A90. A compound according to embodiment A89, wherein R" is selected from hydrogen, C1$-alkyl, aryl, carbamoyl, aryl-Cl.B-alkylene-, C1.8-alkyl-NH-C(O)-, aryl-C1$-alkylene-NH-C(O)-, C1.8-alkyl-SO2-, aryl-C1.8-alkylene-SOz-, aryl-SOz=, SO2-, C,4-alkyl-C(O)-, aryl-C14-alkylene-C(O)-, N(Rt3)(R14)-C1.e-alkylene-Y , and R15-W2 C1.8-alkylene-Y , wherein Y and W2 independently of each other are a direct bond, -CH2-, -SOz-, -N(H)CO-, -N(H)SOr, or -O-C(O)-;
R13 and R14 are hydrogen; and R15 is selected from the group consisting of aryl, heteroaryl, cycloalkyl, heterocyclyl, C1.8--alkyl, or aryl-C14-alkylene-.

Embodiment A91. A compound according to embodiment A90, wherein R11 is selected from hydrogen, C1$-alkyl, aryl, carbamoyl, aryl-C14-alkylene-, C1.6-alkyl-NH-C(0)-, aryl-C1.6-alkylene-NH-C(O)-, C14-alkyl-SO2-, aryl-C14-alkylene-SO2-, aryl-SOZ-, SO2-, C14-alkyl-C(O)-, aryl-C1$-alkylene-C(O)-, N(R13)(R14)-C14-alkylene-Y-, and R1S-W2-C1$-alkylene-Y-, wherein Y is a direct bond;
W2 is a direct bond, -CH2-, -SO2-, -N(H)CO-, -N(H)SOz-, or -O-C(O)-;
R13 and R14 are hydrogen; and R15 is selected from the group consisting of aryl, heteroaryl, cycloalkyl, heterocyclyl, C1.8-alkyl, or aryl-C,$-alkylene-.

Embodiment A92. A compound according to embodiment A90, wherein R" is selected from hydrogen, C14-alkyl, aryl, carbamoyl, aryl-C1$-alkylene-, C,$-alkyl-NH-C(O)-, aryl-C14-alkylene-NH-C(O)-, C,.e-alkyl-SOr, aryl-Cl.B-alkylene-SOr, aryl-SO2, SOr, C14-alkyl-C(O)-, aryl-C14-alkylene-C(O)-, N(R13)(R14)C,4-alkylene-Y-, and R5-W2-C,4-alkylene-Y , wherein Y is a direct bond, -CH2-, -SO2-, -N(H)CO-, -N(H)SOr, or -O-C(O)-;
W2 is a direct bond;
R13 and R14 are hydrogen; and R15 is selected from the group consisting of aryl, heteroaryl, cycloalkyl, heterocydyl, C1.s-alkyl, or aryl-C1.6-alkylene-.

Embodiment A93. A compound according to any one of the embodiments A90 to A92, wherein R" is selected from hydrogen, C14-alkyl, aryl, carbamoyl, aryl-C1 s-alkylene-, C,4-alkyl-NH-C(O)-, aryl-C,.s-alkylene-NH-C(O)-, C,.e-alkyl-SOr, aryl-C14-alkylene-SO2, aryl-SO2-, SOr, C,a-alkyl-C(O)-, aryl-C14-alkylene-C(O)-, NH2C14-alkylene-, and R15-C1.6-alkylene-, wherein R'5 is selected from the group consisting of aryl, heteroaryl, cycloalkyl, heterocyclyl, C1$-alkyl, or aryl-C14-alkylene-.

Embodiment A94. A compound according to embodiment A93, wherein R" is selected from hydrogen, C1.g-alkyl, aryl, carbamoyl, aryl-C1$-alkylene-, C,$-alkyl-NH-C(O)-, aryl-C1$-alkylene-NH-C(O)-, C1.6-alkyl-SOr, aryl-C,$-alkylene-SO2, aryl-SO2-, SO2-, C,--alkyl-C(O)-, aryl-C,.e-alkylene-C(O)-, and NHz-C1.3-alkylene-.

Embodiment A95. A compound according to embodiment A94, wherein R" is hydrogen or C1. -alkyl.

Embodiment A96. A compound according to embodiment A95, wherein R" is hydrogen.

Embodiment A97. A compound according to any one of the embodiments Al to A96, wherein R12 is hydrogen or C14-alkyl.

Embodiment A98. A compound according to embodiment A97, wherein R12 is hydrogen.

Embodiment A99. A compound according to any one of the embodiments Al to A98, wherein G' Is C14-alkyl, C24-alkenyl, Cwalkynyl, cydoalkyl or heterocydyl, optionally substituted with one or more substituents selected from the group consisting of -CN, -CF3, -OCF3, -OR'8, -NR18R19, C~.,o-cydoalkyl and C14-alkyl, wherein R18 and R19 are as defined In embodiment Al.

Embodiment A100. A compound according to embodiment A99, wherein G1 is C1$-alkyl, CZ--alkenyl, C2$-alkynyl, cydoalkyl or heterocydyl, optionally.
substituted with one or more substituents selected from the group consisting of -CN, -CF3, -OCF3, -OR18, -NR18R19 and C14-alkyl, wherein RT8 and Rt9 are as defined In embodiment Al.

Embodiment A101. A compound according to embodiment A99, wherein G1 is C14-alkyl, C2$-alkenyl, C2.a-alkynyl, C3.1o-cycloalkyl or C3~.1o-heterocydyl, optionally substituted with one or more substituents selected from the group consisting of -CN, -CF3, -OCF3, -OR18, -NRt8R19, C3.10-cydoalkyl and C1.g-alkyl, wherein R18 and R19 are as defined In embodiment Al.

Embodiment Al 02. A compound according to embodiment Al 00 or embodiment Al 01, wherein G' is C1$-alkyl, C24-alkenyl, C24-alkynyl, C3.10-cycloalkyl or C3.10-heterocyclyl, optionally substituted with one or more substituents selected from the group consisting of -CN, -CF3, -OCF3, -OR18, -NOR"' and C18-alkyl, wherein R18 and R19 are as defined in embodiment Al.
Embodiment Al 03. A compound according to any one of the embodiments A99 to Al 02, wherein G' is selected from the group consisting of methyl, ethyl, propyl, butyl, isopropyl, isobutyl, sec-butyl, tent butyl, 3-pentyl, 2-pentyl, 3-methyl-butyl, 2-propenyl, cydopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, oxetanyl, tetrahydrofuranyl, tetrahydropyranyl, azetidyl, pyrrolidyl, piperidyl, hexahydroazepinyl, thiolanyl, tetrahydrothiopyranyl, thiepanyl, 1,4-oxathianyl, 1,3-dioxolanyl, 1,2-dithiolanyl, 1,3-dithiolanyl, hexahydro-pyridazinyl, imidazolidyl, 1,3-5 dioxanyl, morpholinyl, 1,3-dithianyl, 1,4-dioxanyl, 1,4-dithianyl, or thiomorpholinyl.
Embodiment A104. A compound according to embodiment A103 wherein G' is selected from the group consisting of methyl, ethyl, propyl, butyl, isopropyl, isobutyl, sec-butyl, ter- butyl, cyclopropyl, cyclobutyl, cyclopentyl, cydohexyl, cycloheptyl, tetrahydrofuranyl, tetrahydropyranyl, pyrrolidyl, piperidyl, 10 hexahydroazepinyl, thiolanyl, tetrahydrothiopyranyl, or thiepanyl .
Embodiment Al 05. A compound according to embodiment Al 04 wherein G1 is selected from the group consisting of methyl, ethyl, propyl, butyl, isopropyl, isobutyl, cydopentyl, cyclohexyl, tetrahydrofuranyl, tetrahydropyranyl, piperidyl, or hexahydroazepinyl.
15 Embodiment Al 06. A compound according to embodiment A105 wherein G' is selected from the group consisting of isobutyl, cyclopentyl, and piperidyl.
Embodiment Al 07. A compound according to embodiment A105 wherein G' is isobutyl.
Embodiment A108. A compound according to embodiment A105 wherein 20 G' is cyclopentyl.
Embodiment A109. A compound according to embodiment A105 wherein G' is piperidyl.

Embodiment Al 10. A compound according to any one of the embodiments A99 to Al 02, wherein 25 R18 and R19, independently of each other, are hydrogen, C14-alkyl, heteroaryl-C14-alkylene-, aryl-C1$-alkylene-, C1$-alkyl-arylene-, C1.6-alkyl-heteroarylene-, heteroaryl, or aryl.

Embodiment Al 11. A compound according to embodiment Al 10, wherein We and R19, independently of each other, are hydrogen, C,$-alkyl, 30 C3.,o-heteroaryl-C,$-alkylene-, C3.10-aryl-C1.6-alkylene-, C,.g-alkyl-C3_,0-arylene-, C1.8-alkyl-C3.10-heteroarylene-, C3.,o-heteroaryl, or C3_70-aryl.

Embodiment Al 12. A compound according to embodiment Al 11, wherein R18 and R19, independently of each other, are hydrogen or C,$-alkyl.
Embodiment Al 13. A compound according to embodiment Al 12, wherein We is hydrogen.

Embodiment Al 14. A compound according to embodiment Al 12 or Al 13, wherein R'9 Is hydrogen.

Embodiment A115. A compound according to embodiment A100 or embodiment A102, wherein Rf a and R19, when attached to the same nitrogen atom, together with the said nitrogen atom forms a 3 to 8 membered heterocyclic ring optionally containing one or two further heteroatoms selected from nitrogen, oxygen and sulfur, and optionally containing one or two double bonds.

.Embodiment Al 16. A compound according to any one of the embodiments Al to A98, wherein G' is alkyl or cycloalkyl, optionally substituted with one or more substituents selected from the group consisting of -CN, -CF3, -OCF3, -OR78, -NR18R19 and C14-alkyl, or G' is aryl optionally substituted with one or more substituents R40, R41, and R42, wherein R18, R19, R40, R41, and R42 are as defined in embodiment Al.
Embodiment Al 17. A compound according to embodiment Al 16, wherein G' is C1.6-alkyl or C3.10-cycloalkyl, optionally substituted with one or more substituents selected from the group consisting of -CN, -CF3, -OCF3, -OR'8, NR18R18 and C1.6-alkyl, or G' is 03.10-aryl optionally substituted with one or more substituer R40, R41, and R42, wherein R18, R'9, R40, R41, and R42 are as defined in embodiment Al.
Embodiment Al 18. A compound according to embodiment Al 17, wherein G' Is C,4-alkyl or C3.10-cycloalkyl, optionally substituted with one or more substituents selected from the group consisting of -CN, -CF3, -OCF3, -OR1e, -NRt8R19 and C,$-alkyl, or G' is phenyl optionally substituted with one or more substituents R40, R41, and R42, wherein R18, R'9, R40, R41, and R42 are as defined in embodiment Al.

Embodiment Al 19. A compound according to embodiment Al 16, Al 17, or Al 18, wherein R18 and R19, independently of each other, are hydrogen, C14-alkyl, heteroaryl-C1$-alkylene-, aryl-C1$-alkylene-, C1-e-alkyl-arylene-, C1$-alkyl-heteroarylene-, heteroaryl, or aryl.

Embodiment A120. A compound according to embodiment A119, wherein R18 and R19, independently of each other, are hydrogen, C1$-alkyl, C3.t0-heteroaryl-Cl.4-alkylene-, C3.10-aryl-C1$-alkylene-, C1.6-alkyl-C3.10-arylene-, C1.8-alkyl-C3.10-heteroarylene-, C310-heteroaryl, or C3.10-aryl.

Embodiment Al 21. A compound according to embodiment Al 20, wherein R18 and R19, independently of each other, are hydrogen or C1--alkyl.
Embodiment Al 22. A compound according to embodiment Al 21, wherein R18 Is hydrogen.

Embodiment A123. A compound according to embodiment A121 or A122, wherein R19 is hydrogen.

Embodiment Al 24. A compound according to embodiment Al 16 or embodiment Al 17, wherein R18 and R19, when attached to the same nitrogen atom, together with the said nitrogen atom forms a 3 to 8 membered heterocyclic ring optionally containing one or two further heteroatoms selected from nitrogen, oxygen and sulfur, and optionally containing one or two double bonds.

Embodiment A125. A compound according to any one of the embodiments A116 to A124, wherein R40, R41, and R42 independently of each other are halogen, -CN, -NO2, C1$-alkyl, -CHF2, -CF3, -OR54, -NR4R55, -SR54, -NR54S(O)2R55, -S(O)2NR54R55, -S(O)NR54R55, -S(O)R54, -S(O)2R54, -C(O)NR54R55, -OC(O)NR54R55, -NR54C(O)R55, -CH2C(O)NR4R55, -CH2C(O)OR54, -OCH2C(O)NR54R55, -CH2OR14, -CH2NR54R55, and -C(O)OR54; or C24-alkenyl and C2.s-alkynyl, which may optionally be substituted with one or more substituents selected from -CN, -CF3, -OCF3, -OR54, -NR54e and C1.6-alkyl, wherein RM and e independently of each other are hydrogen, C1$-alkyl, C,.8-alkyl-arylene-, C,$-alkyl-heteroarylene-, aryl-C14-alkylene-, heteroaryl-C1 -alkylene-, heteroaryl, or aryl;
or R54 and e, when attached to the same nitrogen atom, together with the said nitrogen atom may form a 3 to 8 membered heterocyclic ring optionally, containing one or two further heteroatoms selected from nitrogen, oxygen and sulfur, and optionally containing one or two double bonds.
Embodiment A126. A compound according to embodiment A125, wherein R40, R41, and R42 independently of each other are halogen, -CN, C,$-alkyl, -CF3, -OR54, -Nee, SR04, -NeS(O)2R$, -S(O)RM, -S(O)2RM, -CH2C(O)ORM, -CH2Oe, -CH2NeR66, and -C(O)OR54;
wherein e and R55 independently of each other are hydrogen, C1.8-alkyl, C,$-alkyl-arylene-, C1.6-alkyl-heteroarylene-, aryl-C,.a-alkylene-, heteroaryi-C,.g-alkylene-, heteroaryl, or aryl;
or Rs` and R50, when attached to the same nitrogen atom, together with the said nitrogen atom may form a 3 to 8 membered heterocyclic ring optionally containing one or two further heteroatorns selected from nitrogen, oxygen and sulfur, and optionally containing one or two double bonds.
Embodiment Al 27. A compound according to embodiment Al 26 wherein R40, R", and R42 independently of each other are halogen, or -OR54 wherein RM is hydrogen, C14-alkyl, C14-alkyl-arylene-, C14-alkyl-heteroarylene-, aryl-C,4-alkylene-, heteroaryl-C1$-alkylene-, heteroaryl, or aryl.
Embodiment Al 28. A compound according to embodiment Al 26, wherein e and W5 independently of each other are hydrogen, or C,$-alkyl, C,.g-alkyl-C3_10-arylene-, C14-alkyl-C3.10-heteroarylene-, 03.10-aryl-C,$-alkylene-, C3_10-heteroaryl-C,4-alkylene-, C3.10-heteroaryl, or C3.10-aryl.

Embodiment A129. A compound according to embodiment A128, wherein Rs4 and e independently of each other are hydrogen or C1.g-alkyl.
Embodiment A130. A compound according to embodiment A129, wherein R54 is hydrogen.

Embodiment Al 31. A compound according to embodiment A129 or embodiment A130, wherein . e is hydrogen.
Embodiment A132. A compound according to embodiment A127 wherein e is methyl.

Embodiment A133. A compound according to any one of the embodiments Al to A98, wherein G' is aryl or heteroaryl, optionally substituted with one or more substituents R40, R41, and R42, wherein R40, R41, and R42 are as defined in embodiment Al.

Embodiment Al 34. A compound according to embodiment Al 33, wherein G' is C3.10-aryl or C3.10-heteroaryl, optionally substituted with one or more substituents R40, R41, and R42, wherein R40, R41, and R42 are as defined in embodiment Al.
Embodiment Al 35. A compound according to embodiment Al 33, wherein G' is aryl, optionally substituted with one or more substituents R40, R41, and R42, wherein R40, R41, and R42 are as defined in embodiment Al.
Embodiment Al36. A compound according to embodiment A135, wherein G' is C3_,0-aryl, optionally substituted with one or more substituents R40, R41, and R42, wherein R40, R41, and R42 are as defined in embodiment Al.
Embodiment Al 37. A compound according to embodiment Al 36, wherein G' is phenyl, optionally substituted with one or more substituents R40, R41, and R42, wherein R40, R41, and R42 are as defined in embodiment Al.

Embodiment A138. A compound according to any one of the embodiments A133 to A137, wherein R40, R41, and R42 independently of each other are halogen, -CN, -NO2, C1.0-alkyl, -CHF2, -CF3i -0R54, -NR4R5S, -SR54, -NR54S(0)2R55, S(O)2NR54R55, -S(O)NR54R55, -S(O)R54, -S(O)2R54, -C(O)NR54R56, -OC(O)NR54R55.
-NR54C(O)R55, -CH2C(O)NR64R55, _CH2C(O)OR54, -OCH2C(O)NR54R55, -CH2OR54, CH2NR54R55, and -C(O)OR54; or C2.g-alkenyl and C2-0-alkynyl, which may optionally be substituted with one or more substituents selected from -CN, -CF3, -OCF3, -OR54, -NR54R65 and C1;6-alkyl, wherein R54 and R55 independently of each other are hydrogen, C1.g-alkyl, C14-alkyl-arylene-, C1.g-alkyl-heteroarylene=, aryl-C1.g-alkylene-, heteroaryl-C1.s-alkylene-, heteroaryl, or aryl;
or e and R55, when attached to the same nitrogen atom, together with the said nitrogen atom may form a 3 to 8 membered heterocyclic ring optionally containing one or two further heteroatoms selected from nitrogen, oxygen and sulfur, and optionally containing one or two double bonds.
Embodiment A139. A compound according to embodiment A138, wherein R40, R41, and R42 independently of each other are halogen, -CN, C1$-alkyl, -CF3, -0R54, -NR54R55, -SR54, -NRMS(O)2R55, -S(O)R54, -S(O)2R54, -CH2C(O)OR54, -CH2OR54, -CH2NR54R55, and -C(O)OR54;
wherein e and e independently of each other are hydrogen, C14-alkyl, C14-alkyl-arylene-, C14-alkyl-heteroarylene-, aryl-C14-alkylene-, heteroaryi-C1.6-alkylene-, heteroaryl, or aryl;
or R54 and e, when attached to the same nitrogen atom, together with the said nitrogen atom may form a 3 to 8 membered heterocyclic ring optionally containing one or two further heteroatoms selected from nitrogen, oxygen and sulfur, and optionally containing one or two double bonds.
Embodiment A140. A compound according to embodiment A139 wherein R40, R41, and R42 independently of each other are halogen, or -ORS' wherein R54 is hydrogen, C1$-alkyl, C1.6-alkyl-arylene-, C14-alkyl-heteroarylene-, aryl-C14-alkylene-, heteroaryl-C1$-alkylene-, heteroaryl, or aryl.

Embodiment A141. A compound according to any one of the embodiments A138 to A139, wherein R54 and e independently of each other are hydrogen, or C1$-alkyl, C1.6-alkyl-C3.10-arylene-, C1.g-alkyl-C3_10-heteroarylene-, C3.10-aryl-Cl-6-alkylene-, C3.10-heteroaryl-Cl--alkylene-, C3.10-heteroaryl, or C310-aryl.

Embodiment A142. A compound according to embodiment A141, wherein R54 and e independently of each other are hydrogen or C,4-alkyl.
Embodiment A143. A compound according to embodiment A142, wherein R54 Is hydrogen.

Embodiment A144. A compound according to embodiment A142 or embodiment A143, wherein R55 is hydrogen.
Embodiment A145. A compound according to embodiment A140 wherein R54 is methyl.

Embodiment A146. A compound according to embodiment Al 35, wherein G' is R Re wherein R56, R57, RS , R, and R80, independently of each other, are hydrogen or halogen, -CN, -NO2, C1.8-alkyl, -CHF2, -CF3r -OCF3, -OCHF2, -OCH2CF3, -OCF2CHF2, -S(0)2CF3, -SCF3, -OR8', -NR6'R 2, -SR 1, -NR 1S(O)2R82, -S(O)2NR 'R 2, -S(O)NR61R62, -S(O)R6', -S(O)2R6', C(O)NR61R82, -OC(O)NR 1R62, -NR61C(O)R62, -CH2C(O)NR61R62, -CH2C(O)OR61, -OCH2C(O)NR81R62, -CH20R61, -CH2NR 1R62, -OC(O)R81, -C(O)RB7 and -C(O)OR 6';
or C2.6-alkenyl and C2$-alkynyl, which may optionally be substituted with one or more substituents selected from -CN, -CF3, -OCF3, -OR81, -NR 'R62 and C1. -alkyl;
C3.1o-cycloalkyl, C"-cycloalkenyl, heterocyclyl, C3.10-cycloalkyl-C1.6-alkylene-, C3-10-cyclo-alkyl-Cla-alkoxy-, C3.10-cycloalkyloxy, C3.10-cydoalkyl-C1$-alkylthio-, C3.10-cycloalkylthio, C3_10-cydoalkyl-C2.6-alkenylene-, C3.10-cydoalkyl-C2.8-alkynylene-, C,,e-cycloalke-nyl-C1 -alkylene-, C¾6-cydoalkenyl-C2$-alkenylene-, C44-cydoalkenyl-C2$-alkynylene-, heterocyclyl-C14-alkylene-, heterocydyl-C2$-alkenylene-, heterocyclyl-C2.6-alkynylene-; or aryl, aryloxy, aryloxycarbonyl, aroyl, aryl-Cl.6-alkoxy-, aryl-C1$-alkylene-, aryl-C2.8-alkenylene-, aryl-C2.6-alkynylene-, heteroaryl, heteroaryl-C1$-alkylene-, heteroaryl-C2_6-alkenylene- and heteroaryl-C24-alkynylene-, of which the aryl and heteroaryl moieties optionally may be substituted with one or more substituents selected from halogen, C(O)OR81, -CN, -CF3, -OCF3, -NO2, -ORG7, -NR01R62 or C14-alkyl, wherein R61 and R62 independently of each other are hydrogen, C1.6-alkyl, C14-alkyl-arylene-, C1.6-alkyl-heteroarylene-, aryl-Cl6-alkylene-, heteroaryl-C1$-alkylene-, heteroaryl, or aryl;
or R81 and e, when attached to the same nitrogen atom, together with the said nitrogen atom may form a 3 to 8 membered heterocyclic ring optionally containing one or two further heteroatoms selected from nitrogen, oxygen and sulfur, and optionally containing one or two double bonds.

Embodiment A147. A compound according to embodiment A146, wherein e, R57, R58, R59, and R80 independently of each other are halogen, -CN, -NO2, C1$-alkyl, -CHF2, -CF3, -OR t, -NR81R62, -SR 1, -NR61S(O)2R82, -S(O)2NR 1862, -S(O)NR6'R62, -S(O)W', -S(O)2R61, -C(O)NR 1862, -OC(O)NR6'R62, NR81C(O)R62, -CH2C(O)NR 'R62, -CH2C(O)OR61, -OCH2C(O)NR61R 2, -CH2OR61, -CH2NR61RB2, and -C(O)OR81; or C2.6-alkenyl and C2.s-alkynyl, which may optionally be substituted with one or more substituents selected from -CN, -CF3, -OCF3, -OR81, -NR61R82 and C1$-alkyl, wherein R61 and e independently of each other are hydrogen, C1$-alkyl, C1.6-alkyl-arylene-, C1$-alkyl-heteroarylene-, aryl-C1$-alkylene-, heteroaryi-Cl.6-alkylene-, heteroaryl, or aryl;

or R81 and R82, when attached to the same nitrogen atom, together with the said nitrogen atom may form a 3 to 8 membered heterocyclic ring optionally containing one or two further heteroatoms selected from nitrogen, oxygen and sulfur, and optionally containing one or two double bonds.
Embodiment A148. A compound according to embodiment A146 or embodiment A147, wherein R58 or R57 is -OR87.

Embodiment A149. A compound according to embodiment A148 wherein R 1-is methyl.
Embodiment Al 50. A compound according to embodiment Al 47, wherein R81 and R62 independently of each other are hydrogen, or C1.6-alkyl, C1$-alkyl-C3.10-arylene-, C1.8-alkyl-C3.10-heteroarylene-, C3_10-aryl-C1$-alkylene-, C3.10-heteroaryl-C1.6-alkylene-, C3.10-heteroaryl, or C310-aryl.

Embodiment All 51. A compound according to embodiment All 50, wherein Ret and R 62 independently of each other are hydrogen or C1.6-alkyl.
Embodiment All 52. A compound according to embodiment Al 51, wherein R81 is hydrogen.

Embodiment A153. A compound according to embodiment Al 51 or embodiment All 52, wherein R82 is hydrogen.

Embodiment All 54. A compound according to any one of the embodiments A146 to Al 53, wherein at least one of R50, R57, and e are hydrogen.
Embodiment Al 55. A compound according to embodiment Al 54, wherein at least two of R23, R24, R25, and Rte are hydrogen.

Embodiment Al 56. A compound according to embodiment Al 55, wherein at least three of e, R24, e, and R28 are hydrogen.

Embodiment Al 57. A compound according to any one of the embodiments Al to Al 56, wherein L2 is a direct bond, C14-alkylene, C24-alkenylene, C2.$-alkynylene, -N-R20-, -C1$-aIkyiene-N(R20)-, -C2.8-alkenylene-N(R20)-, or -C2_8-alkynylene-N(R20Y, wherein R20 is as defined in embodiment Al.

Embodiment A158. A compound according to any one of the embodiments Al to A153, wherein L2 is -N-R20-, -alkylene-N(RZ0)-, -alkenylene-N(R20)-, or -alkynylene-N(R20}, wherein R20 is as defined in embodiment Al.

Embodiment Al 59. A compound according to embodiment Al 57 or embodiment Al 58, wherein L2 is -N-R20-, -C14-alkylene-N(R20)-, -C2-e-alkenylene-N(RZ0)-, or -C2 -alkynylene-N(R20)-, wherein R20 is as defined in embodiment Al.

Embodiment Al 60. A compound according to embodiment Al 59, wherein L2 Is -N-R20-, wherein RZ0 is as defined in embodiment Al.

Embodiment A161. A compound according to embodiment A157, wherein L2 is a direct bond.

Embodiment A162. A compound according to any one of the embodiments Al to A160, wherein R20 is hydrogen, or R20 is C1.a-alkyl, C2.6-alkenyl, C2$-alkynyl, C3.10-cydoalkyl-W3-, C3 lofietenxydyl-W3-, C3.10-aryl-W3-, or C.10-heteroaryl-W3-, optionally substituted with one or more substituents R30, R", and R32, wherein W3, R30, R31, and R32 are as defined in embodiment Al.
Embodiment A163. A compound according to embodiment A162, wherein W3 is alkylene.

Embodiment A164. A compound according to embodiment A163, wherein W3 is C2.6-alkylene.

Embodiment A165. A compound according to embodiment A162, wherein W3 is a direct bond.

Embodiment A166. A compound according to any one of the embodiments Al to A160, wherein RZ0 is hydrogen, C14-alkyl, C2.g-alkenyl, or C2.6-alkynyl, optionally substituted with one or more substituents R30, R31, and R32, wherein R30, R31, and e are as defined in embodiment Al.

Embodiment Al 67. A compound according to any one of the embodiments Al 62 to Al 66, wherein R20 is hydrogen, or R20 is C14-alkyl, C14-alkenyl, or C14-alkynyl, optionally substituted with one or more substituents R30, R31, and R32, wherein R30, R31, and R32 are as defined in embodiment Al.

Embodiment A168. A compound according to any one of the embodiments Al to A167, wherein R30, R31, and R32 independently of each other are selected from -CHF2, -CF3, -OCF3, -OCHF2, -OCH2CF3, -OCF2CHF2, -S(O)2CF3r -SCF3, -0R52, -NR52R53, -SR 52, -NR2S(0)2R53, -S(O)2NR52R53, -S(O)NR52R53, -S(O)R52, -S(0)2R52, -C(O)NR52R53, -OC(0)NR52R53, _NR52C(0)R53, -CH2C(O)NR2R53, -OCH2C(O)NR52R53, -CH2OR52, CH2NR52R53, -OC(0)R52, -C(0)R52and -C(O)OR52, wherein R52 and e are as defined in embodiment Al.
Embodiment A169. A compound according to embodiment Al 68, wherein R52 and R53, when attached to the same nitrogen atom, together with the said nitrogen atom may form a 3 to 8 membered heterocyclic ring optionally containing one or two further heteroatoms selected from nitrogen, oxygen and sulfur, and optionally containing one or two double bonds.

Embodiment Al70. A compound according to any one of the embodiments Al to A168, wherein R52 and R53 independently of each other are hydrogen, C1$-alkyl, aryl-C14-alkylene-heteroaryl-Cl.e-alkylene- heteroaryl, or aryl.

Embodiment Al 71. A compound according to embodiment Al 70, wherein R52 and e independently of each other are hydrogen, C1$-alkyl, aryl-C14alkylene-or aryl.

Embodiment Al 72. A compound according to embodiment Al 71, wherein R52 and RR independently of each other are hydrogen or C1$-alkyl.
Embodiment Al 73. A compound according to embodiment Al 72, wherein e is hydrogen.

Embodiment A174. A compound according to embodiment A172 or embodiment A173, wherein e is hydrogen.

Embodiment Al 75. A compound according to embodiment Al 67, wherein R20 is hydrogen.

Embodiment Al 76. A compound according to any one of the embodiments Al to A175, wherein L3 is -C(O)-, -C(O)-C(O)- or -C(O)CH2C(O)-.

Embodiment Al 77. A compound according to embodiment Al 76 wherein L3 is -C(O)-.

Embodiment Al 78. A compound according to embodiment Al 76 wherein L3 is -C(O)-C(O)-.

Embodiment A179. A compound according to embodiment A176 wherein L3 is -C(O)CH2C(O)-.

Embodiment Al80. A compound according to any one of the embodiments Al to A179, wherein R' is hydrogen, or R' is C1.8-alkyl, C24-alkenyl, C24-alkynyl, C3.1a-cydoalkyl-W-, C3.10-heterocyclyl W -, C3.1a-aryl-W4-, or Ca.10-heteroaryl-W4-, optionally substituted with one or more substituents R33, R34, and R35, wherein W4, R33, R34, and e are as defined in embodiment Al.
Embodiment A181. A compound according to embodiment A180, wherein W4 is alkylene.

Embodiment A182. A compound according to embodiment Al81, wherein W4 is C2.8-alkylene.

Embodiment A183. A compound according to embodiment A180, wherein W4 is a direct bond.

Embodiment A184. A compound according to any one of the embodiments Al to A176, wherein R' is hydrogen, C1.g-alkyl, C2.e-alkenyl, or C2$-alkynyl, optionally substituted with one or more substituents e, R34, and e, wherein e. R34, and R35 are as defined in embodiment Al.

Embodiment A185. A compound according to any one of the embodiments A180 to A184, wherein R' is hydrogen, C1. -alkyl, C2.8-alkenyl, or C2$-alkynyl, optionally substituted with one or more substituents e, e, and e, wherein R33, R34, and e are as defined in embodiment Al.
Embodiment Al 86. A compound according to embodiment Al 85, wherein R' is hydrogen or C14-alkyl optionally substituted with one or more substituents e, R34, and e, wherein R33, e, and e are as defined in embodiment Al.

Embodiment Al 87. A compound according to any one of the embodiments Al to Al 86, wherein R33, R34, and R3S independently of each other are selected from -CHF2, -CF3, -OCF3, -OCHF2, -OCH2CF3, -OCF2CHF2, -S(O)2CF3, -SCF3, -OR-, -NR52R63, -SR52, -NR52S(O)2R53, -S(O)2NR52R53, -S(O)NR52R53, -S(O)R52, -S(O)2R52, -C(O)NR52RS3, -OC(O)NR52R53, -NR52C(O)R53, -CH2C(O)NR62R63, -OCH2C(O)NRb2R3, -CH2OR52, -CH2NR52R"S, -OC(O)R52, -C(O)R52 and -C(O)OR52, wherein R52 and e are as defined in embodiment Al.
Embodiment Al 88. A compound according to embodiment Al 86, wherein R62 and R53, when attached to the same nitrogen atom, together with the said nitrogen atom may form a 3 to 8 membered heterocyclic ring optionally containing one or two further heteroatoms selected from nitrogen, oxygen and sulfur, and optionally containing one or two double bonds.

Embodiment Al 89. A compound according to embodiment Al 86, wherein R52 and R5s independently of each other are hydrogen. C14-alkyl, aryl-Cl.4-alkylene-heteroaryl-C1$-alkylene- heteroaryl, or aryl.

Embodiment A190. A compound according to embodiment A189, wherein R52 and e independently of each other are hydrogen, C1.6-alkyl, aryl-C1$-alkylene-or aryl.

Embodiment Al 91. A compound according to embodiment Al 90, wherein R52 and R53 independently of each other are hydrogen or C1$-alkyl.
Embodiment A192. A compound according to embodiment Al91, wherein R52 is hydrogen.

Embodiment A193. A compound according to embodiment A191 or embodiment A192, wherein R53 is hydrogen.

Embodiment Al 94. A compound according to embodiment Al 86, wherein R' is hydrogen.

Embodiment A195. A compound according to any one of the embodiments Al to A194, wherein G2 is heteroaryl, fused heterocydylheteroaryl, or fused cycloalkyiheteroaryl, optionally substituted with one or more substituents R43, R44, and R45, wherein said heteroaryl group posesses a nitrogen atom adjacent to the atom joining G2 with -N(R')-, and wherein R43, R", and R45 are as defined in embodiment Al.
Embodiment Al 96. A compound according to embodiment Al 95, wherein G2 is fused cycloalkylheteroaryl optionally substituted with one or more substituents R4S, R44, and R45, wherein said heteroaryl group posesses a-nitrogen atom adjacent to the atom joining G2with N(R'}, and wherein R43, R44, and R45 are as defined in embodiment Al.
Embodiment Al 97. A compound according to embodiment Al 96 wherein G2 is fused cycloalkylthiazolyl optionally substituted with one or more substituents R43, R44, and R45, and wherein R43, R4', and e are as defined in embodiment Al.
Embodiment A198. A compound according to embodiment A197, wherein G2 is fused cycloalkyithiazolyl optionally substituted with -COOH

Embodiment Al 99. A compound according to embodiment Al 95, wherein G2 is heteroaryl optionally substituted with one or more substituents R43, R44, and R45, wherein said heteroaryl group posesses a nitrogen atom adjacent to the atom joining G2 with -N(R')-, and wherein R'3, R44, and R'5 are as defined in embodiment Al.
Embodiment A200. A compound according to embodiment A199, wherein G2 is furanyl, thienyl, thiophenyl, pyrrolyl, imidazolyl, pyrazolyl, triazolyl, tetrazolyl, thiazolyl, oxazolyl, isoxazolyl, oxadiazolyl, thiadiazolyl, isothiazolyl, pyridinyl, pyridazinyl, pyrazinyl, pyrimidinyl, quinotinyl, isoquinolinyl, benzofuranyl, benzothiophenyl, indolyl, or indazolyl, optionally substituted with one or more substituents R43, R44, and R45, wherein R4', e, and e are as defined in embodiment Al.
Embodiment A201. A compound according to embodiment A200 wherein G2 is thiazolyl, optionally substituted with one or more substituents e, R44, and R4S, wherein R43, R44, and R4s are as defined in embodiment Al.
Embodiment A202. A compound according to embodiment A201 wherein G2 is it N R43 N R
S ~
R44 or R
wherein R43 and R44 are as defined in embodiment Al.
Embodiment A203. A compound according to embodiment A202 wherein G2 is Nai S
wherein R43 is as defined in embodiment Al.
Embodiment A204. A compound according to embodiment A202 wherein G2 is S

wherein R43 and e are as defined in embodiment Al.
Embodiment A205. A compound according to embodiment A200 wherein G2 is N_ 43 S-N
wherein e is as defined in embodiment Al.
Embodiment A206. A compound according to embodiment A202 wherein G2 is R"
wherein R44 is as defined in embodiment Al.

Embodiment A207. A compound according to any one of the embodiments Al to A206, wherein R43, R44, and R45 independently of each other are selected from -CN, -NO2, -SCF3, -OR54, -NR54R65, -SR4, -S(O)2NR54R55, -S(O)NR54R56, -S(O)R54, -S(O)2R54, -C(O)NR54R55, -OC(O)NR54R55, -NR54C(O)R55, halogen, -S-C14-alkylene-OR54, -S(O)2-C,$-alkylene-OR54, -C14-alkylene-S-RM, -C1. -alkylene-S(O)R54, -C13-alkylene-S(O)2R54, -C,.S-alkylene-N(R54)S(O)2R55, -N(R54)S(O)2R56, -C,$-alkylene-C(O)NR54R55, -C1.6-alkylene-N(R54)C(0)R56, -N(R54)C(O)R56, -C, e-alkylene-N(R54)C(0)NR55R5e, C,.e-alkylene-NHC(=NR54)NR66R58, -C14-alkylene-N(R64)C(O)OR65, -N(R54)C(O)OR55, -C,$-alkylene-C(O)OR64, -OCH2C(O)NR54R56, -O(CH2)130R54, -C,.6-alkylene-O-R54, -C1$-alkylene-C(O)R54, -C,.e-alkylene-NR64R55, -C,.6-alkylene=N-O-R54, -C,$-alkylene-N(R54)S(0)2NR56R55, _N(R54)S(O)2NR55R58, -N(R54)S(O)2NR65R5e, -OC(O)R54, -C(O)N(R54)S(0)2Res, -C,$-alkylene-C(R54)=N-OR56, -NHC(=NR54)NR56R56, -Ct.6-alkylene-N=C(N(Rs4R56))2, -N=C(N(R54R65))2r -C(0)R54 and -C(O)ORb4; or C1 -alkyl or C2$-alkenyl , each of which may optionally be substituted with one or more substituents independently selected from halogen, e, -CN, -CF3, -OCF3, -OR54, -C(O)OR54, -NR54R55 and C13-alkyl; or C3_10-cydoalkyl, heterocydyl, C3_,o-cydoalkyl-C1.e-alkylene-, Ca_10-cycloalkyl-C14-alkoxy-, C3.10-cycloalkyloxy, heterocyclyl-C,4-alkylene-, of which the heterocyclyl moieties optionally may be substituted with one or more substituents independently selected from R70; or aryl, aryloxy, aryl-C,_g-alkoxy-, aryl-C1$-alkylene-, heteroaryl, heteroaryl-CI.g-alkylene-, of which the aryl and heteroaryl moieties optionally may be substituted with one or more substituents selected from halogen, -C(O)OR54, -CN, -CF3, -OCF3, -NO2, -OR54, -NR54R55 or C14-alkyl, wherein R54. R55 and e are as defined in embodiment Al.

Embodiment A208. A compound according to embodiment A207, wherein R43, R44, and e independently of each other are selected from -OR54, -NR54R5 i, -SR54, -S(O)R54, -S(O)2R54, -C(O)NRMR5', halogen, -S-C1.g-alkylene-ORS4, -C,$-alkylene-S-R54, -C1$-alkylene-S(O)R54, -C1$-alkylene-S(0)2R54, -C1..8-alkylene-N(R54)S(O)2R55, -C18-alkyIene-C(O)NR54R55, -C1.g-alkylene-N(R54)C(O)R55, -C,4-alkylene-N(R54)C(O)NR56R5 , C14alkylene-NHC(=NR54)NR55R5B, -C,$-alkylene-N(R64)C(O)ORbS, -C,.e-alkylene-C(O)OR54, -C,--alkylene-O-R54, -C,$-alkylene-C(O)R54, -C1$-alkylene-NR54R55, -C1$-alkylene=N-O-R54, -C14-alkylene-N=C(N(R54R55))2, -N=C(N(R54R55))2, _C(O)R54 and -C(O)OR54; or CI-6-alkyl optionally substituted with one or more substituents independently selected from halogen, R54, -CN, -CF3, -OCF3, -0R54, -C(O)OR54, -Nee- and C,-e-alkyl; or Heterocyclyl or heterocyclyl-C1.6-alkylene-, of which the heterocyclyl moieties optionally may be substituted with one or more substituents Independently selected from R70; or aryl, aryl-C,$-alkylene-, heteroaryl, heteroaryl-C14-alkylene-, of which the aryl and heteroaryl moieties optionally may be substituted with one or more substituents selected from halogen, -C(O)OR54, -CN, -CF3, -OCF3, -NO2, -OR 54, -NR54R55 or C14-alkyl, wherein R54. R55, R65, and R70 are as defined in embodiment Al.
Embodiment A209. A compound according to embodiment A208, wherein R43, R44, and R45 Independently of each other are selected from -SR54, -S(O)RS4, -S(O)2R54, halogen, -C,$-alkylene-S-R54, -C1$-alkylene-S(O)R54, -C14-alkylene-S(O)2R54, -C,$-alkylene-N(R54)C(O)ORSS, -C,$-alkylene-C(O)OR54, -C14-alkylene-O-R54, -C1.s-alkylene-NR5'R55, -C,$-alkylene-C(O)R54, -C(O)RS4 and -C(O)OR54; or C1$-alkyl optionally substituted with one or more substituents independently selected from halogen, e, -CN, -CF3, -OCF3, -OR54, -C(O)OR54, -Nee and C1$-alkyl; or Heterocydyl or heterocyclyl-C1.6-alkylene-, of which the heterocyclyl moieties optionally may be substituted with one or more substituents independently selected from R70; or heteroaryl or heteroaryl-C,4-alkylene-, of which the aryl and heteroaryl moieties optionally may be substituted with one or more substituents selected from halogen, -C(O)ORS`, -CN, -CF3, -OCF3, -NO2, -0R50, -NR54R55 or C,$-alkyl, wherein R54. R, R, and km are as defined in embodiment Al.

Embodiment A21 0. A compound according to embodiment A209, wherein R43, R44, and R45 independently of each other are selected from -SR54, -S(O)2R64, halogen,-C,$-alkylene-C(O)OR54, and -C(O)OR54; or Heterocyclyl or heterocyclyl-C14-alkylene-, of which the heterocyclyl moieties optionally may be substituted with one or more substituents Independently selected from R70; or heteroaryl or heteroaryl-C,4-alkylene-, of which the heteroaryl moieties optionally may be substituted with one or more substituents selected from halogen, -C(O)ORS`, -CN, -CF3, -OCF3, -NO2, -0RS`, -NR4R55 or C,.e-alkyl, wherein R54, R55, R, and R70 are as defined In embodiment Al.

