WO1999051231A1 - Antagonists of gonadotropin releasing hormone - Google Patents

Antagonists of gonadotropin releasing hormone Download PDF

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Publication number
WO1999051231A1
WO1999051231A1 PCT/US1999/006713 US9906713W WO9951231A1 WO 1999051231 A1 WO1999051231 A1 WO 1999051231A1 US 9906713 W US9906713 W US 9906713W WO 9951231 A1 WO9951231 A1 WO 9951231A1
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Prior art keywords
alkyl
substituted
aryl
compound
hydrogen
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PCT/US1999/006713
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French (fr)
Inventor
Thomas F. Walsh
Feroze Ujjainwalla
Mark T. Goulet
Jonathan R. Young
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Merck & Co., Inc.
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Priority claimed from GBGB9811286.5A external-priority patent/GB9811286D0/en
Application filed by Merck & Co., Inc. filed Critical Merck & Co., Inc.
Priority to JP2000542002A priority Critical patent/JP2002510628A/en
Priority to AU31178/99A priority patent/AU3117899A/en
Priority to EP99912919A priority patent/EP1067929A1/en
Priority to CA002325995A priority patent/CA2325995A1/en
Publication of WO1999051231A1 publication Critical patent/WO1999051231A1/en

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D519/00Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00Drugs for genital or sexual disorders; Contraceptives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00Drugs for genital or sexual disorders; Contraceptives
    • A61P15/08Drugs for genital or sexual disorders; Contraceptives for gonadal disorders or for enhancing fertility, e.g. inducers of ovulation or of spermatogenesis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P15/00Drugs for genital or sexual disorders; Contraceptives
    • A61P15/18Feminine contraceptives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P5/00Drugs for disorders of the endocrine system
    • A61P5/24Drugs for disorders of the endocrine system of the sex hormones

Definitions

  • the gonadotropin-releasing hormone also referred to as luteinizing hormone-releasing hormone (LHRH)
  • LHRH luteinizing hormone-releasing hormone
  • the hormone is released from the hypothalamus and acts on the pituitary gland to stimulate the biosynthesis and secretion of luteinizing hormone (LH) and follicle- stimulating hormone (FSH).
  • LH released from the pituitary gland is primarily responsible for the regulation of gonadal steroid production in both sexes, whereas FSH regulates spermatogenesis in males and follicular development in females.
  • GnRH agonists and antagonists have proven effective in the treatment of certain conditions which require inhibition of LH/FSH release.
  • GnRH-based therapies have proven effective in the treatment of endometriosis, uterine fibroids, polycystic ovarian disease, precocious puberty and several gonadal steroid-dependent neoplasia, most notably cancers of the prostate, breast and ovary.
  • GnRH agonists and antagonists have also been utilized in various assisted fertilization techniques and have been investigated as a potential contraceptive in both men and women.
  • the compounds of the invention may also be used in combination with bisphosphonates (bisphosphonic acids) and other agents, such as growth hormone secretagogues, for the treatment and the prevention of disturbances of calcium, phosphate and bone metabolism, in particular, for the prevention of bone loss during therapy with the GnRH antagonist, and in combination with estrogens, progesterones, antiestrogens, antiprogestins and/or androgens for the prevention or treatment of bone
  • a compound of the present invention may be co-administered with a 5a-reductase 2 inhibitor, such as finasteride or epristeride; a 5a-reductase 1 inhibitor such as 4,7b-dimethyl-4-aza-5a- cholestan-3-one, 3-oxo-4-aza-4,7b-dimethyl-16b-(4-chlorophenoxy)-5a- androstane, and 3-oxo-4-aza-4,7b-dimethyl-16b-(phenoxy)-5a-androstane as disclosed in WO 93/23420 and WO 95/11254; dual inhibitors of 5a- reductase 1 and 5a-reductase 2 such as 3-oxo-4-aza-17b-(2,5- trifluoromethylphenyl-carbamoyl)-5a-androstane as disclosed in WO 95/07927; antiandrogens such as flutamide, casodex and c
  • a compound of the present invention may be used in combination with growth hormone, growth hormone releasing hormone or growth hormone secretagogues, to delay puberty in growth hormone deficient children, which will allow them to continue to gain height before fusion of the epiphyses and cessation of growth at puberty.
  • a compound of the present invention may be used in combination or co-administered with a compound having luteinizing hormone releasing activity such as a peptide or natural hormone or analog thereof.
  • peptide compounds include leuprorelin, gonadorelin, buserelin, triptorelin, goserelin, nafarelin, histrelin, deslorelin, meterlin and recirelin.
  • a compound of the present invention may be used as described in U.S. Patent No. 5,824,286 which discloses the administration of peptide GnRH antagonists such as Antide and azaline B to premenopausal women to enhance the readability of mammographic film relative to a mammogram effected in the absence of the administration.
  • peptide GnRH antagonists such as Antide and azaline B
  • GnRH antagonists are GnRH-like decapeptides which are generally administered intravenously or subcutaneously presumably because of negligible oral activity. These have amino acid substitutions usually at positions one, two, three, six and ten.
  • Non-peptide GnRH antagonists offer the possible advantage of oral adminstration.
  • Non-peptide GnRH antagonists have been described in European Application 0 219 292 and in De, B. et al., J. Med. Chem., 32, 2036-2038 (1989), in WO 95/28405, WO 95/29900 and EP 0679642 all to Takeda Chemical Industries, Ltd.
  • Substituted indoles known in the art include those described in the following patents and patent applications.
  • US Patent No. 5,030,640 discloses alpha-heterocyclic ethanol aminoalkyl indoles which are potent ⁇ -agonists.
  • US Patent No. 4,544,663 discloses indolamine derivatives which are allegedly useful as male anti-fertility agents.
  • WO 90/05721 discloses alpha-amino-indole-3-acetic acids useful as anti-diabetic, anti-obesity and anti-atherosclerotic agents.
  • French patent 2,181,559 discloses indole derivatives with sedative, neuroleptic, analgesic, hypotensive, antiserotonin and adrenolytic activity.
  • Belgian patent 879381 discloses 3-aminoalkyl-lH-indole-5-thioamide and carboxamide derivatives as cardiovascular agents used to treat hypertension, Raynaud's disease and migraine.
  • U.S. Patent Nos. 5,756,507, 5,780,437 and 5,849,764 also disclose substituted arylindoles as non-peptide antagonists of GnRH.
  • the present invention relates to compounds which are non-peptide antagonists of GnRH which can be used to treat a variety of sex-hormone related conditions in men and women, to methods for their preparation, and to methods and pharmaceutical compositions containing said compounds for use in mammals.
  • the compounds of the present invention are useful to treat a variety of sex-hormone related conditions in both men and women. These conditions include endometriosis, uterine fibroids, polycystic ovarian disease, hirsutism, precocious puberty, gonadal steroid- dependent neoplasias such as cancers of the prostate, breast and ovary, gonadotrophe pituitary adenomas, sleep apnea, irritable bowel syndrome, premenstrual syndrome and benign prostatic hypertophy.
  • the compounds of the invention are also useful as an adjunct to treatment of growth hormone deficiency and short stature, and for the treatment of systemic lupus erythematosis.
  • the compounds of the invention may be useful in in vitro fertilization and as contraceptives.
  • the compounds may also be useful in combination with androgens, estrogens, progesterones, antiestrogens and antiprogestogens for the treatment of endometriosis, fibroids and in contraception. They may also be useful in combination with testosterone or other androgens or antiprogestogens in men as a contraceptive.
  • the compounds may also be used in combination with an angiotensin-converting enzyme inhibitor such as Enalapril or Captopril, an angiotensin Il-receptor antagonist such as Losartan or a renin inhibitor for the treatment of uterine fibroids.
  • an angiotensin-converting enzyme inhibitor such as Enalapril or Captopril
  • an angiotensin Il-receptor antagonist such as Losartan or a renin inhibitor
  • the compounds of the invention may also be used in combination with bisphosphonates (bisphosphonic acids) and other agents, for the treatment and the prevention of disturbances of calcium, phosphate and bone metabolism, in particular, for the prevention of bone loss during therapy with the GnRH antagonist, and in combination with estrogens, progesterones and/or androgens for the prevention or treatment of bone loss or hypogonadal symptoms such as hot flashes during therapy with the GnRH antagonist.
  • a compound of the present invention may be co-administered with a 5a-reductase 2 inhibitor, such as finasteride or epristeride; a 5a-reductase 1 inhibitor such as 4,7b-dimethyl-4-aza-5a- cholestan-3-one, 3-oxo-4-aza-4,7b-dimethyl-16b-(4-chlorophenoxy)-5a- androstane, and 3-oxo-4-aza-4,7b-dimethyl-16b-(phenoxy)-5a-androstane as disclosed in WO 93/23420 and WO 95/11254; dual inhibitors of 5a- reductase 1 and 5a-reductase 2 such as 3-oxo-4-aza-17b-(2,5- trifluoromethylphenyl-carbamoyl)-5a-androstane as disclosed in WO 95/07927; antiandrogens such as flutamide, casodex and c
  • a compound of the present invention may be used in combination with growth hormone, growth hormone releasing hormone or growth hormone secretagogues, to delay puberty in growth
  • a compound of the present invention may be used in combination or co-administered with a compound having luteinizing hormone releasing activity such as a peptide or natural hormone or analog thereof.
  • a compound having luteinizing hormone releasing activity such as a peptide or natural hormone or analog thereof.
  • peptide compounds include leuprorelin, gonadorelin, buserelin, triptorelin, goserelin, nafarelin, histrelin, deslorelin, meterlin and recirelin.
  • a compound of the present invention may be used as described in U.S. Patent No. 5,824,286 which discloses the administration of peptide GnRH antagonists such as Antide and azaline B to premenopausal women to enhance the readability of mammographic film relative to a mammogram effected in the absence of the administration.
  • peptide GnRH antagonists such as Antide and azaline B
  • the present invention relates to compounds of the general formula
  • A is Ci-C ⁇ alkyl, substituted CI-CQ alkyl, C3-C7 cycloalkyl, substituted C3-C7 cycloalkyl, C3-C6 alkenyl, substituted C3-C6 alkenyl, C3-C6 alkynyl, substituted C3-C6 alkynyl, C1-C6 alkoxy, or C0-C5 alkyl-S(O) n -Co-C5 alkyl, C0-C5 alkyl- O-C0-C5 alkyl, C0-C5 alkyl-NR]_8-Co-C5 alkyl where R]_8 and the C0-C5 alkyl can be joined to form a ring, ⁇ ⁇ N-(CH 2 ) p -
  • R ⁇ is hydrogen, C1-C6 alkyl, substituted Ci-C ⁇ alkyl, wherein the substituents are as defined below; aryl, substituted aryl, aralkyl or substituted aralkyl, wherein the substituents are as defined for R3, R4 and R5.
  • R2 is hydrogen, Ci-C ⁇ alkyl, substituted Ci-C ⁇ alkyl, aralkyl, substituted aralkyl, aryl, substituted aryl, alkyl -ORn,
  • R7 is hydrogen, C1-C6 alkyl, or substituted C1-C6 alkyl, unless X is hydrogen or halogen, then R7 is absent;
  • R8 is hydrogen, C(O)OR9, C(0)NRnRi2, NR11R12, C(O)Rn,
  • NRi2C(0)Rn NRi2C(O)NRnRi2, NRi2S(O) 2 Rll, NRi2S(O)2NRnRi2, OC(0)Rn, OC(0)NRnRi2, ORn,
  • R9 and R9a are independently hydrogen, C1-C6 alkyl, substituted Ci-C ⁇ alkyl; aryl or substituted aryl, aralkyl or substituted aralkyl when m ⁇ O; or
  • RlO and RlOa taken together form a carbocyclic ring of 3-7 atoms or ;
  • R9 and RlO taken together form a carbocyclic ring of 3-7 carbon atoms or a heterocyclic ring containing one or more heteroatoms when m ⁇ O; or
  • R9 and R2 taken together form a heterocyclic ring containing 3-7 carbon atoms and one or more heteroatoms when m ⁇ O; or
  • RlO and R2 taken together form a heterocyclic ring containing 3-7 carbon atoms and one or more heteroatoms;
  • RlO and A taken together form a heterocyclic ring containing 3-7 carbon atoms and one or more heteroatoms; or
  • Rll and R12 are independently hydrogen , C1-C6 alkyl, substituted C1-C6 alkyl, aryl, substituted aryl, aralkyl, substituted aralkyl, a carbocyclic ring of 3-7 atoms or a substituted carbocyclic ring containing 3-7 atoms; Rll and R12 taken together can form an optionally substituted ring of 3-7 atoms; Rl3 is hydrogen, OH, NR7R8, NRnSO2(Ci-C6 alkyl),
  • Rl4 and R15 are independently hydrogen, C1-C6 alkyl, substituted Cl-C ⁇ alkyl, C2-C6 alkenyl, substituted C2-C6 alkenyl, CN, nitro, C1-C3 perfluoroalkyl, C1-C3 perfluoroalkoxy, aryl, substituted aryl, aralkyl, substituted aralkyl, RnO(CH2)p-, RllC(0)0(CH2)p-, RllOC(O)(CH 2 ) p -, -(CH 2 )pS(O) n Rl7,
  • R17 is hydrogen, Ci-C ⁇ alkyl, C1-C3 perfluoroalkyl, aryl or substituted aryl
  • Rl6 is hydrogen, Ci-C ⁇ alkyl, substituted C1-C6 alkyl, or
  • Ri8 is hydrogen, C1-C6 alkyl, substituted C1-C6 alkyl, C(O)OR9,
  • C(0)NRnRi2, C(0)Rn, S(O) n Rll; Rl9 is either the definition of R13 or R14;
  • X is hydrogen, halogen, N, O, S(0) n , C(O), (CRnRi2) P ; C2-C6 alkenyl, substituted C2-C6 alkenyl,C2-C ⁇ alkynyl, or substituted C2-C6 alkynyl; when X is hydrogen or halogen,
  • R7 and R ⁇ are absent; when X is O, S(O)n, C(O), or CR11R12 only R7 or Rs is possible; Z is O, S, or NR11; m is 0-3; n is 0-2; p is 0-4; and the alkyl, alkenyl and alkynyl substituents are selected from C1-C6 alkyl, C3-C7 cycloalkyl, aryl, substituted aryl, aralkyl, substituted aralkyl, hydroxy, oxo, cyano, C1-C6 alkoxy, fluoro, C(O)ORn ) aryl C1-C3 alkoxy, substituted aryl C1-C3 alkoxy, and the aryl substituents are as defined for R3, R4 and R5; or a pharmaceutically acceptable addition salt and/or hydrate thereof, or where applicable, a geometric or optical isomer or racemic mixture thereof.