Embodiment A211. A compound according to embodiment A210, wherein R43, R44, and R45 independently of each other are selected from -SR54, -S(O)2R54, halogen,-C,4-alkylene-C(O)ORS4, and -C(O)OR54; or heterocyclyl-C,.e-alkylene-, wherein heterocyclyl is selected from imidazolyl, piperidyl, piperazinyl, and morpholnyl, and of which the heterocydyl moieties optionally may be substituted with one or more substituents independently selected from R70; or heteroaryl or heteroaryl-C,.6-alkylene-, wherein heteroaryl is selected from thiazolyl, triazolyl, or tetrazolyl, and of which the heteroaryl moieties optionally may be substituted with one or more substituents selected from halogen, -C(O)OR54, -CN, -CF3, -OCF3, -NO2, -0R54, -NR54R55 or C,4-alkyl, wherein RS4, IV, R. and R70 are as defined in embodiment Al.
Embodiment A212. A compound according to embodiment A209, wherein R43, R44, and e independently of each other are selected from -C,4-alkylene-S-R54,-C,.6-alkylene-O-R54, -C,.g-alkylene-S(O)2R54 or -C,.84kylene-NR54R55, wherein R54 and R56 are as defined in embodiment Al.
Embodiment A213. A compound according to embodiment A209, wherein R43 is -C,.e-alkylene-S-W`, wherein R54 is as defined in embodiment Al.
Embodiment A214. R43 is -C1 e-alkylene-O-R54, wherein e Is as defined in embodiment Al.
Embodiment A215. R43 is -C1-o-alkylene-NR54R55, wherein R54 and e are as defined in embodiment Al.
Embodiment A216. R43 is -C1.e-aikylene-S(O)2RM, wherein e is as defined in embodiment Al.
Embodiment A217. A compound according to any one of the embodiments A207 to wherein R43 is heteroaryl or heteroaryl-C14-alkyiene- optionally substituted with one or more substituents selected from halogen, -C(O)OR54, -CN, -CF3, -OCF3, -NO2, -ORS4, -NR54R56 or C1.e-alkyl, wherein R54 and R55 are as defined in embodiment Al.
Embodiment A218. A compound according to embodiment A217 wherein R43 is heteroaryl optionally substituted with one or more substituents selected from halogen, -C(O)OR54, -CN, -CF3, -OCF3, -NO2, -OR54, -NR54R5b or C1.8-alkyl, wherein e and e are as defined in embodiment Al.
Embodiment A21 9. A compound according to embodiment A217 wherein R43 is heteroaryl-Cl.e-alkylene- optionally substituted with one or more substituents selected from halogen, -C(O)OR54, -CN, -CF3, -OCF3i -NO2, -OR", -NR54R55 or C1$-alkyl, wherein R54 and e are as defined in embodiment Al.
Embodiment A220. A compound according to any one of the embodiments A207 to wherein e is =0, methyl or C(O)OR75.
Embodiment A221. A compound according to any one of the embodiments A207 to wherein R70 is -C(O)OH
Embodiment A222. A compound according to any one of the embodiments A207 to wherein R70 is -(CH2)14C(O)OH.
Embodiment A223. A compound according to any one of the embodiments A207 to wherein R70 is -S(O)2CH3.
Embodiment A224. A compound according to embodiment A211 wherein R43 Is -C1.e-alkylene-C(O)OR54.
Embodiment A225. A compound according to embodiment A224 wherein R43 is -CH2-C(O)OR54.
Embodiment A226. A compound according to embodiment A211 wherein R44 is -SR54.
Embodiment A227. A compound according to embodiment A211 wherein R44 is -S(O)2R54.
Embodiment A228. A compound according to embodiment A211 wherein R44 is halogen.

Embodiment A229. A compound according to any one of the embodiments Al to A228 wherein e, e and e independently of each other are hydrogen, C1. -alkyl, aryl-C1. -alkylene-, heteroaryl-C14-alkylene-, heterocydyl, heterocydyl-Cl.e-alkylene-, heteroaryl, or aryl, each of which is optionally substituted with one or more substituents independently selected from R";
or RSa and e independently of each other are hydrogen or -(CHR72)u (CHR73)v-W6, or R54 and We, when attached to the same nitrogen atom, together with the said nitrogen atom may form a 3 to 8 membered heterocyclic ring optionally containing one or two further heteroatoms selected from nitrogen, oxygen and sulfur,.and optionally containing one or two double bonds, and optionally substituted with one or more C14-alkyl groups, wherein R71, R72, R79, u, v, and We are as defined in embodiment Al.
Embodiment A230. A compound according to embodiment A229 wherein R54, e and R5 independently of each other are hydrogen, C1.ealkyl, heterocydyl, heterocydyl-C14-alkylene-, heteroaryl, or aryl, each of which is optionally substituted with one or more substituents independently selected from R71;
or RS4 and RSS independently of each other are hydrogen or -(CHR7)õ(CHR73),,-W , wherein R77, R72, R3, u, v, and We are as defined in embodiment Al.
Embodiment A231. A compound according to any one of the embodiments Al to A230 wherein Rr4, R66 and e independently of each other are hydrogen, methyl, ethyl, propyl, butyl, isopropyl, isobutyl, sec butyl, tert-butyl, 3-pentyl, 2-pentyl, or 3-methyl-butyl.
Embodiment A232. A compound according to embodiment A231 wherein R', e and R56 independently of each other are hydrogen, methyl, ethyl, propyl, butyl, isopropyl, isobutyl, sec-butyl, or tert-butyl.
Embodiment A233. A compound according to embodiment A232 wherein R54, e and RS8 independently of each other are hydrogen, methyl, ethyl, propyl, butyl. isopropyl, isobutyi, sec-butyl, or Pert butyl.
Embodiment A234. A compound according to embodiment A233 wherein R5`, e and R58 independently of each other are hydrogen, methyl or ethyl.
Embodiment A235. A compound according to embodiment A234 wherein e is hydrogen.
Embodiment A236. A compound according to any one of the embodiments Al to A230 wherein e, e and e independently of each other are oxetanyl, tetrahydrofuranyl, tetrahydropyranyl, oxepanyl, azetidyl, pyrrolidyl, piperidyl, hexahydroazepinyl, thietanyl, thiolanyl, tetrahydrothiopyranyl, thiepanyl,1,4-oxathianyl, 1,3-dioxolanyl, 1,2-dithiolanyl, 1,3-dithiolanyl, hexahydro-pyridazinyl, imidazolidyl, 1,3-dioxanyl, morpholinyl,l,3-dithianyl,1,4-dioxanyl,1,4-dithianyl, or thiomorpholinyl, each of which is optionally substituted with one or more substituents independently selected from R71, wherein R71 Is as defined in embodiment Al.
Embodiment A237. A compound according to embodiment A236 wherein RM, e and e independently of each other are tetrahydropyranyl, oxepanyl, piperidyl, hexahydroazepinyl, tetrahydrothiopyranyl, thiepanyl, 1,4-oxathianyl, 1,3=
dithiolanyt, hexahydro-pyridazinyl,1.3-dioxanyl, morpholinyl, 1,3-dithianyl, 1,4-dioxanyl,1,4-dithianyl, or thiomorpholinyl, each of which is optionally substituted with one or more substituents independently selected from R", wherein R" is as defined In embodiment Al.
Embodiment A238. A compound according to embodiment A237 wherein RR', R55 and R56 independently of each other are tetrahydropyranyl, piperidyl, tetrahydrothiopyranyl, 1,4-oxathianyl, hexahydro-pyridazinyl, morpholinyl, 1,4-dioxanyl, 1,4-dithianyl, or thiomorpholinyl, each of which is optionally substituted with one or more substituents independently selected from R", wherein e is as defined in embodiment Al.
Embodiment A239. A compound according to embodiment A238 wherein e, e and e independently of each other are tetrahydropyranyl, piperidyl, tetrahydrothiopyranyl, or morpholinyl, each of which is optionally substituted with one or more substituents independently selected from R", wherein R" Is as defined in embodiment Al.
Embodiment A240. A compound according to embodiment A239 wherein R5', R55 and R58 independently of each other are piperidyl or morpholinyl, each of which is optionally substituted with one or more substituents independently selected from R", wherein R" is as defined in embodiment Al.
Embodiment A241. A compound according to embodiment A240 wherein R~', R and R56 independently of each other are piperidyl or morpholinyl.

242.
Embodiment A243. A compound according to any one of the embodiments Al to A230 wherein R54, R55 and R58 independently of each other are furanyl, thienyl, thiophenyl, pyrrolyl, imidazolyl, pyrazolyl, triazolyl, tetrazolyl, thiazolyl, oxazolyl, isoxazolyl, oxadiazolyl, thiadiazolyl, isothiazolyl, pyridinyl, pyridazinyl, pyrazinyl, pyrimidinyl, quinolinyl, isoquinoiinyl, benzofuranyl, benzothiophenyl, indolyl, purinyl, or indazolyl, each of which is optionally substituted with one or more substituents independently selected from R", wherein R" is as defined in embodiment Al.
Embodiment A244. A compound according to embodiment A243 wherein RSt, e and R5 independently of each other are furanyl, thienyl, thiophenyl, pyrrotyl, imidazolyl, pyrazotyl, triazolyl, tetrazolyl, thiazolyl, oxazolyl, isoxazolyl, oxadiazolyl, thiadiazolyl, isothiazolyl, pyridinyl, pyridazinyl, pyrazinyl, pyrimidinyl, benzofuranyl, indolyl, or purinyl, each of which is optionally substituted with one or more substituents independently selected from R", wherein R" is as defined in embodiment Al.
Embodiment A245. A compound according to embodiment A244 wherein R5`, e and e independently of each other are imidazolyl, triazolyl, tetrazolyl, thiazolyl, pyridinyl, pyrimidinyl, benzofuranyt, indolyl, or purinyl, each of which is optionally substituted with one or more substituents independently selected from R", wherein R" is as defined in embodiment Al.
Embodiment A246. A compound according to embodiment A245 wherein R54, R55 and R55 Independently of each other are.imidazolyl, triazolyl, tetrazolyl, thiolyl, pyridinyl, pyrimidinyl, or purinyl, each of which is optionally substituted with one or more substituents independently selected from R", wherein R" Is as defined In embodiment Al.
Embodiment A247. A compound according to embodiment A246 wherein e, R55 and R58 independently of each other are imidazolyl, triazolyl, tetrazolyl, thiazolyl, pyridinyl, pyrimidinyl, each of which is optionally substituted with one or more substituents independently selected from R", wherein R" is as defined in embodiment Al.
Embodiment A248. A compound according to embodiment A247 wherein e is imidazolyl optionally substituted with one or more substituents independently selected from R", wherein R" is as defined in embodiment Al.

Embodiment A249. A compound according to embodiment A247 wherein R54 is triazolyl optionally substituted with one or more substituents independently selected from R71, wherein R71 is as defined in embodiment Al.
Embodiment A250. A compound according to embodiment A247 wherein e is tetrazolyl optionally substituted with one or more substituents independently selected from R71, wherein R71 is as defined in embodiment Al.
Embodiment A251. A compound according to embodiment A247 wherein e is thiazolyl optionally substituted with one or more substituents independently selected from R71, wherein R71 is as defined in embodiment Al.
Embodiment A252. A compound according to embodiment A247 wherein e. is pyndinyl optionally substituted with one or more substituents independently selected from R71, wherein R71 is as defined in embodiment Al.
Embodiment A253. A compound according to embodiment A247 wherein e is pyrimidinyl optionally substituted with one or more substituents independently selected from R71, wherein R71 is as defined in embodiment Al., Embodiment A254. A compound according to embodiment A246 wherein R54 is purinyl optionally substituted with one or more substituents independently selected from R71, wherein R7' Is as defined in embodiment Al.
Embodiment A255. A compound according to any one of the embodiments Al to A254 wherein R71 is methyl or =0.
Embodiment A256. A compound according to any one of the embodiments Al to A254 wherein R71 is -C(O)OH
Embodiment A257. A compound according to any one of the embodiments Al to A254 wherein R7' is -(CH2)13C(O)OH.
Embodiment A258. A compound according to any one of the embodiments Al to A254 wherein e is -(CH2)1.3NR75R76.
Embodiment A259. A compound according to any one of the embodiments Al to A230 wherein u is 0 or 1.
Embodiment A260. A compound according to embodiment A259 wherein u is 0.
Embodiment A261. A compound according to embodiment A259 wherein u is 1.
Embodiment A262. A compound according to any one of the embodiments Al to A230 wherein v is 0 or 1.
Embodiment A263. A compound according to embodiment A262 wherein v is 0.
Embodiment A264. A compound according to embodiment A262 wherein v is 1.

Embodiment A265. A compound according to any one of the embodiments Al to A230 wherein u is 0 and v is 1.
Embodiment A266. A compound according to any one of the embodiments Al to A230 wherein u and v are both 0.
Embodiment A267. A compound according to any one of the embodiments Al to A230 or A259 to A266 wherein R72 and R73 are independently selected from hydrogen, hydroxy or -C(O)OR75.
Embodiment A268. A compound according to embodiment A267 wherein R72 and R73 are independently selected from hydrogen or -C(O)OR75, wherein R75 is as defined in embodiment Al.
Embodiment A269. A compound according to embodiment A267 wherein R72 and R73 are hydrogen.
Embodiment A270. A compound according to any one of the embodiments Al to A230 or A259 to A269 wherein We is -O-R75, -C(O)O-R75, -C(O)-R75, -NR75R76, -NHCH2C(O)R75, -NHC(O)R75, -S(O)2R75, -NHS(O)2R76, or We is heterocyclyl, wherein R75 and R7 are as defined in embodiment Al.
Embodiment A271. A compound according to embodiment A270 wherein We is -0-R75, -C(O)O-R75, -C(O)-R75, -NR75R76, -NHCH2C(O)R'S, -NHC(O)R75, -S(O)2R75, -NHS(O)2R75, or We is oxetanyl, tetrahydrofuranyl, tetrahydropyranyl, oxepanyl, azetidyl, pyrrolidyl, piperidyl, hexahydroazepinyl, thietanyl, thiolanyl, tetrahydrothiopyranyl, thiepanyl, 1,4-oxathianyl, 1,3-dioxolanyl, 1,2-dithiolanyl, 1,3-dithiolanyl, hexahydro-pyridazinyl, imidazolidyl, 1,3-dioxanyl, morpholinyl, 1,3-dithianyl, 1,4-dioxanyl, 1,4-dithianyl, or thiomorpholinyl, wherein R75 and R78 are as defined in embodiment Al.
Embodiment A272. A compound according to embodiment A270 wherein We is -O-R75, -C(O)O-R75, -C(O)-R75, -NR75R7 , -NHCH2C(O)R75, -NHC(O)R75, -S(O)2R75, -NHS(O)2R75, or We is tetrahydropyranyl, oxepanyl, piperidyl, hexahydroazepinyl, tetrahydrothiopyranyl, thiepanyl, 1,4-oxathianyl, morpholinyl, 1,4-dioxanyl, 1,4-dithianyl, or thiomorpholinyl, wherein R75 and R78 are as defined in embodiment Al.
Embodiment A273. A compound according to embodiment A272 wherein W is -O-R75, -C(O)O-R75, -C(O)-R'5, -NR75R76, -NHCH2C(O)R75, -NHC(O)R75, -S(O)2R75, -NHS(O)2R75, or We is tetrahydropyranyl, piperidyl, tetrahydrothiopyranyl, or morpholinyl, wherein R75 and R76 are as defined in embodiment Al.
Embodiment A274. A compound according to embodiment A273 wherein W is -0-R75, -C(O)O-R75, -NR75R78, -NHC(O)R75, -S(O)2R75, or we is tetrahydropyranyl, piperidyl, tetrahydrothiopyranyl, or morpholinyl, wherein R75 and R7e are as defined in embodiment Al.
Embodiment A275. A compound according to embodiment A274 wherein V %P -O-R75, or -C(O)O-R75, wherein R75 is as defined in embodiment Al.
Embodiment A276. A compound according to embodiment A275 wherein WO is -C(0)0-e, wherein R7S is as defined in embodiment Al..
Embodiment A277. A compound according to any one of the embodiments Al to A230 or A259 to A276 wherein R75 and R78 are independently selected from hydrogen, -OH, or C1 -alkyl optionally substituted with -NH2.
Embodiment A278. A compound according to embodiment A277 wherein R75 and R78 are independently selected from hydrogen, -OH, or methyl.
Embodiment A279. A compound according to embodiment A278 wherein R75 and R78 are independently selected from hydrogen or -0H.
Embodiment A280. A compound according to embodiment A279 wherein R75 is hydrogen.
Embodiment A281. A compound according to any one of the embodiments Al to A280, which compound is an activator of glucokinase, when tested in the Glucokinase Activation Assay (I) disclosed herein at a glucose concentration of 2 mM.

Embodiment A282. A compound according to any one of the embodiments Al to A281, which compound is an activator of glucokinase, when tested in the Glucokinase Activation Assay (I) disclosed herein at a glucose concentration of from 10 to 15 mM.

Embodiment A283. A compound according to any one of the embodiments Al to A282, which compound, at a concentration of 30 NM, is capable of providing an at least 1.5, such as at least 1.7, for instance at least 2.0 fold activation of glucokinase in the Glucokinase Activation Assay (I) disclosed herein at a glucose concentration of 2 mM.

Embodiment A284. A compound according to any one of the embodiments Al to A283.
which compound, at a concentration of 30 NM, is capable of providing an at least 1.5, such as at least 1.7, for instance at least 2.0 fold activation of glucokinase in the Glucokinase Activation Assay (I) disclosed herein at a glucose concentration of from 10 to 15 mM.

Embodiment A285. A compound according to any one of the embodiments Al to A284, which at a concentration of 5 lM is capable of providing an at least 1.5, such as at least 1.7, for instance at least 2.0 fold activation of glucokinase in the Glucokinase Activation Assay (I) disclosed herein at a glucose concentration of 2 mM.

Embodiment A286. A compound according to any one of the embodiments Al to A285, which at a concentration of 5 pM is capable of providing an at least 1.5, such as at least 1.7, for instance at least 2.0 fold activation of glucokinase in the Glucokinase Activation Assay (1) disclosed herein at a glucose concentration of from 10 to 15 mM.

Embodiment A287. A glucose kinase activator compound defined as a compound which at a compound concentration of at or below 30 pM at a glucose concentration of 2 mM
in the Glucokinase Activation Assay (I) disclosed herein gives 1.5 - fold higher glucokinase activity than measured at a glucose concentration of 2 mM in the Glucokinase Activation Assay (I) without compound, where the Increase in glucokinase activity provided by the compound increases with increasing concentrations of glucose.

Embodiment A288. A compound according to any one of the embodiments Al to A286, which compound provides an increase in glucokinase activity, where the increase in glucokinase activity provided by the compound increases with increasing concentrations of glucose.

Embodiment A289. A compound according to embodiment A287 or embodiment A288, which provides an increase in glucokinase activity in Glucokinase Activation Assay (I) disclosed herein at a glucose concentration of 15 mM, which increase is significantly higher than the increase in glucokinase activity provided by the compound in Glucokinase Activation Assay (I) disclosed herein at a glucose concentration of 5 mM.

Embodiment A290. A compound according to any one of the embodiments A287 to A289, which at a compound concentration of 10 pM provides an increase in glucokinase activity in Glucokinase Activation Assay (I) disclosed herein at a glucose concentration of 15 mM, which increase is significantly higher than the increase In glucokinase activity provided by the compound at a compound concentration of 10 pM In Glucokinase Activation Assay (I) disclosed herein at a glucose concentration of 5 mM.

Embodiment A291. A compound according to any one of the embodiments A287 to A290, which at a compound concentration of 10 pM provides an increase in glucokinase activity in Glucokinase Activation Assay (I) disclosed herein at a glucose concentration of 15 mM, which increase is at least 1.1 fold higher, such as at least 1.2 fold higher, for instance at least 1.3 fold higher, such as at least 1.4 fold higher, for instance 1.5 fold higher, such as at least 1.6 fold higher, for instance at least 1.7 fold higher, such as at least 1.8 fold higher, for instance at least 1.9 fold higher, such as at least 2.0 fold higher than the increase in glucokinase activity provided by the compound at a compound concentration of 10 pM in Glucokinase Activation Assay (I) disclosed herein at a glucose concentration of 5 mM.
Embodiment A292. A glucose kinase activator compound defined as a compound which at a compound concentration of at or below 30 pM at a glucose concentration of 2 mM
in the Glucokinase Activation Assay (I) disclosed herein gives 1.5 - fold higher glucokinase activity than measured at a glucose concentration of 2 mM in the Glucokinase Activation Assay (I) without compound, which glucose kinase activator compound increases glucose utilization in the liver without inducing any increase in insulin secretion in response to glucose.

Embodiment A293. A glucose kinase activator compound defined as a compound which at a compound concentration of at or below 30 pM at a glucose concentration of 2 mM
in the Glucokinase Activation Assay (I) disclosed herein gives 1.5 - fold higher glucokinase activity than measured at a glucose concentration of 2 mM in the Glucokinase Activation Assay (1) without compound, which glucokinase activator compound shows a significantly higher activity in isolated hepatocytes compared to the activity of the glucokinase compound in Ins-1 cells.

Embodiment A294. A compound according to any one of the embodiments Al to A291, which compound increases glucose utilization in the liver without inducing any increase in insulin secretion in response to glucose.

Embodiment A295. A compound according to any one of the embodiments Al to A291, which compound shows a significantly higher activity in isolated hepatocytes compared to the activity of the compound in ins-1 cells.

Embodiment A296. A compound according to any one of the embodiments A292 to A295, which compound shows a significantly higher activity in isolated hepatocytes measured as described in the Glucokinase Activity Assay (II) compared to the activity of the compound in Ins-1 cells measured as described in the Glucokinase Activity Assay (III).

Embodiment A297. A compound according to embodiment A296, which compound shows an activity in isolated hepatocytes measured as described in the Glucokinase Activity Assay (II) which activity is at least 1.1 fold higher, such as at least 1.2 fold higher, for instance at least 1.3 fold higher, such as at least 1.4 fold higher, for instance 1.5 fold higher, such as at least 1.6 fold higher, for instance at least 1.7 fold higher, such as at least 1.8 fold higher, for instance at least 1.9 fold higher, such as at least 2.0 fold higher, for instance at least a 3.0 fold higher, such as at least a 4.0 fold higher, for instance at least 5.0 fold higher, such as at least 10 fold higher than the activity of the compound in Ins-1 cells measured as described in the Glucokinase Activity Assay (III).

Embodiment A298. A compound according to embodiment A296, which compound shows no activity in the Ins-1 cells measured as described in the Glucokinase Activity Assay (Ill).
Embodiment A299. A method of preventing hypoglycaemia comprising administration of a compound according to any one of the embodiments Al to A298.
Embodiment A300. The use of a compound according to any one of the embodiments Al to Embodiment A298 for the preparation of a medicament for the prevention of hypoglycaemia.
Embodiment A301. A. compound according to any one of embodiments Al to A298, which is an agent useful for the treatment of an indication selected from the group consisting of hyperglycemia, IGT, insulin resistance syndrome, syndrome X, type 2 diabetes, type l diabetes, dyslipidemia, hypertension, and obesity.

Embodiment A302. A compound according to any one of embodiments Al to A301 for use as a medicament.

Embodiment A303. A compound according to any one of embodiments Al to A301 for treatment of hyperglycemia, for treatment of IGT, for treatment of Syndrome X, for treatment of type 2 diabetes, for treatment of type I diabetes, for treatment of dyslipidemia, for treatment of hyperlipidemia, for treatment of hypertension, for treatment of obesity, for lowering of food intake, for appetite regulation, for regulating feeding behaviour, or for enhancing the secretion of enteroincretins, such as GLP-1.

Embodiment A304. A pharmaceutical composition comprising, as an active ingredient, at least one compound according to any one of embodiments Al to 303 together with one or more pharmaceutically acceptable carriers or excipients.

Embodiment A305. A pharmaceutical composition according to embodiment A304 in unit dosage form, comprising from about 0.05 mg to about 1000 mg, preferably from about 0.1 mg to about 500 mg and especially preferred from about 0.5 mg to about 200 mg of the compound according to any one of embodiments Al to 303.

Embodiment A306. Use of a compound according to any one of the embodiments Al to 303 for increasing the activity of glucokinase.

Embodiment A307. Use of a compound according to any one of embodiments Al to A303 for the preparation of a medicament for the treatment of metabolic disorders, for blood glucose lowering, for the treatment of hyperglycemia, for the treatment of IGT, for the treatment of Syndrome X, for the treatment of impaired fasting glucose (IFG), for the treatment of type 2 diabetes, for the treatment of type 1 diabetes, for delaying the progression of impaired glucose tolerance (IGT) to type 2 diabetes, for delaying the progression of non-insulin requiring type 2 diabetes to insulin requiring type 2 diabetes, for the treatment of dys-lipidemia, for the treatment of hyperlipidemia, for the treatment of hypertension, for lowering of food intake, for appetite regulation, for the treatment of obesity, for regulating feeding behaviour, or for enhancing the secretion of enteroincretins.

Embodiment A308. Use of a compound according to any one of embodiments Al to A303 for the preparation of a medicament for the adjuvant treatment of type I diabetes for preventing the onset of diabetic complications.

Embodiment A309. Use of a compound according to any one of embodiments Al to A303 for the preparation of a medicament for increasing the number and/or the size of beta cells in a mammalian subject, for treatment of beta cell degeneration, in particular apoptosis of beta cells, or for treatment of functional dyspepsia, in particular irritable bowel syndrome.

Embodiment A310. Use according to any one of the embodiments A307 to A309 in a regimen which comprises treatment with a further antidiabetic agent.

Embodiment A31 1. Use according to any one of the embodiments A307 to A31 0 in a regimen which comprises treatment with a further antihyperlipidemic agent.

Embodiment A312. Use according to any one of embodiments A307 to A311 in a regimen which comprises treatment with a further antiobesity agent.

Embodiment A313. Use according to any one of embodiments A307 to A312 in a regimen which comprises treatment with a further antihypertensive agent.

Embodiment A314. Use of a compound according to any one of the embodiments Al to A303 or a pharmaceutical composition according to embodiment A304 or embodiment A305 for the treatment of metabolic disorders, for blood glucose lowering, for the treatment of hyperglycemia, for treatment of IGT, for treatment of Syndrome X, for the treatment of impaired fasting glucose (IFG), for treatment of type 2 diabetes,for treatment of type 1 diabetes, for delaying the progression of impaired glucose tolerance (IGT) to type 2 diabetes, for delaying the progression of non-insulin requiring type 2 diabetes to insulin requiring type 2 diabetes, for treatment of dyslipidemia, for treatment of hyperlipidemia, for treatment of hypertension, for the treatment or prophylaxis of obesity, for lowering of food intake, for appetite regulation, for regulating feeding behaviour, or for enhancing the secretion of enteroincretins.

Embodiment A315. Use of a compound according to any one of the embodiments Al to A303 or a pharmaceutical composition according to embodiment A304 or embodiment A305 for the adjuvant treatment of type 1 diabetes for preventing the onset of diabetic complications.
Embodiment A316. Use of a compound according to any one of the embodiments Al to A303 or a pharmaceutical composition according to embodiment A304 or embodiment A305 for increasing the number and/or the size of beta cells in a mammalian subject, for treatment of beta cell degeneration, in particular apoptosis of beta cells, or for treatment of functional dyspepsia, In particular irritable bowel syndrome.
Further embodiments are clear from the appended claims.
Included within the scope of the present invention are the individual enantiomers of the compounds represented by formula (1) above as well as any wholly or partially racemic mixtures thereof. The present invention also covers the individual enantiomers of the compounds represented by formula (I) above as mixtures with diastereoisomers thereof in which one or more stereocenters are inverted.
The present invention provides glucose sensitive glucokinase activators, that is glucokinase activators, for Instance of the general formula (I), which provides a higher increase in glucokinase activity at lower concentrations of glucose. This should be taken to mean that when the glucose concentration is low, then the glucose sensitive glucokinase activator provides an increase in the glucokinase activity, which increase is higher than the increase in glucokinase activity provided by the compound when glucose concentration is high. The compound may for instance provide a 4.0 fold increase in glucokinase activity at a glucose concentration of 5 mM and a 2.0 fold increase in glucokinase activity at a glucose concentration of 15 mM, thus providing an increase in glucokinase activity at a glucose concentration of 5 mM, which increase is 2.0 fold higher than the increase in glucokinase activity provided by the compound at a glucose concentration of 15 mM. For the purpose of describing the present invention, the glucose sensitivity may be assayed by use of Glucokinase Activity Assay (1) where the activity of the glucokinase activator is measured at different concentrations of glucose.
The glucose sensitivity of a glucokinase activator may for instance be measured at a glucose concentration of 5 mM and at a glucose concentration of 15 mM using the same concentration of glucokinase activator, such as a concentration of 10 pM. The two measurements may then be compared and if the fold activity at a glucose concentration of 5 mM (the lower glucose concentration) - in the above example 4.0 fold - is significantly higher than the fold activity at a glucose concentration of 15 mM (the higher glucose concentration -in the above example 2.0 fold - then the glucokinase activator is deemed to be a glucose sensitive glucokinase activator. In the above example, the increase in glucokinase activity at a glucose concentration of 5 mM is 2.0 fold higher than the increase in glucokinase activity at a glucose concentration of 15 mM. The increase in glucokinase activity provided by the glucokinase activator at 5 mM glucose may for instance be at least 1.1 fold higher, such as at least 1.2 fold higher, for instance at least 1.3 fold higher, such as at least 1.4 fold higher, for instance 1.5 fold higher, such as at least 1.6 fold higher, for instance at least 1.7 fold higher, such as at least 1.8 fold higher, for instance at least 1.9 fold higher, such as at least 2.0 fold higher than the activity of the glucokinase activator at 15 mM glucose.
The present invention provides liver specific glucokinase activators, that is, glucokinase activators, for instance of the general formula (I), which increase glucose utilization in the liver (i.e. Increase glycogen deposition) without inducing any increase in insulin secretion in response to glucose. For the purpose of describing this invention, the potential liver selectivity of a glucokinase activator may be assayed by comparison of the results obtained in response to the glucokinase activator in isolated hepatocytes and the results obtained in response to the glucokinase activator in Ins-1 cells.
Glucokinase activators, which show a significantly higher activity in Isolated hepatocytes measured as described in the Glucokinase Activity Assay (II) compared to the activity in Ins-1 cells measured as described in the Glucokinase Activity Assay (I11), are deemed to be liver specific glucokinase activators. The activity of the glucokinase activator in Glucokinase Activity Assay (II) (hepatocytes) may for instance be at least 1.1 fold higher, such as at least 1.2 fold higher, for instance at least 1.3 fold higher, such as at least 1.4 fold higher, for instance 1.5 fold higher, such as at least 1.6 fold higher, for instance at least 1.7 fold higher, such as at least 1.8 fold higher, for instance at least 1.9 fold higher, such as at least 2.0 fold higher, for instance at least a 3.0 fold higher, such as at least a 4.0 fold higher, for instance at least 5.0 fold higher, such as at least 10 fold higher than the activity of the glucokinase activator in Glucokinase Activity Assay (III) (Ins-1 cells). Alternatively, the glucokinase activator may show no activity in the Ins-1 cells measured as described in the Glucokinase Activity Assay (ill), while showing a significant activity In hepatocytes measured as described in the Glucokinase Activity Assay (II).
Such liver-specific glucokinase activators may be particularly useful in patients that are at risk of experiencing hypoglycaemia. Since liver glucokinase is highly sensitive to the serum concentration of glucose, the blood glucose-decreasing effect of the GK
in the liver will only occur when the serum concentration of glucose is relatively high.
When the serum concentration of glucose is relatively low, the effect of the GK in the liver decreases, and thus does not further lower the glucose concentration in the blood. This mechanism remains even when the liver GK is affected by a GK activator. The effect of GK on the pancreatic beta cells is not similarly glucose-sensitive. Therefore a GK activator which affects both liver and beta cells may have a glucose-lowering effect even at low serum glucose concentration, resulting in a risk of hypoglycaemia. A GK activator which affects only, or which primarily effects, the liver GK will thus provide a treatment with a lower risk of hypoglycaemia.
Thus the invention provides a method of preventing hypoglycaemia comprising administration of a liver-specific glucokinase activator, as well as the use of a liver-specific glucokinase activator for the preparation of a medicament for the prevention of hypoglycaemia.
Examples of liver specific glucokinase activators are 2-{3-[2-(2,3-dimethoxyphenoxy)-5-fluorophenyl]ureido}thiazole-4-carboxylic acid ethyl ester, (2-{3-[2-(2,3-dimethoxyphenoxy)-5-fluorophenyl]ureido}thiazol-4-yl)acetic acid ethyl ester, (2-(3-[5-fluoro-2-(2-fluono-6-methoxyphenoxy)phenyljureido}thiazol-4-yl)acetic acid, 2-{3-[2-(2,3-dimethoxyphenoxy)-5-fluorophenyl]ureido}thiazole-4-carboxylic acid, 2-(2-(3-[5-fluoro-2-(2-fluoro-6-methoxyphenoxy)phenyl]ureido)thiazol-4-yl) N-(2-morpholin-4-ylethyl)acetamide, [2-(2-{3-[5-fluoro-2-(2-fluoro-6-methoxyphenoxy)phenyl)ureido}thiazol-4-yl)acetylamino]acetic acid, {2-[3-(2-cyclopentanecarbonyl-4-methyl-phenyl)-ureido]-thiazol-4-yl}acetic acid, and {2-[3-(4-methyl-2-[2-methylpropoxy]phenyl)-ureido]-thiazol-4-yl}-acetic acid.
In one embodiment, a compound according to the present invention is for use as a medicament in the treatment of hyperglycemia.
In one embodiment, a compound according to the present invention is for use as a medicament in the treatment of IGT. -In one embodiment, a compound according to the present invention is for use as a medicament in the treatment of Syndrome X.
In one embodiment, a compound according to the present invention is for use as a medicament in the treatment of type 2 diabetes.
In one embodiment, a compound according to the present invention is for use as a medicament in the treatment of type 1 diabetes.
In one embodiment, a compound according to the present invention is for use as a medicament in the treatment of hyper(ipidemia.
In one embodiment, a compound according to the present invention is for use as a medicament in the treatment of dyslipidemia.
In one embodiment, a compound according to the present invention is for use as a medicament in the treatment of hypertension.
In one embodiment, a compound according to the present invention is for use as a medicament in the treatment of obesity.
In one embodiment, a compound according to the present invention is for use as a medicament for lowering of food intake.

In one embodiment, a compound according to the present invention is for use as a medicament for appetite regulation.
In one embodiment, a compound according to the present invention is for use as a medicament for regulating feeding behaviour.
In one embodiment, a compound according to the present invention is for use as a, medicament for enhancing the secretion of enteroincretins, such as GLP-1.
The present compounds are activators of glucokinase and are as such useful for the activation of glucokinase.
Accordingly, the present invention provides a method for activating glucokinase in a patient in need thereof, which method comprises administering to a subject in need thereof a compound according to the present Invention, preferably in a pharmacologically effective amount, more preferably in a therapeutically effective amount. The present invention also provides a method.for lowering blood glucose in a patient in need thereof, which method comprises administering to a subject in need thereof a compound according to the present invention, preferably in a pharmacologically effective amount, more preferably in a.
therapeutically effective amount. The present invention also provides a method for prevention and/or treatment of glucokinase deficiency-mediated human diseases, the method comprising administration to a human in need thereof a therapeutically effective amount of a compound according to the present invention. As used herein, the phrase "a subject in need thereof includes mammalian subjects, preferably humans, who either suffer from one or more of the aforesaid diseases or disease states or are at risk for such.
Accordingly, in the context of the therapeutic method of the present invention, this method also is comprised of a method for treating a mammalian subject prophylactically, or prior to the onset of diagnosis such disease(s) or disease state(s).
In one embodiment, the present Invention provides a method for the treatment of hyperglycemia, the method comprising administering to a subject in need thereof an effective amount of a compound or a pharmaceutical composition according to the present Invention.
In one embodiment, the present invention provides a method for the treatment of IGT, the method comprising administering to a subject In need thereof an effective amount of a compound or a pharmaceutical composition according to the present invention.
In one embodiment, the present invention provides a method for the treatment of Syndrome X, the method comprising administering to a subject in need thereof an effective amount of a compound or a pharmaceutical composition according to the present invention.
In one embodiment, the present invention provides a method for the treatment of type 2 diabetes, the method comprising administering to a subject in need thereof an effective amount of a compound or a pharmaceutical composition according to the present invention.
In one embodiment, the present invention provides a method for the treatment of type 1 diabetes, the method comprising administering to a subject in need thereof an effective amount of a compound or a pharmaceutical composition according to the present invention.
In one embodiment, the present invention provides a method for the treatment of dyslipidemia or hypertipidemia, the method comprising administering to a subject in need thereof an effective amount of a compound or a pharmaceutical composition according to the present invention.
In one embodiment, the present invention provides a method for the treatment of obesity, the method comprising administering to a subject in need thereof an effective amount of a compound or a pharmaceutical composition according to the present invention.
In one embodiment, the effective amount of the compound is in the range of from about 0.05 mg to about 2000 mg, preferably from about 0.1 mg to about 1000 mg and especially preferred from about 0.5 mg to about 500 mg per day.
In one embodiment, the method according to the present invention is part of a regimen, which comprises treatment with a further antidlabetic agent, for example an antidiabetic agent such as insulin or an insulin analogue, a suiphonylurea, a biguanide, a meglitinide, an insulin sensitizer, a thiazolidinedione insulin sensitizer, an a-glucosidase inhibitor, a glycogen phosphorylase inhibitor, or an agent acting on the ATP-dependent potassium channel of the pancreatic .8-cells, In one embodiment, the method according to the present Invention is part of a regimen, which comprises treatment with a further antihyperlipidemic agent, for example an antihyperlipidemic agent such as cholestyramine, colestipol, dofibrate, gemfibrozil, lovastatin, pravastatin, simvastatin, probucol or dextrothyroxine.
In one embodiment, the method according to the present invention is part of a regimen, which comprises treatment with a further antihypertensive agent.
In one embodiment, the method according to the present invention is part of a regimen, which comprises treatment with a further antiobesity or appetite regulating agent.
In one embodiment, the method according to the present invention is part of a regimen, which comprises treatment with a further antihypertensive agent.
Other embodiments of such methods will be dear from the following description.
Compounds according to the present invention are useful for the treatment of disorders, diseases and conditions, wherein the activation of glucokinase is beneficial.