  • alkyl is intended to include both branched- and straight-chain saturated aliphatic hydrocarbon groups having the specified number of carbon atoms, e.g., methyl (Me), ethyl (Et), propyl, butyl, pentyl, hexyl, heptyl, octyl, nonanyl, decyl, undecyl, dodecyl, and the isomers thereof such as isopropyl (i-Pr), isobutyl (i-Bu), secbutyl (s-Bu), tertbutyl (t-Bu), isopentane, isohexane, etc.
  • aryl includes phenyl and naphthyl. In a preferred embodiment, aryl is phenyl.
  • halogen or halo is intended to include fluorine, chlorine, bromine and iodine.
  • composition is intended to encompass a product comprising the specified ingredients in the specified amounts, as well as any product which results, directly or indirectly, from combination of the specified ingredients in the specified amounts
  • connecting group A can be bonded to any of the available carbon or heteroatoms of the heteroaromatic groups Rl, including both rings of the benzo-fused heterocyclic groups and, likewise, R13, R14, and R15 can be bonded to any of the available carbon atoms of the heteroaromatic groups Ri.
  • optical isomeric forms that is mixtures of enantiomers or diasteromers, e.g., racemates, as well as individual enantiomers or diastereomers of the instant compound are included.
  • These individual enantiomers are commonly designated according to the optical rotation they effect by the symbols (+) and (-), (L) and (D), (1) and (d) or combinations thereof.
  • These isomers may also be designated according to
  • the individual optical isomers may be prepared using conventional resolution procedures, e.g., treatment with an appropriate optically active acid, separating the diastereomers and then recovering the desired isomer.
  • the individual optical isomers may be prepared by asymmetric synthesis.
  • a given chemical fomula or name shall encompass pharmaceuticaly acceptable addition salts thereof and solvates thereof, such as hydrates.
  • the compounds of the present invention while effective themselves, may be formulated and administered in the form of their pharmaceutically acceptable addition salts for purposes of stability, convenience of crystallization, increased solubility and other desirable properties.
  • the compounds of the present invention may be administered in the form of pharmaceutically acceptable salts.
  • pharmaceutically acceptable salt is intended to include all acceptable salts
  • acid salts are hydrochloric, nitric, sulfuric, phosphoric, formic, acetic, trifluoroacetic, propionic, maleic, succinic, malonic, methanesulfonic, benzenesulfonic and the like which can be used as a dosage form for modifying the solubility or hydrolysis characteristics or can be used in sustained release or pro-drug formulations.
  • salts of the compounds of this invention include those formed from cations such as sodium, potassium, aluminum, calcium, lithium, magnesium, zinc, and from bases such as ammonia, ethyl enediamine, N-m ethyl - glutamine, lysine, arginine, ornithine, choline, N,N'- dibenzylethylenediamine, chloroprocaine, diethanolamine, procaine, N- benzylphenethylamine, diethylamine, piperazine, tris(hydroxymethyl) aminomethane, and tetramethylammonium hydroxide.
  • bases such as ammonia, ethyl enediamine, N-m ethyl - glutamine, lysine, arginine, ornithine, choline, N,N'- dibenzylethylenediamine, chloroprocaine, diethanolamine, procaine, N- benzylphenethylamine, diethy
  • esters can be employed, e.g. methyl, ethyl, butyl, acetate, maleate, pivaloyloxymethyl, and the like, and those esters known in the art for modifying solubility or hydrolysis characteristics for use as sustained release or prodrug formulations.
  • the compounds of the present invention may have chiral centers other than those centers whose stereochemistry is depicted in formula I, and therefore may occur as racemates, racemic mixtures and as individual enantiomers or diastereomers, with all such isomeric forms being included in the present invention as well as mixtures thereof.
  • crystalline forms for compounds of the present invention may exist as polymorphs and as such are intended to be included in the present invention.
  • some of the compounds of the instant invention may form solvates with water or common organic solvents. Such solvates are encompassed within the scope of this invention.
  • a preferred method for the synthesis of the substituted tryptamines described in this invention utilizes a palladium-catalyzed cross coupling reaction as a key step as shown in Scheme A.
  • This 7- azaindole synthesis involves the reaction of a suitably functionalized 3- iodo-2-aminopyridine (1) with substituted acetylenes such as 2 in the presence of a base like sodium carbonate, lithium chloride, and a palladium catalyst such as (dppf)PdCl 2 *CH 2 Cl 2 .
  • the reaction is conducted in an inert organic solvent such as dimethylformamide at elevated temperatures, for instance at 100°C, and the reaction is conducted for a period of about 30 minutes to about 24 hours.
  • the acetylene utilized in this reaction may be a terminal acetylene (2a) or be optionally substituted on the terminal carbon atom with a substituent Z (2b, 2c).
  • the substituent abbreviated PG j indicates an alcohol protecting group such as a benzyl ether, tert-hu yl ether or the
  • the nature of the Z substituent determines the distribution of the 7- azaindole isomers (3 and 4) produced in the reaction. For example, if the substituent Z on the acetylene is a hydrogen atom then the isomer 4a is the major product of the reaction. When the substituent Z is chosen to be a substituted silyl group such as trimethylsilyl, triethylsilyl (as shown), or the like, then isomer 3b is formed almost exclusively. When Z is a substituted aryl group, then both isomers 3c and 4c may be formed and the product mixture is separated using chromatographic or crystallization techniques to afford the individual isomers.
  • Scheme B illustrates the preparation of substituted 3- iodo-2-aminopyridines (1) which are utilized in the Larock 7-azaindole synthesis described in Scheme A.
  • the 3-iodo-2-aminopyri dines (1) may be prepared in several ways described in the literature of organic synthesis.
  • a preferred method involves the or ⁇ /io-iodination of substituted 2-aminopyridine derivatives of general formula 9 with an electrophilic iodination reagent such as iodine, iodine monochloride, N-iodosuccinimide or the like.
  • 2-aminopyridine derivatives such as 9 may be commercially available or alternatively they may be prepared using methodologies known in organic chemistry. For instance, application of methodology reported by Wachi and Terada (Wachi, K.; Terada, A. Chem. Pharm. Bull. 1980, 28, 465) allows the conversion of pyridines of general formula 5 to 2-aminopyridines of general formula 9 as shown at the top of Scheme B. In this synthetic transformation, a substituted pyridine (5) is first converted to the corresponding N-oxide (6) with a suitable oxidant such as eto-chloroperbenzoic acid.
  • a suitable oxidant such as eto-chloroperbenzoic acid.
  • the substituted pyridine iV-oxide 6 is reacted with 4-chloro-2,2-dimethyl- 2H-l,3-benzoxazine (7) in an inert high boiling solvent such as 1,2- dichloroethane.
  • An adduct initially formed in this reaction undergoes a thermal rearrangement and the ⁇ T-pyridyl substituted 4-oxo-4H-l,3- benzoxazine 8 is produced.
  • the substituted benzoxazine 8 is hydrolyzed with concentrated hydrochloric acid at elevated temperature to afford the substituted 2-aminopyridines of general formula 9.
  • Acetylenic compounds of general structure 2 are prepared using one of several methods depending upon the choice of the desired substituents.
  • substituents R 9 , R 9a , R 10 and R 10a are selected to be hydrogen or lower alkyl groups
  • compounds of formula 2 may be prepared from known acetylenic alcohols such as 3-butyn-l-ol, 4-pentyn- 2-ol or similar acetylenic alcohols reported in the chemical literature.
  • the conversion of acetylenic alcohols of general formula 10 to acetylene derivatives of general formula 2 is shown in Scheme C.
  • the hydroxyl protecting group (PG j ) illustrated in Scheme C is exemplified as an O-benzyl ether.
  • reaction of 10 with O-benzyl-2,2,2- trichloroacetimidate in the presence of a catalytic amount of a strong acid such as trifluoromethanesulfonic acid and in a suitable inert
  • acetylenes (2b) of general formula 2 wherein Z is a trialkylsilyl group by deprotonation of the acetylene with a base such as /z-butyllithium in an inert organic solvent like tetrahydrofuran followed by reaction with a trialkylsilyl chloride such as triethylchlorosilane.
  • the deprotonation and silylation reactions are generally conducted at low temperatures, for instance between about -78°C and room temperature, and after standard workup and purification a silylacetylene of formula 2b is obtained.
  • acetylenes of general formula 2c wherein Z is an aryl or substituted aryl group are also useful in the 7- azaindole synthesis illustrated in Scheme A.
  • Arylacetylenes 2c may be prepared using a coupling reaction of cuprous acetylides derived from acetylenic alcohols of formula 2a with various aryl halides or aryl triflates (11). Such coupling reactions produce aryl acetylenes of general formula 12 as shown at the bottom of Scheme C.
  • acetylenic compounds of general formula 2a employs an ethynylation reaction sequence of aldehydes of general formula 16 as shown in Scheme D.
  • the aldehydes (16) used in the ethynylation sequence may be prepared using various methods known in organic synthesis starting with hydroxyesters of general formula 13, from protected hydroxyesters of formula 14, or from alcohols related to the mono-hydroxyl protected diols of formula 15. The choice of preferred starting material depends upon the nature of the substituents R 9 , R 9a , R 10 , and R 10a selected. Scheme D illustrates this strategy begining with the generalized hydroxy ester 13.
  • the ester group of compounds of formula 14 can then be converted to an aldehyde of formula 16 either directly using a reagent like diisobutylaluminum hydride in a solvent like toluene, or through a two step process. In the two step process, reduction of the ester group with a reagent such as
  • lithium aluminum hydride in tetrahydrofuran affords alcohols of formula 15 which are then subjected to reoxidation, for instance using a Swern-Moffatt oxidation, to afford the desired aldehydes of formula 16.
  • aldehydes of formula 16 The ethynylation of aldehydes of formula 16 is accomplished in two steps. First, aldehydes (16) are reacted with carbon tetrabromide and triphenylphosphine in an inert organic solvent like dichloro- methane to produce the dibromo olefins of formula 17. Next, the dibromo olefins (17) are treated with two equivalents of a strong base such as tt-butyllithium in tetrahydrofuran at low temperature, for instance at about -78°C.
  • a strong base such as tt-butyllithium in tetrahydrofuran at low temperature, for instance at about -78°C.
  • the strong base induces dehydrohalogenation and metal- halogen exchange to afford lithium acetylides which upon quenching and workup afford acetylenes of general formula 2a.
  • the intermediate lithium acetylides formed in the reaction may be treated with a trialkylsilyl chloride, such as triethylchlorosilane, to afford silylacetylenes of general formula 2b.
  • the conversion of 2-silyl-substituted 7-azaindoles of general formula 3b to 2-aryl-substituted 7-azaindoles of general formula 3c may be accomplished in two steps as shown in Scheme E.
  • the first step is a
  • the second step is a palladium-catalyzed cross coupling reaction of the 2-halo-7-azaindole 18 with a suitable aryl or substituted aryl organometallic reagent 19.
  • Scheme E illustrates this process with an aryl or substituted arylboronic acid as the organometallic reagent, however, other organometallic reagents known to participate in palladium-catalyzed cross-coupling reactions such as arylboronic esters or arylstannanes may also be employed.
  • a 2-iodo-7- azaindole of general formula 18 is coupled with a generalized boronic acid (19) using a catalyst such as [l,l'-bis(diphenylphosphino)ferrocene] dichloropalladium(II) complex with dichloromethane (shown), tetrakis (triphenylphosphine)-palladium(O) or the like.
  • a catalyst such as [l,l'-bis(diphenylphosphino)ferrocene] dichloropalladium(II) complex with dichloromethane (shown), tetrakis (triphenylphosphine)-palladium(O) or the like.
  • the reaction is usually conducted at temperatures between room temperature and about 100 °C, for instance at about 80°C.
  • This palladium catalyzed cross-coupling reaction may be effected using various combinations of palladium catalysts and solvent compositions known in organic chemistry, and the selection of the conditions is made depending upon the type of organometallic reagent (19) used and the identity of the substituent groups in the two starting materials.
  • organometallic reagent is a boronic acid or boronate ester
  • a preferred solvent mixture consists of toluene, ethanol and an aqueous solution of a base like cesium or sodium carbonate.
  • the organometallic reagent 19 is an arylstannane, then no additional base is required, and a polar aprotic solvent such as tetrahydrofuran or dimethylformamide is employed.