Accordingly, the present compounds are useful for the treatment of hyperglycemia, IGT (impaired glucose tolerance), insulin resistance syndrome, syndrome X, type 1 diabetes, type 2 diabetes, dyslipidemia, dyslipoproteinemia (abnormal lipoproteins in the blood) including diabetic dyslipidemia, hyperlipidemia, hyperlipoproteinemia (excess of lipoproteins in the blood) including type I, II-a (hypercholesterolemia), II-b, III, IV
(hypertriglyceridemia) and V (hypertriglyceridemia) hyperlipoproteinemias, and obesity. Furthermore, they may be useful for the treatment of albuminuria, cardiovascular diseases such as cardiac hypertrophy, hypertension and arteriosclerosis including atherosclerosis; gastrointestinal disorders; acute pancreatitis; and appetite regulation or energy expenditure disorders.
Accordingly, in a further aspect the invention relates to a compound according to the present invention for use as a medicament.
The invention also relates to pharmaceutical compositions comprising, as an active ingredient, at least one compound according to the present invention together with one or more pharmaceutically acceptable carriers or excipients.
The pharmaceutical composition is preferably in unit dosage form, comprising from about 0.05 mg to about 1000 mg, preferably from about 0.1 mg to about 500 mg and especially preferred from about 0.5 mg to about 200 mg of the compound according to the present invention.
In one embodiment, the pharmaceutical composition according to the present invention comprises a further antidiabetic agent, for example an antidiabetic agent such as insulin, an insulin derivative or an insulin analogue, a sulphonylurea, a biguanide, a meglitinide, an insulin sensitizer, a thiazolidinedione insulin sensitizer, an a-glucosidase inhibitor, a glycogen phosphorylase inhibitor, or an agent acting on the ATP-dependent potassium channel of the pancreatic.8 cells.
In one embodiment, the pharmaceutical composition according to the present invention comprises a further antihyperlipidemic agent, for example an antihyperlipidemic agent such as cholestyramine, colestipol, clofibrate, gemfibrozil, lovastatin, pravastatin, simvastatin, probucol or dextrothyroxine.
In one embodiment, the pharmaceutical composition according to the present invention comprises a further antiobesity or appetite regulating agent.
In one embodiment, the pharmaceutical composition according to the present invention comprises a further antihypertensive agent.
In one embodiment of the present invention, the pharmaceutical composition according to the present invention comprises a compound according to the present invention in combination with one or more of the agents mentioned above eg in combination with metformin and a sulphonylurea such as glyburide; a sulphonylurea and acarbose;
nateglinide and metformin; acarbose and metformin; a sulfonylurea, metformin and troglitazone; insulin and a sulfonylurea; insulin and metformin; insulin, metfomiin and a sulfonylurea; insulin and troglitazone; insulin and lovastatin; etc.
In one embodiment of the present invention, the present compounds are used for the preparation of a medicament for the treatment of hyperglycemia. As used herein hyperglycemia Is to be taken as generally understood in the art, with reference for example to the Report of the Expert Committee of the Diagnosis and Classification of Diabetes Mellitus, published in Diabetes Care 20, 1183-1197, (1997), but is usually taken to mean an elevated plasma glucose level exceeding about 110 mg/dl. The present compounds are effective in lowering the blood glucose both in the fasting and postprandial.
stage.
In one embodiment of the present invention, the present compounds are used for the preparation of a pharmaceutical composition for the treatment of IGT.
In one embodiment of the present invention, the present compounds are used for the preparation of a pharmaceutical composition for the treatment of Syndrome X.
In one embodiment of the present invention, the present compounds are used for the preparation of a pharmaceutical composition for the treatment of type 2 diabetes. Such treatment includes is treatment for the purpose of the delaying of the progression from IGT to type 2 diabetes as well as delaying the progression from non-insulin requiring type 2 . diabetes to insulin requiring type 2 diabetes.
In one embodiment of the present invention the present compounds are used for the preparation of a pharmaceutical composition for the treatment of type 1 diabetes. Such therapy is normally accompanied by insulin administration.
In one embodiment of the present invention the present compounds are used for the preparation of a pharmaceutical composition for the treatment of dyslipidemia and hyper-lipidemia.
In one embodiment of the present invention the present compounds are used for the preparation of a pharmaceutical composition for the treatment of obesity.
In another aspect of the present invention treatment of a patient with the present compounds are combined with diet and/or exercise.
The present invention provides methods of activating glucokinase activity in a mammal, which methods comprise administering, to a mammal in need of activation of glucokinase activity, a therapeutically defined amount of a compound according to the present invention defined above, as a single or polymorphic crystalline form or forms, an amorphous form, a single enantiomer, a racemic mixture, a single stereoisomer, a mixture of stereoisomers, a single diastereoisomer, a mixture of diastereoisomers, a solvate, a pharmaceutically acceptable salt, a solvate, a prodrug, a biohydrolyzable ester, or a biohydrolyzable amide thereof.
The present invention provides a method of activating glucokinase, comprising the step of administering to a mammal in need thereof a pharmacologically effectve amount of a compound according to the present invention. The invention further provides a pharmaceutical composition comprising a pharmaceutically acceptable carrier and a pharmacologically effective amount of a compound according to the present invention sufficient to activate glucokinase. A glucokinase - activating amount can be an amount that reduces or Inhibits a PTPase activity in the subject.
Additionally provided by the present invention is a pharmaceutical composition comprising a pharmaceutically acceptable carrier and a pharmacologically effective amount of a compound according to the present invention sufficient to treat type I
diabetes.
Also provided by the present invention is a pharmaceutical composition comprising a pharmaceutically acceptable carrier and a pharmacologically effective amount of a compound according to the present invention sufficient to treat type Ii diabetes.
The compounds of the present invention can be administered to any mammal in need of activation of glucokinase activity. Such mammals can include, for example, horses, cows, sheep, pigs, mice, dogs, cats, primates such as chimpanzees, gorillas;
rhesus monkeys, and, most preferably humans.
In a further aspect of the present invention the present compounds are administered in combination with one or more further active substances in any suitable ratios. Such further active agents may be selected from antidiabetic agents, antihyperlipidemic agents, antiobesity agents, antihypertensive agents and agents for the treatment of complications resulting from or associated with diabetes.
Suitable antidiabetic agents include insulin, GLP-1 (glucagon like peptide-1) derivatives such as those disclosed in WO 98/08871 (Novo Nordisk A/S) as well as orally active hypoglycemic agents.
Suitable orally active hypoglycemic agents preferably include imidazolines, sulfonylureas, biguanides. meglitinides, oxadiazoiidinediones, thiazolidinediones, insulin sensitizers, a-gluoosidase inhibitors, agents acting on the ATP-dependent potassium channel of the pancreatic p-cells eg potassium channel openers such as those disclosed in WO
97/26265, WO 99/03861 and, WO 00/37474 (Novo Nordisk A/S) potassium channel openers, such as ormitiglinide, potassium channel blockers such as nateglinide or BTS-67582, glucagon antagonists such as those disclosed in WO 99/01423 and WO 00/39088 (Novo Nordisk A/S and Agouron Pharmaceuticals, Inc.), GLP-1 agonists such as those disclosed in WO 00/42026 (Novo Nordisk A/S and Agouron Pharmaceuticals, Inc.), DPP-IV (dipeptidyl peptidase-IV) inhibitors, PTPase (protein tyrosine phosphatase) inhibitors, inhibitors of hepatic enzymes involved in stimulation of gluconeogenesis and/or glycogenolysis, glucose uptake modulators, GSK-3 (glycogen synthase kinase-3) inhibitors, compounds modifying the lipid metabolism such as antihyperlipidemic agents and antilipidemic agents, compounds lowering food intake, and PPAR (pero)dsome proliferator-activated receptor) and RXR (retinoid X
receptor) agonists such as ALRT-268, LG-1268 or LG-1069.
In one embodiment of the present invention, the present compounds are administered in combination with insulin, insulin derivatives or insulin analogues.
In one embodiment of the present invention, the present compounds are administered in combination with a sulphonylurea eg tolbutamide, chlorpropamide, tolazamide, glibendamide, glipizide, glimepiride, glicazide or glyburide.
In one embodiment of the present invention, the present compounds are administered in combination with a biguanide eg metformin.
In one embodiment of the present invention, the present compounds are administered in combination with a meglitinide eg repaglinide or senaglinide/nateglinide.
In one embodiment of the present invention, the present compounds are administered in combination with a thiazolidinedione insulin sensitizer eg troglitazone, ciglitazone, pioglitazone, rosiglitazone, isaglitazone, darglitazone, englitazone, CS-011/CI-1037 or T 174 or the compounds disclosed in WO 97/41097 (DRF-2344), WO
97/41119, WO
97/41120, WO 00/41121 and WO 98/45292 (Dr. Reddy's Research Foundation).
In one embodiment of the present invention the present compounds may be administered in combination with an insulin sensitizer eg such as GI 262570, YM-440, MCC-555, JTT-501, AR-H039242, KRP-297, GW-409544, CRE-16336, AR-H049020, LY510929, MBX-102, CLX-0940, GW-501516 or the compounds disclosed in WO 99/19313 (NN622/DRF-2725), WO 00/50414, WO 00/63191, WO 00/63192, WO 00/63193 (Dr.
Reddy's Research Foundation) and WO 00/23425, WO 00/23415, WO 00123451, WO
00/23445, WO 00/23417, WO 00/23416, WO 00/63153, WO 00163196, WO 00/63209, WO
00/63190 and WO 00/63189 (Novo Nordisk A/S);

In one embodiment of the present invention the present compounds are administered in combination with an a-glucosidase inhibitor eg voglibose, emiglitate, miglitol or acarbose.
In one embodiment of the present invention the present compounds are administered in combination with a glycogen phosphorylase inhibitor eg the compounds described in WO 97/09040 (Novo Nordisk AIS).
In one embodiment of the present invention the present compounds are administered in combination with an agent acting on the ATP-dependent potassium channel of the pancreatic $-cells eg tolbutamide, glibendamide, glipizide, glicazide, BTS-67582 or repaglinide.
In one embodiment of the present invention the present compounds are administered in combination with nateglinide.
In one embodiment of the present invention the present compounds are administered in combination with an antihyperlipidemic agent or a antilipidemic agent eg cholestyramine, colestipol, dofibrate, gemflbrozil, lovastatin, pravastatin, simvastatin, probucol or dextrothyroxine.
In another aspect of the present invention, the present compounds are administered in combination with more than one of the above-mentioned compounds eg in combination with metformin and a suiphonylurea such as glyburide; a suiphonylurea and acarbose;
nateglinide and metformin; acarbose and metformin; a sulfonylurea, metformin and troglitazone; insulin and a sulfonylurea; insulin and metformin; insulin, metformin and a sulfonylurea; insulin and troglitazone; insulin and lovastatin; etc.
Furthermore, the compounds according to the invention may be administered in combination with one or more antiobesity agents or appetite regulating agents.
Such agents may be selected from the group consisting of CART (cocaine amphetamine regulated transcript) agonists, NPY (neuropeptide Y) antagonists, (melanocortin 3) agonists, MC4 (melanooortin 4) agonists, orexin antagonists, TNF (tumor necrosis factor) agonists, CRF (corticotropin releasing factor) agonists, CRF
BP
(corticotropin releasing factor binding protein) antagonists, urocortin agonists, $3 adrenergic agonists such as CL-316243, AJ-9677, GW-0604, LY362884, LY377267 or AZ-40140, MSH
(melanocyte-stimulating hormone) agonists, MCH (melanocyte-concentrating hormone) antagonists, CCK (cholecystokinin) agonists, serotonin reuptake inhibitors (fluoxetine, seroxat or citalopram), serotonin and norepinephrine reuptake inhibitors, 5HT
(serotonin) agonists, bombesin agonists, galanin antagonists, growth hormone, growth factors such as prolactin or placental tactogen, growth hormone releasing compounds, TRH
(thyreotropin releasing hormone) agonists, UCP 2 or 3 (uncoupling protein 2 or 3) modulators, leptin agonists, DA (dopamine) agonists (bromocriptin, doprexin), lipase/amylase inhibitors, PPAR
modulators, RXR modulators, TR R agonists, adrenergic CNS stimulating agents, AGRP
(agouti related protein) inhibitors, H3 histamine antagonists such as those disclosed in WO
00/42023, WO 00/63208 and WO 00/64884, exendin-4, GLP-1 agonists and ciliary neurotrophic factor. Further antiobesity agents are bupropion (antidepressant), topiramate (anticonvulsant), ecopipam (dopamine antagonist) and naltrexone (opioid antagonist).
In one embodiment of the present invention the antiobesity agent is leptin.
In one embodiment of the present invention the antiobesity agent is a serotonin and norepinephrine reuptake Inhibitor eg sibutramine.
In one embodiment of the present invention the antiobesity agent Is a lipase Inhibitor eg orlistat.
In one embodiment of the present invention the antiobesity agent Is an adrenergic CNS stimulating agent eg dexamphetamine, amphetamine, phentermine, mazirldol phendimetrazine, diethyipropion, fenfluramine or dexfenfluramine.
Furthermore, the present compounds may be administered In combination with one or more antihypertensive agents. Examples of antihypertensive agents are p-Mockers such as aiprenolol, atenolol, timolol, pindolol, propranolol and metoprolol, ACE
(angiotensin converting enzyme) Inhibitors such as benazepril, captopril, enalapril, fosinopril, lisinopril, quinapril and ramipril, calcium channel bloc leers such as nifedipine, felodipine, nicardipine, isradipine, nimodipine, diltiazem and verapamil, and a-blockers such as doxazosin, urapidil, prazosin .and terazosin. Further reference can be made to Remington: The Science and Practice of Pharmacy, 19th Edition, Gennaro, Ed., Mack Publishing Co., Easton, PA, 1995.
In a further aspect the invention provides a pharmaceutical preparation comprising an activator of glucokinase and an insulin derivative.
In one embodiment of the invention the insulin derivative Is selected from the group consisting of B29-N`-myristoyl-des(B30) human insulin, B29-N`-palmitoyl-des(B30) human insulin, B29-N`-myristoyl human insulin, B29-N`-palmitoyl human Insulin, B28-N`-myristoyl LysB2 PO" human insulin, B28-N`-palmitoyl LyeB2 Pro829 human insulin, B30-N`-myristoyl-Thr828Lys30 human Insulin, 630-N`-palmitoyl-ThrO"t ye90 human Insulin, B29-W-(N-palmitoyl1-glutamyl)-des(B30) human insulin, B29-N`-(N-lithocholy1 y-glutamyl)-des(B30) human insulin, B29-N`-(w-carboxyheptadecanoyl)-des(B30) human Insulin and B29-N`4w-carboxyheptadecanoyl) human insulin.

In another embodiment of the invention the insulin derivative is B29-N`-myristoyl-des(B30) human insulin.
It should be understood that any suitable combination of the compounds according to the invention with diet and/or exercise, one or more of the above-mentioned compounds and optionally one or more other active substances are considered to be within the scope of the present invention.

PHARMACEUTICAL COMPOSITIONS
The compounds of the present invention may be administered alone or In combination with pharmaceutically acceptable carriers or excipients, In either single or multiple doses. The pharmaceutical compositions according to the invention may be formulated with pharmaceutically acceptable carriers or diluents as well as any other known adjuvants and excipients in accordance with conventional techniques such as those disclosed in Remington: The Science and Practice of Pharmacy, 19M Edition, Gennaro, Ed., Mack Publishing Co., Easton, PA, 1995.
The pharmaceutical compositions may be specifically formulated. for administration by any suitable route such as the oral, rectal, nasal, pulmonary, topical (including buccal and sublingual), transdemlal, intracistemal, intraperitoneal, vaginal and parenteral (including subcutaneous, intramuscular, intrathecal,.intravenous and intradermal) route, the oral route being preferred. It will be appreciated that the preferred route will depend on the general condition and age of the subject to be treated, the nature of the condition to be treated and the active ingredient chosen.
Pharmaceutical compositions for oral administration include solid dosage forms such as hard or soft capsules, tablets, troches, dragees, pills, lozenges, powders and granules. Where appropriate, they can be prepared with coatings such as enteric coatings or -they can be formulated so as to provide controlled release of the active ingredient such as sustained or prolonged release according to methods well known in the art.
Liquid dosage forms for oral administration include solutions, emulsions, aqueous or oily suspensions, syrups and elixirs.
Pharmaceutical compositions for parenteral administration include sterile aqueous and non-aqueous injectable solutions, dispersions, suspensions or emulsions as well as sterile powders to be reconstituted in sterile injectable solutions or dispersions prior to use.
Depot injectable formulations are also contemplated as being within the scope of the present invention.

Other suitable administration forms include suppositories, sprays, ointments, cremes, gels, inhalants, dermal patches, implants etc.
A typical oral dosage is in the range of from about 0.001 to about 100 mg/kg body weight per day, preferably from about 0.01 to about 50 mg/kg body weight per day, and more preferred from about 0.05 to about 10 mg/kg body weight per day administered in. one or more dosages such as 1 to 3 dosages. The exact dosage will depend upon the frequency and mode of administration, the sex, age, weight and general condition of the subject treated, the nature and severity of the condition treated and any concomitant diseases to be treated and other factors evident to those skilled in the art.
The formulations may conveniently be presented in unit dosage form by methods known to those skilled in the art. A typical unit dosage form for oral administration one or more times per day such as 1 to 3 times per day may contain from 0.05 to about 1000 mg, preferably from about 0.1 to about 500 mg, and more preferred from about 0.5 mg to about 200 mg.
For parenteral routes such as intravenous, intrathecal, intramuscular and similar administration, typically doses are in the order of about half the dose employed for oral administration.
The compounds of this invention are generally utilized as the free substance or as a pharmaceutically acceptable salt thereof. Examples are an acid addition salt of a compound having the utility of a free base and a base addition salt of a compound having the utility of a free acid. The term "pharmaceutically acceptable salts" refers to non-toxic salts of the compounds of this invention which are generally prepared by reacting the free base with a suitable organic or inorganic acid or by reacting the acid with a suitable organic or inorganic base. When a compound according to the present invention contains a free base such salts are prepared in a conventional manner by treating a solution or suspension of the compound with a chemical equivalent of a pharmaceutically acceptable acid. When a compound according to the present invention contains a free acid such salts are prepared in a conventional manner by treating a solution or suspension of the compound with a chemical equivalent of a pharmaceutically acceptable base. Physiologically acceptable salts of a compound with a hydroxy group include the anion of said compound in combination with a suitable cation such as sodium or ammonium ion. Other salts which are not pharmaceutically acceptable may be useful in the preparation of compounds of the present invention and these form a further aspect of the present invention.
For parenteral administration, solutions of the novel compounds of the formula (I) in sterile aqueous solution, aqueous propylene glycol or sesame or peanut oil may be employed. Such aqueous solutions should be suitably buffered if necessary and the liquid diluent first rendered isotonic with sufficient saline or glucose. The aqueous solutions are particularly suitable for intravenous, intramuscular, subcutaneous and intraperitoneal administration. The sterile aqueous media employed are all readily available by standard techniques known to those skilled in the art.
Suitable pharmaceutical carriers include inert solid diluents or fillers, sterile aqueous solution and various organic solvents. Examples of solid carriers are lactose, terra alba, sucrose, cydodextrin, talc, gelatine, agar, pectin, acacia, magnesium stearate, stearic acid and lower alkyl ethers of cellulose. Examples of liquid carriers are syrup, peanut oil, olive oil, phospholipids, fatty acids, fatty acid amines, polyoxyethylene and water.
Similarly, the carrier or diluent may include any sustained release material known In the art, such as glyceryl monostearate or glyceryl distearate, alone or mixed with a wax. The pharmaceutical compositions formed by combining the novel compounds of the present invention and the pharmaceutically acceptable carriers are then readily administered in a variety of dosage forms suitable for the disclosed routes of administration. The formulations may conveniently be presented in unit dosage form by methods known in the art of pharmacy.
Formulations of the present invention suitable for oral administration may be presented as discrete units such as capsules or tablets, each containing a predetermined amount of the active ingredient, and which may include a suitable excipient.
Furthermore, the orally available formulations may be in the form of a powder or granules, a solution or suspension in an aqueous or non-aqueous liquid, or an oil-in-water or water-in-oil liquid emulsion.
Compositions intended for oral use may be prepared according to any known method, and such compositions may contain one or more agents selected from the group consisting of sweetening agents, flavoring agents, coloring agents, and preserving agents in order to provide pharmaceutically elegant and palatable preparations. Tablets may contain the active ingredient in admixture with non-toxic pharmaceutically-acceptable excipients which are suitable for the manufacture of tablets. These excipients may be for example, inert diluents, such as calcium carbonate, sodium carbonate, lactose, calcium phosphate or sodium phosphate; granulating and disintegrating agents, for example corn starch or alginic acid; binding agents, for example, starch, gelatin or acacia; and lubricating agents, for example magnesium stearate, stearic acid or talc. The tablets may be uncoated or they may be coated by known techniques to delay disintegration and absorption in the gastrointestinal tract and thereby provide a sustained action over a longer period. For example, a time delay material such as glyceryl monostearate or glyceryl distearate may be employed.
They may also be coated by the techniques described in U.S. Patent Nos. 4,356,108;
4,166,452; and 4,265,874, to form osmotic therapeutic tablets for controlled release.

Formulations for oral use may also be presented as hard gelatin capsules where the active ingredient is mixed with an inert solid diluent, for example, calcium carbonate, calcium phosphate or kaolin, or a soft gelatin capsules wherein the active ingredient is mixed with water or an oil medium, for example peanut oil, liquid paraffin, or olive oil.
Aqueous suspensions may contain the active compounds in admixture with excipients suitable for the manufacture of aqueous suspensions. Such excipients are suspending agents, for example sodium carboxymethylcellulose, methylcellulose, hydroxypropylmethylcellulose, sodium alginate, polyvinylpyrrolidone, gum tragacanth and gum acacia; dispersing or wetting agents may be a naturally-occurring phosphatide such as lecithin, or condensation products of an alkylene oxide with fatty acids, for example polyoxyethylene stearate, or condensation products of ethylene oxide with long chain aliphatic alcohols, for example, heptadecaethyl-eneoxycetanol, or condensation products of ethylene oxide with partial esters derived from fatty acids and a hexitol such as polyoxyethylene sorbitol monooleate, or condensation products of ethylene oxide with partial esters derived from fatty adds and hexitol anhydrides, for example polyethylene sorbitan monooleate. The aqueous suspensions may also contain one or more coloring agents, one or more flavoring agents, and one or more sweetening agents, such as sucrose or saccharin.
Oily suspensions may be formulated by suspending the active ingredient in a vegetable oil, for example arachis oil, olive oil, sesame oil or coconut oil, or in a mineral oil such as a liquid paraffin. The oily suspensions may contain a thickening agent, for example beeswax, hard paraffin or cetyl aichol. Sweetening agents such as those set forth above, and flavoring agents may be added to provide a palatable oral preparation. These compositions may be preserved by the addition of an anti-oxidant such as ascorbic acid.
Dispersible powders and granules suitable for preparation of an aqueous suspension by the addition of water provide the active compound In admixture with a dispersing or wetting agent, suspending agent and one or more preservatives.
Suitable dispersing or wetting agents and suspending agents are exemplified by those already mentioned above. Additional excipients, for example, sweetening, flavoring, and coloring agents may also be present.
The pharmaceutical compositions of the present invention may also be in the form of oil-in-water emulsions. The oily phase may be a vegetable oil, for example, olive oil or arachis oil, or a mineral oil, for example a liquid paraffin, or a mixture thereof. Suitable emulsifying agents may be naturally-occurring gums, for example gum acacia or gum tragacanth, naturally-occurring phosphatides, for example soy bean, lecithin, and esters or partial esters derived from fatty acids and hexitol anhydrides, for example sorbitan monooleate, and condensation products of said partial esters with ethylene oxide, for example polyoxyethylene sorbitan monooleate. The emulsions may also contain sweetening and flavoring agents.
Syrups and elixirs may be formulated with sweetening agents, for example glycerol, propylene glycol, sorbitol or sucrose. Such formulations may also contain a demulcent, a preservative and flavoring and coloring agents. The pharmaceutical compositions may be in the form of a sterile injectible aqueous or oleaginous suspension. This suspension may be formulated according to the known methods using suitable dispersing or wetting agents and suspending agents described above. The sterile injectable preparation may also be a sterile injectable solution or suspension in a non-toxic parenterally-acceptable diluent or solvent, for example as a solution in 1,3-butanediol. Among the acceptable vehicles and solvents that may be employed are water, Ringer's solution, and isotonic sodium chloride solution. In addition, sterile, fixed oils are conveniently employed as solvent or suspending medium. For this purpose, any bland fixed oil may be employed using synthetic mono- or diglycerides. In addition, fatty acids such as oleic acid find use in the preparation of injectables.
The compositions may also be in the form of suppositories for rectal administration of the compounds of the present invention. These compositions can be prepared by mixing the drug with a suitable non-irritating excipient which is solid at ordinary temperatures but liquid at the rectal temperature and will thus melt in the rectum to release the drug. Such materials include cocoa butter and polyethylene glycols, for example.
For topical use, creams, ointments, jellies, solutions of suspensions, etc., containing the compounds of the present invention are contemplated. For the purpose of this application, topical applications shall include mouth washes and gargles.
The compounds of the present invention may also be administered in the form of liposome delivery systems, such as small unilamellar vesicles, large unilamellar vesicles, and multilamellar vesicles. Liposomes may be formed from a variety of phospholipids, such as cholesterol, stearylamine, or phosphatidyicholines.
In addition, some of the compounds of the present invention may form solvates with water or common organic solvents. Such solvates are also encompassed within the scope of the present invention.
Thus, in a further embodiment, there is provided a pharmaceutical composition comprising a compound according to the present invention, or a pharmaceutically acceptable salt, solvate, or prodrug therof, and one or more pharmaceutically acceptable carriers, excipients, or diluents.
If a solid carrier is used for oral administration, the preparation may be tabletted, placed in a hard gelatine capsule in powder or pellet form or it can be in the form of a troche or lozenge. The amount of solid carrier will vary widely but will usually be from about 25 mg to about 1 g. If a liquid carrier is used, the preparation may be in the form of a syrup, emulsion, soft gelatine capsule or sterile injectable liquid such as an aqueous or non-aqueous liquid suspension or solution.
A typical tablet that may be prepared by conventional tabletting techniques may contain:
Core:
Active compound (as free compound or salt thereof) 5.0 mg Lactosum Ph. Eur. 67.8 mg Cellulose, microcryst. (Avicel) 31.4 mg 15. Amberlite IRP88* 1.0 mg Magnesii stearas Ph. Eur. q.s.
Coating:
Hydroxypropyl methylcellulose approx. 9 mg Mywacett 9-40 T** approx. 0.9 mg * Polacrillin potassium NF, tablet disintegrant, Rohm and Haas.
** Acylated monoglyceride used as plasticizer for film coating.

If desired, the pharmaceutical composition of the present invention may comprise a compound according to the present invention in combination with further active substances such as those described in the foregoing.
The present invention also provides a method for the synthesis of compounds useful as intermediates in the preparation of compounds of formula (I) along with methods for the preparation of compounds of formula (I). The compounds can be prepared readily according to the following reaction Schemes (in which all variables are as defined before, unless so specified) using readily available starting materials, reagents and conventional synthesis procedures. In these reactions, it is also possible to make use of variants which are themselves known to those of ordinary skill in this art, but are not mentioned in greater detail.

ABBREVIATIONS
Abbreviations used in the Schemes and Examples are as follows:
d = days g = grams h = hours Hz = hertz kD = kiloDalton L = liters M = molar mbar = millibar mg = milligrams min = minutes ml = milliliters mM = millimolar mmol ' = millimoles mol = moles N = normal ppm = parts per million psi = pounds per square inch APCI = atmospheric pressure chemical ionization ESI = electrospray ionization i.v. = intravenous m/z = mass to charge ratio mp = melting point MS = mass spectrometry NMR = nuclear magnetic resonance spectroscopy P.O. = per oral Rr = relative TLC mobility rt = room temperature S.C. = subcutaneous TLC = thin layer chromatography tr = retention time BOP = (1-benzotriazolyloxy)tris(dimethylamino)phosphonium hexafluorophosphate DCM = dichloromethane DIEA = diisopropylethylamine DMF = N, N-dimethylformamide DMPU = 1,3-dimethypropylene urea DMSO = dimethylsulfoxide EDC =1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide hydrochloride ether = diethyl ether EtOAc = ethyl acetate HMPA = hexamethyiphosphoric triamide HOBt =1-hydroxybenzotriazole LAH = lithium aluminum hydride LDA = lithium diisopropylamide MeOH = methanol NMM = N-methylmorpholine, 4-methylmorpholine TEA = triethylamine TFA = trifluoroacetic acid THE = tetrahydrofuran THP = tetrahydropyranyl TTF = Fluoro-N,N,N'-tetramethylformamidinium hexafluorophosphate REACTION SCHEMES
Unless otherwise specified, the variables in the Schemes are as defined for formula (I).
Scheme 1 describes the preparation of compounds of formula (74).

Scheme 1 1) 0 (72) G' H K_jt,K L

1100 ' ~ A

(71) 2) G' -1 R101 R1oo L
H (73) (74) N

1 1) (72) G' L' K K L' O
H q2 Al 110, 2) A2 -N N~o~ Roo Roo R
(73) (71) (74) A2 is heteroaryl, fused heterocyclylheteroaryl, or fused cydoalkylheteroaryl.
R100 and R101, independently of each other, are substituents such as, but not limited to, H, alkyl, alkenyl, alkynyl, -alkylene-aryl, alkylene-cycloalkyl, and the like.
K is halogen or 1-imidazolyl.
The amine (71) may be treated with carbonyldiimidazole, 4-nitrophenyl chloroformate, phosgene or a derivative of phosgene such as diphosgene or tiphosgene, in a solvent such as DCM or DCE. DMAP may be used as a catalyst in this reaction.
The reaction may be conducted at a temperature of from 0 C to 100 C. The reaction mixture may be then be treated with the compound (73) and the whole may be incubated at a temperature of from 25 C to 100 C to afford the urea (75). It is also understood that (73) may be treated with the reagent (72) under similar conditions, followed by treatment with the amine (71), to afford (74).

Scheme 2 describes the preparation of a compound of formula (79).
Scheme 2 (76) GI
Lg1 L11 (77) Al N02 G 1 L H NO2 (75) G
G' Lip L
H
N

(78) (79) L" has the meaning of L' in formula (I), with the provisio that when L" is -D-alkylene-E-, -D-alkenylene-E-, -D-alkynylene-E-, -D-cycloalkylene-E-, or -D-heterocyclylene-E-, then D is selected from -0- or -S-, and that L" is not -S(O)-, S(O)2-, -C(O}, or -C(=N-OR12)-.
Lg1 is a leaving group such as F, Cl, Br, or I.
R101 is a substituent such as but not limited to H, alkyl, alkenyl, alkynyl, -alkylene-aryl, alkylene-cycloalkyl, and the like.
A nitro-substitued aryl or heteroaryl ring compound such as (75) may be treated with (76) in the presence of a base such as NaH or potassium tert-butoxide, in a solvent such as THF, DMF, or NMP at a temperature of from 0 C to 100 C, to afford (77). The resulting adduct (77) may be treated with tin(II) chloride in ethanol or other alcoholic solvent, at a temerature of from 25 C to 100 C, in the presence of aqueous HCI, to afford the amine (78).
The amine (78) may, is desired, be treated with an alkyl halide R101-Lg2, wherein Lg2 is a leaving group such. as Br, I, or p-toluenesulfonate, and a base such as DBU or sodium hydride, to afford (79). Alternatively, (78) may be treated with a reagent R102-C(O)-R'03, wherein R102 and R103 independently of each other are substituents such as, but not limited to, H, alkyl, alkenyl, alkynyl, -alkylene-aryl, alkylene-cydoalkyl, and the like, in the presence of a reducing agent such as sodium cyanoborohydrode or sodium triacetoxyborohydride, to afford (79) wherein R101 should be understood as R102-C(H)(R103)-.

Alternatively, (78) may be treated with a reagent Rt02C(O)-OH in the presence of a dehydrating agent such as EDC, to afford an intermediate amide, which may be reduced with a reagent such as DIBAL or LAH, in a solvent such as THF, at a temperature of from 0 C to 80 C, to afford (71) wherein R102 should be understood as -CHrR102.
Alternatively, (79) wherein R101 is -CH3 may be prepared by treatment of (78) with a reagent R102-O-CO-CI, or R102O-CO-O-CO-O-R102, in the presence of a base such as TEA or aqueous alkali, to afford an intermediate which may be reduced as above employing DIBAL or LAH giving (79).
Compound (79) may be employed in the same manner as is compound (73) according to the chemistry in Scheme (1).

Scheme 3 describes the synthesis of a compound of formula (71).
Scheme 3 ? H

(80) (71) A2 is (un)substituted heteroaryl, (un)substituted fused heterocyclylheteroaryl, or (un)substituted fused cycloalkylheteroaryl.
R100 is a substituent such as, but not limited to, H, (un)substituted alkyl, (un)substituted alkenyl, (un)substituted alkynyl, (un)substituted -alkylene-aryl, (un)substituted -alkylene-cycloalkyl, and the like.
The amine (80) may, if desired, be treated with an alkyl halide R700-Lg2, wherein Lg2 is a leaving group such as Br, I, or p-toluenesulfonate, and a base such as DBU or sodium hydride, to afford (71). Alternatively, (80) may be treated with a reagent R102-C(O)-R703 wherein R102 and R103, independently of each other, are substituents such as, but not limited to, H, alkyl, alkenyl, alkynyl, -alkylene-aryl, -alkylene-cycloalkyl, and the like, in the presence of a reducing agent such as sodium cyanoborohydrode or sodium triacetoxyborohydride, to afford (71) wherein R100 should be understood as R10Y-C(H)(R103)-.
Alternatively, (78) may be treated with a reagent such as R702C(O)-CI and a base such as TEA, or R102C(O)-OH in the presence of a dehydrating agent such as EDC, to afford an intermediate amide, which may be reduced with a reagent such as DIBAL or LAH, in a solvent such as THF, at a temperature of from 0 C to 80 C, to afford (71) wherein R1Q0 should be understood as -CH2-R102. Alternatively, (71) wherein R100 is -CH3 may be prepared by treatment of (78) with a reagent R102-0-C(O)-CI, or R1020-C(O)-O-C(O)-O-R102, in the presence of a base such as TEA or aqueous alkali, to afford an intermediate which may be reduced as above employing DIBAL or LAH giving (71).

Scheme 4 describes the synthesis of a compound of formula (81).
Scheme 4 G1 O ' A 1 L Cl NCO L' 0 O
H ) Az N A~ 11o1 2) A- N Al 1101 H R1oo (73) (71) (81) A2 is (un)substituted heteroaryl, (un)substituted fused heterocyclylheteroaryl, or (un)substituted fused cycloalkylheteroaryl.
R100and R101 are, independently of each other, substituents such as but not limited to H, (un)substituted alkyl, (un)substituted alkenyl, (un)substituted alkynyl, (un)substituted -alkylene-aryl, (un)substituted -alkylene-cycloalkyl, and the like.
The amine (73) may be treated with the reagent chlorocarbonyl isocyanate in the presence of a base such as DIEA, in a solvent such as THF, DCE, or dioxane, at a temperature of from - 60 C to 25 C. The intermediate thus formed may be treated at a temperature of from 0 C to 80 C with (71) to afford (81).

Scheme 5 describes the preparation of an intermediate of formula (87).

Scheme 5 0 0 (84) OH 0 _R104 GMI
/
A' NH2 A' N
(82) (83) Al R104 A+ NH2 (85) 0 (86) L" is, in this instance, a group such as (un)substituted alkylene or a direct bond.
R104 is a substituent such as but not limited to (un)substituted alkyl, (un)substituted aryl, (un)substituted alkenyl, (un)substituted alkynyl, (un)substituted -alkylene-aryl, (un)substituted -alkyiene-cydoalkyl, and the like.
The anthranilic acid (82) may be treated with an acid chloride R'04-CO-CI In the presence of a base such as TEA or aqueous alkali to afford an amide Intermediate, which may be treated with a dehydrating agent such as POCI3 or SOCI2 in a solvent such as DCE, at a temperature of from 0 C to 80 C, to afford (83). A reagent (84) derived from an active metallating agent such as lithium or magnesium metal and G'-L"-Br or G'-L"-l may be prepared. For example, where G' is aryl and L" is a direct bond. G'-L"-Br may be treated with n-butyllithium in a solvent such as ether, at a temperature of from - 78 C to 0 C, to afford the reagent (84) where M' is Li. (84) may be treated with (83) in a solvent such as THF, at a temperature of from - 78 C to 50 C, to afford (85). The amide (85) may be treated with aqueous alkali in a solvent such as ethanol, at a temperature of from 25 C to 100 C, to afford (86).

Scheme 6 describes an alternate synthesis of a compound of formula (88).

Scheme 6 1 G

O o Gt-011 CI
At NHR101 At (>_NHR101 BC~
(87) GaCI3 (88) L12 is, in this instance, a group such as but not limited to (un)substituted alkylene, (un)substituted cycloalkylene, or a direct bond.
An amine compound (87) may be treated with an acid chloride, or other acid halide, in the presence of boron trichloride at a temperature of from -40 C to 25 C, followed by treatment with gallium (Ill) chloride and chlorobenzene and heating at a temperature of from 50 C to 150 C, to afford (88).

Scheme 7 describes synthesis of intermediates of formulae (91), (92), (93),'(94), and (95).

Scheme 7 G G' G
\ '3 \L'3 '3 A' -NO2 ----~ A' -NO2 A' N02 H3C Br , 11 (89) (90) O,? (91) G\ 13 A' NOT G\ \ 13 R' s L' N A' NO2 RAl NO2 (92) 1s HS L (93) (91) 1105 R' 8--H
GL'3 GL13 A' -NO2 O A' '-NO2 R1 e/S `2 R107 (94) (95) L13 is a group such as oxygen, or may be a group broadly defined as for L72 and L11.
R106, RI 07 and 11108 are groups such as but not limited to (un)substituted alkyl, (un)substituted -alkylene-aryl, or H.

The nitrotoluene (89) can be brominated with a reagent such as N-bromosuccinimide in carbon tetrachloride to get the bromide intermediate (90).
The methyl group in (89) may also be a more elaborate alkyl broup with hydrogen(s) on the carbon adjacent to A'. The bromide (90) may be treated with sodium methanesulfinate to afford intermediate (91) and with secondary or primary amines to obtain the intermediate (92).
Alternately, the R106 and R'07 groups in the compound R'0 R107NH may be taken together for constitute an heteroaryl or heterocyclic group, and treatment of (90) with such a compound in the presence of a base such as potassium tert-butoxide affords (92) where the R106 and R707 groups are taken together for constitute a heteroaryl or heterocyclic group.
Alternately, (90) may be treated with sodium thiolacetate, followed by hydrolysis with aqueous alkali, to afford the thiol (91). From (91), various compounds may be prepared. For example, treatment of (91) with an alkylating agent such as an alkyl bromide in the presence of base such as sodium hydride affords (93) where L14 is S and R105 is alkyl. Oxidation of this species with a reagent such as m-chloroperbenzoic acid may afford the compound where L14 is -SOr , Compound (92) where R106 is H may be treated with a compound R'08SO2CI in the presence of a base such as pyridine to form (95). Alternately, (92) where R108 is H may be treated with, a carboxylic acid R108COOH in the presence of a peptide coupling agent such as dicyclohexylcarbodiimide to form (94).

Scheme 8 describes synthesis of compounds of formula (97).

Scheme 8 G' ^1 5}7 L18 L1e (A' --NR 10i A' NR 101 X15 ~1s 0 R109 R 'N~R109 R1t1 (96) (97) L18 is oxygen. G' and L18, in this instance, preferably contain no ketone, aldehyde, or primary or secondary amine groups.
R109, R10, and R"' are groups such as but not limited to (un)substituted alkyl, H, or (un)substituted alkylene-aryl. R70 and R"' may optionally be taken together to constitute a heterocyclic ring.

Ureas of formula (91) can be reductively aminated using amines Rf 10NHR1f and a reagend such as sodium triacetoxyborohydride in a solvent such as 1,2-dichloroethane in the presence or absence of acetic acid to obtain compounds of formula (92).

Scheme (9) describes synthesis of compounds of formulae (100) and (101).
Scheme 9 G' L"
O
I N N

(98) G' L" O
".,A 2 NN
R1 R 101 RIao (99) G' \G1 O L i7 ,AZ O z NI `N
1 ~o1 1 100 Y101 ~NR -N Roo H R

R"L18 R R 14 (100) (101) L" is carbonyl or sulfonyl group.
Nitrophenylureas (98) can be reduced to aniline derivatives of formula (99).
Treatment of intermediate (99) with acid chlorides or sulfonyl chlorides can yield compounds of formula (100). Alkylation of intermediate (99) using aldehydes or ketones in the presense of sodium triacetoxyborohydride affords (101). Alternately. (99) may be treated with a dialkyl halide and a base such as DIEA to afford (101) where R13 and R14 and the nitrogen to which they are attached constitute a ring.

Scheme 10 ' L i p L1 ll A2 p 2 Lt9 R1o1 R1oo L19 R1o1 R100 Cp2H ~=O
R11s (102) 8116 (103) L19 in this instance is a group such as (un)substituted alkylene. R1 and R"8 are independently, groups such as (un)substituted alkyl, (un)substituted alkylene-aryl, or H.
Alternately, R15 and R118 may be taken together to constitute a heterocyclic ring.

The acid (102) may be coupled with an amine R"SNHR16 in the presence of a coupling agent such as dicyclohexylcarbodlimide in a solvent such as THE or dichloromethane to afford (103).

Scheme 11 Scheme 11 G' +
G
A N N N N
Rim Rtoo R101 R+oo (104) (105) L' ps~~S=O
N^N/ R+n A101 Rtoo (106) A3 is a group such as (un)substituted heteroarylene, (un)substituted fused heterocydyiheteroarylene, or (un)substituted fused cycloalkylheteroarylene.

R' 17 is a group such as (un)substituted alkyl, (un)substituted alkylene-aryl, (un)substituted aryl, or (un)substituted heteroaryl.

The compound (104) may be treated with a thiol reagent in the presence of a base such as DIEA at temperatures of from 50 C to 150 C to afford the thioether (105). (105) may be oxidized with a oxidizing reagent such as m-chloroperbenzoic acid in a solvent such as dichloromethane to afford the sulfone (106).
Where only one equivalent of the oxidant is employed, the suffoxide may be obtained.
Where 2 or more equivalents of oxidant are employed, the sulfone is obtained.

Scheme 12 describes the synthesis of compounds of formula (109).

Scheme 12 H, R
S_Rõ7 L /A3-L\ /A3 -LJLN L92 NI`N\20 N R1o1 1100 R1o1 R7oo (108) (107) G' L 0 A3-L2o \
NJLN/ OS` Rh,7 Rt01 A100 0 (109) A3 is a group such as (un)substituted heteroarylene, (un)substituted fused heterocyclylheteroarylene, or (un)substituted fused cycloalkylheteroarylene.
L20 in this instance is a group such as (un)substituted alkylene. R' 17 is a group such as (un)substituted alkyl, (un)substituted alkylene-aryl, (un)substituted aryl, or (un)substituted heteroaryl. Lg2 is a leaving group such as chloride, methanesulfonate, or p-toluenesulfonate.

The compound (107) where Lg2 is methanesulfonate may be synthesized from the precursor where Lg2 is hydroxyl by treatment with methanesulfonyl chloride in the presence of pyridine. (107) then may be treated with a thiol reagent in the presence of a base such as DIEA, potassium tert-butoxide, or sodiun hydride, to afford the displacement product (108).
The thioether product (108) may be oxidized to the sulfoxide or sutfone (109) as described In Scheme 11.
Scheme 13 describes the synthesis of compounds of formula (111).

Scheme 13 G' G' L' 0 A3`_L21 L 0 3`L 21 8115 Al N~N~ CO2H N_N O// N R,1e R1o1 R1oo R R
1o1 too (110) (111) L21 in this instance is a group such as alkylene. R15 and R16 may have the meaning denoted previously, or may be, independently, groups such as (un)substituted alkyl, (un)substituted alkylene-aryl, (un)substituted aryl, H. or (un)substituted heteroaryl. A3 is a group such as (un)substituted heteroarylene, (un)substituted fused heterocydylheteroarylene, or (un)substituted fused cycloalkylheteroarylene.

The acid (110) may be coupled with an amine R115NHR"8 in the presence of a coupling agent such as dicydohexylcarbodiimide to afford (111).

Scheme 14 describes a synthesis of intermediates of formula (113).
Scheme 14 Br 8119 (112) 8119 R11a S
O H2N-~\
H2N NH2 ,. N R'18 (113) We and R19 may be, Independently, groups such as (un)substituted alkyl, (un)substituted alkylene-aryl, (un)substituted aryl, H, or (un)substituted heteroaryl.

Thiourea may be condensed with the bromo carbonyl compound (112) in the presence or absence of a mild base such as potassium carbonate or triethylamine, in a solvent such as ethanol, at a temperature of from 25 C to 120 C, to afford (113). The bromo compound (112) may be accessed by a variety of methods known in art For example, bromination of the ketone with pyrrolidinium hydrotribromide in THE
or N-bromosuccinimide in THE in the presence of a mild base such as potassium carbonate affords (112).