  • R 10 R 10 a imidazole, CH 2 Cl 2 rt, 1-24 h
  • the hydroxyl protecting group (PG j ) is anO-benzyl ether as illustrated previously in Schemes C and D
  • the 7-azaindole may be protected as a carbamate derivative such as a er -butylcarbamate (BOC).
  • BOC er -butylcarbamate
  • the BOC-protected 7-azaindole is stable under the hydrogenolysis conditions which are used to remove the O-benzyl ether and it may be conveniently removed at the end of the synthesis using acidic conditions. If it is desired to synthesize compounds of formula (I) wherein R 0 is alkyl, substituted alkyl or the like, then it is possible to introduce that substituent at this point and the use of a protecting group and its subsequent removal is not required.
  • An alcohol of general formula 21 may be converted to a primary amine of general formula 23 using a variety of methods known in the literature of organic chemistry.
  • the bottom of Scheme F illustrates a process where the alcohol 21 is first converted to an azide of general formula 22, followed by reduction to afford the amine derivative 23.
  • the synthesis of an azide of general formula 22 from alcohols like 21 is best accomplished by performing a Mitsunobu reaction in the presence of an appropriate azide source such as diphenylphosphoryl azide or zinc azide pyridine complex.
  • Scheme F illustrates the reaction of alcohol 21 with triphenylphosphine, diethylazodicarboxylate, zinc azide pyridine complex and a proton source such as imidazole in an inert solvent like methylene chloride or tetrahydrofuran.
  • the reaction is usually conducted at room temperature for periods between 1-24 hours, typically overnight or about 15 hours, and affords the azide of general formula 22 in good yield.
  • an azide of formula 22 may then be reduced to an amine of formula 23 using one of several methods common in organic synthesis.
  • One preferred method is catalytic hydrogenation in a solvent like methanol or ethanol in the presence of a catalyst such as 10% palladium on carbon.
  • azides like 22 may be reacted with triphenylphosphine to form an iminophosphorane which upon hydrolysis with water affords the amine of formula 23 and triphenylphophine oxide.
  • the final stage of the synthesis of the novel 7-azaindole derivatives (I) involves elaboration of the sidechain at the C-3 position of the 7-azaindole core.
  • One method for the completion of the synthesis is illustrated in Scheme G.
  • the 2-aryltryptamine (23) may be condensed with a carboxylic acid of type 24 using the coupling reagent l-(3-dimethylamino-propyl)-3-ethylcarbodiimide hydrochloride (EDC), 1,3-dicyclohexyl-carbodiimide (DCC) or the like with or without 1- hydroxybenzotriazole (HOBt) and a tertiary amine base such as N- methylmorpholine (NMM), triethylamine or the like in an inert organic solvent such as methylene chloride, chloroform, dimethylformamide, or mixtures thereof at or near room temperature for a period of 3-24 hours to provide the corresponding amide
  • 2- aryltryptamine 23 can be treated with an active ester or acid chloride of formula 26 in an inert organic solvent such as methylene chloride, chloroform, tetrahydrofuran, diethyl ether, or the like and a tertiary amine base such as triethylamine, diisopropylethylamine, pyridine or the like at a temperature of 0°-25°C for 30 minutes to 4 hours to give compound 25.
  • an inert organic solvent such as methylene chloride, chloroform, tetrahydrofuran, diethyl ether, or the like
  • a tertiary amine base such as triethylamine, diisopropylethylamine, pyridine or the like
  • the amide carbonyl of 25 can be reduced by treatment with borane, lithium aluminum hydride, or equivalent hydride sources in an inert organic solvent such as tetrahydrofuran, diethyl ether, 1,4-dioxane or the like at about 25° to about 100°C, preferably about 65°C, for a period of 1-8 hours to give the corresponding amine 27.
  • borane, lithium aluminum hydride, or equivalent hydride sources in an inert organic solvent such as tetrahydrofuran, diethyl ether, 1,4-dioxane or the like at about 25° to about 100°C, preferably about 65°C, for a period of 1-8 hours to give the corresponding amine 27.
  • the 2-aryltryptamine 23 can be modified by treatment with an aldehyde or ketone of type 28 in the presence of a weak acid such as trifluoroacetic acid (TFA), acetic acid or the like, with or without a dessicant such as 3A molecular sieves or magnesium sulfate, and a hydride source such as sodium borohydride or sodium cyanoborohydride, in an inert organic solvent such as methanol, ethanol, isopropanol, tetrahydrofuran, dichloromethane,
  • a weak acid such as trifluoroacetic acid (TFA), acetic acid or the like
  • a dessicant such as 3A molecular sieves or magnesium sulfate
  • a hydride source such as sodium borohydride or sodium cyanoborohydride
  • the tryptamine 23 can be modified using the Fukuyama modification of the Mitsunobu reaction (Fukuyama, T.; Jow, C.-K.; Cheung, M. Tetrahedron Lett. 1995, 36, 6373- 74).
  • the tryptamine 23 may be reacted with an arylsufonyl chloride such as 2-nitrobenzene-sulfonyl chloride, 4-nitrobenzenesulfonyl chloride or 2,4-dinitrobenzene-sulfonyl chloride and a hindered amine base such as 2,4,6-collidine, 2,6-lutidine or the like in an inert organic solvent such as methylene chloride to provide the corresponding sulfonamide 30.
  • an arylsufonyl chloride such as 2-nitrobenzene-sulfonyl chloride, 4-nitrobenzenesulfonyl chloride or 2,4-dinitrobenzene-sulfonyl chloride and a hindered amine base such as 2,4,6-collidine, 2,6-lutidine or the like
  • an inert organic solvent such as methylene chloride
  • the sulfonamides can be further modified by reaction with an alcohol of type 31 in the presence of triphenylphosphine and an activating agent such as diethylazodicarboxylate (DEAD), diisopropylazodicaboxylate or the like in an inert organic solvent such as benzene, toluene, tetrahydrofuran or mixtures thereof to give the dialkylsulfonamide adduct. Removal of a dinitrobenzenesulfonyl group is accomplished by treatment
  • nucleophilic amine such as rc-propylamine or the like in an inert organic solvent such as methylene chloride to give secondary amines of type 32.
  • an inert organic solvent such as methylene chloride
  • the removal of the sulfonamide is accomplished with a more nucleophilic reagent such as thiophenol or mercaptoacetic acid in combination with lithium hydroxide in DMF.
  • Reaction Scheme K illustrates a method that is complimentary to reaction Scheme J for completing the synthesis of the novel compounds of formula (I).
  • Scheme K also employs the Fukuyama modification of the Mitsunobu reaction similar to that illustrated in reaction Scheme J.
  • the alcohol partner employed is a 2-aryltryptophol of general formula 21 which has been decribed previously in reaction Scheme F.
  • the 2-aryltryptophol (21) is reacted with a substituted sulfonamide of general formula 33, triphenylphosphine and diethylazodicarboxylate in a suitable inert organic solvent such as benzene, tetrahydrofuran, 1,4-dioxane or the like.
  • the reaction is generally conducted at room temperature for a
  • the product is an N,N-disubstituted sulfonamide which is then separately subjected to reaction with a base such as n-propylamine which removes the sulfonamide substituent and furnishes a secondary amine related to formula 32.
  • the sulfonamides of formula 33 employed are readily obtained from a primary amine and either 2-nitrobenzenesulfonyl chloride, 4-nitrobenzenesulfonyl chloride or 2,4-dinitrobenzenesuTfonyl chloride (as shown) in the presence of a hindered amine base such as 2,4,6-collidine, 2,6-lutidine or the like in an inert organic solvent such as methylene chloride.
  • the final stage of the synthesis requires removal of the protecting group on the 7-azaindole nitrogen atom (PG 2 ) which produces a compound of general formula 32 wherein R 0 is a hydrogen atom.
  • PG 2 7-azaindole nitrogen atom
  • the compounds of the present invention are useful in the treatment of various sex-hormone related conditions in men and women. This utility is manifested in their ability to act as antagonists of the neuropeptide hormone GnRH as demonstrated by activity in the following in vitro assays.
  • the ligand binding assay is conducted with the human GnRH receptor (hGnRHR) obtained from CHO-Kl cells stably expressing the cloned receptor. Crude membrane suspensions are prepared from large batches of hGnRHR-CHO-Kl cells and stored as aliquots at -80° C .
  • the radioactive peptide ligand [5-( 1 5 Iodo-Tyr)-Buserelin] is obtained from Woods Assays (Portland, Oregon) and has a radioactive specific activity of 1000 Ci/mmol.
  • the membranes and the radioligand are diluted in assay buffer which consists of 50 mM Tris-HCl (pH 7.5), 2 mM MgCl 2 and 0.1% bovine serum albumin.
  • assay buffer which consists of 50 mM Tris-HCl (pH 7.5), 2 mM MgCl 2 and 0.1% bovine serum albumin.
  • the ligand binding assay is performed at 22°C for 1 hour in 96-well polypropylene plates in a final volume of 200 ul. Each well in the assay plate contains 0.1 nM 125 I-
  • Chinese hamster ovary cell lines expressing the human GnRH receptor functionally coupled to phospholipase C were established and seeded at a concentration of 60,000 cells/mL/well in inositol-free F12 medium containing 10% dialyzed fetal bovine serum, 1% Pen/Strep, 2 mM glutamine, 500 ⁇ g/mL G418 and 1 ⁇ Ci ( 3 H)inositol in 24-well tray. Forty-eight hours after seeding, cells were washed with 3 x 1 L of PBS containing 10 mM LiCl and treated with various concentrations of GnRH antagonist for 2 hrs at 37°C before the addition of 0.5 nM GnRH.
  • the compounds of formula I are useful in a number of areas affected by GnRH. They may be useful in sex-hormone related conditions, sex-hormone dependent cancers, benign prostatic hypertrophy or myoma of the uterus. Sex-hormone dependent cancers which may benefit from the administration of the compounds of this invention include prostatic cancer, uterine cancer, breast cancer and pituitary gonadotrophe adenomas. Other sex-hormone dependent conditions which may benefit from the administration of the compounds of this invention include endometriosis, polycystic ovarian disease, uterine fibroids and precocious puberty. The compounds may also be used in
  • angiotensin-converting enzyme inhibitor such as Enalapril or Captopril
  • an angiotensin H-receptor antagonist such as Losartan or a renin inhibitor for the treatment of uterine fibroids.
  • the compounds of the invention may also be useful for controlling pregnancy, as a contraceptive in both men and women, for in vitro fertilization, in the treatment of premenstrual syndrome, in the treatment of lupus erythematosis, in the treatment of hirsutism, in the treatment of irritable bowel syndrome and for the treatment of sleep disorders such as sleep apnea.
  • a further use of the compounds of this invention is as an adjunct to growth hormone therapy in growth hormone deficient children.
  • the compounds may be administered with growth hormone or a compound which increases the endogenous production or release of growth hormone.
  • Certain compounds have been developed which stimulate the release of endogenous growth hormone.
  • Peptides which are known to stimulate the release of endogenous growth hormone include growth hormone releasing hormone, the growth hormone releasing peptides GHRP-6 and GHRP-1 (described in U.S. Patent No. 4,411,890, PCT Patent Pub. No. WO 89/07110, and PCT Patent Pub. No. WO 89/07111) and GHRP-2 (described in PCT Patent Pub. No.
  • Representative preferred growth hormone secretagoues employed in the present combination include the following:
  • the compounds of the invention may also be used in combination with bisphosphonates (bisphosphonic acids) and other agents, such as growth hormone secretagogues, for the treatment and the prevention of disturbances of calcium, phosphate and bone metabolism, in particular, for the prevention of bone loss during therapy with the GnRH antagonist , and in combination with estrogens, progesterones and or androgens for the prevention or treatment of bone loss or hypogonadal symptoms such as hot flashes during therapy with the GnRH antagonist.
  • bisphosphonates bisphosphonic acids
  • other agents such as growth hormone secretagogues
  • Bisphosphonates (bisphosphonic acids) are known to inhibit bone resorption and are useful for the treatment of bone lithiasis as disclosed in U.S. Patent 4,621,077 to Rosini, et al.
  • the literature discloses a variety of bisphosphonic acids which are useful in the treatment and prevention of diseases involving bone resorption. Representative examples may be found in the following: U.S. Patent No. 3,251,907; U.S. Patent No. 3,422,137; U.S.
  • Patent No. 4,578,376 U.S. Patent No. 4,621,077; U.S. Patent No. 4,624,947; U.S. Patent No. 4,746,654; U.S. Patent No. 4,761,406; U.S. Patent No.
  • bisphosphonates are selected from the group of the following compounds: alendronic acid, etidrononic acid, clodronic acid, pamidronic acid, tiludronic acid, risedronic acid, 6-amino-l- hydroxy-hexylidene-bisphosphonic acid, and 1-hydroxy- 3(methylpentylamino)-propylidene-bisphosphonic acid; or any pharmaceutically acceptable salt thereof.
  • a particularly preferred bisphosphonate is alendronic acid (alendronate), or a pharmaceutically acceptable salt thereof.
  • An especially preferred bisphosphonate is alendronate sodium, including alendronate sodium trihydrate. Alendronate sodium has received regulatory approval for marketing in the United States under the trademark FOSAMAX®.
  • a compound of the present invention may be co-administered with a 5 ⁇ -reductase 2 inhibitor, such as finasteride or epristeride; a 5 ⁇ -reductase 1 inhibitor such as 4,7 ⁇ -dimethyl-4-aza-5 ⁇ - cholestan-3-one, 3-oxo-4-aza-4,7 ⁇ -dimethyl-16 ⁇ -(4-chlorophenoxy)-5 ⁇ - androstane, and 3-oxo-4-aza-4,7 ⁇ -dimethyl-16 ⁇ -(phenoxy)-5 ⁇ -androstane as disclosed in WO 93/23420 and WO 95/11254; dual inhibitors of 5 ⁇ - reductase 1 and 5 ⁇ -reductase 2 such as 3-oxo-4-aza-17 ⁇ -(2,5- trifluoromethylphenyl-carbamoyl)-5 ⁇ -androstane as disclosed in WO 95/07927; antiandrogens such as flutamide, casodex and c
  • a compound of the present invention may be used in combination with growth hormone, growth hormone releasing hormone or growth hormone secretagogues, to delay puberty in growth hormone deficient children, which will allow them to continue to gain height before fusion of the epiphyses and cessation of growth at puberty. Further, a compound of the present invention may be
  • a compound having luteinizing hormone releasing activity such as a peptide or natural hormone or analog thereof.
  • peptide compounds include leuprorelin, gonadorelin, buserelin, triptorelin, goserelin, nafarelin, histrelin, deslorelin, meterlin and recirelin.
  • the active agents may be administered separately or in conjunction.
  • the administration of one element may be prior to, concurrent to, or subsequent to the administration of the other agent.
  • compositions containing the active ingredient may be in a form suitable for oral use, for example, as tablets, troches, lozenges, aqueous or oily suspensions, dispersible powders or granules, emulsions, hard or soft capsules, or syrups or elixirs.
  • Compositions intended for oral use may be prepared according to any method known to the art for the manufacture of pharmaceutical compositions 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 contain the active ingredient in admixture with non-toxic pharmaceutically acceptable excipients which are suitable for the manufacture of tablets.
  • 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.
  • a time delay material such as glyceryl monostearate or glyceryl distearate may be employed. They may also be coated by the technique described in the U.S. Patent 4,256,108; 4,166,452; and 4,265,874 to form osmotic therapeutic tablets for control release.
  • Formulations for oral use may also be presented as hard gelatin capsules wherein the active ingredient is mixed with an inert solid diluent, for example, calcium carbonate, calcium phosphate or kaolin, or as soft gelatin capsules wherein the active ingredient is mixed with water or an oil medium, for example peanut oil, liquid paraffin, or olive oil.
  • an inert solid diluent for example, calcium carbonate, calcium phosphate or kaolin
  • water or an oil medium for example peanut oil, liquid paraffin, or olive oil.
  • Aqueous suspensions contain the active material in admixture with excipients suitable for the manufacture of aqueous suspensions.
  • excipients are suspending agents, for example sodium carboxymethyl-cellulose, methylcellulose, hydroxy-propylmethy- cellulose, sodium alginate, polyvinyl-pyrrolidone, gum tragacanth and gum acacia; dispersing or wetting agents may be a naturally-occurring phosphatide, for example 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 heptadecaethylene-oxycetanol, 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 acids and hexitol anhydrides, for example polyethylene
  • the aqueous suspensions may also contain one or more preservatives, for example ethyl, or n-propyl, p-hydroxybenzoate, one or more coloring agents, one or more flavoring agents, and one or more sweetening agents, such as sucrose, saccharin or aspartame.
  • 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 mineral oil such as liquid paraffin.
  • the oily suspensions may contain a thickening agent, for example beeswax, hard paraffin or cetyl alcohol. 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
  • the pharmaceutical compositions of the invention may also be in the form of an 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 liquid paraffin or mixtures of these.
  • Suitable emulsifying agents may be naturally-occurring phosphatides, for example soy beans, lecithin, and esters or partial esters derived from fatty acids and hexitol anhydrides, for example sorbitan monooleate, and condensation products of the said partial esters with ethylene oxide, for example polyoxyethylene sorbitan monooleate.
  • the emulsions may also contain sweetening and flavouring 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 injectable aqueous or oleagenous suspension. This suspension may be formulated according to the known art using those suitable dispersing or wetting agents and suspending agents which have been mentioned 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-butane diol.
  • compositions can be prepared by mixing the drug with a suitable non-reacted non-reacted non-reacted non-reacted non-reacted non
  • the compounds for the present invention can be administered in intranasal form via topical use of suitable intranasal vehicles, or via transdermal routes, using those forms of transdermal skin patches well known to those of ordinary skill in the art.
  • the dosage administration will, of course, be continuous rather than intermittent throughout the dosage regimen.
  • Compounds of the present invention may also be delivered as a suppository employing bases such as cocoa butter, glycerinated gelatin, hydrogenated vegetable oils, mixtures of polyethylene glycols of various molecular weights and fatty acid esters of polyethylene glycol.
  • the dosage regimen utilizing the compounds of the present invention is selected in accordance with a variety of factors including type, species, age, weight, sex and medical condition of the patient; the severity of the condition to be treated; the route of administration; the renal and hepatic function of the patient; and the particular compound thereof employed.
  • a physician or veterinarian of ordinary skill can readily determine and prescribe the effective amount of the drug required to prevent, counter, arrest or reverse the progress of the condition.
  • Optimal precision in achieving concentration of drug within the range that yields efficacy without toxicity requires a regimen based on the kinetics of the drug's availability to target sites. This involves a consideration of the distribution, equilibrium, and elimination of a drug.
  • doses of the compound of structural formula I useful in the method of the present invention range from 0.01 to 1000 mg per adult human per day. Most preferably, dosages range from 0.1 to 500 mg/day.
  • the compositions are preferably provided in the form of tablets containing 0.01 to 1000 milligrams of the active ingredient, particularly 0.01, 0.05, 0.1, 0.5, 1.0, 2.5, 5.0, 10.0, 15.0, 25.0, 50.0, 100 and 500 milligrams of the active ingredient for the symptomatic adjustment of the dosage to the patient to be treated.
  • An effective amount of the drug is ordinarily supplied at a dosage level of from about 0.0002 mg/kg to about 50 mg/kg of body weight per day. The range is more particularly from about 0.001 mg/kg to 1 mg/kg of body weight per day.
  • the active agent of the present invention may be administered in a single daily dose, or the total daily dosage may be administered in dividend doses of two, three or four times daily.
  • the amount of active ingredient that may be combined with the carrier materials to produce a single dosage form will vary depending upon the host treated and the particular mode of administration.
  • Step 1A Methyl (S)-2-[3-(2-benzyloxy-l-methylethyl)-2-triethylsilyl- lH-pyrrolor2.3-b1pyridin-5-yll-2-methylpropanoate
  • Step IB Methyl (S)-2-[3-(2-benzyloxy-l-methylethyl)-2-iodo-lH- pyrrolo [2.3-61 pyridin-5-yll -2-methylpropanoate
  • Step IC Methyl (S)-2-[3-(2-benzyloxy-l-methylethyl)-2-(3,5-dimethyl- phenyl)-lH-pyrrolor2.3-fclpyridin-5-yl1-2-methylpropanoate
  • methyl (S)-2-[3-(2- benzyloxy-l-methylethyl)-2-iodo-lH-pyrrolo[2,3-6]pyridin-5-yl]-2- methylpropanoate (4.00 g, 8.12 mmol), 2,5-dimethylphenylboronic acid (1.83 g, 12.2 mmol) and Pd(dppf)Cl 2 *C ⁇ 2 Cl 2 (0.33 g, 0.406 mmol) in toluene/MeOH (5:2; 140 mL) was degassed via three vacuum/nitrogen ingress cycles and the resulting mixture was heated to approximately 80°C.
  • reaction mixture was acidified to p ⁇ 6 with 2N ⁇ C1 and extracted with ethyl acetate (x3).
  • the combined organic extract was washed with brine, dried (MgSO 4 ) and concentrated in vacuo. The crude residue was used without further purification in the subsequent reaction.
  • Step IE (S -l-(N,N-Diisobutylamino)-2-[3-(2-benzyloxy-l-methyl- ethyl)-2-(3,5-dimethylphenyl)-lH-pyrrolo[2,3-&]pyridin- 5-yll-2-methylpropan-l-one
  • Step 1G (S)-l-( ⁇ yV ⁇ Diisobutylamino)-2-[3-(2-hydroxy-l-methyl- ethyl)-2-(3,5-dimethylphenyl)-lH-l-(£er -butoxycarbonyl)- pyrrolo [2.3-61 pyridin-5-yll -2-methylpropan-l-one
  • Step lH (5)-l-(N r N-Diisobutylamino)-2-[3-(2-azido-l-methylethyl)-2- (3,5-dimethylphenyl)-lH-l-( er£-butoxycarbonyl)pyrrolo- r2.3-61pyridin-5-yll-2-methylpropan-l-one DEAD is added dropwise via syringe to a stirred solution of (S)-l-(NN-diisobutylamino)-2-[3-(2-hydroxy-l-methylethyl)-2-(3,5- dimethylphenyl)- IH- l-(ter£-butoxycarbonyl)pyrrolo [2,3-6] -pyridin-5-yl] - 2-methylpropan-l-one, ZnN 6 # 2py, PPh 3 and imidazole in C ⁇ 2 C1 2 at approximately 0°C.
  • reaction mixture is allowed to warm to room temperature overnight, and is then filtered through celite ® washing copiously with CH 2 C1 2 .
  • the filtrate is poured into water and extracted with CH 2 C1 2 .
  • the combined organic extract is washed with brine, dried (MgSO 4 ) and concentrated in vacuo.
  • the residue is purified by flash chromatography on silica gel (gradient elution; 25-40% ethyl acetate/hexanes as eluent) to give the title compound.
  • Step II (S)-l-( ⁇ N-Diisobutylamino)-2-[3-(2-amino-l-methyl- ethyl)-2-(3,5-dimethylphenyl)-lH-l-(ter£-butoxycarbonyl)- pyrrolo [2.3-61 pyridin-5-yll -2-methylpropan-l-one
  • Step U (S)-l-(iV ⁇ V-Diisobutylamino)-2-[3-(2-(2,4-dinitrobenzene- sulfonylamino)-l-methylethyl)-2-(3,5-dimethylphenyl)-lH-l- ( er -butoxycarbonyl)pyrrolo[2,3-6]pyridin-5-yl]-2-methyl- propan-1-one
  • 2,4-Dinitrobenzenesulfonyl chloride is added in one portion to a stirred solution of (SVl- ⁇ j N-diisobutylamino ⁇ -fS- -amino-l- methyl-ethy ⁇ - ⁇ -dimethylpheny -lH-l- er ⁇ -butoxycarbonyl ⁇ pyrrolo [2,3-6] -pyridin-5-yl] -2-methylpropan-l-one and 2,4,6-collidine in C ⁇ 2 C1 2 at approximately 0°C. After 5 min., the resulting mixture is warmed to ambient temperature and aged for 2h. The reaction mixture is poured into water and extracted with ethyl acetate.
  • Step IK (S)-6- ⁇ 2-[N-(5-[2-(N ⁇ -Diisobutylamino)-l,l-dimethyl-2- oxoethyl]-2-(3,5-dimethylphenyl)-lH-l-( ⁇ er ⁇ -butoxycarbonyl)- pyrrolo [2,3-6] pyridin-3-yl] propyl)-AT-(2,4-dinitrobenzene- sulfonyl)]aminoethyl ⁇ -3-(2-trimethylsilylethoxymethyl)-3H- imidazo[4.5-61pyridine DEAD is added dropwise via syringe to a stirred solution of (S)-l-(N ' r N-diisobutylamino)-2-[3-(2-(2,4-dinitrobenzenesulfonylamino)- l-methylethyl)-2-(3,5-dimethylphenyl)-lH
  • Step IL (5)-6- ⁇ 2- [2- [5- [2-(N,N-Diisobutylamino)- 1 , l-dimethyl-2-oxo- ethyl]-2-(3,5-dimethylphenyl)-lH-l-(ter£-butoxycarbonyl)- pyrrolo [2,3-6] pyridin-3-yl]propylamino]ethyl ⁇ -3-(2-trim ethyl - silylethoxymethyl)-3H-imidazo[4.5-61pyridine n-Propylamine is added to a stirred solution of crude
  • Step 1M (S)-l-(iV,N-Diisobutylamino)-2- ⁇ 2-(3,5-dimethylphenyl)- 3-[l-methyl-2-(imidazo[4,5-6]pyridin-6-yl)ethyl]-lH- pyrrolo [2.3-61 pyridin-5-yl)-2-methylpropan-l-one
  • reaction mixture After cooling to room temperature, the reaction mixture is adjusted to p ⁇ 9 with 5N NaO ⁇ and extracted with ethyl acetate. The combined organic extract is washed with brine, dried (MgSO 4 ) and concentrated in vacuo. The residue is purified by preparative thin layer chromatography on silica gel (100% ethyl acetate as eluent) to give the title compound.
  • Step A Ethyl 2-methyl-2-(pyridin-3-yl)propanoate A solution of ethyl-3-pyridylacetate (10.0 g, 60.5 mmol) in
  • Step B Ethyl 2-methyl-2-(pyridin-3-yl)propanoate-N-oxide eta-chloroperoxybenzoic acid (55%; 21.3 g, 67,9 mmol) was added in one portion to a vigorously stirred emulsion of ethyl 2- methyl-2-(pyridin-3-yl)propanoate and NaHCO 3 (17.5 g, 0.209 mmol) in water/chloroform (1:1; 500 mL) at ambient temperature. After approximately 12 h, the organic phase was separated and the aqueous phase extracted with chloroform (x3). The combined organic extract was washed with brine, dried (MgSO 4 ) and concentrated in vacuo. The residue (10.9 g, 100%) was judged pure by a combination of TLC and H nmr analysis and was used without further purification in the subsequent reaction.