Scheme 15 describes synthesis of intermediates of formula (117) Scheme (15) O
HO OEt O or G\L~ R20 HOy-'OEt G\L+ R20 NH O O
N- jF1(CH2)fl...i.OEt EDC, HOW O O n=0,1 (114) (115) R' G
GL, R20 HN, \L, 20 Li R
N r(CH2)n"i(OH G an 0 PyBOP ENY_(CH2)n(N
' O O G
(116) (117) Scheme 15 shows the synthetic route to diamides of the type (117), where A', L', R20, R', G', G2 are as defined in Formula (I). Amine (114) can be coupled with an activated oxalic or malonic esters using EDC/HOBt to give amide (115). Deprotection of the t-butyl ester of B is done with lithium hydroxide to give the carboxylic acid (116), which can be coupled using standard amide coupling reagents (eg. PyBOP) to give diamides of the type (115).

The intermediates in the above Schemes may be substituted with amino, hydroxyl, or carboxyl groups which may require protection and deprotection during the course of preparation of Example compounds.

"Amino protection" refers to substituents of the amino group commonly employed to block or protect the amino functionality while reacting other functional groups on the compound. Examples of such amino-protecting groups include the formyl group, the trityl group, the phthalimido group, the tnchloroacetyl group, the chloroacetyl, bromoacetyl and iodoacetyl groups, urethane-type blocking groups such as benzyloxycarbonyl, 4-phenylbenzyloxycarbonyl, 2-methylbenzyloxycarbonyl, 4-methoxybenzyloxycarbonyl, 4-fluorobenzyloxycarbonyl, 4-chlorobenzyloxycarbonyl, 3-chlorobenzyloxycarbonyl, chlorobenzyloxycarbonyl, 2,4-dithlorobenzyloxycarbonyl, 4-bromobenzyloxycarbonyl, 3-bromobenzyloxycarbonyl, 4-nitrobenzyloxycarbonyl, 4-cyanobenzyloxy-carbonyl, 2-(4-xenyl)iso-propoxycarbonyl, 1,1-diphenyleth-1-yloxycarbonyl,1,1-diphenylprop-l-yloxycarbonyl, 2-phenylprop-2-yloxycarbonyl, 2-(p-toluyl)prop-2-yloxycarbonyl, cydopentanyloxycarbonyl, 1-methylcyclopentanyloxycarbonyl, cydohexanyloxycarbonyl, 1-methylcyclohexanyloxycarbonyl, 2-methylcyclohexanyloxycarbonyl, 2-(4-toluylsulfonyl)ethoxycarbonyl, 2(methylsulfonyl)ethoxycarbonyl, 2-(triphenylphosphino)ethoxycarbonyl, 9-fluorenylmethoxycarbonyl ("FMOC"), t-butoxycarbonyl ("BOC"), 2-(tnmethylsilyl)ethoxycarbonyl, allyloxycarbonyl, 1-(trimethylsilylmethyl)prop-1-enyloxycarbonyl, 5-benzisoxalylmethoxycarbonyl, 4-acetoxybenzyloxycarbonyl, 2,2,2-trichloroethoxycarbonyl, 2-ethynyl-2-propoxycarbonyl, cydopropylmethoxycarbonyl, 4 (decyloxy)benzyloxycarbonyl, isobomyloxycarbonyl, 1-piperidyloxycarbonyl and the like; the benzoylmethylsulfonyl group, the 2-(nitro)phenylsulfenyl group, the diphenylphosphine oxide group and like amino-protecting groups. The species of amino-protecting group employed is not critical so long as the derivatized amino group is stable to the condition of subsequent reaction(s) on other positions of the compound of Formula (I) and can be removed at the desired point without disrupting the remainder of the molecule. Preferred amino-protecting groups are the allyloxycarbonyl, the t-butoxycarbonyl, 9-fluorenylmethoxycarbonyl, and the trityl groups. Similar amino-protecting groups used in the cephalosporin, penicillin and peptide art are also embraced by the above terms. Further examples of groups referred to by the above terms are described by J. W. Barton, "Protective Groups In Organic Chemistry", J. G. W. McOmie, Ed., Plenum Press, New York, N.Y., 1973, and T. W. Greene, "Protective Groups in Organic Synthesis", John Wiley and Sons, New York, N.Y., 1981. The related term 'protected amino' defines an amino group substituted with an amino-protecting group discussed above.

"Hydroxyl protection" refers to substituents of the alcohol group commonly employed to block or protect the alcohol functionality while reacting other functional groups on the compound. Examples of such alcohol -protecting groups include the 2-tetrahydropyranyl group, 2-ethoxyethyl group, the trityl group, the trichloroacetyl group, urethane-type blocking groups such as benzyloxycarbonyl, and the trialkylsilyl group, examples of such being trimethylsilyl, tert-butyidimethylsilyl, phenyldimethylsilyl, triiospropyisilyl and thexyldimethylsilyl. The choice of of alcohol-protecting group employed is not critical so long as the derivatized alcohol group is stable to the condition of subsequent reaction(s) on other positions of the compound of the formulae and can be removed at the desired point without disrupting the remainder of the molecule. Further examples of groups referred to by the above terms are described by J. W. Barton, "Protective Groups In Organic Chemistry", J. G.
W. McOmie, Ed., Plenum Press, New York, N.Y., 1973, and T. W. Greene, "Protective Groups in Organic Synthesis", John Wiley and Sons, New York, N.Y., 1981.. The related term "protected hydroxyl" or "protected alcohol" defines a hydroxyl group substituted with a hydroxyl - protecting group as discussed above.

"Carboxyl protection" refers to substituents of the carboxyl group commonly employed to block or protect the -OH functionality while reacting other functional groups on the compound. Examples of such alcohol -protecting groups include the 2-tetrahydropyranyl group, 2-ethoxyethyl group, the trityl group, the ally! group, the trimethytsilylethoxymethyl group, the 2,2,2-trichioroethyl group, the benzyl group, and the trialkylsilyl group, examples of such being trimethylsilyl, tert-butyldimethylsilyl, phenyddimethylsilyl, triiospropylsilyl and thexyldimethylsilyl. The choice of carboxyl protecting group employed is not critical so long as the derivatized alcohol group is stable to the condition of subsequent reaction(s) on other positions of the compound of the formulae and can be removed at the desired point without disrupting the remainder of the molecule. Further examples of groups referred to by the above terms are described by J. W. Barton, "Protective Groups In Organic Chemistry", J. G.
W. McOmie, Ed., Plenum Press, New York, N.Y., 1973, and T. W. Greene, "Protective Groups in Organic Synthesis", John Wiley and Sons, New York, N.Y., 1981. The related term "protected carboxyl" defines a carboxyl group substituted with a carboxyl -protecting group as discussed above.

EXAMPLES
General Procedure A: Preparation of 1-Arvioxy-2-nitrobenzenes.1-Arvlsulfanyl-2-nitrobenzenes and 2 Arvloxv-3-nitropyridines To a solution of potassium t-butoxide (0.62 g, 5.5 mmol) in anhydrous DMF (10 ml) was added a phenol, arylmercaptan or 2-mercaptopyridine (5.5 mmol) at room temperature and the mixture was stirred for 30 min. A 1-fluoro-2-nitrobenzene derivative or 2-bromo-3-nitropyridine (5.0 mmol) was added and the contents were heated at 80 C for 12 h. The contents were poured into water and extracted with ethyl acetate. The organic layer was washed (dil. NaOH, water, brine), dried (Na2SO4) and concentrated. In general, the desired products were of >90% pure and were used as such for further manipulations.

General Procedure B: Preparation of 2-Arvloxvanilines. 2 Arvlsulfanvlanilines and 3-amino-2-arvloxvpvridines The crude 2-substituted-l-nitrobenzene from procedure A was dissolved in ethanol (10 ml). To this solution were added anhydrous tin(Il) chloride (3.8 g, 20 mmol) and conc HCI
(0.2 ml). The resulting mixture was heated at 80 C for 10 h, cooled and concentrated. The residue was diluted with water (100 ml), neutralized to pH 8-9. To the suspension, ethyl acetate (40 ml) was added, stirred for 5 min and filtered through celite. The layers were separated and the aqueous layer was extracted with ethyl acetate (2x10 ml).
The combined organic layer was washed with brine, dried (Na2SO4) and concentrated under reduced pressure to obtain the desired aniline in 60-70% yield. In general, the desired anilines were of >85% pure (LC-MS) and were used as such for further manipulations.

General Procedure C for Preparation of 2 AMoxvanilines and 2-Arvlsulfanvlanilines The crude 2-substituted-l-nitrobenzene (-5 mmol) was dissolved in methanol (10 ml) In a 100 ml round-bottom flask. To this solution was added 10% palladium on charcoal (300 mg) and the flask was evacuated. The flask was filled with hydrogen with the aid of a balloon and the contents were stirred overnight. The mixture was filtered through oelite and concentrated to obtain desired aniline (>90% purity by LC-MS).

General Procedure D: Preparation of urea A mixture of 1,1'-carbonyldiimidazole (98 mg, 0.6 mmol), 2-aminoheteroarene (0.6 mmol) and 4-(N,N-dimethylamino)pyridine (5 mg) in dichloroethane (5 ml) was heated at 80 C for 2 h. The reaction mixture was cooled to room temperature and was added solution of a substituted aniline (0.5 mmol) in dichloroethane (2 ml). The resulting suspension was heated at 80 C for 10 h and concentrated. The residue was purified by column chromatography (silica, CH2CI2 then 10-30% ethyl acetate in CH2CI2) to afford the desired urea in 60-80% yield.

General Procedure E: Preparation of urea A mixture of isocyanate (0.5 mmol) and 2-aminoheteroarene (0.5 mmol) in dichloroethane (4 ml) was heated at 80 C for 12 h. The reaction mixture was concentrated under reduced pressure. The residue was purified by column chromatography (silica, CH2CI2 then 10-30% ethyl acetate in CH2CI2) to afford the desired urea in 60-80%
yield.

General Procedure F: for Preparation of 2-Arvloxv-1-nitrobenzenes To a solution of potassium t-butoxide (0.62 g, 5.5 mmol) in anhydrous THE (20 ml) was added a phenol (5.5 mmol) at -10 C and the mixture was stirred for 30 min.
A fluoro-1-nitrobenzene derivative (5.0 mmol) was added at -10 C and stirred for 12 h at room temperature. The contents were poured into water (25 ml) and extracted with ethyl.acetate (3x20 ml). The organic layer was washed (dil. NaOH, water, brine), dried (Na2SO4) and concentrated to give the desired products with >90% purity by LC-MS and were used as such in the next step.

General Procedure G: for Preparation of 1-Alkoxy-2-nitrobenzenes To a suspension of NaH (60%; 0.20 g, 5.0 mmol) in anhydrous THE (10 ml) was added an alcohol (5.0 mmol) dropwise at room temperature and the mixture was stirred for min. 1-Fluoro-2-nitrobenzene (5.0 mmol) was added and the contents were heated at 60 C for 12 h. The contents were poured into water and extracted with ethyl acetate. The organic layer was washed (dil. NaOH, water, brine), dried (Na2SO4) and concentrated. In general, the desired products were of >90% pure and were used as such in the further 25 manipulations.

General procedure H: General procedure for preparation of compounds of general formula I
that contain a urea moiety in the central core.
One equivalent of a mono- di- or tri.substituted aniline is dissolved in an organic solvent such as ethyl acetate, toluene, or dichloromethane and hydrochloride dissolved In an 30 organic solvent such as ethyl acetate, toluene or dichloromethane is added.
The mixture is concentrated in vacuo to give the hydrochloride of the aniline. The residue Is dissolved or suspended in a non protic organic solvent such as toluene or dichloromethane and excess (e.g. 2 to 5 equivalents) of diphosgene or another phosgene equivalent is added. The mixture is either run at room temperature or heated (up to reflux temperature of the solvent) for 5 to 20 hours. The reaction mixture is concentrated in vacuo and the intermediate residue used in the next step without further purification.
The crude intermediate isocyanate is dissolved in an organic solvent such as ethyl acetate, toluene, dichloromethane, dioxane, DMSO or DMF and one equivalent of a heterocyclic amine is added. The reaction mixture is run at either room temperature or heated until the reaction is taking place. The reaction temperature will depend on the reactivity of the isocyanate and the nucleophilicity of the amine and can be followed either using HPLC or TLC. The reaction mixture is diluted with an organic solvent such as ethyl acetate, toluene or didoromethane and the mixture extracted with water. The product is purified using standard procedures as described In the art or as exemplified below.
General Procedure H1 : Preparation of amides from carboxylic acids prepared using procedure H:
One equivalent of a N-substituted aminothiazol-4-ylcarboxylic acid or N-substituted aminothiazol-4-ylacetic acid prepared by using general procedure H is dissolved in an organic solvent such as 1,2-dichloropropane, dimethylformamide or a mixture of two organic solvents such as a mixture of 1,2-dichloropropane and dimethylformamide. One equivalent of PyBOP (benzotriazole-1-yl-oxy-tris-pyrrolidino-phosphonium hexafluorophosphate) is added, the reaction mixture is left standing for 20 minutes followed by addition of two equivalents of an appropriate amine and DIPEA (diisopropylethylamine), and the mixture is left overnight.
The reaction mixture is diluted with ethylacetate and extracted using a general washing procedure such as washing twice with water, twice with 4N HCI, once with water, twice with 50% saturated sodiumhydrogencarbonate, and three times with water.
The organic solvent is evaporated in vacuo giving an amorphous product The product is purified by either recrystalization in an organic solvent such as diethylether or by HPLC (e.g. a Waters Deltprep 4000).
In case the isolated product contains a carboxylic acid ester functionality, the ester group can be hydrolysed to the corresponding acid by dissolving the compound in ethanol 96% and adding 2N NaOH. The mixture is left standing for some time (e.g. 2 hours) whereafter the ethanol is evaporated in vacuo, water is added, and pH is adjusted to acidic with 2N HCI. The mixture is extracted with an organic solvent such as ethylacetate and the combined organic phases are evaporated in vacuo giving an amorphous product.

General procedure H2: Preparation of intermediate isocyanates:
2-Benzylphenyl isocyanate a___9 N=0 2-Benzylaniline (2.0 g, 11 mmol) was dissolved in ethylacetate (5 ml) and hydrochloride in ethylacetate (3N, 5 ml) was added. After 2 hrs the organic solvent was removed in vacuo giving a solid residue. Toluene (50 ml) was added, then diphosgene (2.2 g, 33 mmol) and the reaction-mixture was heated at 110 C for 16 hours. The solvent and excess diphosgene was removed in vacuo giving an residual oil that was used for the next step without further purification.
The following isocyanates were prepared using the same procedure used for preparation of benzylphenyl isocyanate:
(5-Chloro-2-isocyanatophenyl)phenyl methanone CI

OY

2-(2-Methylphenoxy)phenyl isocyanate JP

2-(4-Methoxvpheno )-5-(trifluoromethvl)phenvl isocyanate C

F
OOXF
N--O
2-(Phenylsulfonyl)phenyl isocyanate \ 20 0 0 N=--O

General Procedure I: Preparation of 2-acyl anilines A solution of 1 M borontrichkxide in dichloromethane (110 mL, 0.11 mol) was cooled to -20 C. To this solution was added a solution of aniline (0.1 mol) in dichloromethane (100 mL). The mixture was warmed to room temperature and was stirred for 3 h. The mixture was re-cooled to -20 C. Alkyl nitrile (0.1 mol) was added over 5 min, followed by I M solution of (anhydrous) GaCI3 (100 mL, 0.1 mol) in dichloromethane. To this solution was added chlorobenzene (300 mL) and the mixture was heated to reflux for 24 h. After being cooled to room temperature, the mixture was poured into ice water (1 L) and the mixture was stirred for 3 h. The organic layerwas separated and the aqueous layer was extracted with dichloromethane (4 x 400 mL). The combined organic layer was washed with water (4 x 500 ml), brine (2 x 500 mL), dried over anhydrous Na2SO4. The aqueous layer was then basifled to pH 7.5 with Na2CO3 and the mixture was extracted with dichloromethane (2 x 400 ml).
The organic layer was washed with water (4 x 500 mL), brine (2 x 500 mL), dried over anhydrous Na2SO4. Both organic layers were combined and concentrated in-vacuo.
The crude mixture was purified by column chromatography with hexanes-ethyl acetate (9:1) as eluent to give the 2-amino-alkylphenones in 10-50% yield.

General Procedure J: Preparation of adds from esters The ester (1 mmol) was dissolved in 1:1 mixture of THE and methanol (5 mL). To this solution was added 2 M solution of LiOH (2 mL, 4 mmol). The mixture was stirred for 1 h and was concentrated. The residue was diluted with water (10 mL) and the aqueous layer was washed with ether (2 x 10 mL). The water layer was acidified with HCI to pH 6.0 and precipitated acid was extracted with ethyl acetate (2 x 50 mL). The organic layer was washed with water (2 x 20 ml), dried (Na2SO4) and concentrated in vacuo to furnish the desired acid in almost quantitative yield.

General Procedure K: Preparation of amides A mixture of acid (0.5 mmol) and HBTU (0.5 mmol) was dissolved in anhydrous DMF (2 mL). To this solution was added DIEA (0.6 mmol) and stirred for 2-3 minutes. A
solution of alkyl amine (0.5 mmol) in DMF (1 mL) was added and the mixture was stirred at room temperature for 30 min. The mixture was poured into water (20 mL) and was extracted with ethyl acetate (2 x 20 mL). The organic layer was washed with saturated solution of citric acid (5 mL), NaHCO3 (2 x 10 mL) water (2 x 0 mL), brine (2 x 10 mL), dried (Na2SO4) and concentrated in vacuo to give the desired amide. The crude mixture was purified by column chromatography (silica, CH2CI2 then 10-50% ethyl acetate in CH2CI2) to furnish amide in 50-75% yield.

General Procedure L: Preparation of sulfonamides/amides To a solution of acid (1.0 mmol) and DIEA (1.5 mmol) in anhydrous THE (20 mL) was added diphenylphosphoroyl azide (1.5 mmol) and was heated to reflux for 8-12 hours.
The reaction mixture was then concentrated in vacuo to give crude isocyanate.
To this crude product was added dilute HCI (1.2 M, 20 ml-) and the mixture was heated to reflux for 2 hours. The reaction mixture was neutralized with Na2CO3 and the aqueous layer was extracted with ethyl acetate (3 x30 mL). The organic layer was washed with water (2 x 30 mL), brine (1 x 30 mL) and dried (anhydrous Na2SO4) and concentrated in vacuo to give the desired amine. This crude amine (1.0 mmol) was reacted with aryl/alkylsulfonyl chloride (1 mmol) and Et3N (2 mmol) to give the desired sulfonamides. The amides were prepared as described in procedure K. The crude product was purified by silica gel chromatography [hexanes:EtOAc/MeOH (70:30:0 to 5:90:5)] to furnish the desired sulfonamides in 20-30%
yield.

General Procedure M: Preparation of bis-ureas or carbamates A mixture of acid (1.0 mmol) and DIEA (1.5 mmol) was dissolved in anhydrous THE
or CH3CN (30 mL). Then dipenylphosphoroyl azide (1.5 mmol) added to the reaction mixture.
Reaction mixture was refluxed for 8-12 hours. The reaction mixture was then concentrated in vacuo to give crude isocyanate. To this crude product desired amines or alcohols(2.0 mmol) were added and stirred at rt for 2h. The reaction mixture was then concentrated in vacuo.
The crude reaction mixture was then purified by silica gel chromatography (hexanes:EtOAc 70:30 to 10:90) to furnish the desired bis-ureas or carbamates in 30-45%
yield.

General Procedure N: Preparation of alcohols To a solution of ethyl-2-amino-4-thiazolyl acetate or ethyl-2-amino-4thiazoyl carboxylate (100 mmol) in anhydrous THF (100 ml-) was added lithiumborohydride (200 mmol, 2.0 M solution in THF) at -10 C, and the mixture was allowed to warm up to ambient temperature and stirred for 8-10 h. The mixture was then concentrated in vacuo. Methanol (200 mL) was added to quench excess lithiumborohydride and filtered through with a plug of silica gel to afford the amino alcohol.
To this crude amino alcohol (100 mmol) and imidazole (500 mmol) in anhydrous DMF (50 ml) was added tent-butyldimethylsilyl chloride (500 mmol) and stirred at rt for 6 h.
= The reaction mixture was then washed with water (5x100 ml-) and brine (2x100 mL) and extracted with ethylacetate (3x200 mL), dried over Na2SO4r and concentrated in vacuo to give TBS-protected amino alcohol.
TBS-protected amino alcohol (50 mmol) was subjected to urea formation following general procedure D to give desired urea. This crude urea (25 mmol) was then treated with = TBAF (50 mmol, 1.0 M solution in THF) and stirred at rt for 4 h. The reaction mixture was poured in to water and extracted with ethyl acetate. The organic extracts were combined, washed (water), dried (Na2SO4) and concentrated in vacuo_ The crude mixture was purified by silica gel chromatography [hexanes:EtOAc (70:30 to 10:90)] to afford the desired alcohol in 70-80 % yield.
General Procedure 0: Preparation of Amines by Reductive Amination . To the aldehyde (0.11mmol) in dichloroethane or THF (5 ml) was added the respective amine (0.11 mmol) and stirred at room temperature for 15 min. To this solution was added sodium triacetoxyborohydride (0.16 mmol). After stirring at room temperature overnight, the mixture was concentrated in vacuo and purified by column chromatography (silica, 2-8% MeOH in DCM) to obtain the desired product in 30-50 % yield.

General Procedure P: Preparation of Arylethers by Mitsunobu Reaction To a solution of 1-[2-(cyclopentanecarbonyl-4-methyl-phenyl]-3-[4-(2-hydroxy-ethyl)-thiazol-2-yl]-urea (0.268 mmol), phenol (0.536 mmol) and triphenylphosphine (0.268mmo1) in THF (2 ml) was added diisopropyl azodicarboxylate (0.268mmo1) at 0 C. The resulting solution was stirred at it overnight, The mixture was concentrated and purified by flash chromatography on silica gel (10-50% EtOAct hexane) to give the desired product in 28-40%
yield.

General procedure Q: Synthesis of 1-(2-cyclocentanovl-4-methyl-ahenyl)73-(5-alky thio-2-thiazolyl)ureas A mixture of 1-(2-cyclopentanoyl-4-methyl-phenyl)-3-(5-bromol-2-thiazolyl)urea (1 mmol), alkylthiol (2 mmol) and DIEA (2 mmol) in DMF (5 ml-) was heated at 80 C
for 3 h.
The mixture was poured into water (20 ml-) and was extracted with ethyl acetate (3 x 25 mL).
The organic layer was washed with water (2 x 30 mL), brine (1 x 30 mL), dried (anhydrous Na2SO4) and concentrated in vacuo to furnish a residue containing 1-(2-cydopentanoyl-4-methyl-phenyl)-3-(5-alkythio-2-thiazolyl)urea along with 1-(2-cyclopentanoyl-4-methyl-phenyl)-3-(thiazol-2-yl)urea. The crude product was purified by column chromatography (silica, CH2CI2 then 5-20% ethyl acetate in CH2CI2) to afford the desired product in 25-35 %
yield Same procedure was adopted for the synthesis of 1-(2-cydopentanoyl-4-methyl-phenyl)-3-(5-arylthio-2-thiazolyl)ureas. The crude products were purified by column chromatography (silica, CH2CI2 then 5-20% ethyl acetate in CH2CI2 and 2% MeOH
in'CH2CI2) to afford the desired product in 25-35 % yield. .
General Procedure R: Oxidation of alkyl and arvlthio substituted thiazolyl ureas Alkyl or arylthio substituted thiazolyl urea (0.5 mmol) was dissolved in CH2CI2 (5 ml-) and was cooled to 0 C in an ice bath. To this solution was added m-cpba (133 mg, 0.75 mmol) in CH2CI2 (3 mL). The mixture was stirred at 0 C for 4 h and was diluted with CH2CI2 (30 mL). The organic layer was washed with saturated solution of NaHCO3 (2 x 20 mL), water (3 x 20 mL), brine (1 x 20 mL), dried (anhydrous Na2SO4) and concentrated in vacuo.
The crude mixture was purified by column chromatography (silica, CH2CI2 then 5-20% ethyl acetate In CH2CI2 and 2% MeOH in CH2CI2) to give the desired alkyl or aryl sulfone in 60-80% yield.
General Procedure S: Preparation of 2-Amino Arviphenones To a solution of 2-amino benzoic add (10 mmol) in THE was added benzoyl chloride (2.8 g, 20 mmol) followed by pyridine (1.58 g, 20 mmol). The mixture was stirred for I h at room temperature. The 2-phenyl-benzo[d][1,3]oxazin-4-one formed was filtered and the residue was washed with water and dried in vaccuum desiccator.
To a solution of 2-phenyl-benzo[d][1,3]oxazin-4-one (5 mmol) in dry CH2CI2 (20 ml-) was added 1 N solution of aryl magnesium bromide in THE (5 ml-) at 0 C. The mixture was stirred at room temperature for 2 h and poured into water (30 mL).
The aqueous layer was extracted with ethyl acetate (3 x 30 ml-) and was washed with water (3 x 50 mL), brine (1 x 50 mL), dried (anhydrous Na2SO4) and concentrated in vacuo to afford N-(2-benzoyl-phenyl)-benzamide in 60-70% yield.

To a solution of the crude N-(2-benzoyl-phenyl)-benzamide (2 mmol) in THE (10 mL) was added 10 N solution of NaOH (5 mL) and was heated to reflux for 18 h. The mixture was poured into water (50 mL) and was extracted with ethyl acetate (3 x30 mL). The organic layer was washed with water (3 x 50 mL), brine (1 x 50 mL), dried (anhydrous Na2SO4) and concentrated in vacuo to afford 2-amino arylphenone. The crude product was purified by column chromatography (silica, hexanes then 5-20% ethyl acetate) to furnish the desired product in 28-40 % yield.
General Procedure T: Preparation of Amides/Sulfonamides To a solution of amine (0.5 mmol) in DCM (5 mL) was added triethylamine (1 mmol) and cooled the reaction mixture to 0 C. Acid chloride or sulfonyl chloride (0.5 mmol) was added drop-wise and stirred for overnight The reaction mixture was concentrated in vacuo and the residue was purified by column chromatography [silica, DCM:ethyl acetate (80:20 to 20:80)] to yield desired amides or sulfonamides respectively.

General Procedure U: Preparation of Hydantoins from Amino Acids:
To a solution of Boc-Gly-Merrifield resin (1.2 g, 0.96 mmol) was added trifluoroacetic acid (5 ml, 20% in DCM), then the resin was washed with three cycles of DMF, methanol, and DCM. To this resin in DCM (20 ml-) was slowly added phosgene (10 mL, 20%
in toluene, 2.0 mmol)) and triethylamine (0.56 ml, 4.0 mmol) at -20 C. The reaction mixture was allowed to warm up to room temperature. The excess phosgene was washed away with there cycles of DCM. To this resin in DCM (20 mL) was added 1-(4-aminomethyl-thiazol-2-yl)-3-(2-cydopentanecarbonyl-4-methyl-phenyl)-urea (0.9 g, 2.5 mmol) in DCM
(10 ml-) and the reaction mixture was placed in a shaker and reacted for 4 h to give the corresponding urea. The resin was then washed with three cycles of DMF, methanol and DCM and dried over 2 h. To the resin was added triethylamine (10 mL, 20% solution in THF) and the reaction mixture was heated for 16 h. The mixture was filtered and the filtrate was concentrated in vacuo to afford hydantoins in 60-75% overall yields.

General Procedure V: Preparation of Specific 2-Aminothiazole Analogs:
To a solution of 1,3-dichloroacetone, 1,3-dibromoacetone, 1-acetoxy-3-chloroacetone, bromomalonaldehyde or 1,4-dibromobutan-2,3-dione (100 mmol) in methanol (100 ml) was added thiourea (7.6 g, 100 mmol) and the mixture was stirred at rt. for 3h. The reaction mixture was concentrated in vacuo to give the desired products in almost quantitative yields.

4-Chloromethyl-thiazole-2-ylamine (172 mg, 1.0 mmol) was reacted with arylthiols (2 mmol) and DIEA (2 mmol) in THE (5 mL) following the general procedure Z. These Intermediates were coupled with CDI and 2-amino-5-methyl-phenyl)-cydopentyl-methanone (203 mg, 1.0 mmol) following the general procedure D.
General Procedure W: Preparation of alkylamino nitrobenzenes 1-Fluoro-2-nitrobenzene derivative (5.0 mmol) and an amine (10 mmol) in THE
(25 mL) were heated at 60 C for 12 h. The contents were poured into water and extracted with ethyl acetate. The organic layer was washed (water, brine), dried (Na2SO4) and concentrated. The residue was dissolved in methanol (25 mL) and subjected reduction following the general procedure C. In general, the desired products were of >90% pure and were used as such in the further manipulations.

General Procedure X: Preparation of Alkenes by Wittig Reaction The aldehyde (0.10g, 0.28mmol) and (carbethoxymethylene)-triphenylphosphorane (0.12g, 0.34mmol) were stirred at room temperature in benzene overnight. The reaction mixture was concentrated under vacuum and purified by column chromatography (silica, 15%
EtOAc/hexanes) to obtain the product in 80% yield.

General procedure Y: Synthesis of 1-(2-cvdopentanoyl-4-methyl-phenvl)-3-(5-arvithio-2-thiazolyl)ureas A mixture of 1-(2-cyclopentanoyl-4-methyl-phenyl)-3-(5-bromol-2-thiazolyl)urea (1 mmol), arylthiol (2 mmol) and tert. BuOK (2 mmol; 4 equivalent of tert.BuOK
was used for arylthlo carboxylic acids) In DMF (5 mL) was heated at 80 C for 3 h. The mixture was poured into water (20 mL). Urea containing arylthio carboxylic acid was neutralized with saturated NaHCO3 solution. The aqueous layer was extracted with ethyl acetate (3 x 25 mL). The organic layer was washed with water (2 x 30 mL), brine (1 x 30 mL), dried (anhydrous Na2SO4) and concentrated in vacuo to furnish a residue containing 1-(2-cydopentanoyl-4-methyl-phenyl)-3-(5-arylthio-2-thiazolyl)urea along with 1-(2-cyclopentanoyl-4-methyl-phenyl)-3-(2-thiazolyl)urea. The crude product was purified by column chromatography (silica, CH2CI2 then 5-20% ethyl acetate in CH2Cl2and 2% MeOH in CH2CI2) to afford the desired product in 25-35 % yield.

General procedure Z: Synthesis of 1-(2-cyclopentanecarbonyl-4-methvl-phenyl)-344-(arv{-sulfanylmethA)-thiazol-2-vll-areas and 1-(2-cvdopentanecarbonyl-4-methyl-phenyl -3-t44arylsulfanyl)-ethvf-thiazol-2-vl}-ureas A mixture of 1-(4-chloromethyl-thiazoi-2-yl)-3-(2-cydopentanecarbonyl-4-methyl-phenyl)-urea (1 mmol), arylthiol (2 mmol) and DIEA (2 mmol) In THE (5 mL) was heated at 80 C for 3 h. The mixture was poured into water (20 mL) and was extracted with ethyl acetate (3 x 25 mL). The organic layer was washed with water (2 x 30 mL).
brine (1 x 30 mL), dried (anhydrous Na2SO4) and concentrated in vacuo to furnish a residue containing 1-(2-cydopentanecarbonyl-4methyl-phenyl)-3-[4-(arylsulfanylmethyl)-thiazol-2-yl-urea. The crude product was purified by column chromatography (silica, CH2CI2 then 5-20%
ethyl acetate in CH2Cl2 and 2% MeOH in CH2CI2) to afford the desired product in 79-85 %=yield Similarly, synthesis of 1-(2-cydopentanecarbonyl-4-methyl-phenyl)-3-{4-[arylsulfanyl)-ethyl]-thiazol-2-yl}-urea was carried out by reacting methanesulfonic add 2-{2-[3-(2-cydopentanecarbonyl-4-methyl-phenyl)-ureido]-thiazol-4-yl]-ethyl ester with arylthiol and Et3N. This afforded the desired product in 60-80 % yield.
General Procedure AA: Preparation of urea.
A mixture of 1,1'-carbonyldiimidazole (98 mg, 0.6 mmol), (2-aminothiazol-4-yl)acetic add ethyl ester (0.6 mmol) and 4-(N,N-dimethylamino)pyridine (2 mg) in dichloromethane (5 ml) was stirred at room temperature for 2 h. A solution of a substituted aniline derivative (0.6 mmol) in dichloromethane (1 ml) was added and stirring was continued at room temperature for 24 h. The reaction mixture was concentrated and the residue was purified.
by column chromatography (silica, CH2Ci2 then 10-30% ethyl acetate in CH2CI2) to afford the desired urea.

HPLC-MS (Method A) The following instrumentation is used:
= Hewlett Packard series 1100 G1312A Bin Pump = Hewlett Packard series 1100 Column compartment = Hewlett Packard series 1100 G1315A DAD diode array detector = Hewlett Packard series 1100 MSD
= Sedere 75 Evaporative Light Scattering detector The instrument Is controlled by HP Chemstation software.
The HPLC pump is connected to two eluent reservoirs containing:
A: 0.01% TFA in water B: 0.01% TFA in acetonitrile The analysis is performed at 40 C by injecting an appropriate volume of the sample (preferably 1 pl) onto the column which is eluted with a gradient of acetonitrile:
The HPLC conditions, detector settings and mass spectrometer settings used are giving in the following table.
Column: Waters Xterra MS C-18 X 3 mm id 5 Om Gradient: 5% - 100% acetonitrile linear during 7.5 min at 1.5ml/min Detection: 210 nm (analogue output from DAD (diode array detector)) ELS (analogue output from ELS) MS ionisation mode API-ES
Scan 100-1000 amu step 0.1 amu After the DAD the flow is divided yielding approx I mimin to the ELS and 0.5 mImin to the MS.

Example 1 N-(2-Phenoxyphenyl)-N'-(thiazol-2-yl)urea ao H H
N ~
yN " S
/ O N~
N-(2-Phenoxyphenyl}N'-(thiazol-2-yl)urea (0.59 g, 94.9%) was prepared from 2-phenoxyaniline (0.37 g, 2.00 mmol) and 2-aminothiazole (0.20 g, 2.00 mmol) following the general procedure D.
LC-MS (m/z): 313 (M+1)`.
1H NMR (400 MHz, acetone-de): 6 6.76 (d, J = 13.8 Hz, 1 H), 6.98-7.04 (m, 4H), 7.11 (t, J =
4.8 Hz, 2H), 7.32 (t, J = 8.0 Hz, 2H), and 8.35 (dd, J =1.6, 8.0 Hz, 1 H), 10.2 (br, 2H).

Example 2 N-[2-(2,3-Dimethoxyphenoxy)-5-Fluorophenyl]-N'-(thizol-2-yl)sulfamide D,CH3 / yO*CH

O
ZINI
H H

TNI
F
To a solution of sulfuryl chloride (2.0 ml, 2.0 mmol, 1.0 M solution in dichioro-methane) were added p-nitrophenol (0.55 g, 4.0 mmol) in dichioromethane and N,N-diisopro-pylethylamine (0.71 ml, 4.0 mmol) at -78 C. The reaction mixture was stirred for 1 hour at -78 C and 2-(2,3-dimethoxyphenoxy)-5-fluoroaniline (0.52 g, 2.0 mmoi) in dichloromethane (5 ml) was added. The reaction mixture was stirred for 10 min and 2-aminothiazole (0.2 g, 2.0 mmol) was added. The reaction mixture was allowed to warm up slowly to ambient temperature. The mixture was concentrated under reduced pressure. The residue was dissolved in ethyl acetate and was washed (dil. NaOH, water, brine), dried (Na2SO4) and concentrated under reduced pressure. The crude product was treated with Dowex-50 acidic resin in ethyl acetate-methanol (1:1) to remove unreacted 2-aminothiazole. The filtrate was concentrated and the residue was purified by silica gel column chromatography (ethylacetate:hexanes, from 50:50 to 90:10 as eluent system) to afford the title compound (0.42 g, 49%).
LC-MS (m/z): 427 (M+1)'.
1H NMR (400 MHz, acetone-d6): 6 3.12 (br, 2H), 3.71 (s, 3H), 3.86 (s, 3H), 6.56 (dd, J = 7.6, 1.6 Hz, I H), 6.66 (m,1 H), 6.77-6.87 (m, 3H), 6.99 (t, J = 3.6 Hz, I H), 7.26 (d, J = 4.8 Hz, 1 H), and 7.38 (dd, J =10.8, 3.2 Hz, I H) Example 3 1-(2-phenoxyphenyl)-5-(thiazol-2-yl)biuret ao 6 / H H H~
\ NYNYN " S
0 0 N~

To a solution of 2-phenoxyaniline (0.46 g, 2.50 mmol) in tetrahydrofuran (20 ml) was added diisopropylethylamine (0.89 ml, 5.00 mmol) and the solution was cooled to -30 C, then N-(chlorocarbonyl)isocyanate (0.3 ml, 3.75 mmol) was slowly added. The mixture was then allowed to warm up to the room temperature during 30 min. 2-Aminothiazole (0.375 g, 3.75 mmol) was added to the reaction mixture and stirred at room temperature for 6 hours.
The reaction mixture was concentrated under reduced pressure to afford crude product, which was purified by silica gel chromatography (hexanes:ethyl acetate from 80:20 to 30:70) to afford title compound (0.49 g, 55%) as pale yellow solid.
LC-MS (m/z): 356 (M+1).
'H NMR (400 MHz, acetone-de): d 6.92 (dd, J = 1.6, 7.6 Hz, 1 H), 7.06 (m, 5H), 7.40 (m, 3H), 8.32 (d, J = 4.8 Hz, 1 H), 8.45 (d, J = 5.6 Hz, 1 H), 9.02 (br, 1 H), 9.78 (br, 1 H), and 10.46 (br, 1H).

Example 4 2-[(U(2-Phenoxyanilino)sulfonyl]amino]carbonyl)amino]thiazole C~O
N- '0 N S
0 , " Oy To a solution of chiorosulfonyl isocyanate (0.22 ml, 2.5 mmol) in tetrahydrofuran (25 ml) were added 2-phenoxyaniline (0.37 g, 2.0 mmol) and DIEA (0.89 ml, 5.0 mmol) at -78 C.
The solution was stirred and slowly allowed to warmed up to 0 C. To this reaction mixture, was added 2-amino thiazole (0.20 g, 2.0 mmol) and continued stirring at room temperature for 3 h. The reaction mixture was concentrated under reduced pressure and the crude product was purified by column chromatography (ethylacetate:hexanes, from 50:50 to 90:10 as eluent system) to afford the title compound (0.52 g, 66%).
LC-MS (m/z): 392 (M+1)'.
'H NMR (400 MHz, acetone-d6): 6 6.85 (dd, J = 8.8, 1.6 Hz, 1 H), 6.88 (dd, J
=1.6, 8.8 Hz, 1H), 7.00-7.16 (m, 5H), 7.29-7.39 (m, 4H), 10.33 (br, I H), 10.88 (br, 2H).

Example 5 N-(2-Phenylsulfanylphenyl}N'-(thiazol-2-yl)urea as N
S
Y

N-(2-Phenylsulfanylphenyl)-N'-(thiazol-2-yl)urea (116 mg, 71%) was prepared from 2-phenylsulfanylaniline (100 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 329 (M+1)'.
'H NMR (400 MHz, acetone-de): 6 7.03 (d, J = 3.6 Hz,1 H), 7.10-7.18 (m, 4H), 7.25-7.31 (m, 3H), 7.48 (m, 1 H), 7.59 (dd, J = 3.6, 1.6 Hz,1 H). 8.44 (dd, J = 8.4, 1.2 Hz, 1 H), 9.00 (br, 1 H), 10.44 (br, 1 H).

Example 6 N-(2-Phenylsulfonylphenyl)-N'-(thiazol-2-yl)urea 1 \
/ , SAO H H
NTI) NN-(2-Phenylsulfonylphenyl)-N'-(thiazol-2-yl)urea (98 mg, 55%) was prepared from 2-phenylsulfonylaniline (116 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 361 (M+1)+.

1H NMR (400 MHz, acetone-de): 6 7.07 (d. J = 3.6 Hz, I H), 7.33-7.37 (m,1 H), 7.40 (d, J =
3.6 Hz, 1 H), 7.55-7.60 (m, 2H), 7.63-7.71 (m, 2H), 7.98-8.01 (m, 2H), 8.12 (d, J = 8.0 Hz, 1 H), 8.22-8.25 (m, 1 H), 9.26 (br, 1 H), 10.99 (br, 1 H).

Example 7 N-(2-Benzylphenyl)-N'-(thiazol-2-yl)urea H H
NYNS
\ O ~NJ

N-(2-Benzylphenyl)-N'-(thiazol-2-yl) urea (111 mg, 72 %) was prepared from commercially available 2-benzylaniline (91 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 311 (M+1)`.
' H NMR (400 MHz, acetone-d6): 6 4.08 (s, 2H), 7.02 (d, J = 3.2 Hz,1 H), 7.06-7.14 (m, 2H), 7.14-7.19 (m, 4H), 7.23-7.29 (m, 4H), 7.96 (d, J = 8.4 Hz, 1 H), 8.75 (br, 1 H), 10.01 (br, 1 H).
Example 8 N-(2-Benzoylphenyl)-N'-(thiazol-2-yl)urea O
H
6)TNI) N-(2-Benzoylphenyl)-N'-(thiazol-2-yl)urea (100 mg, 63%) was prepared from 2-aminobenzophenone (97 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 325 (M+1)'.
'H NMR (400 MHz, acetone-de): 6 7.05 (s, 1 H), 7.16 (s, 1 H), 7.35 (d, J = 3.6 Hz, 1H), 7.54 (d, J = 7.2 Hz, 2H), 7.65 (s, 1 H), 7.75 (s, 1 H), 8.45 (s, 1 H), 10.18 (br, 1 H), 10.85 (br, 1 H).

Example 9 N-[2-(Phenylamino)phenyl]-N'-(thiazol-2-yl)urea aNH

H (5fi) N-[2-(Phenylamino)phenyn-N'-(thiazol-2-yl)urea (75 mg, 49%) was prepared from (N-Phenylamino)aniline (92 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 312 (M+1)' 'H NMR (400 MHz, acetone-de): 6 6.75-6.79 (m, 3H), 6.86 (br, 1 H), 7.01 (d, J
= 3.6 Hz, 1 H), 7.05-7.09 (m, 1 H), 7.15-7.19 (m, 3H), 7.24-7.28 (m, 2H), 8.16 (d, J = 8.0, 1.2 Hz, 1 H), 8.65 (br, I H), 10. 15 (br, I H).