  • Step C Ethyl 2-[6-(2,2-dimethyl-4-oxo-4H-l,3-benzoxazin-3-yl)- pyridin-3-yn-2-methylpropanoate
  • Step F Methyl 2-(6-amino-5-iodopyridin-3-yl)-2-methylpropanoate
  • Step AA Methyl (.S)-3-benzyloxy-2-methylpropanoate
  • Step BB CS-3-Benzyloxy-2-methylpropan-l-ol
  • Step CC GS-3-Benzyloxy-2-methylpropanal
  • An oven dried three-necked 2 L round bottom flask was equipped with a mechanical stirrer, a thermometer, an N 2 inlet, and a septum.
  • the flask was charged with 24.050 g (0.189 mol) of oxalyl chloride and 425 mL CH 2 C1 2 .
  • the reaction mixture was stirred under an N 2 atmosphere and cooled to -78°C with an external dry ice-acetone bath.
  • a solution of methyl sulfoxide (29.607 g; 0.379 mol) in 85 mL CH 2 C1 2 was then added over 5 min to the reaction mixture via cannula.
  • Step DD CS -4-Benzyloxy-l,l-dibromo-3-methylbutene
  • Step EE GS0-(4-benzyloxy-3-methylbut-l-ynyl)triethylsilane
  • An oven dried 100 mL single-necked round bottom flask was equipped with a magnetic stir bar and a septum then charged with 5.171 g (15.5 mmol) of (S)-4-benzyloxy-l,l-dibromo-3-methylbutene and 20 mL of anhydrous THF.
  • the reaction mixture was stirred at -78°C under an N 2 atmosphere and 12.4 mL of a 2.5 M solution of rc-butyllithium (31.0 mmol) was added dropwise via syringe over 15 min.
  • Step DDD 6-Bromo-3-(2-trimethysilylethoxymethyl) -3H-imidazo
  • Step EEE 6-Ethenyl-3-(2-trimethysilylethoxymethyl)-3H-imidazo-
  • Step FFF 6-(2-Bromo-l-hydroxyethyl)-3-(2-trimethysilyl- ethoxymethyP- 3H-imidazo [4.5-61 -pyridine
  • Step HHH 2-[3-(2-Trimethylsilylethoxymethyl)-3H-imidazo-
  • 6-Oxiranyl-3-(2-trimethylsilylethoxymethyl)-3H-imidazo- [4,5-6] pyridine 918 mg, 3.15 mmol
  • 10% Pd/C 400 mg
  • ammonium formate 993 mg, 15.75 mmol
  • the reaction mixture was heated to 70°C for 2.5 h. After cooling to ambient temperature, the mixture was filtered through celite ® , eluted with methanol, concentrated in vacuo.

Abstract

There are disclosed compounds of formula (I) and pharmaceutically acceptable salts thereof which are useful as antagonists of GnRH and as such may be useful for the treatment of a variety of sex-hormone related and other conditions in both men and women.

Description

TITLE OF THE INVENTION
ANTAGONISTS OF GONADOTROPIN RELEASING HORMONE
BACKGROUND OF THE INVENTION The gonadotropin-releasing hormone (GnRH), also referred to as luteinizing hormone-releasing hormone (LHRH), is a decapeptide that plays a key role in human reproduction. The hormone is released from the hypothalamus and acts on the pituitary gland to stimulate the biosynthesis and secretion of luteinizing hormone (LH) and follicle- stimulating hormone (FSH). LH released from the pituitary gland is primarily responsible for the regulation of gonadal steroid production in both sexes, whereas FSH regulates spermatogenesis in males and follicular development in females. GnRH agonists and antagonists have proven effective in the treatment of certain conditions which require inhibition of LH/FSH release. In particular, GnRH-based therapies have proven effective in the treatment of endometriosis, uterine fibroids, polycystic ovarian disease, precocious puberty and several gonadal steroid-dependent neoplasia, most notably cancers of the prostate, breast and ovary. GnRH agonists and antagonists have also been utilized in various assisted fertilization techniques and have been investigated as a potential contraceptive in both men and women. They have also shown possible utility in the treatment of pituitary gonadotrophe adenomas, sleep disorders such as sleep apnea, irritable bowel syndrome, premenstrual syndrome, benign prostatic hyperplasia, hirsutism, as an adjunct to growth hormone therapy in growth hormone deficient children, and in murine models of lupus. The compounds of the invention may also be used in combination with bisphosphonates (bisphosphonic acids) and other agents, such as growth hormone secretagogues, for the treatment and the prevention of disturbances of calcium, phosphate and bone metabolism, in particular, for the prevention of bone loss during therapy with the GnRH antagonist, and in combination with estrogens, progesterones, antiestrogens, antiprogestins and/or androgens for the prevention or treatment of bone
- 1 loss or hypogonadal symptoms such as hot flashes during therapy with the GnRH antagonist.
Additionally, a compound of the present invention may be co-administered with a 5a-reductase 2 inhibitor, such as finasteride or epristeride; a 5a-reductase 1 inhibitor such as 4,7b-dimethyl-4-aza-5a- cholestan-3-one, 3-oxo-4-aza-4,7b-dimethyl-16b-(4-chlorophenoxy)-5a- androstane, and 3-oxo-4-aza-4,7b-dimethyl-16b-(phenoxy)-5a-androstane as disclosed in WO 93/23420 and WO 95/11254; dual inhibitors of 5a- reductase 1 and 5a-reductase 2 such as 3-oxo-4-aza-17b-(2,5- trifluoromethylphenyl-carbamoyl)-5a-androstane as disclosed in WO 95/07927; antiandrogens such as flutamide, casodex and cyproterone acetate, and alpha-1 blockers such as prazosin, terazosin, doxazosin, tamsulosin, and alfuzosin.
Further, a compound of the present invention may be used in combination with growth hormone, growth hormone releasing hormone or growth hormone secretagogues, to delay puberty in growth hormone deficient children, which will allow them to continue to gain height before fusion of the epiphyses and cessation of growth at puberty. Further, a compound of the present invention may be used in combination or co-administered with a compound having luteinizing hormone releasing activity such as a peptide or natural hormone or analog thereof. Such peptide compounds include leuprorelin, gonadorelin, buserelin, triptorelin, goserelin, nafarelin, histrelin, deslorelin, meterlin and recirelin. Additionally, a compound of the present invention may be used as described in U.S. Patent No. 5,824,286 which discloses the administration of peptide GnRH antagonists such as Antide and azaline B to premenopausal women to enhance the readability of mammographic film relative to a mammogram effected in the absence of the administration.
Current GnRH antagonists are GnRH-like decapeptides which are generally administered intravenously or subcutaneously presumably because of negligible oral activity. These have amino acid substitutions usually at positions one, two, three, six and ten.
- 2 Non-peptide GnRH antagonists offer the possible advantage of oral adminstration. Non-peptide GnRH antagonists have been described in European Application 0 219 292 and in De, B. et al., J. Med. Chem., 32, 2036-2038 (1989), in WO 95/28405, WO 95/29900 and EP 0679642 all to Takeda Chemical Industries, Ltd.
Substituted indoles known in the art include those described in the following patents and patent applications. US Patent No. 5,030,640 discloses alpha-heterocyclic ethanol aminoalkyl indoles which are potent β-agonists. US Patent No. 4,544,663 discloses indolamine derivatives which are allegedly useful as male anti-fertility agents. WO 90/05721 discloses alpha-amino-indole-3-acetic acids useful as anti-diabetic, anti-obesity and anti-atherosclerotic agents. French patent 2,181,559 discloses indole derivatives with sedative, neuroleptic, analgesic, hypotensive, antiserotonin and adrenolytic activity. Belgian patent 879381 discloses 3-aminoalkyl-lH-indole-5-thioamide and carboxamide derivatives as cardiovascular agents used to treat hypertension, Raynaud's disease and migraine. U.S. Patent Nos. 5,756,507, 5,780,437 and 5,849,764 also disclose substituted arylindoles as non-peptide antagonists of GnRH.
SUMMARY OF THE INVENTION
The present invention relates to compounds which are non-peptide antagonists of GnRH which can be used to treat a variety of sex-hormone related conditions in men and women, to methods for their preparation, and to methods and pharmaceutical compositions containing said compounds for use in mammals.
Because of their activity as antagonists of the hormone GnRH, the compounds of the present invention are useful to treat a variety of sex-hormone related conditions in both men and women. These conditions include endometriosis, uterine fibroids, polycystic ovarian disease, hirsutism, precocious puberty, gonadal steroid- dependent neoplasias such as cancers of the prostate, breast and ovary, gonadotrophe pituitary adenomas, sleep apnea, irritable bowel syndrome, premenstrual syndrome and benign prostatic hypertophy. They are also useful as an adjunct to treatment of growth hormone deficiency and short stature, and for the treatment of systemic lupus erythematosis. Further, the compounds of the invention may be useful in in vitro fertilization and as contraceptives. The compounds may also be useful in combination with androgens, estrogens, progesterones, antiestrogens and antiprogestogens for the treatment of endometriosis, fibroids and in contraception. They may also be useful in combination with testosterone or other androgens or antiprogestogens in men as a contraceptive. The compounds may also be used in combination with an angiotensin-converting enzyme inhibitor such as Enalapril or Captopril, an angiotensin Il-receptor antagonist such as Losartan or a renin inhibitor for the treatment of uterine fibroids. Additionally, the compounds of the invention may also be used in combination with bisphosphonates (bisphosphonic acids) and other agents, for the treatment and the prevention of disturbances of calcium, phosphate and bone metabolism, in particular, for the prevention of bone loss during therapy with the GnRH antagonist, and in combination with estrogens, progesterones and/or androgens for the prevention or treatment of bone loss or hypogonadal symptoms such as hot flashes during therapy with the GnRH antagonist.
Additionally, a compound of the present invention may be co-administered with a 5a-reductase 2 inhibitor, such as finasteride or epristeride; a 5a-reductase 1 inhibitor such as 4,7b-dimethyl-4-aza-5a- cholestan-3-one, 3-oxo-4-aza-4,7b-dimethyl-16b-(4-chlorophenoxy)-5a- androstane, and 3-oxo-4-aza-4,7b-dimethyl-16b-(phenoxy)-5a-androstane as disclosed in WO 93/23420 and WO 95/11254; dual inhibitors of 5a- reductase 1 and 5a-reductase 2 such as 3-oxo-4-aza-17b-(2,5- trifluoromethylphenyl-carbamoyl)-5a-androstane as disclosed in WO 95/07927; antiandrogens such as flutamide, casodex and cyproterone acetate, and alpha- 1 blockers such as prazosin, terazosin, doxazosin, tamsulosin, and alfuzosin.
Further, a compound of the present invention may be used in combination with growth hormone, growth hormone releasing hormone or growth hormone secretagogues, to delay puberty in growth
4 - hormone deficient children, which will allow them to continue to gain height before fusion of the epiphyses and cessation of growth at puberty.
Further, a compound of the present invention may be used in combination or co-administered with a compound having luteinizing hormone releasing activity such as a peptide or natural hormone or analog thereof. Such peptide compounds include leuprorelin, gonadorelin, buserelin, triptorelin, goserelin, nafarelin, histrelin, deslorelin, meterlin and recirelin.
Additionally, a compound of the present invention may be used as described in U.S. Patent No. 5,824,286 which discloses the administration of peptide GnRH antagonists such as Antide and azaline B to premenopausal women to enhance the readability of mammographic film relative to a mammogram effected in the absence of the administration.
DETAILED DESCRIPTION OF THE INVENTION
The present invention relates to compounds of the general formula
R2 N-(A)-
R 10a
R-.
Figure imgf000007_0001
(I)
wherein A is Ci-Cβ alkyl, substituted CI-CQ alkyl, C3-C7 cycloalkyl, substituted C3-C7 cycloalkyl, C3-C6 alkenyl, substituted C3-C6 alkenyl, C3-C6 alkynyl, substituted C3-C6 alkynyl, C1-C6 alkoxy, or C0-C5 alkyl-S(O)n-Co-C5 alkyl, C0-C5 alkyl- O-C0-C5 alkyl, C0-C5 alkyl-NR]_8-Co-C5 alkyl where R]_8 and the C0-C5 alkyl can be joined to form a ring, \ ^N-(CH2)p-
R16 , or a single bond,
Rθis hydrogen, C1-C6 alkyl, substituted Ci-Cβ alkyl, wherein the substituents are as defined below; aryl, substituted aryl, aralkyl or substituted aralkyl, wherein the substituents are as defined for R3, R4 and R5.
Rl is
YS ι\u
^ ^
^R -n 11 Riq
I . xj 13 I. N 13
R V x- R li13
14 R 15 R14 R15 R 14 R 15
N, .Z. .Z
*/V\/\/\ r/^\/V N N' N'
^R 13 λ- -NRl3
R14 R13 R 14 Ri. R14 R15
R14s
Tr iΛ Λ/W
*ΛΛΛ NΛΛΛ/> R ni I|"13
13 ' =AJ -INf N V
K14 R15 R 14 R 13 R15 RH 7 Ri
Figure imgf000008_0001
%Λ/WΛ r_^ΛΛ
11 nio ^ n R N N V 13
N V
R 15 Rl5 R13
.z. Z.
^R„3 — __ RI3 , n» -R 13 κ14 Ri R14 R15 R14 R15
"^ i. IIR "13 *ΛΛΛ NΛΛΛ "^R >*ι V -NRl3
"14 R13 R14N R R Xi4Nλ' R
- 6 51231
R 14\.N.
N' W -^
* S\S/\/ s*
RI l|R13
X 3 N
R ~M N.-\ N^λ'
"14 R 15 R N R 13 R 15
R14\.N. R l1i \N, R14\N.
~^R °t R li13 I -Nf
N \' -NRl3 N \
R 15 R 15 R 13
-N ,N .N>
^Y ^ -R ^ " —"n -R
13 ""13 'ft -R
-N 13
Rl4N R1fN R15 R14N R15
.N, .N. .N l
R ,JR13
4!. 13
R R^f R14
"14 N' R R15 R-I4
13
N' — "Rl3
Rl5 N^R14
Figure imgf000009_0002
N. .N
^i R
Figure imgf000009_0003
Rl5 R-I4
RlL .N
Rl3
Figure imgf000009_0001
N' R14
Figure imgf000009_0004
7 - /51231
R
.N. N
-÷R 13
N' R 14
Figure imgf000010_0001
Figure imgf000010_0002
'VV' R,.
*N'
Figure imgf000010_0003
"14
R
IN rw> I '
*www*
N
R '14
Rι^ N'Z MA 14
.N r^ N-^
^N- /<R13
N
^. N l\T, N
Figure imgf000010_0004
N R 14
13 ^NI^R13
^ 3 r^r'
N
I* R14l14 13
R 13
N^ N-^ ^N- /Ri3 N πi4 R 1'4 RuN
13
3 N^
R
R *1 3 N 4 14
R R13
N ^A Ik
If R^N N
Figure imgf000010_0006
κ14
'14
Figure imgf000010_0007
N^ N" N'V R 13 l . '
Rι R "^14
- 8 the nitrogen atoms contained in the Ri heteroaromatic rings may exist either as drawn or, when chemically allowed, in their oxidized (N→O) state; R2 is hydrogen, Ci-Cβ alkyl, substituted Ci-Cβ alkyl, aralkyl, substituted aralkyl, aryl, substituted aryl, alkyl -ORn,
Ci-C6(NRnRi2), Ci-C6(CONRnRi2) or C(NRnRi2)NH; R2 and A taken together form a ring of 5-7 atoms; R3, R4 and R5 are independently hydrogen, Cl-Cβ alkyl, substituted
Ci-Cβ alkyl, C2-C6 alkenyl, substituted C2-C6 alkenyl, CN, nitro, C1-C3 perfluoroalkyl, C1-C3 perfluoroalkoxy, aryl, substituted aryl, aralkyl, substituted aralkyl, RnO(CH2)p-, RllC(O)O(CH2)p-, RnOC(0)(CH2)p-, -(CH2)pS(O)nRl7, -(CH2)pC(O)NRnRi2 or halogen; wherein R17 is hydrogen, Ci-Cβ alkyl, C1-C3 perfluoroalkyl, aryl or substituted aryl; R3 and R4 taken together form a carbocyclic ring of 3-7 carbon atoms or a heterocyclic ring containing 1-3 heteroatoms selected from N, O and S; R6 is hydrogen, Ci-Cβ alkyl, substituted C1-C6 alkyl, aryl, substituted aryl, C1-C3 perfluoroalkyl, CN, NO2, halogen, RnO(CH2)p-, NRi2C(0)Rn, NRi2C(O)NRnRi2 or SOnRli;
R7 is hydrogen, C1-C6 alkyl, or substituted C1-C6 alkyl, unless X is hydrogen or halogen, then R7 is absent; R8 is hydrogen, C(O)OR9, C(0)NRnRi2, NR11R12, C(O)Rn,
NRi2C(0)Rn, NRi2C(O)NRnRi2, NRi2S(O)2Rll, NRi2S(O)2NRnRi2, OC(0)Rn, OC(0)NRnRi2, ORn,
SOnRll, S(0)nNRnRi2, Ci-Cβ alkyl or substituted Ci-Cβ alkyl, unless X is hydrogen or halogen, then R8 is absent; or R7 and Rδ taken together form a carbocyclic ring of 3-7 atoms; R9 and R9a are independently hydrogen, C1-C6 alkyl, substituted Ci-Cβ alkyl; aryl or substituted aryl, aralkyl or substituted aralkyl when m≠O; or
O
R9 and Rga taken together form a carbocyclic ring of 3-7 atoms or when m≠O;
- 9 R9 and A taken together form a heterocyclic ring containing 3-7 carbon atoms and one or more heteroatoms when m≠O; or RlO and RlOa are independently hydrogen, Ci-Cβ alkyl, substituted C1-C6 alkyl, aryl, substituted aryl, aralkyl or substituted aralkyl; or
O
RlO and RlOa taken together form a carbocyclic ring of 3-7 atoms or ; R9 and RlO taken together form a carbocyclic ring of 3-7 carbon atoms or a heterocyclic ring containing one or more heteroatoms when m≠O; or R9 and R2 taken together form a heterocyclic ring containing 3-7 carbon atoms and one or more heteroatoms when m≠O; or RlO and R2 taken together form a heterocyclic ring containing 3-7 carbon atoms and one or more heteroatoms; RlO and A taken together form a heterocyclic ring containing 3-7 carbon atoms and one or more heteroatoms; or
Rll and R12 are independently hydrogen , C1-C6 alkyl, substituted C1-C6 alkyl, aryl, substituted aryl, aralkyl, substituted aralkyl, a carbocyclic ring of 3-7 atoms or a substituted carbocyclic ring containing 3-7 atoms; Rll and R12 taken together can form an optionally substituted ring of 3-7 atoms; Rl3 is hydrogen, OH, NR7R8, NRnSO2(Ci-C6 alkyl),
NRnSO2(substituted C1-C6 alkyl), NRnS02(aι l), NRnSO2(substituted aryl), NRnSO2(Ci-C3 perfluoroalkyl); Sθ2NRn(Ci-C6 alkyl), SO2NRn(substituted Ci-Cβ alkyl),
SO2NRii(aryl), SO2NRn(substituted aryl), SO2NRn(Ci-C3 perfluoroalkyl); SO2NRn(C(O)Ci-C6 alkyl); SO2NRn(C(O)- substituted C1-C6 alkyl); SO2NRn(C(O)-aryl); Sθ2NRn(C(O)-substituted aryl); S(O)n(Cι-C6 alkyl); S(O)n ( substituted Ci-Cβ alkyl), S(O)n(aryl), S(O)n(substituted aryl), C1-C3 perfluoroalkyl, C1-C3 perfluoroalkoxy, C1-C6 alkoxy, substituted C1-C6 alkoxy, COOH, halogen, NO2 or CN;
10 Rl4 and R15 are independently hydrogen, C1-C6 alkyl, substituted Cl-Cβ alkyl, C2-C6 alkenyl, substituted C2-C6 alkenyl, CN, nitro, C1-C3 perfluoroalkyl, C1-C3 perfluoroalkoxy, aryl, substituted aryl, aralkyl, substituted aralkyl, RnO(CH2)p-, RllC(0)0(CH2)p-, RllOC(O)(CH2)p-, -(CH2)pS(O)nRl7,
-(CH2)pC(O)NRnRi2 or halogen; wherein R17 is hydrogen, Ci-Cρ alkyl, C1-C3 perfluoroalkyl, aryl or substituted aryl; Rl6 is hydrogen, Ci-Cβ alkyl, substituted C1-C6 alkyl, or
N(RnRl2); Ri8 is hydrogen, C1-C6 alkyl, substituted C1-C6 alkyl, C(O)OR9,
C(0)NRnRi2, C(0)Rn, S(O)nRll; Rl9 is either the definition of R13 or R14;
X is hydrogen, halogen, N, O, S(0)n, C(O), (CRnRi2)P; C2-C6 alkenyl, substituted C2-C6 alkenyl,C2-Cβ alkynyl, or substituted C2-C6 alkynyl; when X is hydrogen or halogen,
R7 and Rδ are absent; when X is O, S(O)n, C(O), or CR11R12 only R7 or Rs is possible; Z is O, S, or NR11; m is 0-3; n is 0-2; p is 0-4; and the alkyl, alkenyl and alkynyl substituents are selected from C1-C6 alkyl, C3-C7 cycloalkyl, aryl, substituted aryl, aralkyl, substituted aralkyl, hydroxy, oxo, cyano, C1-C6 alkoxy, fluoro, C(O)ORn) aryl C1-C3 alkoxy, substituted aryl C1-C3 alkoxy, and the aryl substituents are as defined for R3, R4 and R5; or a pharmaceutically acceptable addition salt and/or hydrate thereof, or where applicable, a geometric or optical isomer or racemic mixture thereof.
Unless otherwise stated or indicated, the following definitions shall apply throughout the specification and claims.
When any variable (e.g., aryl, heterocycle, Ri, etc.) occurs more than one time in any constituent or in formula I, its definition on
11 - each occurrence is independent of its definition at every other occurrence. Also, combinations of substituents and/or variables are permissible only if such combinations result in stable compounds.
The term "alkyl" is intended to include both branched- and straight-chain saturated aliphatic hydrocarbon groups having the specified number of carbon atoms, e.g., methyl (Me), ethyl (Et), propyl, butyl, pentyl, hexyl, heptyl, octyl, nonanyl, decyl, undecyl, dodecyl, and the isomers thereof such as isopropyl (i-Pr), isobutyl (i-Bu), secbutyl (s-Bu), tertbutyl (t-Bu), isopentane, isohexane, etc. The term "aryl" includes phenyl and naphthyl. In a preferred embodiment, aryl is phenyl.
The term "halogen" or "halo" is intended to include fluorine, chlorine, bromine and iodine.
As used herein, the term "composition" is intended to encompass a product comprising the specified ingredients in the specified amounts, as well as any product which results, directly or indirectly, from combination of the specified ingredients in the specified amounts
It is intended that the connecting group A can be bonded to any of the available carbon or heteroatoms of the heteroaromatic groups Rl, including both rings of the benzo-fused heterocyclic groups and, likewise, R13, R14, and R15 can be bonded to any of the available carbon atoms of the heteroaromatic groups Ri.
In addition, it is well known to those skilled in the art that many of the foregoing heterocyclic groups can exist in more than one tautomeric form. It is intended that all such tautomers be included within the ambit of this invention.
The optical isomeric forms, that is mixtures of enantiomers or diasteromers, e.g., racemates, as well as individual enantiomers or diastereomers of the instant compound are included. These individual enantiomers are commonly designated according to the optical rotation they effect by the symbols (+) and (-), (L) and (D), (1) and (d) or combinations thereof. These isomers may also be designated according
- 12 to their absolute spatial configuration by (S) and (R), which stands for sinister and rectus, respectively.
The individual optical isomers may be prepared using conventional resolution procedures, e.g., treatment with an appropriate optically active acid, separating the diastereomers and then recovering the desired isomer. In addition, the individual optical isomers may be prepared by asymmetric synthesis.
Additionally, a given chemical fomula or name shall encompass pharmaceuticaly acceptable addition salts thereof and solvates thereof, such as hydrates.
The compounds of the present invention, while effective themselves, may be formulated and administered in the form of their pharmaceutically acceptable addition salts for purposes of stability, convenience of crystallization, increased solubility and other desirable properties.
The compounds of the present invention may be administered in the form of pharmaceutically acceptable salts. The term "pharmaceutically acceptable salt" is intended to include all acceptable salts Examples of acid salts are hydrochloric, nitric, sulfuric, phosphoric, formic, acetic, trifluoroacetic, propionic, maleic, succinic, malonic, methanesulfonic, benzenesulfonic and the like which can be used as a dosage form for modifying the solubility or hydrolysis characteristics or can be used in sustained release or pro-drug formulations. Depending on the particular functionality of the compound of the present invention, pharmaceutically acceptable salts of the compounds of this invention include those formed from cations such as sodium, potassium, aluminum, calcium, lithium, magnesium, zinc, and from bases such as ammonia, ethyl enediamine, N-m ethyl - glutamine, lysine, arginine, ornithine, choline, N,N'- dibenzylethylenediamine, chloroprocaine, diethanolamine, procaine, N- benzylphenethylamine, diethylamine, piperazine, tris(hydroxymethyl) aminomethane, and tetramethylammonium hydroxide. These salts may be prepared by standard procedures, e.g. by reacting a free acid
- 13 - with a suitable organic or inorganic base, or alternatively by reacting a free base with a suitable organic or inorganic acid.
Also, in the case of an acid (-COOH) or alcohol group being present, pharmaceutically acceptable esters can be employed, e.g. methyl, ethyl, butyl, acetate, maleate, pivaloyloxymethyl, and the like, and those esters known in the art for modifying solubility or hydrolysis characteristics for use as sustained release or prodrug formulations. The compounds of the present invention may have chiral centers other than those centers whose stereochemistry is depicted in formula I, and therefore may occur as racemates, racemic mixtures and as individual enantiomers or diastereomers, with all such isomeric forms being included in the present invention as well as mixtures thereof. Furthermore, some of the crystalline forms for compounds of the present invention may exist as polymorphs and as such are intended to be included in the present invention. In addition, some of the compounds of the instant invention may form solvates with water or common organic solvents. Such solvates are encompassed within the scope of this invention.
The compounds of the invention are prepared according to the following reaction schemes. All of the substituents are as defined above unless indicated otherwise.
14 Reaction Scheme A
Re
Pd(dppf)Cl2-CH2Cl2
(CR9R9a) ^PGT LiCl, Na2CQ5,
Re— r DMF, heat
Figure imgf000017_0001
Figure imgf000017_0002
Rio Rio3
NH2 2a Z = H 2b Z = Et3Si
R.