Example 10 N-[2-Fluoro-6-(4-methoxyphenoxy)benzyl]-N'-(thiazol-2-yl)urea H3C'O /
\ O O S
H H N
N-[2-Fluoro-6-(4-methoxyphenoxy)benzyl]-N'-(thiazol-2-yl)urea (0.61 g, 81%) was prepared from 2-fluoro-6-(4-methoxyphenoxy)benzylamine (0.494 g, 2.00 mmol) and 2-aminothiazole (0.20 g, 2.00 mmol) following the general procedure D.
LC-MS (m/# 327 (M+1) 'H NMR (400 MHz, acetone-de): d 3.06 (br, 1 H), 3.78 (s, 3H), 4.67 (d, J = 4.8 Hz, 2H), 6.52 (d, J = 8.4 Hz, 1 H), 6.85 (t, J = 9.6 Hz, 1 H), 6.95 (m, 3H), 7.05 (m, 2H), 7.24 (m, 2H), 10.06 (br, 1H).

Example 11 N-(2-Benzyloxyphenyl)-N'-(thiazoi-2-yl)urea O
H H
NyNS
o NJ

N-(2-Benzyloxyphenyl)-N'-(thiazol-2-yl)urea (0.56 g, 86%) was prepared from 2-benzyloxyaniline (0.40 g, 2.00 mmol) and 2-aminothiazole (0.20 g, 2.00 mmol) following the general procedure D.
LC-MS (m/z): 327 (M+1).
'H NMR (400 MHz, CDCI3): d 4.00 (br, 2H), 5.15 (s, 2H), 6.85 (dd, J =1.6, 8.8 Hz, 2H), 6.97 (dd, J =1.6, 7.2 Hz, 1 H), 6.98 (dd, J = 2.0, 6.0 Hz, 1 H), 7.37 (m, 2H), 7.46 (t, J = 7.2 Hz, I H), 7.52 (d, J = 5.6 Hz, 2H), and 7.56 (d, J = 6.8 Hz, 2H) Example 12 N-[2-(2,3,4-Trimethoxybenz)loxy)phenyl]-N'-(thiazoi-2-yl)urea (LOCH 3 N y N
H HTN/
S
O 2-(2,3,4-Trimethoxybenzyloxy)-1-nitrobenzene (0.46 g, 72 %) was prepared from 2,3,4-trimethoxybenzyl alcohol (0.35 ml, 2.0 mmol) and 1-fluoro-2-nitrobenzene (0.21 ml, 2.0 mmol) following the general procedure G. This was reduced to 2-(2,3,4-trimethoxybenzyl-oxy)aniline (0.26 g, 65 %) following the general procedure B. N-[2-(2,3,4-trimethoxybenzyl-oxy)phenyl]-N'-(thiazol-2-yl)urea (240 mg, 65 %) was prepared from 2-(2,3,4-trimethoxy-benzyloxy)aniline (0.26 g, 0.9 mmol) and 2-aminothiazole (140 mg, 1.4 mmol) following the general procedure D.
LC-MS (m/z): 417 (M+1)`.
'H NMR (400 MHz, acetone-de): 6 3.72 (s, 3H), 3.73 (s, 3H), 3.81 (s, 3H), 3.88 (s, 2H), 6.73-7.36 (m, 7H), 8.15 (t, J = 8.4 Hz, 1 H), 8.90 (br,1 H), 10.10 (br,1 H).

Example 13 N-(2-Ethoxyphenyl}N'-(thiazol-2-yl)urea ~'H3 N Y N S
o N-(2-Ethoxyphenyl}N'-(thiazol-2-yl)urea (95 mg, 72%) was prepared from commercially available 2-ethoxyaniline (68 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 265 (M+1 Y.
'H NMR (400 MHz, acetone-da): 6 1.29 (t, J = 7.0 Hz, 3H), 3.94-3.98 (q, J =
7.0 Hz, 2H), 6.74-6.88 (m, 4H), 7.27 (d, J = 5.2 Hz, 1 H), 8.17 (dd, J = 1.6, 8.0 Hz, 1 H), 8.42 (br, 1 H), 10.92 (br, 1H).

Example 14 N-(2-Phenoxyphenyl}N'-(pyridin-2-yl)urea ao N
Y p N-(2-Phenoxyphenyl)-N'-(pyridin-2-yl)urea (109 mg, 72%) was prepared from 2-phenoxyphenylisocyanate (106 mg, 0.5 mmol) and 2-aminopyridine (60 mg, 0.6 mmol) following the general procedure E.
LC-MS (m/z): 307 (M+1)~.

'H NMR (400 MHz, DMSO-de): 6 6.88-6.91 (m, 1H), 6.96-7.08 (m, 4H), 7.15-7.19 (m, 2H), 7.32-7.36 (m, 2H), 7.65-7.69 (m, 1 H), 7.88 (d, J = 4.0 Hz, I H), 8.36 (d, J =
8.0 Hz, 1 H), 9.84 (s,1 H), 11.5 (br, 1 H).

Example 15 N-(2-Phenoxyphenyl)-N'-[(4-methoxycarbonylmethyl)thiazol-2-yqurea ao H H
\ NyN I S
O N
O

N-(2-Phenoxyphenyl)-N'-[(4-methoxycarbonylmethyl)thiazol-2-yqurea (130 mg, 65%) was prepared from 2-phenoxyphenylisocyanate (106 mg, 0.5 mmol) and methyl 2-aminothiazole-4-acetate (104 mg, 0.6 mmol) following the general procedure E.
LC-MS (m/z): 401 (M+1)`.
'H NMR (400 MHz, acetone-de): 6 3.58 (s, 2H), 3.61 (s, 3H), 6.84-6.89 (m, 2H), 7.01-7.05 (m, 3H), 7.13-7.18 (m, 2H), 7.38-8.42 (m, 2H), 8.40 (d, J = 8.0 Hz, 1 H), 8.91 (br,1 H), 10.12 (br, 1H).

Example 16 N-Methyl-N-(2-phenoxyphenyl)-N'-(thiazol-2-yl)urea NY NS
ONJ
2-Phenoxyaniline (0.93 g, 5.00 mmol) and di-tent--butyl dicarbonate (2.18 g, 10.0 mmol) were dissolved in anhydrous dioxane (50 ml), then the reaction mixture was refluxed for 3 h. The mixture was concentrated under reduced pressure to quantitatively give 2-phenoxy-N-(t butoxycarbonyl)aniline (1.43 g). The product was confirmed by LC-MS and subjected to next reaction without further purification.
To a solution of 2-phenoxy-N-(t-butoxycarbonyl)aniline (1.43 g, 5.0 mmol) in anhydrous tetrahydrofuran (50 ml) was added lithium aluminumhydnde (10 ml, 10.0 mmol, 1.0 M solution in tetrahydrofuran) at -10 C. The mixture was then refluxed at 65 C overnight.
The reaction mixture was quenched with slow addition of MeOH (10 mi) and concentrated under reduced pressure. The reaction mixture was then poured into water (50 ml) and extracted with ethyl acetate (3x100 ml). Organic extracts were combined and washed with brine (2x100 ml) and dried over (Na2SO4), concentrated under reduced pressure to give N-methyl-2-phenoxyaniline (0.94 g, 94.0%) as a pale yellow oil. The product was confirmed by LC-MS and subjected to next reaction without further purification.
To a solution of 2-aminothiazole (0.20 g. 2.00 mmol) in dichloroethane (20 ml) was added 1,1'-carbonyldiimidazole (0.40 g, 2.5 mmol) and N,N-dimethylaminopyridine (0.05 g, 0.4 mmol) then the solution was refluxed at 80 C for I h. N-Methyl-2-phenoxyaniline (0.40 g, 2.00 mmol) was added to the solution. The reaction mixture was then stirred overnight at 80 C. The reaction was monitored by LC-MS and TLC, then concentrated under reduced pressure to afford crude product which subsequently was subjected to silica gel chromatography (hexanes:ethyl acetate from 80:20 to 50:50 as eluent system) to afford title product (0.48 g, 73%) as orange solid.
LC-MS (m/z): 327 (M+1)*.
'H NMR (400 MHz, CDC13): 6 3.30 (s, 3H), 6.84 (d, J= 4.8 Hz,1 H), 6.97 (m, 3H), 7.16 (m, 2H), 7.29 (m, 5H), and 7.74 (br, 1H).

Example 17 N-isopropyl-N-(2-phenoxyphenyl)-N'-(thiazoh2-yl)urea CJL.H3CNJCHH

~NYNYS
O NJ
To a solution of 2-phenoxyaniline (0.93 g, 5.0 mmol) in dichloroethane (50 ml) was added anhydrous acetone (0.73 ml, 10.0 mmol) and acetic acid (0.1 ml, 2.0 mmol). The mixture was stirred for 30 min, and sodium triacetoxyborohydride (3.18 g, 15.0 mmol) was added in one portion. The reaction mixture was stirred overnight at ambient temperature. The reaction mixture was quenched by slow addition of MeOH (10 ml) and concentrated under reduced pressure. The residue was poured into water (50 ml) and extracted with ethyl acetate (3x1 00 ml). Organic extracts were combined and washed with brine (2x100 ml) and dried (Na2SO4), concentrated under reduced pressure to give N-isopropyl-2-phenoxyaniline (1.05 g, 91%) as colorless oil.
To a solution of 2-aminothiazole (0.20 g, 2.00 mmol) in dichloroethane (20 ml) was added 1,1'-carbonyldiimidazole (0.40 g, 2.5 mmol) and N,N-dimethylaminopyridine (0.05 g, 0.4 mmol) then the solution was refluxed at 80 C for I h. N-Isopropyl-2-phenoxyaniline (0.46 g, 2.0 mmol) was added and the reaction mixture was then stirred overnight at 80 C. The reaction mixture was concentrated under reduced pressure to afford crude product, which was purified by silica gel chromatography (hexanes:ethyl acetate from 80:20 to 50:50 as eluent system ) to afford title product (0.56 g, 79%).
LC-MS (m/z): 355 (M+1)'.
'H NMR (400 MHz, acetone-de): d 1.22 (d, J= 6.4 Hz, 6H), 4.81 (m, 1H), 6.91 (m, 2H), 7.10-7.24 (m, 5H), 7.39 (m, 4H), and 9.00 (br,1 H).

Example 18 N-[2-(4-Methoxyphenoxy)phenyl)-N'-(thiazol-2-yl)urea 1-13C '0 a H H
NuNTNI S
o ~
2-(4-Methoxyphenoxy)-1-nitrobenzene (0.98 g, 80 %) was prepared from 4-methoxyphenol (0.62 g, 5.0 mmol) and 1-fluoro-2-nitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This was reduced to 2-(4-methoxyphenoxy)aniline (0.32 9, 60%, 2.5 mmol scale) following the general procedure B. N-[2-(4-Methoxyphenoxy)phenyl)-N'-(thiazol-2-yl)urea (256 mg, 75%) was prepared from 2-(4-methoxyphenoxy)aniline (215 mg, 1.0 mmol) and 2-aminothiazole (100 mg, 1.0 mmol) following the general procedure D.
LC-MS (m/z): 343 (M+1);.
'H NMR (400 MHz, acetone-d8): 6 3.80 (s, 3H), 6.80 (d, J = 8.0 Hz, 1 H), 6.98-7.05 (m, 6H), 7.10 (m, 1 H), 7.32 (d, J = 3.6 Hz, 1 H), 8.40 (d, J = 8.0 Hz, 1 H), 8.90 (br, 1 H), 10.23 (br, 1 H).

Example 19 N-[2-(4-Fluorophenoxy)phenyl]-N'-(thiazol-2-yl)urea F \

O
H H

O"YI) 2-(4-Fluorophenoxy)-1-nitrobenzene (0.87 g, 75%) was prepared from 4-fluoro-phenol (0.62 g, 5.5 mmol) and 1-fluoro-2-nitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This was reduced to 2-(4-fluorophenoxy)aniline (0.51 g, 68%) following general procedure B. N-[2-(4-Fluorophenoxy)phenyl]-N'-(thiazol-2-yl)urea (118 mg, 72%) was prepared from 2-(4-fluorophenoxy)aniline (102 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 331 (M+1)+
1H NMR (400 MHz, acetone-4a):,6 6.89 (dd, J = 8.4, 1.2 Hz, 1 H), 7.01-7.11 (m, 4H), 7.14-7.29 (m, 3H), 7.31 (d, J = 3.6 Hz. 1 H), 8.42 (dd, J = 8.0, 1.6 Hz, 1 H), 9.12 (br,1 H), 10.19 (br, 111).

Example 20 N-[2-(4-Chlorophenoxy)phenyl]-N'-(thiazol-2-yl)urea Cl \

O
H H
NyNYS, O ''NII ~1 2-(4-Chlorophenoxy)-1-nitrobenzene (0.88 g. 71%) was prepared from 4-chlorophenol (0.70 g, 5.5 mmol) and 1-fluoro-2-nitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This was reduced to 2-(4-chlorophenoxy)aniline (0.50 g, 65%) following general procedure B. N-[2-(4-Chlorophenoxy)phenyl]-N'-(thiazol-2-yl)urea (106 mg, 620/9) was prepared from 2-(4-chlorophenoxy)aniline (109 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 347 (M+1)'.

'H NMR (400 MHz, acetone-de): 6 6.98 (d, J = 7.6 Hz,1 H), 7.04-7.09 (m, 4H), 7.19-7.23 (m, I H), 7.31 (d, J = 3.6 Hz, 1 H), 7.39-7.43 (m, 2H), 8.44 (dd, J = 8.4, 1.6 Hz, 1 H), 8.90 (br, 1 H), 10.13 (br, 11-1).

Example 21 N-[2-(4-Cyanophenoxy)phenyl]-N'-thiazolylurea N

ao S
N

y "'*' ED

2-(4-Cyanophenoxy)-1-nitrobenzene (0.82 g, 69%) was prepared from 4-cyan phenol (0.66 g, 5.5 mmol) and 1-fluoro-2-nitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This was reduced to 2-(4-cyanophenoxy)aniline (0.47 g, 65%) following general procedure B. N-[2-(4-Cyanophenoxy)phenyl]-N'-thiazolylurea (110 mg, 65%) was prepared from 2-(4-cyanophenoxy)aniline (105 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 338 (M+1 )'.
'H NMR (400 MHz, acetone-de): 6 6.04 (d, J = 8.0 Hz, 1 H), 7.13-7.18 (m, 4H), 7.28-7.33 (m, 2H), 7.78-7.81 (m, 2H), 8.47 (d, J = 8.0 Hz, 1 H), 8.95 (br,1 H), 10.43 (br,1 H).

Example 22 N-[2-(4-Methoxycarbonylphenoxy)phenyl]-N'-(thiazol-2-yl)urea H3C'0 H H
&NTNT>
2-(4-Methoxycarbonylphenoxy)-1-nitrobenzene (0.79 g, 58%) was prepared from methyl 4-hydroxybenzoate (0.84 g, 5.5 mmol) and 1-fluoro-2-nitrobenzene (0.71 g. 5.0 mmol) following the general procedure A. This was reduced to 2-(4-methoxycarbonylphenoxy)-aniline (0.46 g, 66%) following general procedure B. N-[2-(4-Methoxycarbonylphenoxy)-phenyl]-N'-(thiazoi-2-yl)urea (100 mg, 55%) was prepared from 2-(4-methoxycarbonyl-phenoxy)aniline (122 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z):'371 (M+1)'.
'H NMR (400 MHz, acetone-de): d 3.85 (s, 3H), 7.03 (d, J= 3.6 Hz, 1H), 7.07-7.14 (m, 4H), 7.25-7.29 (m, 2H), 8.01-4.04 (m, 2H), 8.46 (dd, J = 8.1, 1.2 Hz, 1 H), 8.76 (br, 1 H), 10.07 (br, 1 H).

Example 23 N-[2-(4-Isopropylphenoxy)phenyq-N'-(thiazol-2-yl)urea O

H TNI Ny S
O -2-(4-isopropylphenoxy}1-nitrobenzene (0.95 g, 75 %) was prepared from 4-isopro-pylphenol (0.68 g, 5.0 mmol) and 1-fluoro-2-nitrobenzene (0.71 g. 5.0 mmol) following the general procedure A. This was reduced to 2-(4-isopropylphenoxy)aniline (0.34 g, 60 %, 2.5 mmol scale) following general procedure B. N-[2-(4-Isopropylphenoxy)phenyl]-N'-(thiazol-2-yi)urea (247 mg, 70 %) was prepared from 2-(4-isopropylphenoxy)aniline (227 mg, 1.0 mmol) and 2-aminothiazole (100 mg, 1.0 mmol) following the general procedure D.
LC-MS (m!z): 355 (M+1)'.
'H NMR (400 MHz, acetone-d6): 6 1.17 (d, J = 7.2 Hz, 3H), 1.22 (d, J = 6.8 Hz, 3H), 2.88 (m, 1 H), 6.74 (d, J = 6.6 Hz, 1 H), 6.88 (d, J = 8.0 Hz, 1 H), 6.94-7.15 (m, 4H), 7.28 (m, 2H), 8.43 (d, J = 8.2 Hz. 1 H),10.15 (br, 2H).

Example 24 N-[2-(3,4-Difluorophenoxy)phenyl]-N'-(thiazol-2-yl)urea F

F O

/ 2-(3,4-Dicuorophenoxy)-1-nitrobenzene (0.76 g, 60 %) was prepared from 3,4-difluorophenol (0.65 g, 5.5 mmol) and 1-fluoro-2-nitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This was reduced to 2-(3,4-dicuorophenoxy)aniline (0.33 g, 60 %, 2.5 mmol scale) following general procedure B. N-[2-(3,4-Difluorophenoxy)phenyq-N'-(thia-zol-2-yl)urea (312 mg, 60 %) was prepared from 2-(3,4-difluorophenoxy)aniline (330 mg, 1.5 mmol) and 2-aminothiazole (150 mg, 1.5 mmol) following the general procedure D.
LC-MS (m/z): 349 (M+1) 'H NMR (400 MHz, acetone-do): 6 6.88 (m, 1 H), 7.01 (d, J = 8.0 Hz, 1 H), 7.04-7.12 (m, 4H), 7.22 (m, 1 H), 7.30-7.42 (m, 2H), 8.43 (d, J = 8.2 Hz, 1 H), 10.16 (br, 2H).

Example 25 N-[2-(3,4-Dichlorophenoxy)phenyl]-N'-(thiazol-2-yl)urea CI

CI O H
NyNS
~ I O N-J
2-(3,4-Dichlorophenoxy)-1-nitrobenzene (1.15 g, 81%) was prepared from 3,4-dichlorophenol (0.9 g, 5.5 mmol) and 1-fluoro-2-nitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This was reduced to 2-(3,4-dichlorophenoxy)aniline (0.69 g, 68%) following general procedure B. N-(2-(3,4-Dichlorophenoxy)phenyl]-N'-(thiazol-2-yl)urea (129 mg, 68%) was prepared from 2-(3,4-dichlorophenoxy)aniline (127 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 382 (M+1) .
'H NMR (400 MHz, acetone-do): d 6.99-7.13 (m, 4H), 7.24-7.28 (m, 2H), 7.30 (d, J = 3.6 Hz, I H), 7.57 (d, J = 9.2 Hz,1 H), 8.44 (dd, J = 8.4, 1.2 Hz, I H), 9.20 (br,1 H), 10.09 (br, I H).

Example 26 N-[2-(4-Chloro-3-methylphenoxy)phenyl]-N'-(thiazol-2-yl)urea Cl H3C O
H H
N y N
S O
TNI
N-[2-(4-Chloro-3-methylphenoxy)phenyQ-N'-(thiazol-2-yl)urea (233 mg, 65 %) was prepared from 2-(4-chloro-3-methytphenoxy)aniline (233 mg, 1.0 mmol) and 2-aminothiazole (100 mg, 1.0 mmol) following the general procedure D.
LC-MS (m/z): 361 (M+1)'.
'H NMR (400 MHz, acetone-de): 6 2.36 (s, 3H), 6.94-6.98 (m, 2H), 7.05 (m, 4H), 7.19 (m, 1 H), 7.31 (d, J = 4.0 Hz, 1 H), 7.37 (d, J = 8.4 Hz, 1 H), 8.43 (d, J = 8.4 Hz, 1 H), 10.23 (br, 2H).

Example 27 N-[2-(3,4-Dimethoxyphenoxy)phenyl]-N'-(thiazol-2-yl)urea CH3 O~CH3 O

O
6111) 2-(3,4-Dimethoxyphenoxy)-1-nitrobenzene (0.93 g, 68%) was prepared from 3,4-dimethoxyphenol (0.85 g, 5.5 mmol) and 1-fluoro-2-nitrobenzene (0.71 g, 5.0 mmoi) following the general procedure A. This was reduced to 2-(3,4-dimethoxyphenoxy)aniline (0.51 g, 62%) following general procedure B. N-[2-(3,4-Dimethoxyphenoxy)phenyl]-N'-(thiazol-2-yl)urea (128 mg, 69%) was prepared from 2-(3,4-dimethoxyphenoxy)aniline (123 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 373 (M+1)'.
'H NMR (400 MHz, acetone-de): 6 3.80 (s, 6H), 6.54 (dd, J = 8.4, 2.4 Hz,1 H), 6.78 (d, J = 2.4 Hz,1 H), 6.82 (d, J = 8.0 Hz, 1 H), 6.97 (d, J = 8.0 Hz,1 H), 6.99-7.01 (m, 1 H), 7.04 (d, J = 3.6 Hz, 1 H), 7.07-7.12 (m, 1 H), 7.33-7.34 (d, J = 3.6 Hz, 1 H), 8.39 (dd, J =
8.0, 1.2 Hz, 1 H), 8.90 (br, 1H), 10.23 (br,1 H).

Example 28 N-[2-(3,4-Methylenedioxyphenoxy)phenyl]-N'-(thiazol-2-yl)urea /'-0 O
H H
NN
O
2-(3,4-Methylenedioxyphenoxy)-1-nitrobenzene (0.75 g, 58%) was prepared from 3,4-methylenedioxyphenoi (0.76 g, 5.5 mmol) and 1-fluoro-2-nitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This was reduced to 2-(3,4-methylenedioxyphenoxy)-aniline (0.47 g, 71%) following general procedure B. N-[2-(3,4-Methylenedioxyphenoxy)-phenyl]-N'-(thiazol-2-yl)urea (120 mg, 68%) was prepared from 2-(3,4-methylenedioxy-phenoxy)aniline (115 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 357 (M+1)'.
'H NMR (400 MHz, acetone-de): 6 6.06 (s, 2 H), 6.51 (dd, J = 8.4, 2.4 Hz,1 H), 6.67 (d, J =
2.4 Hz, 1 H), 6.84-6.87 (m, 2H), 6.99-7.05 (m, 2H), 7.10-7.14 (m, 1 H), 7.32-7.33 (d, J = 3.6 Hz, I H), 8.39 (dd, J = 8.0, 1.2 Hz, 1 H), 8.95 (br,1 H), 10.22 (br, I H).

Example 29 N-[2-(2,4-Dichlorophenoxy)phenyl]-N'-(thiazol-2-yl)urea CI CI

O H H
OTNI) N-[2-(2,4-Dichlorophenoxy)phenyl]-N'-(thiazol-2-yl)urea (125 mg, 67%) was prepared from 2-(2,4-dichlorophenoxy)aniline (127 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.

LC-MS (m!z): 382 (M+1)+.
'H NMR (400 MHz, acetone-dg): 6 6.86 (d, J = 8.0 Hz, 1 H) 7.03-7.08 (m, 3H), 7.19-7.23 (m, 1 H), 7.30 (d, J = 4.0 Hz,1 H), 7.38 (dd, J = 8.8, 2.8 Hz, 1 H), 7.65 (d, J =
2.4 Hz,1 H), 8.43 (dd, J = 8.0, 1.2 Hz, 1 H), 8.87 (br, 1 H), 10.16 (br, 1 H).

Example 30 N-[2-(2,4-Difluorophenoxy)phenyl]-N'-(thiazol-2-yl)urea F

O
H H
F / NyNS
6 ` O Nom'!
2-(2,4-Difluorophenoxy)-1-nitrobenzene (0.95 g, 76%) was prepared from 2,4-di-fluorophenol (0.72 g, 5.5 mmol) and 1-fluoro-2-nitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This was reduced to 2-(2,4-difluorophenoxy)aniline (0.53 g, 63%) following general procedure B. N-[2-(2.4-Difluorophenoxy)phenyl]-N'-(thiazol-2-yl)urea (120 mg, 69%) was prepared from 2-(2,4-difluorophenoxy)anitine (110 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 349 (M+1)`
'H NMR (400 MHz, acetone-d8): 6 6.83 (m,1 H), 7.00-7.30 (m, 6H), 7.32 (d, J =
3.6 Hz, 1 H), 8.42 (dd, J = 8.0, 2.0 Hz, 1 H), 9.00 (br, 1 H), 10.19 (br, 1 H).

Example 31 N-[2-(4-Fluoro-2-methoxyphenoxy)phenyt)-N'-(thiazol-2-yl)urea F / O,CH

~ O

N
y S
(1-511 O

2-(4-Fluoro-2-methoxyphenoxy)-1-nitrobenzene (0.88 g, 67%) was prepared from 4-fluoro-2-methoxyphenol (0.78 g, 5.5 mmol) and 1-fluoro-2-nitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This was reduced to 2-(4-fluoro-2-methoxyphenoxy)-aniline (0.60 g, 78%) following general procedure C. N-[2-(4-Fluoro-2-methoxyphenoxy)-phenyl]-N'-(thiazol-2-yl)urea (127 mg, 71%) was prepared from 2-(4-fluoro-2-methoxy-phenoxy)aniline (116 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 361 (M+1)'.
1H NMR (400 MHz, acetone-d6): 3 3.82 (s, 3H), 6.61 (dd, J = 8.0, 2.8 Hz,1 H), 6.74-6.79 (m, 1 H), 6.89-6.94 (m, I H), 7.00-7.06 (m, 3H), 7.16 (dd, J = 8.8, 5.6 Hz,1 H), 7.33 (d, J = 3.6 Hz, 1 H), 8.43 (dd, J = 8.4, 1.6 Hz, 1 H), 8.85 (br, 1 H), 10.29 (br, 1 H).

Example 32 N-[2-(4-Methoxy-2-methoxycarbonylphenoxy)phenyl]-N'-(thiazol-2-yl)urea O
H C'O OCH3 Q
H H
NyN~S

2-[4-Methoxy-2-methoxycarbonylphenoxy]-1-nitrobenzene (0.78 g, 52%) was prepared from methyl 5-methoxysalicylate (1.0 g, 5.5 mmol) and 1-fluoro-2-nitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This was reduced to 2-[4-methoxy-2-(methoxycarbonyl)phenoxy]aniline (0.47 g, 68%) following general procedure B.
N-[2-(4-Methoxy-2-methoxycarbonylphenoxy)phenyl]-N'-(thiazol-2-yl)urea (130 mg, 66%) was prepared from 2-[4-methoxy-2-(methoxycarbonyl)phenoxy]aniline (136 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 401 (M+1)".
IH NMR (400 MHz, acetone-de): 6 3.69 (s, 3H), 3.84 (s, 3H), 6.61 (dd, J =
8.0,1.6 Hz, 1 H), 6.90-6.95 (m, I H), 7.03-7.09 (m, 2H), 7.16-7.25 (m, 2H), 7.25-7.39 (m, 1H), 7.43-7.44 (m, 1 H), 8.37 (dd, J = 8.4, 1.6 Hz,1 H), 8.96 (br, 1 H), 10.26 (br,1 H).

Example 33 N-[2-(3-Methoxyphenoxy)phenyl]-N'-(thiazol-2-yl)urea O
H H
Ny0TNI NS
~
2- (3-Methoxyphenoxy)-1-nitrobenzene (0.84 g, 69%) was prepared from 3-methoxy-phenol (0.68 g, 5.5 mmol) and 1-fluoro-2-nitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This was reduced to 2-(3-methoxyphenoxy)aniline (0.51 g, 70%) following general procedure B. N-(2-(3-Methoxyphenoxy)phenyl]-N'-(thiazol-2-yl)urea (136 mg, 68%) was prepared from 2-(3-methoxyphenoxy)aniline (108 mg, 0.5 mmol) and 2-amino-thiazole (60 mg, 0.6.mmol) following the general procedure D.
LC-MS (m/z): 343 (M+1)'.
'H NMR (400 MHz, acetone-de): 6 3.78 (s, 3H), 6.55-6.62 (m, 2H), 6.71-6.73 (m,1H), 6.95 (dd, J = 8.0, 1.6 Hz, 1 H), 7.03-7.07 (m, 2 H), 7.16-7.20 (m, 1 H), 7.27 (d, J
= 8.4 Hz, 1 H), 7.31 (d, J = 4.0 Hz, 1 H), 8.43 (dd, J = 8.4, 1.6 Hz, 1 H), 8.84 (br, 1 H), 10.37 (br, 1 H).

Example 34 N-[2-(3-Fluorophenoxy)phenyl]-N'-(thiazol-2-yl)urea F

H Of1) 2-(3-Fluorophenoxy)-1-nitrobenzene (0.85 g, 73%) was prepared from 3-fluoro-phenol (0.62 g. 5.5 mmol) and 1 -fluoro-2-nitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This was reduced to 2-(3-fluorophenoxy)aniline (0.50 g, 68%) following 20 general procedure B. N-[2-(3-Fluorophenoxy)phenyl]-N'-(thiazol-2-yl)urea (110 mg, 68%) was prepared from 2-(3-fluorophenoxy)aniline (102 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m z): 331 (M+1)'.
'H NMR (400 MHz, acetone-de): 6 6.80-6.84 (m, 2H), 6.85-6.93 (m, 1H), 7.03-7.07 (m, 2H), 7.08-7.13 (m, 1 H), 7.30 (d, J = 3.6 Hz, 1 H), 7.38-7.45 (m, 1 H), 8.45 (dd, J
= 8.0, 1.2 Hz, 1 H), 9.06 (br, 1H),10.1 (br 1H).

Example 35 N-[2-(3-Trifluoromethylphenoxy)phenyl]-N'-(thiazol-2-yi)urea F))a O F /
N N g r 0 N J/

2-[3-(Trifluoromethyl)phenoxy]-1-nitrobenzene (0.92 g, 65%) was prepared from hydroxybenzotrifluoride (0.89 g, 5.5 mmol) and 1-fluoro-2-nitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This was reduced to 2-[3-(trifluoromethyl)phenoxy]aniline (0.56 g, 68%) following general procedure B. N-[2-(3-Trifluoromethylphenoxy)phenyq-N'-(thiazol-2-ylurea (120 mg, 62%) was prepared from 2-[3-(trifluoromethyl)phenoxy]aniline (127 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 381 (M+1)`.
'H NMR (400 MHz, acetone-d6): 6 7.04-7.13 (m, 3H), 7.24-7.29 (m, 3H), 7.36 (s, 1 H), 7.47 (d, J = 7.6 Hz, 1 H), 7.63 (t, J = 8.0 Hz,1 H), 8.46 (dd, J = 8.0, 1.2 Hz,1 H), 8.95 (br,1 H), 10.08 (br, 1 H).

Example 36 N-[2-(2-Methylphenoxy)phenyl]-N'-(thiazol-2-yl)urea O
H H
S
Ny NTNI
O

N-[2-(2-Methylphenoxy)phenyl]-N'-(thiazol-2-yl)urea (110 mg, 68%) was prepared from 2-(2-methylphenoxy)aniline (100 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 327 (M+1)'.
'H NMR (400 MHz, acetone-de): 6 2.25 (s, 3H), 6.68 (d, J = 8.4 Hz, I H), 6.89 (d, J = 8.0 Hz, 1 H), 6.96-7.00 (m,1 H), 7.04-7.13 (m, 3H), 7.20-7.34 (m, 3H), 8.42 (dd, J =
8.0, 1.6 Hz, 1 H), 8.95 (br, 1 H), 10.25 (br,1 H).

Example 37 N-[2-(2-Methoxyphenoxy)phenyl]-N'-(thiazol-2-yl)urea 0,CH3 H H
~ys>

2-(2-Methoxyphenoxy}1-nitrobenzene (0.99 g, 81 %) was prepared from 2-methoxy-phenol (0.68 g, 5.5 mmol) and 1-fluoro-2-nitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This was reduced to 2-(2-methoxyphenoxy)aniline (0.63 g, 73%) following general procedure B. N-2-(2 Methoxyphenoxy)phenyl-N'-(thiazol-2-yl)urea (110 g, 65%) was prepared from 2-(2-methoxyphenoxy)aniline (108 mg, 0.5 mmol) and 2-amino-thiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 343 (M+1)'.
'H NMR (400 MHz, acetone-do): 6 3.78 (s, 3H), 6.61 (d, J = 8.0 Hz, I H), 6.91-7.33 (m, 8H), 8.37 (d, J = 8.0 Hz,1 H), 9.13 (br, 1 H), 10.31 (br, 1 H).

Example 38 N-[2-(2-Isopropoxyphenoxy)phenyl]-N'-(thiazol-2-yl)urea aOyCH 3 H H
NuN

2-(2-Isopropoxyphenoxy)-1-nitrobenzene (0.90 g, 69%) was prepared from 2-iso-propoxyphenol (0.84 g, 5.5 mmol) and 1-fluoro-2-nitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This was reduced to 2-(2-methoxyphenoxy)aniline (0.65 g, 81 %) following general procedure B. N-[2-(2-Isopnopoxyphenoxy)phenyl]-N'-(thiazol-2-yl)urea (120 mg, 65%) was prepared from 2-(2-isopropoxyphenoxy)aniline (122 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 371 (M+1)'.
'H NMR (400 MHz, acetone-de): d 1.07 (d, J = 6.0 Hz, 6H), 4.54-4.59 (m, 1 H), 6.64 (dd, J =
8.0, 1.6 Hz, 1 H), 6.88-6.92 (m, 1 H), 6.97-7.06 (m, 3H), 7.12-7.22 (m, 3 H), 7.33 (d, J = 3.6 Hz, 1 H), 8.38 (dd, J = 8.0, 1.6 Hz, 1 H), 8.86 (br, 1 H), 10.3 (br, I H).

Example 39 N-[2-(2-Fluorophenoxy)phenyl]-N'-(thiazol-2-yl)urea a F

O H
NyNS

2-(2-Fluorophenoxy)-1-nitrobenzene (0.94 g, 81%) was prepared from 2-fluoro-phenol (0.62 g, 5.5 mmol) and 1 fluoro-2-nitrobenzene (0.71 g, 5.0 mmol) -following the general procedure A. This was reduced to 2-(2-fluorophenoxy)aniline (0.59 g, 72%) following general procedure B. N-[2-(2-Fluorophenoxy)phenyl]-N'-(thiazol-2-yl)urea (110 mg, 68%) was prepared from 2-(2-fluorophenoxy)aniline (102 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS: 331 (M+1)+
1H NMR (400 MHz, acetone- %): 6 6.84 (d, J = 8.0 Hz, 1 H) 7.05-7.08 (m, 1 H), 7.01-7.06 (m, 2H), 7.12-7.17 (m, 2H), 7.22-7.25 (m, 2H), 7.29-7.36 (m, 2H), 8.43 (dd, J =
8.0, 1.6 Hz, 1 H), 8.95 (br,1 H), 10.17 (br,1 H).

Example 40 N-[2-(2-Methylsulfanylphenoxy)phenyl)-N'-(thiazol-2-yl)urea S`CH3 O
N
S
Y ~
ON/
2-(2-Methylsulfanylphenoxy)-1-nitrobenzene (0.88 g, 68%) was prepared from 2-hydroxythioanisole (0.77 g, 5.5 mmol) and 1-fluoro-2-nitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This was reduced to 2-(2-methylsulfanylphenoxy)aniline (0.53 g, 68%) following general procedure B. N-[2-(2-Methylsulfanylphenoxy)phenyl]-N'-(thiazol-2-yl)urea (115 mg, 65%) was prepared from 2-(2-methylsulfanylphenoxy)aniline (115 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 359 (M+1)'.
'H NMR (400 MHz, acetone-de): 6 2.42 (s, 3H), 6.68 (dd, J = 8.0, 1.2 Hz, 1 H), 6.92 (d, J = 8.0 Hz, 1 H), 6.95-6.99 (m, 1 H), 7.04 (d, J = 3.6 Hz, 1 H), 7.09-7.14 (m, 1 H), 7.17-7.26 (m, 2H), 7.31 (d, J = 3.6 Hz, 1 H), 7.38 (dd, J = 7.6, 1.6 Hz, 1 H), 8.42 (dd, J = 8.0, 1.6 Hz, 1 H), 8.95 (br, 1 H), 10.26 (br, 1 H).

Example 41 N-[2-(2-Methylsulfonylphenoxy)phenyl]-N'-thiazolylurea O:.O
~
"CH3 / I S' \ \ O
H H
N Y N
S

To a solution of 2-(2-methylsulfanylphenoxy)-1-nitrobenzene (1.3 g, 5.0 mmol) in di-chloromethane (30 ml) at 0 C was added mCPBA (70%, 3.68 g, 15.mmol), in portions during 10 min. The contents were stirred for 2 h at room temperature. The precipitate was filtered off and the mother liquor was washed thrice with 10% aq Na2S2O7. The organic layer was washed (dil NaOH, water, brine), dried and concentrated to obtain 2-(2-methylsulfonyl-phenoxy)-1-nitrobenzene (1.0 g, 68%). This was reduced to 2-(2-methylsulfonylphenoxy)-aniline (0.68 g, 76%) following general procedure B. N-[2-(2-Methylsulfonylphenoxy)phenyl]-N'-(thiazol-2-yl)urea (105 mg, 55%) was prepared from 2-(2-methylsulfonylphenoxy)aniline (132 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (mlz): 391 (M+1)'.
1 H NMR (400 MHz, acetone-de): 6 3.44 (s, 3H). 7.02 (d, J = 3.6 Hz, 1 H), 7.06 (d, J = 8.4 Hz, 1 H), 7.12-7.20 (m, 2H), 7.27-7.36 (m, 2H), 7.38-7.40 (m,1 H), 7.67-7.71 (m, 1 H), 8.02 (dd, J
= 8.0, 1.6 Hz, I H), 8.42 (dd, J = 8.4, 1.2 Hz, I H), 9.20 (br, I H), 9.78 (br, I H).

Example 42 N-[2-(2-Tnfluoromethylphenoxy)phenyl]-N'-(thiazol-2-yl)urea F

a'F F
O
N N S
O

2-[2-(Trifluoromethyl)phenoxy]-1-nitrobenzene (0.92 g, 65%) was prepared from hydroxybenzotnfluoride (0.89 g, 5.5 mmol) and 1-fluoro-2-nitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This was reduced to 2-[2-(trifluoromethyl)phenoxy]aniline (0.56 g, 68%) following general procedure B. N-[2-(2-Trifluoromethylphenoxy)phenyl)-N'-(thiazol-2-yl)urea (115 mg, 61%) was prepared from 2-[2-(trifluoromethyl)phenoxy]aniline (127 mg, 0.5 mmol) and 2-aminothlazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 381 (M+1)'.
1H NMR (400 MHz, acetone-de): 6 6.91 (dd, J = 8.0, 1.6 Hz, 1 H), 7.01,06 (m, 2H), 7.08-7.11 (m, I H), 7.22-7.26 (m, 2H), 7.34 (t, J = 7.6 Hz, I H), 7.65 (t, J = 7.6 Hz, I H), 7.81 (dd, J
= 8.0, 1.2 Hz, 1 H), 8.45 (dd, J = 8.4, 1.6 Hz, 1 H), 9.00 (br, 1 H), 10.2 (br, 1 H).

Example 43 N-[2-(2,6-Dimetho)cyphenoxy)phenyl]-N'-(thiazol-2-yl)urea 0,CH3 O
H H
H3C'0 y S

2-(2,6-Dimethoxyphenoxy)-1-nitrobenzene (0.85 g, 63%) was prepared from 2,6-di-methoxyphenol (0.85 g, 5.5 mmol) and 1-fluoro-2-nitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This was reduced to 2-(2,6-dimethoxyphenoxy)aniline (0.51 g, 68%) following general procedure C. N-[2-(2,6-Dimethoxyphenoxy)phenyl]-N'-(thiazol-2-yl)-urea (117 g, 63%) was prepared from 2-(2,6-dimethoxyphenoxy)aniline (123 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 373 (M+1)'.
'H NMR (400 MHz, acetone-d6): 6 3.76 (s, 3 H), 6.49 (dd, J = 8.4, 1.2 Hz, 1 H), 6.80 (d, J =
8.4 Hz, 2H), 6.84-6.88 (m, 1 H), 6.95-6.99 (m, 1 H), 7.04 (d, J = 3.2 Hz, 1 H), 7.22 (t, J = 8.4 Hz, I H), 7.35 (d, J = 3.6 Hz, I H), 8.33 (dd, J = 8.0, 1.6 Hz, I H), 8.85 (br, 1 H), 10.40 (br, 1 H).
Example 44 N-[2-(2,6-difluorophenoxy)phenyl]-N'-(thiazol-2-yl)urea F

'?~
H H
F NyNS
0 N--'/
2-(2,6-difluorophenoxy)-1-nitrobenzene (0.44 g, 70 %) was prepared from 2,6-difluorophenol (0.32 g, 2.5 mmol) and 1-fluoro-2-nitrobenzene (0.36 g, 2.5 mmol) following the general procedure A. This was reduced to 2-(2,6-di luorophenoxy)aniline (0.24 g, 60 %) following general procedure B. N-[2-(2,6-difluorophenoxy)phenyl)-N'-(thiazol-2-yl)urea (133 mg, 60 %) was prepared from 2-(2.6-difluorophenoxy)aniline (206 mg, 0.9 mmol) and 2-aminothlazole (405 mg, 2.5 mmol) following the general procedure D.
LC-MS (m/z): 349 (M+1)'.

'H NMR (400 MHz, acetone-de): d 6.73 (d, J = 8 Hz, 1 H), 6.98 (m, 1 H), 7.06 (d, J = 3.2 Hz, 1 H), 7.12 (m, 1 H), 7.20-7.28 (m, 2H), 7.25 (d, J = 3.6 Hz, 1 H), 7.40 (m, 1 H), 8.43 (d, J = 8.2 Hz, 1 H), 9.05 (br, 1 H), 10.12 (br, 1 H).

Example 45 N-[2-(2-Fluoro-6-methoxyphenoxy)phenyl)-N'-(thiazol-2-yl)urea O, O
H H
S
F NyNTN/

O 2-(2-Fluoro-6-methoxyphenoxy}1-nitrobenzene (0.84 g, 64%) was prepared from fluoro-6-methoxyphenol (0.78 g, 5.5 mmol) and 1-fluoro-2-nitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This was reduced to 2-(2-fluoro-6-methoxyphenoxy)-aniline (0.63 g, 85%) following general procedure C. N-2-(2-Fluoro-6-methoxyphenoxy)-phenyl)-N'-(thiazol-2-yl)urea (114 mg, 63%) was prepared from 2-(2-fluoro-6-methoxy-phenoxy)aniline (117 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 361 (M+1)'.
1H NMR (400 MHz, acetone-d6): d 3. 82 (s, 3H), 6.59 (m, 1H), 6.89-6.96 (m, 2H), 7.02-7.07 (m, 3H), 7.27-7.33 (m, I H), 7.34 (d, J = 3.6 Hz, 1 H), 8.38 (dd, J = 8.4, 1.6 Hz, I H), 8.85 (br, I H), 10.31 (br, I H).

Example 46 N-[2-(2-Methoxy-6-methoxycarbonylphenoxy)phenyl]-N'-(thiazol-2-yl)urea H H
1-13C'0 y S
0 N j 2-(2-Methoxy-6-methoxycarbonylphenoxy)-1-nitrobenzene (1.24 g, 82%) was prepared from methyl 3-methoxysalicylate (1.0 g, 5.5 mmol) and 1-fluoro-2-nitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This compound was reduced to 2-(2-methoxy-6-methoxycarbonylphenoxy)aniline (0.89 g, 80%) following the general procedure C. N-[2-(2-Methoxy-6-methoxycarbonylphenoxy)phenyl]-N'-(thiazol-2-yl)urea (143 mg, 72%) was prepared from 2-(2-methoxy-6-methoxycarbonylphenoxy)aniline (136 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 401 (M+1)'.
'H NMR (400 MHz, acetone-de): d 3.78 (s, 3H), 3.87 (s, 3H), 6.89-6.97 (m, 1H), 7.04-7.23 (m, 3H), 7.36-7.47 (m, 2H), 7.67-7.76 (m, 2H), 8.17 (dd, J = 1.6, 10.8 Hz,1 H), 8.78 (br, 1 H), 10.64 (br, I H).

Example 47 N-[(3-methoxy-2-methoxycarbonylphenoxy)phenyl]-N'-(thiazol-2-yl)urea N y N
S
H HTNL/

O 2-(3-Metho)y-2-methoxycarbonylphenoxy)-1-nitrobenzene (1.21 g, 80%) was prepared from methyl 6-methoxysalicylate (1.09 g, 5.5 mmol) and 1-fluoro-2-nitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This compound was reduced to 2-(3-methoxy-2-methoxycarbonylphenoxy)aniline (0.82 g, 75%) following the general procedure C. N-[(3-metho)y-2-methoxycarbonylphenoxy)phenyl]-N'-(thiazol-2-yl)urea (130 mg, 65%) was prepared from 2-(3-methoxy-2-methoxycarbonylphenoxy)aniline (136 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 401 (M+1)'.
'H NMR (400 MHz, acetone-d8): d 3.66 (s, 3H), 3.80 (s, 3H), 6.44-6.46 (m,1H), 6.83-6.87 (m, 1 H), 6.96-6.99 (m, 1 H), 7.03 (d, J = 3.6 Hz, I H), 7.33 (d, J = 4 Hz, 1 H), 7.37-7.46 (m, 2H), 7.46-7.48 (m, 1 H), 8.32-8.35 (dd, J = 1.6, 8.0 Hz, 1 H), 8.80 (br, 1 H),10.32 (br,1 H).

Example 48 N-[2-(2,3-Dimethoxyphenoxy)phenyl]-N'-(thiazol-2-yl)urea O~CH3 \ O

TNI N~N S
O /
2-(2,3-Dimethoxyphenoxy)-1-nitrobenzene (0.88 g, 64%) was prepared from 2,3-dimethoxyphenol (0.85 g, 5.5 mmol) and 1-fluoro-2-nitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This was reduced to 2-(2,3-dimethoxyphenoxy)aniline (0.57 g, 73%) following general procedure B. N-[2-(2,3-Dimethoxyphenoxy)pheny$-N'-(thiazol-2-yl)urea (131 g, 71%) was prepared from 2-(2,3-dimethoxyphenoxy)aniline (123 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (mlz): 373 (M+1)`.
'H NMR (400 MHz, acetone-de): d 3.66 (s, 3H), 3.88 (s, 3H), 6.66-6.74 (m, 2H), 6.91-6.98 (m, 2H), 7.04-7.16 (m, 3H), 7.32 (d, J = 3.6 Hz, 1 H), 8.39 (dd, J = 8.0, 1.6 Hz, 1 H), 8.90 (br, 1 H), 10.26 (br, 1H).

Example 49 N-[2-(2,3,4-Trichlorophenoxy)phenyl]-N'-(thiazol-2-yl)urea Cl CI CI

N S
YJ

2-(2,3,4-Trichlorophenoxy)-1-nitrobenzene (1.04 g, 65%) was prepared from 2,3,4-trichlorophenol (0.98 g, 5.0 mmol) and 1-fluoro-2-nitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This was reduced to 2-(2,3,4-trichlorophenoxy)aniline (0.42 g, 60%, 2.5 mmol scale) following general procedure B. N-[2-(2,3,4-Trichlorophenoxy)phenyl]-N'-(thiazol-2-yl)urea (343 mg, 55%) was prepared from 2-(2,3,4-trichlorophenoxy)aniline (420 mg, 1.5 mmol) and 2-aminothiazole (150 mg, 1.5 mmol) following the general procedure D.
LC-MS (m/z): 415 (M+1)'.
'H NMR (400 MHz, acetone-de): 6 9.97-7.12 (m, 4H), 7.23-7.28 (m, 2H), 7.58 (d, J 8.8 Hz, 1 H), 8.45 (d, J = 8.0 Hz, 1 H), 10.13 (br, 1 H).

Example 50 N-[2-(2,4,6-Trifluorophenoxy)phenyl]-N'-(thiazol-2-yl)urea F F

O
H H
F / NyN~S
\ I O N-.J
2-(2,4,6-Trifluorophenoxy)-1-nitrobenzene (1.14 g, 85%) was prepared from 2,4,6-trifluorophenoi (0.74 g, 5.0 mmol) and 1-fluoro-2-nitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This was reduced to 2-(2,4,6-trifluorophenoxy)aniline (0.42 g, 70%, 2.5 mmol scale) following general procedure B. N-[2-(2,4,6-Trifluorophenoxy)phenyl]-N'-(thiazol-2-yl)urea (219 mg, 60%) was prepared from 2-(2,4,6-trifluorophenoxy)aniline (237 mg, 1.0 mmol) and 2-aminothiazole (100 mg, 1.0 mmol) following the general procedure D.
LC-MS (m/z): 367 (M+1)'.
'H NMR (400 MHz, acetone-de): 6 6.78 (d, J = 8.4 Hz, 1 H), 7.00-7.21 (m, 5H), 7.36 (d, J =
3.6 Hz, 1 H), 8.42 (d, J = 8.4 Hz, 1 H), 9.05 (br, I H), 10.36 (br, I H).

Example 51 N-[2-(2,4-dichloronaphth-1-oxy)phenyl]-N'-(thiazol-2-yl)urea Cl Cl O

2-(2,4-Dichloronaphth-1-oxy)-1-nitrobenzene (1.17 g, 60%) was prepared from 2,4-dichloronaphth-l-ol (1.06 g, 5.0 mmol) and 1-fluoro-2-nitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This was reduced to 2-(2,4-dichloronaphth-l-oxy)aniline (0.45 g, 60%, 2.5 mmol scale) following general procedure B. N-[2-(2,4-Dichloronaphth-1-oxy)phenylj-N'-thiazolylurea (172 g, 40%) was prepared from 2-(2,4-dichloronaphth-1-oxy)aniline (303 mg, 1.0 mmol) and 2-aminothiazole (100 mg, 1.0 mmol) following the general procedure D.
LC-MS (m/z): 431 (M+1)'.
'H NMR (400 MHz, acetone-de): 6 6.39 (d, J = 8.2 Hz, 1H), 6.86 (m, I H), 7.07 (m, 2H), 7.34 (d, J = 3.6 Hz, 1 H), 7.71-7.88 (m, 3H), 8.00 (d, J = 8.0 Hz, 1 H), 8.32 (d, J
= 8.0 Hz, 1 H), 8.48 (d, J = 8.0 Hz, 1 H), 9.15 (br, 1 H), 10.35 (br, 1 H).

Example 52 N-[2-(2-Methoxyphenoxy)-5-(methylsulfonyl)phenyl]-N'-(thiazol-2-yl)urea O`CH3 O
H H
S
Ny NTNI
O

H3C' 1 1 2-(2-Methoxyphenoxy)-5-(methylsulfonyl}1-nitrobenzene (1.21 g, 75%) was prepared from 2-methoxyphenol (0.68 g, 5.5 mmol) and 1-fluoro-4-methylsulfonyl-2-nitro-benzene (1.09 g, 5.0 mmol) following the general procedure A. This was reduced to 2-(2-methoxyphenoxy)-5-(methylsulfonyl)aniline (0.68 g, 62%) following general procedure B. N-[2-(2-Methoxyphenoxy)-5-(methylsulfonyl)phenyl]-N'-(thiazol-2-yl)urea (136 mg, 65%) was prepared from 2-(2-methoxyphenoxy)-5-(methylsulfonyl)aniline (146 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 421 (M+1)`.
'H NMR (400 MHz, acetone-d6): 6 2.82 (s, 3H), 3.77 (s, 3H), 6.73 (d, J = 8.4 Hz, 1H) 7.05-7.11 (m, 2H), 7.23-7.28 (m, 2H), 7.32-7.37 (m, 2H), 7.50 (dd, J = 8.4, 3.6 Hz, 1 H), 9.02 (d, J
= 2.4 Hz, 1 H), 9.12 (br, 1 H), 10.42 (br, 1 H).

Example 53 N-[5-Cyano-2-(2-methoxyphenoxy)phenyl]-N'-(thiazol-2-yl)urea O, H H
S
N\ /NTN' ~O
N
4-(2-Methoxyphenoxy)-3-nitrobenzonitrile (1.10 g, 81%) was prepared from 2-methoxyphenol (0.68 g, 5.5 mmol) and 4-fluoro-3-nitrobenzonitrile (1.33 g, 5.0 mmol) foilowing.general procedure A. This was reduced to 4-(2-methoxyphenoxy)-3-aminobenzo-nitrite (0.62 g, 63%) following general procedure B. N-[5-Cyano-2-(2-methoxyphenoxy)-phenyl]-N'-(thiazol-2-yl)urea (130 mg, 71 %) was prepared from 4-(2-methoxyphenoxy)-3-aminobenzonitrile (120 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following general procedure D.
LC-MS (m/z): 368 (M+1)'.
'H NMR (400 MHz, acetone-d8): 6 3.79 (s, 3H), 6.69 (d, J = 8.4 Hz, 1 H) 7.05-7.09 (m, 1 H), 7.10 (d, J = 3.6 Hz, 1 H), 7.22-7.27 (m, 2H), 7.32-7.36 (m, 3H), 8.75 (d, J =
2.0 Hz, 1 H), 9.12 (br, I H), 10.38 (br, I H).

Example 54 N-[5-Fluoro-2-(2-methylsulfanylphenoxy)phenyl]-N'-thiazolylurea /O
O
Na O TNI )y F
5-Fluoro-2-(2-methyisulfanylphenoxy)-1-nitrobenzene (0.95 g, 68%) was prepared from 2-hydroxythioanisole (0.77 g, 5.5 mmol) and 2,5-difluoro-1-nitrobenzene (0.80 g, 5.0 mmol) following the general procedure A. This was reduced to 5-fluoro-2-(2-methylsulfanyl-phenoxy)aniline (0.52 g, 62%) following general procedure B. N-[5-Fluoro-2-(2-methyl-sulfanylphenoxy)phenyl]-N'-(thiazol-2-yl)urea (120 mg, 65%) was prepared from 5-fluoro-2-(2-methylsulfanylphenoxy)aniline (125 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 377 (M+1)'.
'H NMR (400 MHz, acetone-de): 6 2.48 (s, 3H), 6.61 (m, 2H), 6.92 (d, J = 7.6 Hz, 1 H), 7.06 (d, J = 3.6 Hz,1 H), 7.16-7.25 (m, 2H), 7.31 (d, J = 3.6 Hz,1 H), 7.39 (dd, J
= 7.6, 2.0 Hz, 1 H), 8.26-8.29 (m, 1 H), 9.00 (br, 1 H), 10.32 (br, 1 H).

Example 55 N-[5-Fluoro-2-(2-fluoro-6-methoxyphenoxy)phenyq-N'-(thiazol-2-yl)urea O, H H
g F NyNTNI/
O F

5-Fluoro-2-(2-fluoro-6-methoxyphenoxy)-1-nitrobenzene (0.91 g, 65%) was prepared from 2-fluoro-6-methoxyphenol (0.78 g, 5.5 mmol) and 2,5-difluoro-1-nitrobenzene (0.80 g, 5.0 mmol) following the general procedure A. This was reduced to 5-fluoro-2-(2-fluoro-6-methoxyphenoxy)aniline (0.66 g, 81 %) following general procedure C.
N-[5-Fluoro-2-(2-fluoro-6-methoxyphenoxy)phenyl-N'-(thiazol-2-yl)urea (130g, 69%) was prepared from 5-fluoro-2-(2 fluoro-6-methoxyphenoxy)aniline (126 mg, 0.5 moral) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 379 (M+1)'.
'H NMR (400 MHz, acetone-d8): 6 3.83 (s, 3H), 6.60-6.70 (m, 2H), 6.92-6.97 (m, I H), 7.03-7.05 (m, I H), 7.09 (d, J = 4.0 Hz, I H), 7.27-7.33 (m, 1 H), 7.36 (d, J = 3.6 Hz, I H), 8.23 (dd, J
=10.8, 3.2 Hz, 1 H), 9.05 (br,1 H), 10.39 (br, 1 H).

Example 56 N-[2-(2,3-Dimethoxyphenoxy)-5-fluorophenyl]-N'(thiazol-2-yl)urea 0. CH3 O,CH3 O
H H
F
2-(2,3-Dimethoxyphenoxy)-5-fluoro-l-nitrobenzene (1.0 g, 68%) was prepared from 2,3-dimethoxyphenol (0.85 g, 5.5 mmol) and 2,5-difluoro-1-nitrobenzene (0.80 g, 5.0 mmol) following the general procedure A. This was reduced to 2-(2,3-dimethoxyphenoxy)-5-fluoro-aniline (0.67 g, 75%) following general procedure C. N-[2-(2,3-Dimethoxyphenoxy)-5-fluoro-phenyl]-N'-(thiazol-2-yI)urea (126 g, 65%) was prepared from 2-(2,3-dimethoxyphenoxy)-5-fluoroaniline (132 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 391 (M+1)*.
'H NMR (400 MHz, acetone-de): 6 3.68 (s, 3H), 3.88 (s, 3H), 6.67 (dd, J = 9.2, 1.2 Hz, 1 H), 6.70-6.79 (m, 2H), 6.92 (dd, J = 8.0, 1.6 Hz, 1 H), 7.05-7.09 (m, 2H), 7.32 (d, J = 3.6 Hz, I H), 8.25 (dd, J = 11.2, 2.8 Hz, 1 H), 9.03 (br,1 H), 10.33 (br, 1 H).

Example 57 N-[2-(3,4-Difluorophenoxy)-5-fluorophenyl]-N'-(thiazol-2-yl)urea F
F

O
H H
Ny NTNI S
O ~
F
2-(3,4-Difluorophenoxy}5-fluoro-l-nitrobenzene (1.05 g, 78%) was prepared from 3,4-difluorophenol (0.72 g, 5.5 mmol) and 2,5=difluoro-1-nitrobenzene (0.8 g, 5.0 mmol) following the general procedure A. This compound was reduced to 2-(3,4-diuorophenoxy)-5-fluoroaniline (0.63 g, 68%) following the general procedure B. N-[2-(3,4-Difluorophenoxy)-5-fluorophenyq-N'-(thiazol-2-yl)urea (132 mg, 72%) was prepared from 2-(3,4-difluoro-phenoxy)-5-fluoroaniline (120 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) 5- following the general procedure D.
LC-MS (m/z): 367 (M+1)+.
'H NMR (400 MHz, acetone-d6): 6 6.81-6.89 (m, 2H), 7.05-7.11 (m, 3H), 7.31-7.38 (m, 2H), 8.28 (dd, J = 2.8, 10.8 Hz, 1 H), 9.10 (br, 1 H), 10.34 (br, 1 H).

Example 58 N-[5-Fluoro-2-(4-fluorophenoxy)phenyl]-N'-(thiazol-2-yl)urea F
o H
NNS
0 j1NI'J

5-Fluoro-2-(4-fluorophenoxy)-1-nitrobenzene (0.94 g, 75%) was prepared from 4-fluorophenol (0.62 g, 5.5 mmol) and 2,5-difluoro-1-nitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This compound was reduced to 2-(4-fluorophenoxy)-5-fluoroaniline (0.53 g, 64%) following the general procedure B. N-[5-Fluoro-2-(4-fluorophenoxy)phenyl]-N'-(thiazol-2-yl)urea (130 mg, 75%) was prepared from 5-fluoro-2-(4-fluorophenoxy)aniline (110 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 349 (M+1)+.
'H NMR (400 MHz, acetone-de): 6 6.78-6.82 (m,1 H), 6.93-6.97 (m, 1 H), 7.06-7.10 (m, 3H), 7.14-7.18 (m, 2H), 7.3 (d, J = 3.2 Hz, 1 H). 8.27 (dd, J = 2.8, 10.8 Hz, 1 H), 8.82 (br,1 H), 10.28 (br, 1 H).

Example 59 N-(2-(2,4-Dichlorophenoxy)-5-fluorophenyl]-N'-(thiazol-2-yl)urea CI \ CI

O
H H
NyND/y SO 2-(2,4-Dichlorophenoxy)-5-fluoro-1-nitrobenzene (1.17 g, 78%) was prepared from 2,4-dichlorophenol (0.89 g, 5.5 mmol) and 2,5-difluoro-l-nitrobenzene (0.8 g, 5.0 mmol) following the general procedure A. This compound was reduced to 2-(2,4-dichlorophenoxy) 5-fluoroaniline (0.68 g, 64%) following the general procedure B. N-[2-(2,4-Dichlorophenoxy)-5-fluorophenyl]-N'-(thiazol-2-yl)urea (150 mg, 76%) was prepared from 2-(2,4-dichloro-phenoxy)-5-fluoroaniline (135 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 399 (M+1)+.
'H NMR (400 MHz, acetone-de): 6 6.79-6.84 (m. 1 H), 6.93 (m, 1 H), 7.03-7.07 (m, 2H), 7.30 (d, J = 3.2 Hz, 1 H), 7.38 (dd, 2.4, 8.8 Hz 1 H), 7.64 (d, J = 2.4 Hz, 1 H), 8.29 (dd, J = 2.4, 11.2 Hz 1 H), 9.00 (br, 1 H), 10.24 (bs, 1 H).

Example 60 N-[5-Fluoro-2-(4-methoxyphenoxy)phenyl]-N'-(thiazol-2-yl)urea O

O

H HTNI
NN S O om'/

5-Fluoro-2-(4-methoxyphenoxy)-1-nitrobenzene (1.05 g, 80%) was prepared from 4-methoxyphenol (0.68 g, 5.5,mmol) and 2,5-difluoro-l-nitrobenzene (0.8 g, 5.0 mmol) following the general procedure A. This compound was reduced to 5-fluoro-2-(4-methoxy-phenoxy)aniline (0.62 g, 66%) following the general procedure B. N-[5-Fluoro-2-(4-methoxy-phenoxy)phenyl]-N'-(thiazol-2-yl)urea (133 mg, 74%) was prepared from 2-(4-methoxy-phenoxy}5-fluoroaniline (117 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 361 (M+1)`.
1H NMR (400 MHz, acetone-d6): J3.79 (s, 3H), 6.75-6.77 (m, 1H), 6.82-6.87 (m, 1H),6.94-7.01 (m, 3H), 7.07 (d, J = 2.1 Hz, 1 H), 7.32 (d, J = 3.6 Hz, I H), 8.26 (dd, J = 3.2, 11.2 Hz, I H), 9.05 (br, 1 H), 10.32 (br, I H).
Example 61 N-[5-Fluoro-2-(2-methoxyphenoxy)phenyl]-N'-(thiazol-2-yl)urea O H H
NyNS
O

5-Fluoro-2-(2-methoxyphenoxy)-1-nitrobenzene (1.07 g, 81%) was prepared from 2-methoxyphenol (0.62 g, 5.5 mmol) and 2,5-difluoro-1-nitrobenzene (0.8 g, 5.0 mmol) following the general procedure A. This compound was reduced to 2-(2-methoxyphenoxy)-5-fluoroaniline (0.58 g, 66%) following the general procedure B. 1-[5-Fluoro-2-(2-methoxy-phenoxy)phenyl)-3-(thiazol-2-yl)urea (129 mg, 72%) was prepared from 5-fluoro-2-(2-methoxyphenoxy)aniline (117 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 361 (M+1)' 'H NMR (400 MHz, acetone-de): 6 3.79 (s, 3H), 6.65-6.7 (m, 2H), 6.98-7.01 (m,1H), 7.05-7.22 (m, 4H), 7.32 (d, J = 3.6 Hz, 1 H), 8.22 (dd, J = 2.8, 10.8 Hz, 1 H), 9.12 (br, 1 H), 10.42 (br, 1 H).

Example 62 N-[5-Fluoro-2-(2-trifluoromethylphenoxy)phenyl]-N'-(thiazol-2-yl)urea F

OF

H H
NyNS
O N
F
5-Fluoro-2-(2-trifluromethylpheno)y}1-nitrobenzene (1.17 g, 78%) was prepared from 2-hydroxybenzotrifluonde (0.89 g, 5.5 mmol) and 2,5-difluoro-1-nitrobenzene (0.8 g, 5.0 mmol) following the general procedure A. This compound was reduced to 5-fluoro-2-(2-tri-fluoromethylphenoxy)-aniline (0.65 g, 62%) following the general procedure B.
N-[5-Fluoro-2-(2-trifluoromethylphenoxy)phenyl]-N'-(thiazol-2-yl)urea (146 mg, 74%) was prepared from 2-(2-trifluoromethylphenoxy)-5-fluoroaniline (135 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (mlz): 399 (M+1)'.
'H NMR (400 MHz, acetone-de): 6 6.81-6.87 (m,1H), 6.95-7.05 (m, 3H), 7.21 (m,1H), 7.31-7.36 (m, 1 H), 7.6-7.65 (m,1 H), 7.79 (d, J = 7.6 Hz, 1 H), 8.30 (dd, J =
3.2,11.2 Hz, 1 H), 8.72 (br, 1 H), 10.24 (br, 1 H).

Example 63 N-[5-Fluoro-2-(naphth-2-oxy)phenyl]-N'-(thiazol-2-yl)urea Nz~

N S
fD/

5-Fluoro-2-(naphth-2-oxy)-1-nitrobenzene (1.13 g, 80%) was prepared from 2-naphthol (0.79 g, 5.5 mmol) and 2,5-difluoro-1-nitrobenzene (0.8 g, 5.0 mmol) following the general procedure A. This compound was reduced to 2-(2-naphth-2-oxy)-5-fluoroaniline (0.64 g, 64%) following the general procedure B. N-[5-Fluoro-2-(naphth-2-oxy)phenyl]-N'-(thiazol-2-yl)urea (123 mg, 65%) was prepared from 5-Fluoro-2-(naphth-2-oxy)-aniline (127 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 381 (M+1)'.
1H NMR (400 MHz, acetone-d6): d 6.83-6.87 (m, 1 H), 7.01(bs, 1 H), 7.08 (m, 1 H), 7.33 (bs, 1 H), 7.42-7.49 (m, 3H), 7.80 (d, J = 7.6 Hz, 1 H), 7.90(d, J = 7.6 Hz, 1 H), 7.97 (d, J = 8.8 Hz, 1 H), 8.32 (d, J = 8.4 Hz, 1 H), 8.62 (br, 1 H), 10.22 (br, 1 H) Example 64 N-[2-(2,3-Dimethoxyphenoxy)-6-fluorophenyl]-N'-(thiazol-2-yl)urea .CH3 / O

~ I
O
O
H H
Ny N~S
/ ON-) F
2-(2,3-Dimethoxyphenoxy)-6-fluoro-nitrobenzene (1.05 g, 72%) was prepared from 2,3-dimethoxyphenol (0.85 g, 5.5 mmol) and 2,6-difluoronitrobenzene (0.80 g, 5.0 mmol) following the general procedure A. This compound was reduced to 2-(2,3-dimethoxy-phenoxy)-6-fluoroaniline (0.66 g, 70%) following the general procedure C N-[2-(2,3-Di-methoxyphenoxy)-6-fluorophenyl]-N'-(thiazol-2-yl)urea (136 mg, 70%) was prepared from 2-(2,3-dimethoxyphenoxy)-6-fluoroaniline (131 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 391 (M+1)`.
'H NMR (400 MHz, acetone-de): 6 3.64 (s, 3H), 3.85 (s, 3H), 6.59 (d, J = 8.0 Hz, I H), 6.68-6.69 (d, J = 8.0 Hz, 1 H), 6.88-7.06 (m, 4H), 7.22-7.22 (m 1 H), 7.30-7.31 (d, J = 3.2 Hz, I H), 8.18 (br, 1 H), 10.26 (br, 1 H).

Example 65 N-[2-(4-Fluoro-2-methoxyphenoxy)phenyl]-N'-(thiazol-2-yl)urea (f' 'cH3 H H
NyN~S
0 N--=~
F
4-Fluoro-2-(2-methoxyphenoxy)-1-nitrobenzene (1.2 g, 91.6%) was prepared from 2-methoxyphenol (0.68 g, 5.5 mmol) and 2,4-difluoro-1-nitrobenzene (0.80 g, 5.0 mmol) following the general procedure F. The product was then reduced to 4-fluoro-2-(2-methoxy-phenoxy)aniline (0.96 g, 73%) following general procedure B. N-(4-Fluoro-2-(2-methoxy-phenoxy)phenyl]-N'-(thiazol-2-yl)urea (0.32 g, 86%) was prepared from 4-fluoro-2-(2-methoxyphenoxy)aniline (0.117 g, 0.5 mmol) and 2-aminothiazole (0.060 g, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 361 (M+1)`.
'H NMR (400 MHz, CDCI3): 5 3.78 (s, 3H), 6.32 (dd, J = 4.0, 14.0 Hz,1 H), 6.35 (dd, J = 2.8, 10.4 Hz, 1 H), 6.61 (t, J = 4.0 Hz, 1 H), 6.80 (m, 2H), 7.05 (m, 2H), 7.18 (m, 2H), 11.46 (br, 2H).

Example 66 N-[2-(2,3-Dimethoxyphenoxy)- 4-fluorophenyl]-N'-(thiazol-2-yl)urea 0~CH3 CH3 bc 0 H H
I \ NyN~S

2-(2,3-Dimethoxyphenoxy)-4-fluoro-1 -nitrobenzene (0.88 g, 60%) was prepared from 2,3-dimethoxyphenol (0.85 g, 5.5 mmol) and 2,4-difluoro-1-nitrobenzene (0.8 g, 5.0 mmol) following the general procedure F. This compound was reduced to 2-(2,3-dimethoxy-phenoxy)-4-fluoroaniline (0.52 g, 66%) following the general procedure C. N-[2-(2,3-di-methoxyphenoxy)-4-fluorophenyl]-N'-(thiazol-2-yl)urea (116 mg, 60%) was prepared from 2-(2,3-dimethoxyphenoxy)-4-fluoroaniline (132 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (mlz): 391 (M+1)'.
'H NMR (400 MHz, acetone-d6): 6 3.68 (s, 3H), 3.89 (s, 3H), 6.46 (dd, J = 2.4, 9.2 Hz, 1H), 6.76 (dd, J = 1.6, 8.0 Hz, I H), 6.82-6.87 (m, 1 H), 6.98 (dd, J = 2.3, 6.8 Hz, I H), 7.04 (d, J =
3.6 Hz, 1 H), 7.1-7.13 (t, J = 8.4 Hz, 1 H), 7.31(d, J = 4.0 Hz, 1 H), 8.33-8.37 (dd, J = 6.4, 9.6 Hz, 1 H), 8.42 (br, 1 H), 10.23 (br, 1 H).

Example 67 N-[4-Fluoro-2-(2-fluoro-6-methoxyphenoxy)phenyl)-N'-(thiazol-2-yl)urea O
O
H H
F NIrNS
O ~10 4-Fluoro-2-(2-fluoro-6-methoxyphenoxy)-1-nitrobenzene (0.91 g, 65%) was prepared from 2-fluoro-6-methoxyphenol (0.78 g, 5.5 mmol) and 2,4-difluoro-1-nitrobenzene (0.8 g, 5.0 mmol) following the general procedure F. This compound was reduced to 4-fluoro-2-(2-fluoro-6-methoxyphenoxy)aniline (0.61 g, 75%) following the general procedure C. N-[4-Fluoro-2-(2-fluoro-6-methoxyphenoxy)phenyl]-N'-(thiazol-2-yl)urea (122 mg, 65%) was prepared from 4-fluoro-2-(2-fluoro-6-methoxyphenoxy)aniline (126 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 379 (M+1)'.
'H NMR (400 MHz, acetone-d6): 6 3.84 (s, 3H), 6.39 (dd, 2.8, 9.6 Hz 1 H), 6.81-6.85 (m, 1 H), 6.95-6.98 (m, 1 H), 7.05-7.07 (m, 2 H) 7.29-7.35 (m, 2H), 8.32-8.36 (m, 1 H), 8.85 (br, 1 H), 10.26 (br, 1H) Example 68 N-[2-(2-Fluoro-6-methoxyphenoxy)-4-methoxyphenyl]-N'-(thiazol-2-yl)urea O
H H
F \ NyN~S
H3C. O O N, /

A mixture of 4-fluoro-2-(2-fluoro-6-methoxyphenoxy)-1-nitrobenzene (1.33 g, 5 mmol) and sodium methoxide (035g, 6 mmol) in DMF (10 ml) was heated at 80 C
for 2 It The mixture was poured into water and was extracted with ethyl acetate (3x20 ml). The combined organic layer was washed with water, brine and dried (Na2SO4). The solution was concentrated under reduced pressure to obtain 2-(2-fluoro-6-methoxyphenoxy)-4-methoxy-1-nitrobenzene (1.02 g, 70%). This compound was reduced to 2-(2-fluoro-6-methoxyphenoxy)-4-methoxyaniline (0.62 g, 73%) following the general procedure C. N-[2-(2-Fluoro-6-methoxyphenoxy)-4-methoxyphenylj-N'-(thiazol-2-yl)urea (136 mg, 70%) was prepared from 2-(2-methoxy-6-fluorophenoxy)-4-methoxyaniline (132 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (Mz): 391 (M+1)'.
'H NMR (400 MHz, CDCI3): 6 3.74 (s, 3H), 6.19 (bs, 1H), 6.46 (dd, J =2.4, 7.6 Hz, 1H), 6.61-6.84 (m, 3H), 7.04-7.19 (m, 1 H), 7.32-7.44 (bs, 1 H), 8.04-8.12 (m, 1 H), 8.20 (br,1 H), 10.22 (br, 1 H).

Example 69 N-[3-Fluoro-2-(2-fluoro-6-methoxyphenoxy)phenyq-N'-(thiazol-2-yl)urea O
O
F H H
F I ~ NYN~S
/ O N-/

Methyl 3-fluoro-2-(2-fluoro-6-methoxyphenoxy)benzoate (0.88 g, 60%) was prepared from methyl 2,3-difluorobenzoate (0.86 g, 5 mmol) and 2-fluoro-6-methoxyphenol (0.78 g, 5.5 mmol) as described in procedure A. Hydrolysis of this ester with LiOH in aqueous methanol furnished 2-(2-metho)cy-6-fluorophenoxy)-3-fluorobenzoic acid (0.86 g, 90%). To a solution of 3-fluoro-2-(2-fluoro-6-methoxyphenoxy)benzoic acid (0.56 g, 2.0 mmol) in 1,2-dichloroethane (10 ml) was added oxalyl chloride (0.18 ml, 2.2 mmol). The solution was stirred at room temperature for 45 min. To this solution was added NaN3 (390 mg, 6 mmol) and the mixture was heated to reflux for 3 h. 2-Aminothiazole (200 mg, 2 mmol) was then added to this mixture and was further refluxed for 3 h. The mixture was concentrated and the residue was purified by column chromatography (silica, CH2CI2 then 10% ethyl acetate in CH2CI2) to afford 1-(3-fluoro-2-(2-fluoro-6-methoxyphenoxy)phenyg-3-(thiazol-2-yl)urea in (414 mg, 55%).
LC-MS (m/z): 379 (M+1)'.
1H NMR (400 MHz, acetone-d6): 6 3.72 (s, 3H), 6.44 (d, J = 8.4 Hz, 1 H), 6.69-6.84 (m, 4H).
7.01-7.12 (m, 2H), 7.35-7.36 (d, J = 4.0 Hz, 1 H), 8.28 (br. 1 H), 10.28 (br,1 H).

Example 70 N-[2-(2,3-Dimethoxyphenoxy)-5-methoxyphenyl)-N'-thiazol-2-ylurea O.,CH3 O`CH3 O
H H
N Y N
S
O N

2-(2,3-Dimethoxyphenoxy)-5-methoxy-1-nitrobenzene (0.85 g, 56%) was prepared from 2,3-dimethoxyphenol (0.85 g, 5.5 mmol) and 4-chloro-3-nitroanisole (0.94 g, 5.0 mmol) following the general procedure A. This was reduced to 2-(2,3-dimethoxyphenoxy)-5-methoxyaniline (0.65 g, 85%) following general procedure C. N-[2-(2,3-Dimethoxyphenoxy) 5-methoxyphenyl]-N'-(thiazol-2-yl)urea (124 g, 62%) was prepared from 2-(2,3-dimethoxy-phenoxy)-5-methoxyaniline (133 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.

LC-MS (m/z): 403 (M+1)`.
'H NMR (400 MHz, acetone-de): 6 3.70 (s, 3H), 3.79 (s. 3H). 3.87 (s, 3H), 6.53-6.57 (m, 2H), 6.75 (d, J = 8.8 Hz, 1 H), 6.85 (dd, J = 8.4, 1.2 Hz, 1 H), 7.00 (d, J = 8.4 Hz, 1 H), 7.04 (d, J =
3.6 Hz, 1 H), 7.30 (d, J = 3.6 Hz, 1 H). 8.10 (d, J = 3.6 Hz, 1 H), 10.26 (br,1 H).

Example 71 N-[2-(2,3-Dimethoxyphenoxy)-4-methylphenyl]-N'-(thiazol-2-yl)urea 0,CH3 o H H
NuN~S
/ `loll IIN((~

3-(2,3-Dimethoxyphenoxy)-4-nitrotoluene (0.92 g, 64%) was prepared from 2,3-di-methoxyphenol (0.85 g, 5.5 mmol) and 3-fluoro-4-nitrotoluene (0.78 g, 5.0 mmol) following the general procedure A. This was reduced to 2-(2,3-dimethoxyphenoxy)-4-methylaniline (0.65 g, 79%) following general procedure C. N-[2 (2,3-Dimethoxyphenoxy)-4-methylphenyl]-N'-(thiazol-2-yl)urea (120 mg, 63%) was prepared from 2-(2,3-dimethoxyphenoxy)-4-methyl-aniline (130 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 387 (M+1)*.
'H NMR (400 MHz, acetone-de): d 2.20 (s, 3H). 3.67 (s. 3H), 3.88 (s, 3H) 6.57 (d, J = 1.2 Hz, 1 H), 6.64 (dd, J = 8.4, 1.6 Hz, I H), 6.89-6.92 (m, 2H), 7.01-7.08. (m, 2H), 7.31 (d, J = 3.6 Hz, 1 H), 8.24 (d, J = 8.4 Hz,1 H), 8.60 (br, 1 H), 10.23 (br,1 H).

Example 72 N-[2-(2,3-Dimethoxyphenoxy)-3-methylphenyq-N'-(thiazol-2-yl)urea O,CH3 / KO
Z~Nll H H
S
H3C NyNTNI
O
2-(2,3-Dimethoxyphenoxy)-3-nitrotoluene (0.80 g, 56%) was prepared from 2,3-dimethoxyphenol (0.85 g, 5.5 mmol) and 2-chloro-3-nitrotoluene (0.85 g, 5.0 mmol) following the general procedure A. This was reduced to 2-(2,3-dimethoxyphenoxy)-3-methylaniline (0.54 g, 76%) following general procedure C. N-(2-(2,3-Dimethoxyphenoxy)-3-methylphenyq-N'-(thiazol-2-yl)urea (116 mg, 61%) was prepared from 2-(2,3-dimethoxyphenoxy)-3-methyl-aniline (130 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
WAS (m/z): 387 (M+1)'.
'H NMR (400 MHz, acetone-de): 6 2.09 (s, 3H), 3.88 (s, 6H), 6.07 (dd, J =
8.4,1.2 Hz, 1 H), 6.73 (dd. J = 8.4,1.2 Hz, 1 H), 6.85-6.89 (m, 1 H), 6.98-7.00 (m, 2H), 7.16-7.20 (m, 1 H), 7.24 (d, J = 3.6 Hz, 1 H), 8.27 (d, J = 8.0 Hz, 1 H), 8.95 (br, 1 H), 10.09 (br, 1 H).

Example 73 N-[2-(2-Chlorophenoxy)-5-chlorophenyl]-N'-(thiazol-2-yl)urea Cl O
H H
NNf S
O :/
Cl N-[2-(2-Chlorophenoxy)-5-chlorophenyq-N'-(thiazol-2-yl)urea (119 mg, 63%) was prepared from 2-(2-chlorophenoxy)-5-chloroaniline (127 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 381 (M+1)'.

'H NMR (400 MHz, acetone-de): 66.76 (d, J = 8.4 Hz, 1 H), 7.04 (dd, J = 8.4, 2.4 Hz, 1 H), 7.07 (d, J = 3.6 Hz, 1 H), 7.17 (d, J = 8.4 Hz, 1 H), 7.24-7.42 (m, 3H), 7.59 (dd, J = 8.0, 1.6 Hz, 1 H), 8.55 (d, J = 2.4 Hz, 1 H), 9.01 (br, 1 H), 10.28 (br, 1 H).

Example 74 N-[5-Chloro-2-(4-chloro-3-methylphenoxy)phenyl]-N'-(thiazol-2-yl)urea Cl 0 H H
NuNS
ON~/
CI
N-[5-Chloro-2-(4-chloro-3-methylphenoxy)phenyl]-N'-(thiazol-2-yl)urea (236 mg, 60%) was prepared from 2-(2-methyl-3-chlorophenoxy)-5-chloroaniline (commercially available, 268 mg, 1.0 mmol) and 2-aminothiazole (100 mg, 1.0 mmol) following the general procedure D.
LC-MS (m/z): 397 (M+1)`
'H NMR (400 MHz, acetone-de): 6 2.35 (s, 3H), 6.90-7.02 (m, 2H), 7.06-7.10 (m, 3H), 7.32 (d, J = 3.6 Hz, 1 H), 7.40 (d, J = 8.8 Hz, 1 H), 8.54 (d, J = 2.4 Hz, 1 H), 10.22 (br, 2H).
Example 75 N-[2-(4-Chlorophenoxy)-5-(trifluoromethyl)phenyg-N'-(thiazol-2-yl)urea CI ) H H
NYNS

F
F F
N-[2-(4-Chlorophenoxy)-5-(trifluoromethyl)phenyl]-N'-(thiazol-2-yl)urea (136 mg, 66%) was prepared from 2-(4-Chlorophenoxy)-5-(trifluoromethyl)aniline (144 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.

LC-MS (m/z): 415 (M+1)'.
1H NMR (400 MHz, acetone-de): 6 5.12 (br, 111), 7.02(d, J= 9 Hz, 1H), 7.09 (d, J=3.6 Hz, 1 H), 7.21 (d, J = 8.8 Hz, 2H), 7.34 (d, J = 3.6 Hz, I H), 7.39 (d, J = 8.8 Hz, 1 H), 7.49 (d, J =
8.8 Hz, 2H), 8.85 (d, J = 1.5 Hz, 1 H), 8.95 (br, 1 H), 10.29 (br, 1 H).

Example 76 N-[4,5-difluoro-2-(2,3-dimethoxyphenoxy)phenyl]-N'-(thiazol-2-yl)urea H H
NyN '~ S
0 N~
F

4,5-Difluoro-2-(2,3-dimethoxyphenoxy)-1-nitrobenzene (1.4 g, 90.3%) was prepared from 2,3-dimethoxyphenol (0.85 g, 5.5 mmol) and 1,3,4-trifluoronitrobenzene (0.885 g, 5.0 mmol) following the general procedure F. The product was then reduced to 2-(2-methoxy-phenoxy)-4,5-difluoroaniline (1.35 g, 96.1%) following general procedure B. N-[4,5-Di luoro-2-(2,3-dimethoxyphenoxy)phenyl]-N'-(thiazol-2-yl)urea (0.181 g, 89%) was prepared from 2-(2,3-dimethoxypheno)y}4,5-difluoroaniline (0.140 g, 0.5 mmol) and 2-aminothiazole (0.060 g, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 361 (M+1)'.
'H NMR (400 MHz, acetone-de): 6 3.71 (s, 3H), 3.88 (s, 3H), 6.63 (dd, J=1.6, 8.4 Hz,1H), 6.89 (dd, J=1.2, 6.4 Hz, 1H), 7.03-7.11 (m, 2H), 7.38 (d, J= 3.6 Hz, 1H), 8.26 (dd, J= 1.6 Hz, 7.6 Hz, 1 H), 8.42 (dd, J = 1.2 Hz, 7.2 Hz, 1 H), 9.13 (br,1 H), 10.22 (br,1 H).