(CR9R9a),
R6- R.ιoRιoa
Figure imgf000017_0003
N
Figure imgf000017_0004
, PvG^i\ H H (CR9R ;
3b Z = Et3Si 4a Z = H 3c Z = 4c Z =
Figure imgf000017_0005
Figure imgf000017_0006
Rs R4 R R4
A preferred method for the synthesis of the substituted tryptamines described in this invention utilizes a palladium-catalyzed cross coupling reaction as a key step as shown in Scheme A. This 7- azaindole synthesis involves the reaction of a suitably functionalized 3- iodo-2-aminopyridine (1) with substituted acetylenes such as 2 in the presence of a base like sodium carbonate, lithium chloride, and a palladium catalyst such as (dppf)PdCl2*CH2Cl2. The reaction is conducted in an inert organic solvent such as dimethylformamide at elevated temperatures, for instance at 100°C, and the reaction is conducted for a period of about 30 minutes to about 24 hours. A standard workup and isolation affords the substituted isomeric indole derivatives 3 and 4, and the isomer of general formula 3 is the preferred isomer. The acetylene utilized in this reaction may be a terminal acetylene (2a) or be optionally substituted on the terminal carbon atom with a substituent Z (2b, 2c). The substituent abbreviated PGj indicates an alcohol protecting group such as a benzyl ether, tert-hu yl ether or the
15 like. The nature of the Z substituent determines the distribution of the 7- azaindole isomers (3 and 4) produced in the reaction. For example, if the substituent Z on the acetylene is a hydrogen atom then the isomer 4a is the major product of the reaction. When the substituent Z is chosen to be a substituted silyl group such as trimethylsilyl, triethylsilyl (as shown), or the like, then isomer 3b is formed almost exclusively. When Z is a substituted aryl group, then both isomers 3c and 4c may be formed and the product mixture is separated using chromatographic or crystallization techniques to afford the individual isomers.
If the synthesis is conducted with a silyl-substituted acetylene 2b to produce a silyl-substituted 7-azaindole 3b, then the silyl group is next converted to an aryl or substituted aryl group of general formula 3c using the reactions described later in Scheme E. The 2- arylsubstituted 7-azaindole derivatives 3c formed either directly from arylacetylenes (2c) as shown in Scheme A or from 2-trialkylsilyl-7- azaindoles using the method of Scheme E are then further elaborated as described below to produce the novel 7-azaindole derivatives described in this invention.
Reaction Scheme B
B8 R8 .X
R7" m-CPBA, Ri R'
Figure imgf000018_0001
N' H2O-CHCl3
C1CH2CH2C1, 90°C, 3 days
100°C Re I2, Ag(CF3C02), h MeOH, rt, 3 h.
N' NH2
Figure imgf000018_0003
Figure imgf000018_0002
- 16 - Scheme B illustrates the preparation of substituted 3- iodo-2-aminopyridines (1) which are utilized in the Larock 7-azaindole synthesis described in Scheme A. The 3-iodo-2-aminopyri dines (1) may be prepared in several ways described in the literature of organic synthesis. A preferred method involves the or^/io-iodination of substituted 2-aminopyridine derivatives of general formula 9 with an electrophilic iodination reagent such as iodine, iodine monochloride, N-iodosuccinimide or the like. The or /io-iodination of 2-aminopyridine derivatives (9) as illustrated in Scheme B employs iodine and silver trifluoroacetate in a suitable organic solvent like methanol at room temperature and 3-iodo-2-aminopyridines of general formula 1 are produced in high yield.
In some cases, 2-aminopyridine derivatives such as 9 may be commercially available or alternatively they may be prepared using methodologies known in organic chemistry. For instance, application of methodology reported by Wachi and Terada (Wachi, K.; Terada, A. Chem. Pharm. Bull. 1980, 28, 465) allows the conversion of pyridines of general formula 5 to 2-aminopyridines of general formula 9 as shown at the top of Scheme B. In this synthetic transformation, a substituted pyridine (5) is first converted to the corresponding N-oxide (6) with a suitable oxidant such as eto-chloroperbenzoic acid. In the next step, the substituted pyridine iV-oxide 6 is reacted with 4-chloro-2,2-dimethyl- 2H-l,3-benzoxazine (7) in an inert high boiling solvent such as 1,2- dichloroethane. An adduct initially formed in this reaction undergoes a thermal rearrangement and the ΛT-pyridyl substituted 4-oxo-4H-l,3- benzoxazine 8 is produced. Finally, the substituted benzoxazine 8 is hydrolyzed with concentrated hydrochloric acid at elevated temperature to afford the substituted 2-aminopyridines of general formula 9.
17 Reaction Scheme C
NH
1) π-BuLi,
P r"~^o'^cci3 THF, -78°C
• (CR9R9a)r^/OH CF3S03H ^
Figure imgf000020_0002
2) Et3SiCl
RloRloa CC -QHw Rιo Rιoa 2a
10
(C 9R9a)^°v
Figure imgf000020_0003
Figure imgf000020_0001
R 10R10a 2b
(CRgRgg OH Pd(OAc)2, PPh3,
Λ RioRioa IQ IO3 ^x. Cul, Et3N,
11 85°C
10
Figure imgf000020_0004
X = Br, I, OS02CF3 R4 R3
NH
(CR9R9a),
Figure imgf000020_0006
Ptr ^O^ X^CCI3
R IQ IO3 CF3SQ3H
2c
CClpCgH^
Figure imgf000020_0005
Acetylenic compounds of general structure 2 are prepared using one of several methods depending upon the choice of the desired substituents. When the substituents R9, R9a, R10 and R10a are selected to be hydrogen or lower alkyl groups, compounds of formula 2 may be prepared from known acetylenic alcohols such as 3-butyn-l-ol, 4-pentyn- 2-ol or similar acetylenic alcohols reported in the chemical literature. The conversion of acetylenic alcohols of general formula 10 to acetylene derivatives of general formula 2 is shown in Scheme C. For clarity the hydroxyl protecting group (PGj) illustrated in Scheme C is exemplified as an O-benzyl ether. Thus, reaction of 10 with O-benzyl-2,2,2- trichloroacetimidate in the presence of a catalytic amount of a strong acid such as trifluoromethanesulfonic acid and in a suitable inert
18 organic solvent like carbon tetrachloride at room temperature affords after 2 to 24 hours the protected acetylenic alcohol 2a. Compounds of formula 2a may in turn be converted to acetylenes (2b) of general formula 2 wherein Z is a trialkylsilyl group by deprotonation of the acetylene with a base such as /z-butyllithium in an inert organic solvent like tetrahydrofuran followed by reaction with a trialkylsilyl chloride such as triethylchlorosilane. The deprotonation and silylation reactions are generally conducted at low temperatures, for instance between about -78°C and room temperature, and after standard workup and purification a silylacetylene of formula 2b is obtained.
As previously stated, acetylenes of general formula 2c wherein Z is an aryl or substituted aryl group, are also useful in the 7- azaindole synthesis illustrated in Scheme A. Arylacetylenes 2c may be prepared using a coupling reaction of cuprous acetylides derived from acetylenic alcohols of formula 2a with various aryl halides or aryl triflates (11). Such coupling reactions produce aryl acetylenes of general formula 12 as shown at the bottom of Scheme C. These reactions are generally carried out in a basic organic solvent like triethylamine at elevated temperatures, typically between about 60°C and about 120°C, and the coupling reaction is catalyzed by copper(I) salts such as cuprous iodide and a palladium catalyst such as palladium acetate in combination with triphenylphosphine. The hydroxyl group of the arylacetylenes of general formula 12 can be protected with a suitable protecting group such as the O-benzyl ether group shown in Scheme C, to afford an arylacetylene (2c) of general formula 2 wherein Z is an aryl or substituted aryl group. It is also recognized that in some cases it may be preferable to reverse the order of the steps illustrated in Scheme C. For instance, acetylenic alcohols (7) may be subjected to silylation or arylation prior to the hydroxyl group protection step.
19 - Reaction Scheme D
NH PhT/^θ''^CCl3
Figure imgf000022_0001
RioRioa Y A LiAlH4, THF
RioRioa
13 14
Figure imgf000022_0002
1) DMSO, (COCl)2,
Ha^ /(CR9R9a)i^ CH2Cb, -50°C (CR9R9a)^0
Figure imgf000022_0003
2) Et3N
H A H R ioRioa o RIQRIO3
16
CBr4, PPh3, . (CR9R9a)s^O CH2CI2, rt H
Figure imgf000022_0006
-
Figure imgf000022_0004
Rio Rioa
Figure imgf000022_0005
n-BuLi, THF, 2a -78°C to 0°C
Another useful approach for the preparation of acetylenic compounds of general formula 2a employs an ethynylation reaction sequence of aldehydes of general formula 16 as shown in Scheme D. The aldehydes (16) used in the ethynylation sequence may be prepared using various methods known in organic synthesis starting with hydroxyesters of general formula 13, from protected hydroxyesters of formula 14, or from alcohols related to the mono-hydroxyl protected diols of formula 15. The choice of preferred starting material depends upon the nature of the substituents R9, R9a, R10, and R10a selected. Scheme D illustrates this strategy begining with the generalized hydroxy ester 13. Protection of the hydroxyl group of 13, for instance as the O-benzylether shown, affords a protected hydroxy ester of formula 14. The ester group of compounds of formula 14 can then be converted to an aldehyde of formula 16 either directly using a reagent like diisobutylaluminum hydride in a solvent like toluene, or through a two step process. In the two step process, reduction of the ester group with a reagent such as
20 lithium aluminum hydride in tetrahydrofuran affords alcohols of formula 15 which are then subjected to reoxidation, for instance using a Swern-Moffatt oxidation, to afford the desired aldehydes of formula 16.
The ethynylation of aldehydes of formula 16 is accomplished in two steps. First, aldehydes (16) are reacted with carbon tetrabromide and triphenylphosphine in an inert organic solvent like dichloro- methane to produce the dibromo olefins of formula 17. Next, the dibromo olefins (17) are treated with two equivalents of a strong base such as tt-butyllithium in tetrahydrofuran at low temperature, for instance at about -78°C. The strong base induces dehydrohalogenation and metal- halogen exchange to afford lithium acetylides which upon quenching and workup afford acetylenes of general formula 2a. Alternatively, the intermediate lithium acetylides formed in the reaction may be treated with a trialkylsilyl chloride, such as triethylchlorosilane, to afford silylacetylenes of general formula 2b.
Reaction Scheme E
R8
R8
(CR9R9a)
.(CR9R9a), Gι
R-ioR-io3
R ioRioa ^
H SiEt,
ICl, AgBF4,
3b MeOH-THF, 0°C 18
18 + I R ioRioa
R5 R4
(dppf)PdCl2«CH2Cl2, 19 toluene-EtOH-2M aq. Na2C03,
80°C
Figure imgf000023_0001
The conversion of 2-silyl-substituted 7-azaindoles of general formula 3b to 2-aryl-substituted 7-azaindoles of general formula 3c may be accomplished in two steps as shown in Scheme E. The first step is a
21 - halodesilylation reaction which converts silyl-substituted 7-azaindoles of formula 3b into 2-halo-7-azaindoles of general formula 18. Scheme E illustrates this process using iodine monochloride so that the product obtained is a 2-iodoindole of general formula 18. Silver tetrafluoroborate is also employed in this example to increase the reactivity of the halogenating reagent. It is possible to effect the halodesilylation reaction with other electrophilic halogenating reagents such as A^-bromo- succinimide in dichloromethane which affords a 2-bromo-7-azaindole derivative. Both 2-bromo and 2-iodo-7-azaindoles of formula 18 are useful in the subsequent step.
The second step is a palladium-catalyzed cross coupling reaction of the 2-halo-7-azaindole 18 with a suitable aryl or substituted aryl organometallic reagent 19. Scheme E illustrates this process with an aryl or substituted arylboronic acid as the organometallic reagent, however, other organometallic reagents known to participate in palladium-catalyzed cross-coupling reactions such as arylboronic esters or arylstannanes may also be employed. In the example, a 2-iodo-7- azaindole of general formula 18 is coupled with a generalized boronic acid (19) using a catalyst such as [l,l'-bis(diphenylphosphino)ferrocene] dichloropalladium(II) complex with dichloromethane (shown), tetrakis (triphenylphosphine)-palladium(O) or the like. The reaction is usually conducted at temperatures between room temperature and about 100 °C, for instance at about 80°C. This palladium catalyzed cross-coupling reaction may be effected using various combinations of palladium catalysts and solvent compositions known in organic chemistry, and the selection of the conditions is made depending upon the type of organometallic reagent (19) used and the identity of the substituent groups in the two starting materials. When the organometallic reagent is a boronic acid or boronate ester then a preferred solvent mixture consists of toluene, ethanol and an aqueous solution of a base like cesium or sodium carbonate. If instead the organometallic reagent 19 is an arylstannane, then no additional base is required, and a polar aprotic solvent such as tetrahydrofuran or dimethylformamide is employed.