Example 77 N-[4,5-Dichloro-2-(2,3-dimethoxyphenoxy)phenyl]-N'-(thiazol-2-yl)urea O..CH3 (OCH3 H H
NyNS
Cl Cl 4,5-Dichloro-2-(2,3-dimethoxyphenoxy)-1-nitrobenzene (1.12 g, 65%) was prepared from 2,3-dimethoxyphenol (0.85 g, 5.5 mmol) and 4,5-dichloro-2 fluoro-l-nitrobenzene (1.05 g, 5.0 mmol) following the general procedure A. This was reduced to 4,5-dichloro-2-(2,3-di-methoxyphenoxy)aniline (0.68 g, 67%) following general procedure B. N-[4,5-Dichloro-2-(2,3-dimethoxyphenoxy)phenyl]-N'-(thiazol-2-yl)urea (136 mg, 62%) was prepared from 4,5-di-chloro-2-(2,3-dimetho)yphenoxy)aniline (157 mg, 0.5 mmol) and 2-aminothiazole (60 mg. 0.6 mmol) following the general procedure D.
LC-MS (m/z): 441 (M+1)'.
'H NMR (400 MHz, acetone-de): 6 3.70 (s, 3H), 3.91 (s, 3H), 6.81-6.83 (m, 2H), 7.01 (dd, J =
8.4, 1.2 Hz, 1 H), 7.09 (d, J = 3.6 Hz, 1 H), 7.15 (t, J = 8.4 Hz, 1 H), 7.34 (d, J = 3.6 Hz, 1 H), 8.65 (s,1 H), 8.95 (br, 1 H), 10.36 (br, 1 H).

Example 78 N-[5-Chloro-2-(2,3-dimethoxyphenoxy)- -dimethylaminophenylJ-N'-(thiazol-2-yl)urea 0,CH3 IIXO,CH3 H H
NuN~S
H3C, N 0 INI~

4,5-Dichloro-2-(2,3-dimethoxyphenoxy)-1 -nitrobenzene (0.35 g, 1.0 mmol) was heated with dimethylamine in tetrahydofuran (4 ml, 2 M) in a sealed vial at 80 C for 48 h. The reaction mixture was cooled to room temperature and dissolved in ethyl acetate (15 ml). The solution was washed (water, brine) and concentrated to obtain the desired nitrobenzene, which was reduced to 5-chloro-2-(2,3-dimethoxyphenoxy)-4-(dimethylamino)aniline (0.23 g, 73%) following general procedure B. N-[5-Chloro-2-(2,3-dimethoxyphenoxy)-4-dimethyl-aminophenyl]-N'-(thiazol-2-yl)urea (136 mg, 61%) was prepared from 5-chloro-2-(2,3-di-methoxyphenoxy)-4-(dimethylamino)aniline (161 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 450 (M+1)+
'H NMR (400 MHz, acetone-de): 6 2.61 (s, 3H), 2.66 (s. 3H), 3.70 (s, 3H), 3.89 (s, 3H), 6.58 (s, 1 H), 6.68 (dd, J = 8.4, 1.2 Hz, 1 H), 6.92 (dd, J = 8.4, 1.6 Hz, 1 H), 7.04-7.10 (m, 2H), 8.44 (s,1 H), 9.20 (br, 1 H), 10.26 (br, 1 H).

Example 79 N-[5-Chloro-2-(2,3-dimethoxyphenoxy)-4-(4-morpholino)phenyl]-N'-(thiazol-2-yl)urea O.CH3 O`CH3 H H
S
NY NTNI
O
OJ CI

4,5-Dichloro-2-(2,3-dimethoxyphenoxy)-1-nitrobenzene (0.35 g, 1.0 mmol) was heated with morpholine (4 ml) In a sealed vial at 100 C for 48 h. The reaction mixture was cooled to rt and dissolved in ethyl acetate (15 ml). The solution was washed (water, brine) and concentrated to obtain the desired nitrobenzene, which was reduced to 5-chloro-2-(2,3-dimethoxyphenoxy)-4-(4-morpholino)aniline (0.22 g, 61%) following general procedure B. N-[5-Chloro-2-(2,3-dimethoxyphenoxy)-4-(4-morpholino)phenyl]-N'-(thiazol-2-yl)urea (127 mg, 52%) was prepared from 5-chloro-2-(2,3-dimethoxyphenoxy)-4-(4-morpholino)aniline (182 mg. 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 492 (M+1)'.

'H NMR (400 MHz, acetone-d6): 6 2.83 (m, 4H), 3.69-3.72 (m, 7H), 3.89 (s, 3H), 6.58 (s, 1 H), 6.69 (dd, J = 8.4, 1.6 Hz, I H), 6.93 (dd, J = 8.4, 1.6 Hz, 1 H), 7.05-7.10 (m, 2H); 7.31 (d, J =
3.2 Hz, 1 H), 8.48 (s, 1 H), 9.02 (br, 1 H), 10.25 (s, 1 H).

Example 80 N-[2-(2,4-Difluorophenoxy)pyridin-3-yl]-N'-(thiazol-2-yl)urea F ,a F

O
H H
yN\ /g N N O ~ND

N-2-(2,4-Difluorophenoxy)pyridin-3-yl-N'-(thiazol-2-yl)urea (112 mg, 65%) was prepared from 3-amino-2-(2,4-difluorophenoxy)pyridine (111 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 350 (M+1)'.
'H NMR (400 MHz, acetone-d6): d 7.08-7.16 (m, 3H), 7.20-7.26 (m, 1 H), 7.36 (d, J = 3.2 Hz, 1 H), 7.40-7.46 (m, 1 H), 7.71 (dd, J = 4.8, 1.6 Hz, 1 H), 8.69 (dd, J = 8.0, 1.6 Hz, 1 H), 9.00 (br, 1 H), 10.31 (br, 1 H).

Example 81 N-[2-(2-Fluorophenoxy)pyridin-3-yl]-N'-[thiazol-2-yqurea F

H H
N NYNYS
I O Nom'/
N-2-(2-Fluorophenoxy)pyndin-3-yl-N'-(thiazol-2-yl)urea (112 mg, 68%) was prepared from 3-amino-2-(2-fluorophenoxy)pyridine (102 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (mfz): 332 (M+1)'.
'H NMR (400 MHz, acetone-de): 17.09 (d, J = 3.6 Hz, 1 H) 7.13 (dd, J = 8.0, 4.8 Hz, 1 H), 7.25-7.39 (m, 5H), 7.71 (dd, J = 4.8, 1.6 Hz, 1 H), 8.69 (dd, J = 8.4, 1.6 Hz, 1 H), 9.00 (br, 1 H), 10.31 (br, 1 H).

Example 82 N-[2-(2-Methoxyphenoxy)pyridin-3-yl]-N'-(thiazol-2-yl)urea O
O
H H

(/ IOI /

2-(2-Methoxy)phenoxy-3-nitropyridine (0.86 g, 70%) was prepared from 2-methoxy-phenol (0.68 g, 5.5 mmol) and 2-bromo-3-nitropyridine (1.05 g, 5.0 mmol) following the general procedure A. This compound was reduced to 2-(2-methoxyphenoxy)-3-amino-pyridine (0.49 g, 65%) following general procedure B. N-[2-(2-Methoxyphenoxy)pyndin-3-yl]-N'-(thiazol-2-yl)urea (126 g, 74%) was prepared from 2-(2-methoxyphenoxy)-3-aminopyridine (108 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 344 (M+1)'.
'H NMR (400 MHz, acetone-de): d 3.69 (s, 3H), 6.74 (d, J = 3.6 Hz, 1 H), 6.99-7.01 (m, 2H), 7.16-7.21 (m, 3H), 7.45 (d, J = 2.8 Hz, 1 H), 7.71 (d, J = 4.0 Hz, 1 H), 8.57-8.59 (d, J = 8.0 Hz, 1 H), 8.89 (br, 1 H), 10.44 (br, 1 H).

Example 83 N-[2-(2,3-Dimethoxyphenoxy)pyridin-3-yl]-N-(thiazol-2-yl)urea O
H H
N 3 NyN I S
/ IOI N~

2-(2,3-Dimethoxy)phenoxy-3-nitropyridine (1.03 g, 75%) was prepared from 2,3-dimethoxyphenol (0.85 g, 5.5 mmol) and 2-bromo-3-nitropyridine (1.05 g, 5.0 mmol) following the general procedure A. This compound was reduced to 2-(2,3-dimethoxyphenoxy)-aminopyridine (0.57 g, 62%) following the general procedure B. N-[2-(2,3-Dimethoxy-phenoxy)pyridin-3-yi]-N'-(thiazol-2-yl)urea (131 mg, 70%) was prepared from 2-(2,3-di-methoxyphenoxy)-3-aminopyridine (123 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 374 (M+1)`.
'H NMR (400 MHz, acetone-de): 6 3.58 (s, 3H), 3.87 (s, 3 H), 6.81 (dd, J= 1.6, 8.0 Hz,1H), 6.95 (dd, J = 1.6, 8.4 Hz, I H), 7.05-7.07 (m, 3H), 7.35 (d, J = 3.2 Hz, 1 H), 7.67-7.79 (m, 1 H), 8.64-8.86 (dd, J = 2.4, 8.0 Hz, 1 H), 8.89 (br, 1 H), 10.26 (br, 1 H).

Example 84 N-[4-Chloro-2-(2-chlorobenzoyl)phenyl]-N'-(thiazol-2-yl)urea Cl O
H H
NyN\ g O N~
CI
N-[4-Chloro-2-(2-chlorobenzoyl)phenyl]-N'-(thiazol-2-yl)urea (0.51 g, 86%) was prepared from 2-amino-2',5-dichlorobenzophenone (0.4 g, 1.50 mmol) and 2-aminothiazole (150 mg, 1.5 mmol) following the general procedure D.
LC-MS (m/z): 394 (M+1),'H NMR (400 MHz, CDCI3): 6 6.45 (br, 1H), 6.79 (dd, J =
1.2, 7.6 Hz, 2H), 7.11 (d, J = 7.2 Hz, 1 H), 7.25-7.49 (m, 1 H), 6.91-7.33 (m, 3H), 8.65 (d, J =
8.8Hz, 1 H), 8.68 (d, J = 9.6 Hz, 1 H), 8.93 (br, 1 H).

Example 85 N-[4-Chloro-2-(2-fluorobenzoyl)phenyl]-N'-(thiazol-2-yl)urea F

O

NN S
H HTNI
O
C
I
N-[4-Chloro-2-(2-fluorobenzoyl)phenyl]-N'-(thiazol-2-yl)urea (116 mg, 62%) was prepared from 2-amino-5-chloro-2'-fluorobenzophenone (125 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.

LC-MS (mhz): 377 (M+1)+.

Example 86 N-[2-(2,4-Difluorophenylsulfanyl)phenyl]-N'-(thiazol-2-yl)urea F F

S
H H
NyNS
O ~'NII

2-(2,4-Difluorophenylsulfanyl)-1-nitrobenzene (1.04 g, 78%) was prepared from 2,4-difluorothiophenol (0.73 g, 5.5 mmol) and 2-fluoronitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This compound was reduced to 2-(2,4-difluorophenylsulfanyl)-aniline (0.64 g, 70%) following the general procedure B. 1-[2-(2,4-Difluorophenylsulfanyl)-phenyq-3-(thiazol-2-yl)urea (130 g, 72%) was prepared from 2-(2,4-difluorophenylsulfanyl)-aniline (118 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 365 (M+1)'.
1H NMR (400 MHz, acetone-de): d 6.69-6.79 (m, 3H), 6.85 (d, J = 3.6 Hz, 1H), 7.04-7.09 (m, 1 H), 7.36-7.40 (m 2H), 7.51-7.53 (dd, J = 1.6, 8.0 Hz, 1 H), 8.42 (d, J = 8.0 Hz, I H), 8.88 (br, 1 H), 10.2 (br, 1 H).

Example 87 1-[2-(2-Fluorophenylsulfanyl)phenyq-3-(thiazol-2-yl)urea F

S H H
S
NyNfD/
O 2-(2-Fluorophenylsulfanyl)nitrobenzene (1.03 g, 83%) was prepared from 2-fluoro-thiophenol (0.70 g, 5.5 mmol) and 2-fluoronitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This compound was reduced to 2-(2-fluorophenylsulfanyl)aniline (0.65 g, 72%) following general procedure B. N-[2-(2-Fluorophenylsulfanyl)phenyl]-N'-(thiazol-2-yl)-urea (129 mg, 75%) was prepared from 2-(2-fluorophenylsulfanyl)aniline (107 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 347 (M+1)`.
'H NMR (400 MHz, acetone-d6): 6 6.74-6.82 (m, 1 H), 7.02-7.07 (m, 2H), 7.14-7.23 (m, 3H), 7.29 (d, J = 3.6 Hz, 1 H), 7.51-7.58 (m, 1 H), 7.60 (dd, J = 1.2, 7.6 Hz, 1 H), 8.43-8.46 (d, J =
8.8 Hz, 1 H), 9.08 (br, 1 H), 10.39 (br, 1 H).

Example 88 N-[2-(2-Chloro-4-fluorophenylsulfanyl)phenyl]-N'-(thiazol-2-yl)urea F ~ CI

S
H H
NyN~S
O Nom'/

2-(2-Chloro-4-fluorophenylsulfanyl)nitrobenzene (1.13 g, 80%) was prepared from 2-chloro-4-fluorothiophenol (0.89 g, 5.5 mmol) and 2-fluoronitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This compound was reduced to 2-(2-chloro-4-fluoro-phenylsulfanyl)aniline (0.76 g, 75%) following the general procedure B. N-[2-(2-Chloro-4-fluorophenylsulfanyl)phenylj-N'-(thiazol-2-yl)urea (144 mg, 76%) was prepared from 2-(2-chloro-4-fluorophenylsulfanyl)aniline (126 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 381 (M+1)+.
'H NMR (400 MHz, acetone-de): 6 6.59-6.68 (m, 1H), 6.96-7.04 (m, 2H), 7.16-7.22 (m, 1H), 7.26 (d, J = 4.0 Hz, 1 H), 7.32-7.38 (m, 1 H), 7.50-7.61 (m, 2H), 8.47 (d, J
=8.0 Hz, 1 H), 9.00 (br, 1 H), 10.23 (br, 1 H).

Example 89 N-[2-(2,3-Dichlorophenylsulfanyl)phenyl]-N'-(thiazol-2-yl)urea &cl S
N y S
o YJ

2-(2,3-Dichlorophenylsulfanyl)nitrobenzene (1.25 g, 84%) was prepared from 2,3-dichlorothiophenol (0.97 g, 5.5 mmol) and 2-fluoronitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This compound was reduced to 2-(2,4-dichlorophenylsulfanyi)-aniline (0.81 g, 72%) following the general procedure B. N-[2-(2,3-Dichlorophenylsulfanyl)-phenyl]-N'-(thiazol-2-yl)urea (154 mg, 78%) was prepared from 2-(2,3-chlorophenylsulfanyl)-aniline (135 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (r fz): 397 (M+1)+
'H NMR (400 MHz, CDCI3): 56.34-6.44(m, 1H),6.72-6.78(m, 1H), 6.88-6.96 (m, I
H), 7.11-7.22 (m, 3H), 7.50-7.57 (m, 2H), 8.51-8.53 (d, J = 6.0 Hz, 1 H), 9.08 (br, 1 H), 10.32 (br, 1 H).
Example 90 N-[2-(3,5-Dimethylphenylsulfanyl)phenyl]-N'-(thiazol-2-yl)urea N
S' / 0 y TNI
2-(3,5-Dimethylphenylsulfanyl)nitrobenzene (1.01 g, 78%) was prepared from 3,5-dimethylthiophenol (0.76 g, 5.5 mmol) and 2-fluoronitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This compound was reduced to 2-(3,5-dimethylphenylsulfanyl)-aniline (0.64 g, 72%) following the general procedure B. N-[2-(3,5-Dimethylphenylsulfanyl-phenyl]-N'-(thiazol-2-yl)urea (131 mg, 74 6) was prepared from 2-(3,5-dimethylphenyl-sulfanyl)aniline (115 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 357 (M+1)' 'H NMR (400 MHz, CDCI3): 6 2.09 (s, 6 H), 6.54-6.86 (m, 4H), 7.04-7.10 (m, IH), 7.27-7.34 (m, 1 H), 7.41-7.46 (m, 1 H), 7.48-7.56 (bs, 1 H), 8.41 (d, J = 8.4 Hz, 1 H), 8.20 (br, 1 H), 11.8 (br,1 H).

Example 91 N-[2-(2-Methoxycarbonylphenylsulfanyl)phenyl)-N'-(thiazol-2-yl)urea O'CH3 S
H H
Ny NS

2-(2-Methoxycarbonylphenylsulfanyl)nitrobenzene (1.15 g, 80%) was prepared from methyl thiosalicylate (0.92 g, 5.5 mmol) and 2-fluoronitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This compound was reduced to 2-(2-methoxycarbonyl-phenylsulfanyl)aniline (0.75 g, 73%) following the general procedure B. N-[2-(2-Methoxy-carbonylphenylsulfanyl)phenyl]-N'-(thiazol-2-yl)urea (142 mg, 74%) was prepared from 2-(2-methoxycarbonylphenylsulfanyl)aniline (130 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 387 (M+1)*.
'H NMR (400 MHz, acetone-d6): 6 3.88 (s, 3H), 6.62-6.82 (m, 2H), 7.02-7.24 (m, 4H), 7.44-7.50 (m, 1 H), 7.55-7.64 (bs, 1 H), 7.87 (d, J = 6.4, 1 H), 8.42 (d, J = 8.0 Hz, 1 H), 8.82 (br, 1 H), 10.9 (br. 1H).

Example 92 N-[2-(2-Methoxyphenylsulfanyl)phenyl]-N'-(thiazol-2-yl)urea O,CH3 S

N y N
H HTNI
S O

2-(2-Methoxyphenyisulfanyl)nitrobenzene (1.07 g, 82%) was prepared from 2-methoxy thiophenol (0.76 g, 5.5 mmol) and 2-fluoronitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This compound was reduced to 2-(2-methoxyphenylsulfanyl)aniline (0.66 g, 70%) following general procedure B. N-[2-(2-Methoxyphenylsulfanyl)phenyl]-N'-(thiazol-2-yl)urea (110 mg, 62 %) was prepared from 2-(2-methoxyphenylsulfanyl)aniline (115 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 359 (M+1)+
1H NMR (400 MHz, acetone-d8): d 3.48 (s, 3H), 6.77-6.89 (m, 2H), 6.90-7.00 (m, 2H), 7.05-7.24 (m, 2H), 7.29 (d, J = 3.6 Hz, 1 H), 7.38-7.42 (m, I H), 7.55 (dd, J =1.6, 8.0 Hz, 1 H), 8.41-8.43. (d, J = 8.4 Hz, 1 H), 8.89 (br,1 H), 10.22 (br, 1 H).

Example 93 N-[2-(2-Pyridinylsulfanyl)phenyl]-N'-(thiazol-2-yl)urea N

S
~ H H
S
/ o 2-(2-Pyridylsulfanyl)nitrobenzene (0.70 g, 60%) was prepared from 2-mercapto-pyridine (0.618, 5.5 mmol) and 2-fluoronitrobenzene (0.71 g, 5.0 mmol) following the general procedure A. This compound was reduced to 2-(2-pyridylsulfanyl)aniline (0.37 g, 62%) following general procedure B. N-[2-(2-Pyridylsulfanyl)phenyl]-N'-(thiazol-2-yl)urea (98 mg, 60%) was prepared from 2-(2-pyridylsulfanyl)aniline (101 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 330 (M+1)'.

'H NMR (400 MHz, CDCI3): 6 6.78-6.80 (d, J = 8.0 Hz, 1 H), 6.96 (d, J = 3.6 Hz, 1 H), 7.03-7.07 (m, 1 H), 7.13-7.18 (m, 1 H), 7.23 (d, J = 2.8 Hz, 1 H), 7.51-7.57 (m, 2H), 7.64 (d, J = 1.6, 7.6 Hz, 1 H), 8.35 (d, J = 4.0 Hz, 1 H), 8.45 (d, J = 8.4 Hz, 1 H), 8.13 (br, 1 H), 10.44 (br, 1 H).
Example 94 N-(2-Propyloxyphenyl)-N'-(thiazol-2-yl)urea H H
&NTNT>
N-(2-Propyloxyphenyl)-N'-(thiazol-2-yl)urea (97 mg, 70%) was prepared from 2-propyloxyaniline (76 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 279 (M+1)'.
'H NMR (400 MHz, acetone-de): 6 1.07 (t, J = 7.6 Hz, 3H), 1.88 (m, 2H), 4.05 (q, J = 7.6 Hz), 6.90-7.01 (m, 3H), 7.05 (d, J = 3.6 Hz), 7.36 (d, J = 3.6 Hz), 8.30 (dd, J =
7.6, 1.6 Hz, 1 H), 8.80 (br, 1 H), 10.24 (br, 1 H).

Example 95 N-(2-Butyloxyphenyl)-N'-(thiazol-2-yl)urea H H
NuNTS
IOI N

N-(2-Butyloxyphenyi)-N'-(thiazol-2-yl)urea (94 mg, 65%) was prepared from 2-butylyloxyaniline (82 mg, 0.5 mmol) and 2-aminothiazole (60 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 293 (M+1)'.

'H NMR (400 MHz, acetone-d6): 6 0.98 (t, J = 7.2 Hz, 3H), 1.54 (m, 2H), 1.84 (quint, J = 6.4 Hz, 2H), 4.10 (t, J = 6.4 Hz, 2H), 6.90-7.03 (m, 3H), 7.05 (d, J = 3.6 Hz, 1 H), 7.25 (d, J = 3.6 Hz, 1 H), 8.30 (dd, J = B.O. 1.2 Hz, 1 H), 9.00 (br, I H), 10.20 (br, 1 H).

Example 96 N-(2-(Cyclopentyloxyphenyl)-N'-(thiazol-2-yl)urea S
N y J

2-(Cydopentyloxy)-1-nitrobenzene (1.04 g. 80%) was prepared from cydopentanol (0.46 ml, 5.0 mmol) and 1-fluoro-2-nitrobenzene (0.71 g, 5.0 mmol) following the general procedure G. This was reduced to 2-(cyclopentyloxy)aniline (0.30 g, 68%, 2.5 mmol scale) following general procedure B. N-(2-Cydopentyloxyphenyl}N'-(thiazol-2-yl)urea (212 mg, 70%) was prepared from 2-(cyclopentyloxy)aniline (177 mg, 1.0 mmol) and 2-aminothiazole (100 mg. 1.0 mmol) following the general procedure D.
LC-MS (m/z): 305 (M+1)`.
'H NMR (400 MHz, acetone-de): d 1.60-2.05 (m, 8H), 4.94 (m,1 H), 6.90-7.05 (m, 4H), 7.35 (d, J = 4.0 Hz, 1 H), 8.30 (d, J = 8.8 Hz, 1 H), 10.20 (br, 2H).

Example 97 N-(2-Isopropo)cyphenyl}N'-(thiazol-2-yl)urea 1-1C ?H3 H H~j NyN " S

2-(Isopropoxy)-1-nitrobenzene (317 mg, 70%) was prepared from isopropyl alcohol (0.24 ml, 3.0 mmol) and 1-fluoro-2-nitrobenzene (0.36 g, 2.5 mmoi) following the general procedure G. This was reduced to 2-(isopropoxy)aniline (198 mg, 75%) following general procedure B. N-(2-Isopropoxyphenyl}N'-thiazolylurea (218 mg, 60%) was prepared from 2-(isopropoxy)aniline (198 mg, 01.3 mmol) and 2-aminothiazole (150 mg, 1.5 mmol) following the general procedure D.

LC-MS (m/z): 279 (M+1)'.
'H NMR (400 MHz, acetone-de): 6 1.36 (d, J = 6.4 Hz, 6H), 4.71 (m, 1 H), 6.90-7.07 (m, 4H), 7.36 (d, J = 3.6 Hz, 1 H), 8.30 (d, J = 8.0 Hz, 1 H), 10.22 (br, 2H) Example 98 N-[2-(2-Methylpropoxy)phenyl]-N'-(thiazol-2-yl)urea H3C\
IY O H H
S
CH3 NyNTNI

2-(2-Methylpropoxy}1-nitrobenzene (0.73 g, 75%) was prepared from 2-methyl-propanol (0.46 ml, 5.0 mmol) and 1-fluoro-2-nitrobenzene (0.71 g, 5.0 mmol) following the general procedure G. This was reduced to 2-(2-methylpropoxy)aniline (0.29 g, 70%, 2.5 mmol scale) following general procedure B. N-[2-(2-Methylpropoxy)phenyl]-N'-(thiazol-2-yl}
urea (189 mg, 65%) was prepared from 2-(2-methylpropoxy)aniline (165 mg, 1.0 mmol) and 2-aminothiazole (100 mg, 1.0 mmol) following the general procedure D.
LC-MS (m/z): 293 (M+1)' 1H NMR (400 MHz, acetone-de): d 1.09 (d, 6H), 2.13 (m, 1 H), 3.86 (d, J = 6.8 Hz, 1 H), 6.90-7.10 (m, 4H), 7.38 (d, J = 3.6 Hz, 1 H), 8.29 (d, J = 7.2 Hz, 1 H), 10.05 (br, -2H).

Example 99 N-[2-(Cyclopentylmethoxy)phenyl]-N'-(thiazol-2-yl)urea H H
N\/NS

2-(Cyclopentylmethoxy)-1-nitrobenzene (443 mg, 80%) was prepared from cyclo-pentanemethanol (0.32 ml, 3.0 mmol) and 1-fluoro-2-nitrobenzene (0.36 g, 2.5 mmol) following the general procedure G. This was reduced to 2-(cydopentylmethoxy)aniline (268 mg, 70%) following general procedure B. N-[2-(Cyclopentylmethoxy)phenyl]-N'-(thiazol-2-yl)-urea (286 mg, 60%) was prepared from 2-(cyclopentylmethoxy)aniline (0.25 g, 1.5 mmol) and 2-aminothiazole (150 mg, 1.5 mmol) following the general procedure D.
LC-MS (m/z): 319 (M+1)`.

1H NMR (400 MHz, acetone-de): 6 1.40 (m, 2H), 1.65 (m, 4H), 1.91 (m, 2H), 2.45 (m, I H), 3.98 (d, J = 7.6 Hz, 1 H), 6.88-7.06 (m, 4H), 7.35 (d, J = 3.6 Hz, 1 H), 8.29 (d, J = 7.6 Hz, I H), 10.14, (br, 2H).

Example 100 N-[2-(3-pentoxy)phenyl]-N'-(thiazol-2-yl)urea H H
Ny NONI/

O2-(3-Pentoxyr1-nitrobenzene (366 mg, 70%) was prepared from 3-pentanol (0.27 ml, 2.5 mmol) and 1-fluoro-2-nitrobenzene (0.36g, 2.5 mmol) following the general procedure G. This was reduced to 2-(3-pentoxy)aniline (0.25 g, 80%) following general procedure B. N-[2-(3-pentoxy)phenyl]-N'-(thiazol-2-yl)urea (0.26 g, 57%) was prepared from 2-(3-pentoxy)-aniline (0.25 g, 1.5 mmol) and 2-aminothiazole (150 mg, 1.5 mmol) following the general procedure D.
LC-MS (m/z): 307 (M+1 'H NMR (400 MHz, acetone-de): 6 0.92 (t, J = 7.2 Hz, 6H), 1.75 (m, 4H), 4.38 (m, 1 H), 6.89-7.06 (m, 4H), 7.36 (d, J = 3.6 Hz, 1 H), 8.32 (d, J = 8.0 Hz, 1 H).

Example 101 N-[2-(2-pentoxy)phenyl]-N'-(thiazol-2-yl)urea CH

H3C" 0 H H
NyNTN S
O //

2-(2-Pentoxy)-1-nitrobenzene (387 mg, 74%) was prepared from 2-pentanol (0.27 ml, 2.5 mmol) and 1-fluoro-2-nitrobenzene (0.36 g, 2.5 mmol) following the general procedure G. This was reduced to 2-(2-pentoxy)aniline (0.26 g, 79%) following general procedure B. N-[2-(2-pentoxy)phenyl]-N'-(thiazol-2-yl)urea (280 mg, 62%) was prepared from 2-(2-pentoxy)aniline (0.25 g, 1.5 mmol) and 2-aminothiazole (150 mg, 1.5 mmol) following the general procedure D.
LC-MS (m/z): 307 (M+1)`.
'H NMR (400 MHz, acetone-de): 6 0.93 (t, J = 7.2 Hz, 3H),1.32 (d, J = 6.0 Hz, 3H), 1.40-1.90 (m, 4H), 4.55 (m, 1 H), 6.85-7.07 (m, 4H), 7.36 (d, J = 3.6 Hz, 1 H), 8.31 (d, J = 8.0 Hz, 1 H), 10.15 (br, 1 H).

Example 102 N-[2-(2-Methoxyethoxy)phenyl]-N'-(thiazol-2-yl)urea H3C' "'-\O
H H
Ny N~S

O10 2-(2-Methoxyethoxy)-1-nitrobenzene (0.25 g, 64%) was prepared from 2-methoxy-ethanol (0.16 ml, 2.0 mmol) and 1-fluoro-2-nitrobenzene (0.21 ml, 2.0 mmol) following the general procedure G. This was reduced to 2-(2-methoxyethoxy)aniline (0.13 g, 60%) following general procedure B. N-[2-(2-Methoxyethoxy)phenyl]-N'-(thiazol-2-yl)urea (115 mg, 55%) was prepared from 2-(2-methoxyethoxy)aniline (115 mg, 0.7 mmol) and 2-amino-thiazole (140 mg, 1.4 mmol) following the general procedure D.
LC-MS (m/z): 295 (M+1)'.
1H NMR (400 MHz, acetone-de): 6 3.37 (s, 3H), 3.78 (t, J = 4.8 Hz, 2H), 4.25 (t, J = 4.8 Hz, 2H), 6.95-7.06 (m, 4H), 7.37 (d, J = 3.6 Hz, 1 H), 8.29 (d, J = 8.0 Hz, 1 H), 8.80 (br, 1 H), 10.20 (br, 1H).

Example 103 (General procedure (H)) (2-[3-(2-Benzylphenyl)ureido]thiazol-4-yl)acetic acid N N

T-) --HO
The intermediate 2-benzylphenyl isocyanate (0.26 g, 1.2 mmol) (general procedure H2) was dissolved in DMF(5 ml) and 2-amino-4-thiazole acetic acid (0.20 g, 1.2 mmol) was added. After 16 hours at 20 C ethylacetate (60 ml) was added and the mixture was extracted with water (5x20 ml). The solvent was removed in vacuo and the remaining oil was purified on Waters Deltprep 4000 giving 150 mg of the title compound.
Preparative system: (gradient 20-90% CH3CN 40min., 20 ml/min., Rt=35 min Solvent A--water, solvent B=CH3CN, solvent C=0,5% TFA/water).
' H-NMR (DMSO-de): 6 10.90 (broad, 1 H); 8.45 (s, 1 H); 7.80 (s, 1 H); 7.20 (multi, 9H); 6.85 (s, 1H); 3.98 (s, 2H); 3.53 (s, 2H).
HPLC-MS (Method A): m/z = 368 (M+1); R = 4.10 min 'H NMR (CDCI3): 6 7.98 (br d, 2H), 7.88-7.70 (m, 4H), 7.50 (t, 3H), 7.18 (d, 1 H), 6.84 (br s, 1 H), 3.71 (br s, 2H), 2.70 (br s, 2H), 2.52 (m, 1 H), 1.90-1.70 (m, 5H),1.45-1.15 (m, 5H).
Example 104 (General procedure (H)) (2-[3-(2-Benzoyl-4-chlorophenyl)ureido)thiazol-4-yl)acetic acid 1lJ1.ro H H

i o s o Cl HO

The title compound was prepared as in example 103 using (5-chloro-2-isocyanato-phenyl)phenyl methanone (general procedure H2) as intermediate isocyanate.
'H-NMR (DMSO-de): Selected data : 6 9.48 (broad, 1 H); 8.12 (broad, 1 H);
(multi, 9H); 6.87 (s, 1 H); 3.57 (s, 2H).
HPLC-MS (method A): m/z = 415 (M+1); R~ = 3.79 min Example 105 (General procedure (H)) (2-[3-(2-(2-Methylphenoxy)phenyl)ureidojthiazol-4-yl)acetic acid O
H H

O O
HO

The title compound was prepared as in example 103 using 2-(2-methylphenoxy)-phenyl isocyanat (general procedure H2) as intermediate isocyanate.
'H-NMR (DMSO-de): 6 11.09 (broad, 1 H); 8.88 (broad, I H); 8.25 (d, 1 H); 7.37 (d, I H); 7.22 (t, I H); 7.11 (multi, 2H); 6.97 (t, I H); 6.89 (d, 1 H); 6.87 (s, 1 H); 6.67 (d, 1 H); 3.53 (s, 2H);
2.23 (s, 3H).
HPLC-MS (method A): m/z = 384 (M+1); R = 4.67 min Example 106 (General procedure (H)) (2-[3-(2-(4-Methoxyphenoxy)-5-(trifluoromethyl)phenyl)ureido]thiazol-4 yl)acetic acid \
H H
Ny N
O S O
F HO
F F
The title compound was prepared as in example 103 using 2-(4-methoxyphenoxy)-5-(trifluoromethyl)phenyl isocyanate (general procedure H2) as intermediate isocyanate.
1H-NMR (DMSO-de): 6 12.32 (broad, 1H); 11.20 (bro ad, 1 H); 9.30 (d, 1 H);
8.62 (d, 1 H); 7.32 (d, 1H); 7.17 (d, 2H); 7.05 (d, 2H); 6.90 (s, 1H); 6.83 (d, 1H); 3.78 (s, 3H);
3.53 (s, 2H).
Example 107 (General procedure (H)) {2-[3-(2-phenoxyphenyl)ureido]thiazol-4-y}acetic add H H
NyN,, o o HO
The title compound was prepared as in example 103 using 2-phenoxyphenyl isocyanate (general procedure H2) as intermediate isocyanate.
'H NMR (CDCI3) selected data: 6 3.47 (2H, s), 6.78 (1H, s), 6.90 (1H, d), 6.97-7.08 (3H, m), 7.09-7.19 (2H, m), 7.38 (2H, t), 8.16 (11-1, brs), HPLC-MS (Method A): m/z =
370 (M+1); Rt =
3.50 min.

Example 108 (General procedure (H)) 2-{3-[5-Fluoro-2-(2-fluoro-6-methoxyphenoxy)phenyl]ureido}thiazole-4-carboxylic acid F

:;:~ O
HC '0 N N N O

F
The title compound was prepared accorrding to general procedure H.
'H NMR (DMSO): d 12.76 (br,1 H), 11.21 (br 1 H), 9.23 (s,1 H), 8.06 (dd.1 H), 7.94 (s, 1 H), 7.33 (d, 1 H), 7.10-7.01 (m, 2H), 6.74 (t, 1 H), 6.55 (dd, 1 H), 3.80 (s,3H).
HPLC-MS (Method B): m!z = 422 (M+1); R1 = 3.90min.
Example 109 (General procedure (H)) 2-{3-[2-(2,3-Dimethoxyphenoxy)-5-fluorophenyl]ureido}thiazole-4-carboxylic acid ethyl ester 0,CH3 O
N O

'H NMR (DMSO): d 11.44 (s, 1H), 8.99{s 1H), 8.06 (dd,1H), 7.99 (s, 1H), 7.09 (t, 1H), 6.94 (d, 1 H), 6.80 (t, 1 H), 6.72 (dd,1 H), 6.67 (d,1 H), 4.25 (q, 2H), 3.84 (s, 3H), 3.67 (s, 3H), 1,28 (t, 3H).
HPLC-MS (Method B): m/z = 462 (M+1); R = 4.53 min.

Example 110 (General procedure (H)) (2-(3-[2-(2,3-Dimethoxyphenoxy)-5-fluorophenyl]ureido)thiazol-4-yl)acebc acid ethyl ester 0..CH3 O
H H
NuN~, IOC S_~

F
'H NMR (DMSO): d 11.16 (br, 1H), 9,09 (br 1H), 8.08 (dd,1H), 7.09 (t, 1H), 6.94 (d, 11-1), 6.92 (s,1 H), 6.78 (t,1 H), 6.70 (dd, 1 H), 6.65(d, 1 H), 4.06 (q, 2H), 3.84 (s, 3H), 3.66 (s, 2H), 3.62 (s, 3H), 1,18 (t, 3H).
HPLC-MS (Method B): m/z = 476 (M+1); R, = 4.43 min.
Example 111 (General procedure (H)) (2-{3-[5-Fluoro-2-(2fuoro-6-methoxyphenoxy)phenyljureido}thiazol-4-yl)acetic acid ~XO"CH3 H H
F NuNV~
''OII 1IS~OH

'H NMR (DMSO): 6 12.27 (br, 1 H), 11.06 (br, 1 H), 9.22 (br,1 H), 8.06 (dd,1 H), 7.32 (dd,1 H), 7.08 (d, 1 H), 7.03 (t, 1 H), 6.90 (s, 1 H), 6.75-6.70 (m,2H), 6.53 (dd, 1 H), 3.79 (s, 3H), 3.55 (s.
2H).
HPLC-MS (Method B): m/z = 436 (M+1); R~ = 3.85 min.

Example 112 (General procedure (H)) 2-{3-[2-(2,3-Dimethoxyphenoxy)-5-fluorophenyl]ureido)thiazole-4-carboxylic acid O,.CH3 O`CH3 O
N yNy~' O OH

'H NMR (DMSO): 6 12.77 (br, 1H), 11.33 (s, 1H), 9.06 (s, 1H), 8.07 (dd,1H), 7.93 (s, 1H), 7.08 (d, 1 H), 7.09 (t, 1 H), 6.95 (dd, 1 H), 6.80 (t, I H), 6.73-6.63 (m,2H), 3.84 (s, 3H), 3.66 (s, 3H).
HPLC-MS (Method B): m/z = 434 (M+1); R, = 3.92 min.
Example 113 (General procedure (H)) (2-{3-[2-(2,3-Dimethoxyphenoxy)-5-fluorophenyl]ureido)thiazol-4-yl)acetic acid O'CH3 O
H H
JNyNN

O
'H NMR (DMSO): 612.30 (br, 1 H), 11.14 (br, 1 H), 9,08 (br 1 H), 8.08 (dd,1 H), 7.08 (t, 1 H), 6.94 (d, 1 H), 6.89 (s, 1 H), 6.78 (t,1 H), 6.70 (dd, 1 H), 6.66(dd, 1 H), 3.84 (s, 3H), 3.66 (s, 3H), 3.54 (s, 2H).
HPLC-MS (Method B): m/z = 448 (M+1); Rt = 3.76 min.

Example 114 (General procedure (H)) 2-{3-[5-Fluoro-2-(2-fluoro-6-methoxyphenoxy)phenyl]ureido)-4-methylthiazole-5-carboxylic acid ethyl ester O,CH3 O
H H
F NN\ N

Y
O S i O
0 \-CH3 'H NMR (DMSO): 6 11.35 (s, 1 H), 9,38 (br 1 H), 8.05 (dd,1 H), 7.32 (dd, 1 H), 7.10-7.02 (m, 2H), 6.76 (t,1 H), 6.56(dd, 1 H), 4.24 (q, 2H), 3.79 (s, 3H), 2.52 (s, 3H), 1,29 (t, 3H).
HPLC-MS (Method B): m/z = 464 (M+1); Rt = 4.91 min.

Example 115 (General procedure (H)) 2-{3-[5-Fluoro-2-(2-fluoro-6-methoxyphenoxy)phenyl]ureido)-4-methylthiazole-5-carboxylic acid jT CH3 O
H H
F NN\ N

Y

OH
O
'H NMR (DMSO): 6 12.79 (br, 1H), 11.29 (br, 1H), 9,38 (br 1H), 8.05 (dd,IH), 7.32 (dd, 1H), 7.10-7.01 (m, 2H), 6.75 (t, 1H), 6.54 (dd, 1H), 3.79 (s, 3H), 2.51 (s, 2H).
HPLC-MS (Method B): m/z = 436 (M+1); Rt = 4.19 min.

Example 116 (General procedure (H1)) N-Ethyl-2-(2-{3-[5-fluoro-2-(2-fluoro-6-methoxyphenoxy)phenyl]ureido)thiazol-4-yi)acetamide O`CH3 O
H H

F Cy5CH
/ O g N
O

'H NMR (DMSO): d 11.03 (s, 1H), 9.22 (br 1H), 8.06 (dd,1H), 7.89 (t, 1H), 7.32 (dd, 1H), 7.10-7.00 (m, 2H), 6.82 (s,1 H), 6.72 (t, 1 H), 6.53(dd, 1 H), 3.79 (s, 3H), 3.39 (s, 2H), 3.07 (q, 2H),1,01 (t, 3H).
HPLC-MS (Method B): m/z = 463 (M+1); R1 = 4.06 min.
Example 117 (General procedure (H1)) 2-(2-{3-[5-Fluoro-2-(2-fluoro-6-methoxyphenoxy)phenyl]ureido}thiazol-4-yl)-N-(2-methoxy-ethyl)acetamide O,CH3 H
O HH O H

F \ N N 1TO-CH3 z~~
F
'H NMR (DMSO): 6 11.03 (br, 1 H), 9.22 (br 1 H), 8.06 (dd,1 H), 7.99 (t, 1 H), 7.32 (dd,1 H), 7.10-7.00 (m, 2H), 6.82 (s,1 H), 6.72 (t, 1 H), 6.53(dd, 1 H), 3.79 (s, 3H), 3.43 (s, 2H), 3.34 (t, 2H), 3.24 (s, 3H), 3.23 (t, 2H).
HPLC-MS (Method B): m/z = 493 (M+1); R, = 4.01 min.

Example 118 (General procedure (H1)) 2-(2-(3-[5-Fluoro-2-(2-fluoro-6-methoxyphenoxy)phenyl]ureido}thiazol-4-yi)-N-(2-morpholin-4-ylethyl)acetamide 0,CH3 F H N'YN
N
y S / N

F ~O
'H NMR (DMSO):selected data: 6 11.01 (br, 1H), 9.77 (br, 1H), 9.23 (br 1H), 8.19 (br, 1H), 8.06 (dd,1 H), 7.32 (dd, 1 H), 7.10-7.00 (m, 2H), 6.88 (s,1 H), 6.72 (t, 1 H), 6.53(dd, 1 H), 3.97 (m, 2H), 3.79 (s, 3H), 3.64 (m, 2H), 3.47 (s, 2H).
HPLC-MS (Method B): m/z = 548 (M+1); R = 3.24 min.
Example 119 (General procedure (H1)) [2-(2-(3-[5-Fluoro-2-(2-fluoro-6-methoxyphenoxy)phenyQureido}thiazol-4-yl)acetylamino]acetic acid methyl ester O, F NYN~ yN - \~

'H NMR (DMSO): Selected data 6 11.06 (br, 1 H), 9.25 (br 1 H), 8.34 (t,1 H), 8.06 (dd, 1 H), 7.31 (dd, I H), 7.10-7.00 (m, 2H), 6.88 (s,1 H), 6.73 (t, I H), 6.53(dd, 11-1), 3.85"(d, 2H), 3.79 (s, 3H), 3.63 (s, 2H), 3.49 (s, 2H).
HPLC-MS (Method B): m/z = 507 (M+1); R, = 3.74 min.

Example 120 (General procedure (H1)) 2-{3-[2-(2,3-Dimethoxyphenoxy)-5-fluorophenyl]ureido}thiazole-4-carboxylic acid (2-methoxyethyl)amide 0,CH3 CH3 \ I ' O HJO
N y N Y N N
I S
0 ~,O

'H NMR (DMSO):Selected data 611.29 (s, 11-1), 9.13 (s IH),8.08 (dd,1H), 7.78 (t,IH), 7.73 (s, 1 H), 7.09 (t,1 H), 6.95 (dd,1 H), 6.80 (t, 1 H), 6.71(dd, 1 H), 6.67 (dd, 1 H), 3.84 (s,'31-1), 3.67 (s, 3H), 3.26 (s, 3H).
HPLC-MS (Method B): m/z = 491 (M+1); Rt = 3.86 min.
Example 121 (General procedure (H1)) [2-(2-{3-[5-Fluoro-2-(2-fluoro-6-methoxyphenoxy)phenyl]ureido}thiazol-4-yl)acetylamino]acetic acid XO'H3 O
F N N N O
\_~
N
O S OH
F
'H NMR (DMSO): 6 12.54 (br, 1H), 11.06 (br, 1H), 9.23 (br 1H),8.21 (t,1 H), 8.06 (dd, IH), 7.31 (dd,1 H), 7.09-7.01 (m, 2H), 6.88 (s,1 H), 6.72 (t, 1 H), 6.53(dd, 1 H), 3.79 (s, 3H), 3.76 (s, 2H), 3.49 (s, 2H).
HPLC-MS (Method B): m/z = 493 (M+1); R1 = 3.47 min.

Example 122 (General procedure (H)) 2-{3-[2-(2,3-Dimethoxyphenoxy)-5-fluorophenyl]ureido}thiazole-4-carboxylic acid ethylamide O,CH3 O,CH3 N 'H NMR (DMSO): 6 11.21 (s, 1H), 9.19 (s 1H),8.08 (dd,IH), 7.89 (t,1H), 7.69 (s, 1H), 7.10 (t,1H), 6.95 (dd,IH), 6.79 (t, 1H), 6.73-6.66 (m, 2H), 3.84 (s, 3H), 3.66 (s, 3H), 3.25 (q, 2H), 1.08 (t, 3H).
HPLC-MS (Method B): m/z = 461 (M+1); R, = 3.96 min.
Microanalysis:
Calculated for : C, 55.09%; H, 4.88%; N, 111.88%.
Found: C, 55.18%; H, 4.67%; N, 12.21%.
Example 123 (General procedure (H1)) [(2-{3-[2-(2,3-Dimethoxyphenoxy)-5-fluorophenyl]ureido}thiazole-4-carbonyl)amino]acetic acid methyl ester 0,CH3 a H H H--O\ CH
Ny YN N 3 -F
'H NMR (DMSO): 611.26 (s, 1H), 9.20 (s 1H), 8.26 (t, 1H), 8.09 (dd,1H), 7.77 (s,IH), 7.10 (t,IH), 6.95 (dd,1H), 6.79 (t, 1H), 6.72-6.67 (m, 2H), 4.01 (d, 2H), 3.84 (s, 3H), 3.66 (s, 3H), 3.65 (s, 3H).

Example 124 (General procedure (H)) (5-{3-[5-Fluoro-2-(2-fluoro-6-methoxyphenoxy)phenyl]ureido)-[1,3,4]thiadiazol-2-yl)acetic acid ethyl ester 0,CH3 H H
F N N N
1 Y ~N

'H NMR (DMSO): 611.35 (s, 1H), 9.31 (s 1H), 8.03 (t,1H), 8.04 (dd, 1H), 7.31 (dd,1H), 7.10-7.02 (m, 2H), 6.75 (t, 1 H), 6.55(dd, 1 H), 4.19-4.14(m, 4H), 3.80 (s, 3H), 1.23 (t, 3H).
HPLC-MS (Method B): m/z = 465 (M+1); Rt = 4.14 min.

Example 125 (General procedure (H1)) [(2-{3-[2-(2,3-Dimethoxyphenoxy)-5-fluorophenyl]ureido}thiazole-4-carbonyl)amino]acetic acid 0,.CH3 ~ I OH
N N Y N Y N
o F
'H NMR(DMSO): 6 12.67 (br, 1H), 11.36 (s, 1 H), 9.24(s 1 H), 8.08 (dd,1 H), 7.78 (s,1 H), 7.10 (t,1H), 6.95 (dd,1H), 6.79 (t, 1H), 6.72-6.67 (m, 2H), 3.93 (d, 2H), 3.84 (s, 3H), 3.67 (s, 3H).
HPLC-MS (Method B): m/z = 491 (M+1); R = 3.58 min.

Example 126 (General procedure (H)) (5-(3-[5-Fluoro-2-(2-fluoro-6-methoxyphenoxy)phenyljureido)-[1,3,4]thiadiazol-2-yl)acetc acid 0`CH3 H H
F NyN\ fN% ~J N

0 S t OH

'H NMR (DMSO): d 12.96 (br,11-1), 11.33 (br, 11-1), 9.31 (s 11-1), 8.04 (dd, 11-1), 7.33 (dd,1 H), 7.11-7.01 (m, 2H), 6.75 (t, IH), 6.55 (dd, 1H), 4.10 (s. 2H), 3.80 (s, 3H).
HPLC-MS (Method B): m/z = 337 (M+1); R~ = 3.47 min.

Example 127 (General procedure (H)) 5-(3-[2-(2,3-Dimethoxyphenoxy)-5-fluorophenyl]ureido)-[1,3,4]thiadiazole-2-carboxylic acid ethyl ester O~CH3 o H H

N
NYN~N`

'H NMR (DMSO): 6 11.91 (s, 1H), 9.26 (s 1H), 8.05 (dd, 1H), 7.10 (t,1H), 6.95 (dd,1H), 6.83 (t, 1H), 6.75-6.67 (m, 2H), 4.40 (q, 2H), 3.84 (s, 3H), 3.66 (s, 3H), 1.35 (t, 3H).
HPLC-MS (Method B): m/z = 463 (M+1); Re = 4.34 min.

Example 128 (General procedure (H)) (5-{3-[2-(2,3-Dimethoxyphenoxy)-5-fluorophenyl]ureido}-[I,3,4]thiadiazol-2-yl) acetic acid ethyl ester O,CH3 H H

T<~/cH3 'H NMR (DMSO): 6 11.42 (s, 1H), 9.17 (s 1H), 8.05 (dd, 1H), 7.09 (t,1 H), 6.95 (dd,1H), 6.81 (t, 1 H), 6.72 (dd, 1 H), 6.67 (dd, 1 H), 4.19-4.13 (m, 4H), 3.84 (s, 3H), 3.66 (s, 3H), 1.22 (t, 3H).
HPLC-MS (Method B): mlz = 477 (M+1); R, = 4.10 min.
Example 129 (General procedure (H1)) 3-[2-(2-{3-[2-(2,3-Dimethoxyphenoxy)-5-fluorophenyl]ureido}thiazol-4-yl)acetylamino]propionic acid methyl ester O~CH3 NO
N N N

0 S:
F
'H NMR (DMSO): 611.11 (s, 1H), 9.07 (br 1H), 8.08 (dd, 1H), 7.98 (t,1H), 7.08 (d,IH), 6.94 (dd,1 H), 6.81 (s, 1 H), 6.77 (dd, 1 H), 6.70 (dd,1 H), 6.65 (dd, 1 H), 3.84 (s, 3H), 3.66 (s, 3H), 3.58 (s, 3H), 3.39 (s, 2H), 3.27 (q, 2H), 2.46 (t, 2H).
HPLC-MS (Method B): m/z = 533 (M+1); R1 = 3.71 min.

Example 130 (General procedure (H 1)) 2-(2-(3-[2-(2,3-Dimethoxyphenoxy)5-fluorophenyl]ureido)thiazol-4-yl)-N-(2-morpholin-4-ylethyl)acetamidee 0,CH3 O
H
N y N N
iNZ
N
O S

~O
'H NMR (DMSO):Selected data 6 11.11 (br, 11-1), 9.08 (br 11-1). 8.07 (dd, 11-1), 7.09 (t,1 H), 6.94 (dd,1 H), 6.86 (s, 1 H), 6.77 (t,1 H), 6.70 (dd, 1 H), 6.66 (dd, 1 H), 3.84 (s. 3H), 3.66 (s, 3H), 3.43 (s, 2H), 3.03-2.99 (m, 4H), 1.74-1.71 (m, 4H).
HPLC-MS (Method B): m/z = 560 (M+1); R~ = 2.75 min.
Example 131 (General procedure (H1)) [(2-{3-[5-Fluoro-2-(2-fluoro-6-methoxyphenoxy)phenyl]ureido}thiazole-4-carbonyl)amino]acetic acid methyl ester 0,CH3 CHO 3 HH
F N N HN
~10 F
'H NMR (DMSO): 6 11.27 (s, 1 H), 9.36 (s 1 H), 8.32 (t, 1 H), 8.07 (dd, 1 H), 7.79 (s, 1 H), 7.33 (dd,1 H), 7.11-7.02 (m, 2H), 6.75 (t,1 H), 6.55 (dd, 1 H), 4.03 (d, 2H), 3.80 (s, 3H), 3.66 (s, 3H).
HPLC-MS (Method B): m/z = 493 (M+1); R~ = 3.91 min.

Example 132 (General procedure (H1)) 3-[2-(2-{3-[2-(2,3-Dimethoxyphenoxy)-5-fluorophenyl]ureido)thiazol-4-yl)acetylamino]propionic acid Oll CH3 0 OH
O O
N N N N
~ Y H
O s F
'H NMR (DMSO): 612.21 (br, 1 H), 11.09 (br, 1 H), 9.06 (br 1 H), 8.07 (dd, 1 H), 7.98 (t,1 H), 7.09 (t, 1 H), 6.94 (dd,1 H), 6.81 (s, 1 H), 6.76 (t, 1 H), 6.71 (t, 1 H), 6.66 (dd,1 H), 3.84 (s, 3H), 3.66 (s, 3H), 3.39 (s, 2H), 3.24 (q, 2H), 2.38 (t, 2H).

Example 133 (General procedure (H1)) [(2-(3-[5-Fluonr2-(2-fluoro-6-methoxyphenoxy)phenyl]ureido}thiazole-4-carbonyl)amino]acetic acid O,CH3 O
O J-OH
F N N H ~N N
o s o F
1 H NMR (DMSO): 6 12.74 (br, 1 H), 11.23 (s, 1 H), 9.31 (s 1 H), 8.17 (t, 1 H), 8.07 (dd, 1 H), 7.78 (s, 1H), 7.33 (dd, 1H), 7.11-7.01 (m, 2H), 6.75 (t,IH), 6.54 (dd,1H), 3.92 (d, 2H), 3.80 (s, 3H).

Example 134 (General procedure (H1)) (R) 3-[(2-{3-[5-Fluoro-2-(2-fluoro-6-methoxyphenoxy)phenyl]ureido}thiazole-4-carbonyl)amino]-2-hydroxy-propionic acid H3C,0 I F 0 H H

\ 00 N \ OH

F NANS O
H H
'H NMR (DMSO): d 12.62 (br, 1H), 11.32 (s, 1H), 9.23 (s 1H), 8.06 (dd, 1H), 7.79-7.76 (m, 2H), 7.33 (dd, 1 H), 7.11-7.02 (m, 2H), 7.06 (dd, 1 H), 6.75 (t,1 H), 6.54 (dd,1 H), 5.62 (br, 1 H), 4.16 (t, 1 H), 3.80 (s, 3H), 3.64-3.52 (m, 1 H), 3.49-3.40 (m, 1 H).
HPLC-MS (Method B): m/z = 509 (M+1); Rt = 3.49 min.
Example 135 (General procedure (H1)) 2-[(2-{3-[5-Fluoro-2-(2fluoro-6-methoxyphenoxy)phenyl]ureido}thiazole-4-carbonyi)amino}3-hydroxy-propionic acid H3C,0 I F 0 H

I \ ON N -X OH
F NANS OH
H H
'H NMR (DMSO): d 12.88 (br, 1 H), 11.42 (s,1 H), 9.17 (s 1 H), 8.06 (dd, 1 H), 7.92 (d,1 H), 7.80 (s, 1 H), 7.32 (dd, 1H), 7.11-7.01 (m, 2H), 6.75 (t,1 H), 6.54 (dd,1 H), 5.10 (br, 1 H), 4.46 -4.43 (m, 1 H), 3.89 (m, 4H).

Example 136 1-(2-Cyclopentanecarbonyl-4-methylphenyl}3-thiazol-2-yl-urea O
H H
NyIN S
I / O TNI

2-Cyclopentanecarbonyl-4-methylaniline (10.2 g) is prepared from p-toluidine (10.7 g, 0.1 mol) and cyclopentanecarbonitrile (9.5 g, 0.1 mol) following the general procedure I.
1-(2-Cydopentanecarbonyl--methyl-phenyl)-3-thiazol-2-yl-urea (132 mg) is prepared from 2-cydopentanecarbonyl-4-methylaniline (102 mg, 0.5 mmol) and 2-aminothlazole (0.060 g, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 330 (M+1)' 'H NMR (400 MHz, CDCI3): d 1.69 (m, 2H), 1.91 (m, 2H), 2.37 (s, 3H), 3.76 (m, 1 H), 6.89 (d, 1 H), 7.35 (d.1 H), 7.71 (s, 2H), 8.42 (d,1 H), 11.57 (br, 1 H) ppm.

Example 137 1-(2-Isobutyryl-4-methylphenyl)-3-thiazol-2-yl-urea H H
I ~ NN~S
/ O Nom 2-Isopropylcarbonyl-4-methylaniline (7.0 g) is prepared from p-toluidine (10.7 g, 0.1 mol) and isobutyronitrile (6.9 g, 0.1 mol) following the general procedure I.1-(2-Isobutyryl-4-methylphenyl)-3-thiazol-2-yl-urea (113 mg) is prepared from 2-isopropylcarbonyl-4-methylaniline (88 mg, 0.5 mmol) and 2-aminothiazole (0.060 g, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 304 (M+1)`
'H NMR (400 MHz, CDCI3): 6 1.97 (d, 6H), 2.37 (s, 3H), 3.72 (m, 1 H), 6.90 (d,1 H), 7.36 (d, 1 H), 7.69 (s, 2H), 8.44 (s, 1 H),11.51 (br,1 H), 11.72 (br, 1 H) ppm.

Example 138 1-[5-Fluoro-2-(3-methylbutyryl)phenyl]-3-thiazol-2-yl-urea H H
~
NuN >
IOI IINII
F
2-[(2-Methyl)-propylcarbonyl]-5-fluoroaniline (6.82.g) is prepared from m-fluoro aniline (11.1 g, 0.1 mol) and 3-methylbutyronitrile (8.3 g, 0.1 mol) following the general procedure I. 1-[5-Fluoro-2-(3-methyl-butyryl)-phenyl]-3-thiazol-2-yl-urea (128 mg) is prepared from 2-[(2-methyl)-propylcarbonyl]-5-fluoroaniline (97 mg, 0.5 mmol) and 2-aminothiazole (0.060 g, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 322 (M+1)`
'H NMR (400 MHz, CDCI3): 6 0.99 (d, 6H), 2.23 (m, 1 H), 2.83 (d, 2H). 6.75 (m,1 H), 6.93 (d, 1 H), 7.62 (d, 1 H), 7.92 (dd, 1 H), 8.43 (dd, 1 H), 11.60 (br, 1 H), 12.04 (br, 1 H) ppm.
Example 139 1-[5-Methyl-2-(3-methylbutyryl)phenyl]-3-thiazol-2-yl-urea H H
S
NuNTNI
o 2-[2-Methylpropylcarbonyl]-5-methylaniline (6.8 g) is prepared from m-toluidine (10.2 g, 0.1 mol) and isobutyronitrile (8.3 g, 0.1 mol) following the general procedure I. 1-[5-Methyl-2-(3-methylbutyryl)phenyl]-3-thiazol-2-yl-urea (114 mg) is prepared from 2-[2-methylpropylcarbonyi]-5-methylaniline (95 mg, 0.5 mmol) and 2-aminothiazole (0.060 g, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 318 (M+1)' 'H NMR (400 MHz, CDC13): 6 0.98 (d, 6H), 2.31 (m, 11-1), 2.37 (s, 3H), 2.44 (d, 2H), 6.91 (m, 1 H), 7.27 (m,1 H), 7.51 (d, 1 H), 7.68 (dd, 1 H), 8.45 (d, 1 H). 11.58 (br, 1 H), 11.60 (br, 1 H) PPM-Example 140 [3-Cyclopentanecarbonyl-4-(3-thiazol-2-yl-ureido)phenyl]acetic acid ethyl ester H H
S

(4-Amino-3-cydopentanecarbonylphenyl)acetic acid ethyl ester (2.7 g) is prepared from (4-aminophenyl)acetic acid ethyl ester (18.0 g, 0.1 mol) and cyclopentanecarbonitrile (9.5 g, 0.1 mol) following the general procedure I. [3-Cyclopentanecarbonyl-4-(3-thiazoi-2-yl-ureido)phenyl]acetic acid ethyl ester (140 mg) is prepared from (4-amino-3-cydopentane-carbonylphenyl)acetic acid ethyl ester (138 mg, 0.5 mmol) and 2-aminothlazole (0.060 g, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 402 (M+1 )' 'H NMR (400 MHz, CDCI3): 6 1.12 (t, 3H), 1.73 (m, 2H). 1.82 (m, 2H), 3.27 (m,1H), 3.62 (s, 2H), 4.15 (q, 2H), 6.89 (d, 1 H), 7.44 (dd, 1 H), 7.62 (d, 1 H), 7.86 (s, 1 H), 8.51 (s, 1 H), 11.62 (br, I H) ppm.

Example 141 [3-Cydopentanecarbonyl-4-(3-thiazol-2-yl-ureido)phenygaoetic acid O
H H
0 NVN~S
/ II>
HO O II N

[3-Cyclopentanecarbonyl-4-(3-thiazol-2-yl-ureido)phenyl]acetic acid (168 mg) is prepared from [3-cyclopentanecarbonyl-4-(3-thiazol-2-yl-ureido)phenyl]acetic acid ethyl ester (201 mg, 0.5 mmol) following the general procedure J.
LC-MS (m/z): 374 (M+1)+

'H NMR (400 MHz, DMSO-d8): 6 1.66 (m, 2H), 1.96 (m, 2H), 3.71 (s, 2H), 3.92 (m, 1 H), 7.05 (d, 1 H), 7.38 (d, 1 H), 7.56 (dd, 1 H), 8.08 (s, 1 H), 8.55 (s, 1 H), 11.26 (br, 1 H) ppm.

Example 142 2-[3-Cyclopentanecarbonyl-4-(3-thiazol-2-yl-ureido)phenyl]-N-methylacetamide O
H H
0 NuN~'S/, H3C, N ffOJJ IINIL

H
2-[3-Cyctopentanecarbonyl-4-(3-thiazol-2-yl-ureido}phenyl]-N-methylacetamide (154 mg) is prepared from [3-cydopentanecarbonyl4-(3-thiazol-2-yl-ureido)phenyljacetic add (186 mg, 0.5 mmol) and I M solution of methylamine in THE (0.5 ml, 0.5 mmol) following the general procedure K.
LC-MS (m/z): 387 (M+1)' 'H NMR (400 MHz, CDCI3/DMSO-de): 6 1.51 (m, 2H), 1.73 (m, 2H), 2.58 (s, 3H), 3.36 (s, 2H), 3.59 (m, 1 H), 6.67 (m, 1 H), 7.21 (m, 2H), 7.71 (s, 1 H), 8.26 (bs, 1 H), 10.95 (br, 1 H) PPM.

Example 143 {2-[3-(2-Cydopentanecarbonyl-4-methyl-phenyl)-ureido]-thiazol-4-yl)-acetic acid ethyl ester H H, \ NyN " S
O N

H3C'/

{2-[3-(2-Cydopentanecarbonyl-4-methyl-phenyl}ureido]-thiazol-4-yl)-acetic acid ethyl ester (154 mg) is prepared from (2-amino-5-methylphenyl)(cyclopentyl)methanone (102 mg, 0.5 mmol) and ethyl-2-amino-4-thiazolyl acetate (93 mg, 0.5 mmol) following the general procedure D.

LC-MS (m/z): 416 (M+1)' 'H NMR (400 MHz, CDCI3): 6 1.23 (t, 3H), 1.67 (m, 2H), 1.87 (m, 2H), 2.34 (s, 3H), 3.70 (s, 2H), 4.18 (m, 3H), 6.68 (s, 1 H), 7.25 (s, 2H), 7.32 (d. 1 H), 7.67 (s, 1 H), 8.45 (s, 1 H), 9.75 (br, 1 H), 11.51 (br, 1 H) ppm.

Example 144 {2-{3-(2-Cyclopentanecarbonyl-4-methyl-phenyl)-ureido]-thiazol-4-yl}acetic acid H H
NyN\ /g 0 iN"

HO

{2-[3-(2-Cyclopentanecarbonyl-4-methylphenyl)-ureido]-thiazol-4-yl}-acetic acid (198 mg) is prepared from {2-[3-(2-cyclopentanecarbonyl-4-methylphenyl)-ureido]-thiazol-4-yl}-acetic acid ethyl ester (208 mg, 0.5 mmol) following the general procedure J.
LC-MS (m/z): 388 (M+1)' 'H NMR (400 MHz,DMSO-d5): d 1.73 (m, 2H), 1.86 (m, 2H), 2.32 (s, 3H), 3.55 (s, 2H), 3.86 (m 1 H), 6.84 (s, 1 H), 7.36 (d, 1 H), 7.84 (d, 1 H), 8.15 (d, 1 H), 10.62 (br, 1H),11.92 (br, 1 H), 12.24 (br, 1 H) ppm.

Example 145 (3-Cyclopentanecarbonyl-4-{3-(4-ethoxycarbonylmethylthiazol-2-yl)-ureido}phenyl)acetic acid ethyl ester H H rt NyN " S

{3-Cyclopentanecarbonyl-4-{3-(4-ethoxycarbonylmethyl-thiazol-2-yl)-ureido}-phenyl}-acetic acid ethyl ester (205 mg) is prepared from (4-amino-3-cyclopentanecarbonyl-phenyl)acetic acid ethyl ester (138 mg, 0.5 mmol) and ethyl-2-amino-4-thiazolyl acetate (93 mg, 0.5 mmol) following the general procedure D.
5. LC-MS (m/z): 488 (M+1)' 'H NMR (400 MHz, CDCI3): 6 1.24 (t, 6H),1.67 (m, 2H), 1.88 (m, 2H), 2.34 (s, 3H), 3.61(s, 2H), 3.71 (s, 2H), 3.73 (m, 1 H), 4.17(m, 4H), 4.18 (m, 3H), 6.69 (s,1 H), 7.42 (d, 2H), 7.85 (s, 1H), 8.53 (s, I H), 11.64 (br, 1 H) ppm.

Example 146 1-(2-Cyclopentanecarbonyl-4-methyl-phenyl)-3-(5-methanesulfonyl-thiazol-2-yl)-urea O

\ \ N NYS 0 I lol N S O
/ i CH

1-(2-Cyclopentanecarbonyl-4-methyl-phenyl)-3-(5-methanesulfonyl-thiazol-2-yl}urea (149 mg) is prepared from 2-cyciopentanecarbonyl-4-methylaniline (102 mg, 0.5 mmol) and 5-methanesulfonyl-thiazol-2-yl-amine (106 mg, 0.6 mmol) following the general procedure D.
LC-MS (m/z): 408 (M+1)`
'H NMR (400 MHz, CDCI3): d 1.65-1.77 (m, 4H), 1.88-1.97 (m, 4H), 2.40 (s, 3H), 3.21 (s, 3H), 3.81 (p,1H), 7.41 (dd,1H), 7.78 (s, 11-1), 8.31 (d, 1H). 8.43 (d, IH), 11.57 (br, IH), 11.95 (br, 1 H) ppm.

Example 147 2-[3-(2-Cyclopentanecarbonyl-4-methylphenyl)-ureido]-thiazole-4-carboxylic add ethyl ester O
H H
I \ N Y N
" S
O N

O

2-[3-(2-Cydopentanecarbonyl-4-methylphenyi}ureido]-thiazole-4-carboxylic acid ethyl ester (3.6 g) is prepared from 2-cydopentanecarbonyl-4-methyl aniline (2.04 g, 10 mmol) and ethyl-2-amino-4-thiazole acetate (1.72 g, 10 mmol) following the general procedure D.
LC-MS (m/z): 402 (M+1)' 'H NMR (400 MHz, CDCI3): 6 1.35 (t, 3H), 1.62-1.78 (m, 4H), 1.83-1.96 (m, 4H), 2.37 (s, 3H), 3.74 (p, 1 H), 4.33 (q, 2H), 7.36 (d, 1 H), 7.72 (s, 1 H), 7.81 (s, 1 H), 8.44 (d, 1 H), 9.25,(br, 1 H), 11.84 (br, 1 H) ppm.

Example 148 2-[3-(2-Cydopentanecarbonyl-4-methylphenyl)-ureido]-thiazole-4-carboxylic add O
H H
I NuN)I_S
ON
H OH
O
2-[3-(2-Cydopentanecarbonyl-4-methylphenyl)-ureido]-thiazole-4-carboxylic acid (3.2 g) is prepared from 2-[3-(2-cyclopentanecarbonyl-4-methyl-phenyl)-ureido]-thiazole-4-carboxylic acid ethyl ester (3.6 g, 8.95 mmol) following the general procedure J.
LC-MS (m/z): 374 (M+1)' 'H NMR (400 MHz, DMSO-de): 6 1.58 (m, 4H), 1.73 (m, 4H), 2.29 (s, 3H), 3.72 (m, 1H), 7.13 (s, 1 H), 7.28 (d, 1 H), 7.63 (d, 1 H), 7.72 (br,1 H), 7.94 (s, 1 H), 8.22 (br, 1 H), 10.92 (br, 1 H) ppm.

Example 149 2-[3-(2-Cydopentanecarbonyl-4-methylphenyl)-ureido]-thiazole-4-carboxamide O
H H
NuN~S
IOI IINI' 2-[3-(2-Cyclopentanecarbonyl-4-methylphenyl)-ureido]-thiazole-4-carboxamide (145 mg) is prepared from 2-[3-(2-cydopentanecarborryl-4-methylphenyl)-ureido]-thiazole-4-carboxylic acid (187 mg, 0.5 mmol) following the general procedure K.
LC-MS (m/z): 373 (M+1)`
'H NMR (400 MHz, DMSO-de): 6 1.61 (m, 4H), 1.73 (m, 2H), 1.88 (m, 2H), 2.32 (s, 3H), 3.86 (m, 1 H), 7.38 (d, 1 H), 7.56 (s, 1 H), 7.68 (s, 1 H), 7.84 (s, I H), 7.93 (s,1 H), 8.14 (d, 1 H), 10.73 (br, 1 H), 11.86 (br, 1 H) ppm.
Example 150 2-{2-[3-(2-Cyclopentanecarbonyl-4-methylphenyl)-ureido]-thiazole-4-yl}-aoetamide O
H H
NyN " S
O N

2-{2-[3-(2-Cyclopentanecarbonyl-4-methylphenyl)-ureido]-thiazole-4-yl}-acetamide (325 mg) is prepared from 2-[3-(2-cyclopentanecarbonyl-4-methylphenyl)-ureido]-thiazol-4-yl acetic acid (386 mg, 1.0 mmol) following the general procedure K.
LC-MS (m/z): 387 (M+1)' 'H NMR (400 MHz, DMSO-d8): a 1.60 (m, 4H), 1.73 (m, 2H), 1.87 (m, 2H), 2.31 (s, 3H), 3.38 (s, 2H), 3.88 (m,1 H), 6.77 (s, 1 H), 6.97 (s, 1 H), 7.38 (d, 2H), 7.83 (s,1 H), 8.15 (d,1 H), 10.63 (br, 1 H), 11.81 (br, 1 H) ppm.

Example 151 2-(2-[3-(2-Cydopentanecarbonyl-4-methylphenyl)-ureido]-thiazol-4-yl}-N-methyl-acetamide H H
NyN\ 'S

2-{2-[3-(2-Cycopentanecarbonyl-4-methylphenyl)-ureido]-thiazol-4-yl}-N-methyl-acetamide (346 mg) is prepared from 2-[3-(2-cydopentanecarbonyl-4-methyl-phenyl -ureido]-thiazol-4-yl acetic acid (386 mg, 1.0 mmol) following the general procedure K.
LC-MS (m/z): 401 (M+1)+
'H NMR (400 MHz, DMSO-d6): d 1.70 (m, 4H), 1.88 (m, 2H), 1.94 (m, 2H), 2.63 (s, 3H), 2.79 (d, 3H), 3.62 (s, 2H), 3.77 (p,1 H), 6.65 (s,1 H), 6.77 (br, 1 H), 7.35 (dd, 1 H), 7.71 (s, 1 H), 8.43 (d, 1 H), 9.15 (br, 1 H), 11.70 (br, I H) ppm.
Example 152 4-(2-{2-[3-(2-Cydopentanecarbonyl-4-methylphenyl)-ureido]-thiazol-4-yl) -acetyl)-1-methyl-piperazinium chloride H H
N-yS
Ny O

= ~ CI
H

4-(2-{2-[3-(2-Cydopentanecarbonyl-4-methylphenyl)ureido]-thiazol-4-yl}-acetyl)-methyl-piperazine (337 mg) is prepared from 2-[3-(2-cyclopentanecarbonyl-4-methyl-phenyl)-ureido]-thiazol-4-ylacetic acid (386 mg, 1.0 mmoi) and N-methylpiperazine following the general procedure K.
4-(2-{2-[3-(2-Cyclopentanecarbonyl-4-methylphenyl}ureidoj-thiazol-4-yi)-acetyl)-1-methyl-piperazinium chloride (392 mg) is prepared from 4-(2-(2-[3-{2-cyclopentanecarbonyl-4-methylphenyl)-ureido]-thiazol-4-yl)-acetyl)-1-methyl-piperazine (386 mg, 1.0 mmol) by treatment with anhydrous hydrogen chloride (5 ml, 4.0 M solution in dioxane) followed by collection of the solid product.
LC-MS (m/z): 471 (M+1)' 'H NMR (400 MHz, DMSO-de): 6 1.60 (m, 4H), 1.72 (m, 2H), 1.87 (m, 2H), 2.32 (s, 3H), 2.47 (s, 3H), 2.76 (d, 2H), 2.94 (m, 2H), 3.37 (m, 2H), 3.73 (d, 2H), 3.84 (m, 2H), 4.22 (d, 1 H), 4.44 (d, 1 H), 6.83 (s, 1 H), 7.36 (d, 1 H), 7.82 (s, 1 H), 8.11 (d, 1 H), 10.63 (br,1 H), 10.82 (br, 1 H) ppm.
Example 153 1-[4-Methyl-2-(2-methylpropoxy)phenyl]-3-thiazol-2-yi-urea H
J:N Y I
/ O N

3-(2-Methylpropoxy)-4-nitrotoluene (0.78 g) is prepared from 2-methylpropanol (0.46 ml, 5.0 mmoi) and 3-fluoro-4-nitrotoluene (0.77 g, 5.0 mmol) following the general procedure G. This is reduced to afford 4-methyl-2-(2-methylpropoxy)aniline (0.47 g) following general procedure C. N-[4-Methyl-2-(2-methylpropoxy)phenyl]-N'-(thiazol-2-yi)urea (210 mg) is prepared from 4-methyl-2-(2-methylpropoxy)aniline (179 mg, 1.0 mmol) and 2-aminothiazole (100 mg, 1.0 mmoi) following the general procedure D.
LC-MS (m/z): 306 (M+1)+
'H NMR (400 MHz, CDC13): 61.01 (d, 6H), 2.16 (m, 1H), 2.32 (s, 3H), 3.78 (d, 2H), 6.70 (s, 1 H), 6.75 (d, 1 H), 6.86 (d, 1 H), 7.40 (d, 1 H), 8.07 (d, 1 H), 9.30 (br, 1 H), 10.72 (br, 1 H) ppm.

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Claims (34)

1. A compound of Formula (I a) wherein R25 is selected from the group consisting of F, C1, Br and methyl;
L1 is a bond, -D-C1-6-alkylene-E-, -0-, -S-, -S(O)-, -S(O)2-, -C(O)-, -N(R11)-, or -C(=N-OR12);

D is a direct bond or -0-;
E is a direct bond or -0-;
R11 is hydrogen;
R12 is hydrogen;
G1 is C1-6-alkyl, C2-6-alkenyl, C2-6-alkynyl, C3-10-cycloalkyl or C3-10-heterocyclyl, optionally substituted with one or more substituents selected from the group consisting of -CN, -CF3, -OCF3, -OR18, -NR 18R19, C3-10-cycloalkyl and C1-6-alkyl;
R18 and R19, independently of each other, are hydrogen or C1-6-alkyl;
L2 is -N-R20-;
L3 is -C(O)-;
R1 is hydrogen;
R20 is hydrogen;
G2 is ;
R43 is -C1-6-alkylene-C(O)OR54 R54 is hydrogen, methyl, ethyl, propyl, butyl, isopropyl, isobutyl, sec-butyl, tert-butyl, 3-pentyl, 2-pentyl, or 3-methyl-butyl;
or a pharmaceutically acceptable salt thereof or solvate of any of the foregoing.
2. The compound according to claim 1, wherein L1 is a bond, -D-C1-6-alkylene-E-, -0-, -C(O)-, -N(R11)-, or -C(=N-OR12)-.
3. The compound according to claim 1, wherein L1 is -0-.
4. The compound according to claim 1, wherein L1 is -S-.
5. The compound according to claim 1, wherein L1 is a bond.
6. The compound according to claim 1, wherein L1 is -C(O)-.
7. The compound according to any one of claims 1 to 6, wherein D is a direct bond.
8. The compound according to any one of claims 1 to 6, wherein D is -0-.
9. The compound according to any one of claims 1 to 8, wherein E is a direct bond.
10. The compound according to any one of claims 1 to 8, wherein E is -o-.
11. The compound according to any one of claims 1 to 10, wherein G1 is selected from the group consisting of methyl, ethyl, propyl, butyl, isopropyl, isobutyl, sec-butyl, tert-butyl, 3-pentyl, 2-pentyl, 3-methyl-butyl, 2-propenyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, oxetanyl, tetrahydrofuranyl, tetrahydropyranyl, azetidyl, pyrrolidyl, piperidyl, hexahydroazepinyl, thiolanyl, tetrahydrothiopyranyl, thiepanyl, 1,4-oxathianyl, 1,3-dioxolanyl, 1,2-dithiolanyl, 1,3-dithiolanyl, hexahydro-pyridazinyl, imidazolidyl, 1,3-dioxanyl, morpholinyl, 1,3-dithianyl, 1,4-dioxanyl, 1,4-dithianyl, and thiomorpholinyl.
12. The compound according to claim 11, wherein G1 is selected from the group consisting of methyl, ethyl, propyl, butyl, isopropyl, isobutyl, sec-butyl, tert-butyl, cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, tetrahydrofuranyl, tetra hydropyranyl, pyrrolidyl, piperidyl, hexahydroazepinyl, thiolanyl, tetrahydrothiopyranyl, and thiepanyl .
13. The compound according to claim 12, wherein G1 is selected from the group consisting of methyl, ethyl, propyl, butyl, isopropyl, isobutyl, cyclopentyl, cyclohexyl, tetrahydrofuranyl, tetrahydropyranyl, piperidyl, and hexahydroazepinyl.
14. The compound according to claim 13, wherein G1 is selected from the group consisting of isobutyl, cyclopentyl, and piperidyl.
15. The compound according to claim 14, wherein G1 is isobutyl.
16. The compound according to claim 14, wherein G1 is cyclopentyl.
17. The compound according to claim 14, wherein G1 is piperidyl.
18. The compound according to any one of claims 1 to 17, wherein R18 and R19 are hydrogen.
19. The compound according to any one of claims 1 to 18, wherein R43 is -CH2-C(O)OR54.
20. The compound according to any one of claims 1 to 19, wherein R54 is hydrogen, methyl, ethyl, propyl, butyl, isopropyl, isobutyl, sec-butyl, or tert-butyl.
21. The compound according to claim 20, wherein R54 is hydrogen, methyl or ethyl.
22. The compound according to claim 21, wherein R54 is hydrogen.
23. The compound according to claim 1, wherein the compound is {2-[3-(2-Cyclopentanecarbonyl-5-methyl-phenyl)-ureido]-thiazol-4-yl}acetic acid, a pharmaceutically acceptable salt thereof, or a solvate of any of the foregoing.
24. The compound according to claim 23, wherein the compound is {2-[3-(2-Cyclopentanecarbonyl-5-methyl-phenyl)-ureido]-thiazol-4-yl}acetic acid, or a pharmaceutically acceptable salt thereof.
25. The compound according to claim 23, wherein the compound is {2-[3-(2-Cyclopentanecarbonyl-5-methyl-phenyl)-ureido]-thiazol-4-yl}acetic acid.
26. Use of a compound as defined in any one of claims 1 to 25 in the manufacture of a medicament for the treatment of metabolic disorders, for blood glucose lowering, for the treatment of hyperglycemia, for treatment of IGT, for treatment of syndrome X, for the treatment of impaired fasting glucose (IFG), for treatment of type 2 diabetes, for treatment of type 1 diabetes, for delaying the progression of impaired glucose tolerance (IGT) to type 2 diabetes, for delaying the progression of non-insulin requiring type 2 diabetes to insulin requiring type 2 diabetes, for treatment of dyslipidemia, for treatment of hyperlipidemia, for treatment of hypertension, for the treatment or prophylaxis of obesity, for lowering of food intake, for appetite regulation, for regulating feeding behaviour, or for enhancing the secretion of enteroincretins.
27. Use of a compound as defined in any one of claims 1 to 25 in the manufacture of a medicament for the treatment of an indication selected from the group consisting of hyperglycemia, IGT, insulin resistance syndrome, syndrome X, type 2 diabetes, type 1 diabetes, dyslipidemia, hypertension and obesity.
28. The use as defined in claim 26 or 27, wherein the medicament further comprises an active substance selected from the group consisting of antidiabetic agents, antihyperlipidemic agents, antiobesity agents, anti hypertensive agents and agents for the treatment of complications resulting from or associated with diabetes.
29. The use as defined in claim 28, wherein the active substance is metformin.
30. A pharmaceutical composition comprising a compound as defined in any one of claims 1 to 25, and one or more pharmaceutically acceptable carriers or excipients.
31. The pharmaceutical composition as defined in claim 30 for the treatment of metabolic disorders, for blood glucose lowering, for the treatment of hyperglycemia, for treatment of IGT, for treatment of syndrome X, for the treatment of impaired fasting glucose (IFG), for treatment of type 2 diabetes, for treatment of type 1 diabetes, for delaying the progression of impaired glucose tolerance (IGT) to type 2 diabetes, for delaying the progression of non-insulin requiring type 2 diabetes to insulin requiring type 2 diabetes, for treatment of dyslipidemia, for treatment of hyperlipidemia, for treatment of hypertension, for the treatment or prophylaxis of obesity, for lowering of food intake, for appetite regulation, for regulating feeding behaviour, or for enhancing the secretion of enteroincretins.
32. The pharmaceutical composition as defined in claim 30 or 31, wherein the composition is in a unit dosage form, comprising from about 0.05 mg to about 1000 mg, or from about 0.1 mg to about 500 mg, or from about 0.5 mg to about 200 mg of the compound.
33. Use of a compound as defined in any one of claims 1 to 25 for the treatment of metabolic disorders, for blood glucose lowering, for the treatment of hyperglycemia, for treatment of IGT, for treatment of syndrome X, for the treatment of impaired fasting glucose (IFG), for treatment of type 2 diabetes, for treatment of type 1 diabetes, for delaying the progression of impaired glucose tolerance (IGT) to type 2 diabetes, for delaying the progression of non-insulin requiring type 2 diabetes to insulin requiring type 2 diabetes, for treatment of dyslipidemia, for treatment of hyperlipidemia, for treatment of hypertension, for the treatment or prophylaxis of obesity, for lowering of food intake, for appetite regulation, for regulating feeding behaviour, or for enhancing the secretion of enteroincretins.
34. Use of a compound as defined in any one of claims 1 to 25 for the treatment of an indication selected from the group consisting of hyperglycemia, IGT, insulin resistance syndrome, syndrome X, type 2 diabetes, type 1 diabetes, dyslipidemia, hypertension and obesity.
CA2744893A 2002-06-27 2003-06-27 Aryl carbonyl derivatives as glucokinase activators Abandoned CA2744893A1 (en)

Applications Claiming Priority (9)

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