22 Reaction Scheme F
G, R6" R10R10a
Figure imgf000025_0002
PPh3, DEAD /OH Zn(N3)2«2pyr,
R 10R10a imidazole, CH2Cl2 rt, 1-24 h
Figure imgf000025_0001
Re
V" \<\^_ /-(CR9R9a)I^ Ri°Ri
10% Pd/C, H2,
22
Figure imgf000025_0003
EtOH, rt 1-12 h
Figure imgf000025_0004
The next stage of the synthesis of the novel 7-azaindole derivatives is illustrated in Scheme F. This sequence of reactions begins with protection of the 7-azaindole with an amine protecting group (PG2) to afford compounds of general formula 20. The protection step is required to avoid competing side rections of the 2-aryltryptophol of formula 21 (where PG2 is H) in the later conversion of compounds of formula 21 to compounds of formula 22. The indole protection is followed by removal of the hydroxyl protecting group (PG^ from the side chain at the C-3 position of the 7-azaindole ring to afford compounds of general formula 21. Finally, the hydroxyl group of 21 is converted to a primary amine of general formula 23 which is then further functionalized as shown below in the following schemes. The choice of an appropriate amine protecting group (PG2) for the 7-azaindole is determined primarily by which protecting group (PG^ is present on the hydroxyl
- 23 - group in the C-3 sidechain, and by consideration of the chemical stability of the amine protecting group (PGj) required in the remaining steps of the synthesis. When the hydroxyl protecting group (PGj) is anO-benzyl ether as illustrated previously in Schemes C and D, the 7-azaindole may be protected as a carbamate derivative such as a er -butylcarbamate (BOC). In this case, the BOC-protected 7-azaindole is stable under the hydrogenolysis conditions which are used to remove the O-benzyl ether and it may be conveniently removed at the end of the synthesis using acidic conditions. If it is desired to synthesize compounds of formula (I) wherein R0 is alkyl, substituted alkyl or the like, then it is possible to introduce that substituent at this point and the use of a protecting group and its subsequent removal is not required.
An alcohol of general formula 21 may be converted to a primary amine of general formula 23 using a variety of methods known in the literature of organic chemistry. The bottom of Scheme F illustrates a process where the alcohol 21 is first converted to an azide of general formula 22, followed by reduction to afford the amine derivative 23. The synthesis of an azide of general formula 22 from alcohols like 21 is best accomplished by performing a Mitsunobu reaction in the presence of an appropriate azide source such as diphenylphosphoryl azide or zinc azide pyridine complex. Scheme F illustrates the reaction of alcohol 21 with triphenylphosphine, diethylazodicarboxylate, zinc azide pyridine complex and a proton source such as imidazole in an inert solvent like methylene chloride or tetrahydrofuran. The reaction is usually conducted at room temperature for periods between 1-24 hours, typically overnight or about 15 hours, and affords the azide of general formula 22 in good yield. Finally, an azide of formula 22 may then be reduced to an amine of formula 23 using one of several methods common in organic synthesis. One preferred method is catalytic hydrogenation in a solvent like methanol or ethanol in the presence of a catalyst such as 10% palladium on carbon. Alternatively, azides like 22 may be reacted with triphenylphosphine to form an iminophosphorane which upon hydrolysis with water affords the amine of formula 23 and triphenylphophine oxide.
- 24 Reaction Scheme G
HOγ(A) Rl
O 24
EDC, HOBt, NMM, CH2Cl2 R8
ΛA) ιo ιoa o
Figure imgf000027_0001
YA) R1
O 26 25
Figure imgf000027_0002
Et3N, CH2C12
The final stage of the synthesis of the novel 7-azaindole derivatives (I) involves elaboration of the sidechain at the C-3 position of the 7-azaindole core. One method for the completion of the synthesis is illustrated in Scheme G. As shown, the 2-aryltryptamine (23) may be condensed with a carboxylic acid of type 24 using the coupling reagent l-(3-dimethylamino-propyl)-3-ethylcarbodiimide hydrochloride (EDC), 1,3-dicyclohexyl-carbodiimide (DCC) or the like with or without 1- hydroxybenzotriazole (HOBt) and a tertiary amine base such as N- methylmorpholine (NMM), triethylamine or the like in an inert organic solvent such as methylene chloride, chloroform, dimethylformamide, or mixtures thereof at or near room temperature for a period of 3-24 hours to provide the corresponding amide derivative (25). Alternatively, 2- aryltryptamine 23 can be treated with an active ester or acid chloride of formula 26 in an inert organic solvent such as methylene chloride, chloroform, tetrahydrofuran, diethyl ether, or the like and a tertiary amine base such as triethylamine, diisopropylethylamine, pyridine or the like at a temperature of 0°-25°C for 30 minutes to 4 hours to give compound 25.
25 - Reaction Scheme H
R2 r
-(A
'Ri R ioRioa O RιoRιoa
Figure imgf000028_0001
BH3, THF
Figure imgf000028_0002
or
LiAlH4, THF
As shown in reaction Scheme H, the amide carbonyl of 25 can be reduced by treatment with borane, lithium aluminum hydride, or equivalent hydride sources in an inert organic solvent such as tetrahydrofuran, diethyl ether, 1,4-dioxane or the like at about 25° to about 100°C, preferably about 65°C, for a period of 1-8 hours to give the corresponding amine 27.
Reaction Scheme I
f2
28
O (A) R 10Rιoa II R 10R10a (A)-Ri
TFA, 3 A sieves
Figure imgf000028_0003
NaCNBH3)
Figure imgf000028_0004
As shown in reaction Scheme I, the 2-aryltryptamine 23 can be modified by treatment with an aldehyde or ketone of type 28 in the presence of a weak acid such as trifluoroacetic acid (TFA), acetic acid or the like, with or without a dessicant such as 3A molecular sieves or magnesium sulfate, and a hydride source such as sodium borohydride or sodium cyanoborohydride, in an inert organic solvent such as methanol, ethanol, isopropanol, tetrahydrofuran, dichloromethane,
26 chloroform, or mixtures thereof at a temperature of about 0° to about 25°C for a period of 1-12 hours to give the corresponding secondary or tertiary amine derivative 29.
Reaction Scheme J
02N. ,Nθ2 /NH2 RioRioβ2CI
2,4,6-collidine, CH2C12
Figure imgf000029_0001
OzN . O,
H
-s" i
I ,NH KJRIO3
R^Rioa l- PPh3, benzene
HO. JKΛ (A)
Figure imgf000029_0003
Figure imgf000029_0002
2. n-propylamine
As shown in reaction Scheme J, the tryptamine 23 can be modified using the Fukuyama modification of the Mitsunobu reaction (Fukuyama, T.; Jow, C.-K.; Cheung, M. Tetrahedron Lett. 1995, 36, 6373- 74). The tryptamine 23 may be reacted with an arylsufonyl chloride such as 2-nitrobenzene-sulfonyl chloride, 4-nitrobenzenesulfonyl chloride or 2,4-dinitrobenzene-sulfonyl chloride and a hindered amine base such as 2,4,6-collidine, 2,6-lutidine or the like in an inert organic solvent such as methylene chloride to provide the corresponding sulfonamide 30. The sulfonamides can be further modified by reaction with an alcohol of type 31 in the presence of triphenylphosphine and an activating agent such as diethylazodicarboxylate (DEAD), diisopropylazodicaboxylate or the like in an inert organic solvent such as benzene, toluene, tetrahydrofuran or mixtures thereof to give the dialkylsulfonamide adduct. Removal of a dinitrobenzenesulfonyl group is accomplished by treatment
- 27 with a nucleophilic amine such as rc-propylamine or the like in an inert organic solvent such as methylene chloride to give secondary amines of type 32. When a mono-nitrobenzenesulfonyl derivative is employed, the removal of the sulfonamide is accomplished with a more nucleophilic reagent such as thiophenol or mercaptoacetic acid in combination with lithium hydroxide in DMF.
Reaction Scheme K
,N02 l. PPh3, DEAD, benzene
2. n-propylamine
33 3. Remove PG2
N\
»
R10 R10a
-R3
Figure imgf000030_0001
R5 R4
Reaction Scheme K illustrates a method that is complimentary to reaction Scheme J for completing the synthesis of the novel compounds of formula (I). Scheme K also employs the Fukuyama modification of the Mitsunobu reaction similar to that illustrated in reaction Scheme J. However in this instance, the alcohol partner employed is a 2-aryltryptophol of general formula 21 which has been decribed previously in reaction Scheme F. The 2-aryltryptophol (21) is reacted with a substituted sulfonamide of general formula 33, triphenylphosphine and diethylazodicarboxylate in a suitable inert organic solvent such as benzene, tetrahydrofuran, 1,4-dioxane or the like. The reaction is generally conducted at room temperature for a
- 28 - period of 2 to 24 hours, typically overnight or for about 12-16 hours. The product is an N,N-disubstituted sulfonamide which is then separately subjected to reaction with a base such as n-propylamine which removes the sulfonamide substituent and furnishes a secondary amine related to formula 32. The sulfonamides of formula 33 employed are readily obtained from a primary amine and either 2-nitrobenzenesulfonyl chloride, 4-nitrobenzenesulfonyl chloride or 2,4-dinitrobenzenesuTfonyl chloride (as shown) in the presence of a hindered amine base such as 2,4,6-collidine, 2,6-lutidine or the like in an inert organic solvent such as methylene chloride. The final stage of the synthesis requires removal of the protecting group on the 7-azaindole nitrogen atom (PG2) which produces a compound of general formula 32 wherein R0 is a hydrogen atom. It will be recognized by individuals skilled in the art of organic synthesis that a preference for utilizing either the synthetic sequences outlined in reaction Schemes J or K will be determined by the substituents selected to be present in the compounds of formula (I).
The compounds of the present invention are useful in the treatment of various sex-hormone related conditions in men and women. This utility is manifested in their ability to act as antagonists of the neuropeptide hormone GnRH as demonstrated by activity in the following in vitro assays.
GnRH receptor binding assay:
The ligand binding assay is conducted with the human GnRH receptor (hGnRHR) obtained from CHO-Kl cells stably expressing the cloned receptor. Crude membrane suspensions are prepared from large batches of hGnRHR-CHO-Kl cells and stored as aliquots at -80° C . The radioactive peptide ligand [5-(1 5Iodo-Tyr)-Buserelin] is obtained from Woods Assays (Portland, Oregon) and has a radioactive specific activity of 1000 Ci/mmol. The membranes and the radioligand are diluted in assay buffer which consists of 50 mM Tris-HCl (pH 7.5), 2 mM MgCl2 and 0.1% bovine serum albumin. The ligand binding assay is performed at 22°C for 1 hour in 96-well polypropylene plates in a final volume of 200 ul. Each well in the assay plate contains 0.1 nM 125I-
29 - buserelin, 10-15 ug of hGnRH receptor-membrane protein and the test compound. Test compounds are examined over a range of concentrations from 0.01 to 10,000 nM. The incubation is terminated by vacuum filtration onto 96-well Packard GF/C Unifilter plates (pretreated with 0.1% polyethyleneimine) and then washed with 2 mL of cold phosphate buffered saline (pH 7.5). The Unifilter plates are dried prior to addition of scintillation fluid and counting in a Packard TopCount detector
Phosphoinositide (PI) turnover assay
Chinese hamster ovary cell lines expressing the human GnRH receptor functionally coupled to phospholipase C were established and seeded at a concentration of 60,000 cells/mL/well in inositol-free F12 medium containing 10% dialyzed fetal bovine serum, 1% Pen/Strep, 2 mM glutamine, 500 μg/mL G418 and 1 μCi (3H)inositol in 24-well tray. Forty-eight hours after seeding, cells were washed with 3 x 1 L of PBS containing 10 mM LiCl and treated with various concentrations of GnRH antagonist for 2 hrs at 37°C before the addition of 0.5 nM GnRH. After incubation at 37°C for an additional 60 min, the medium was removed and the cells were lysed with 1 mL of 0.1 M formic acid. The trays were freeze-thawed once and the cell extract was applied onto a Dowex AG1-X8 column. The column was washed with 2 1 mL H2O to remove free (3H)inositol and (3H)inositol phosphates were eluted with 3 x 1 mL 2 M ammonium formate in 1M formic acid. The eluate was then counted in a scintillation counter.
The compounds of formula I are useful in a number of areas affected by GnRH. They may be useful in sex-hormone related conditions, sex-hormone dependent cancers, benign prostatic hypertrophy or myoma of the uterus. Sex-hormone dependent cancers which may benefit from the administration of the compounds of this invention include prostatic cancer, uterine cancer, breast cancer and pituitary gonadotrophe adenomas. Other sex-hormone dependent conditions which may benefit from the administration of the compounds of this invention include endometriosis, polycystic ovarian disease, uterine fibroids and precocious puberty. The compounds may also be used in
- 30 combination with an angiotensin-converting enzyme inhibitor such as Enalapril or Captopril, an angiotensin H-receptor antagonist such as Losartan or a renin inhibitor for the treatment of uterine fibroids. The compounds of the invention may also be useful for controlling pregnancy, as a contraceptive in both men and women, for in vitro fertilization, in the treatment of premenstrual syndrome, in the treatment of lupus erythematosis, in the treatment of hirsutism, in the treatment of irritable bowel syndrome and for the treatment of sleep disorders such as sleep apnea. A further use of the compounds of this invention is as an adjunct to growth hormone therapy in growth hormone deficient children. The compounds may be administered with growth hormone or a compound which increases the endogenous production or release of growth hormone. Certain compounds have been developed which stimulate the release of endogenous growth hormone. Peptides which are known to stimulate the release of endogenous growth hormone include growth hormone releasing hormone, the growth hormone releasing peptides GHRP-6 and GHRP-1 (described in U.S. Patent No. 4,411,890, PCT Patent Pub. No. WO 89/07110, and PCT Patent Pub. No. WO 89/07111) and GHRP-2 (described in PCT Patent Pub. No.
WO 93/04081), as well as hexarelin (J. Endocrinol Invest.. 15(Suppl 4), 45 (1992)). Other compounds which stimulate the release of endogenous growth hormone are disclosed, for example, in the following: U.S. Patent No. 3,239,345; U.S. Patent No. 4,036,979; U.S. Patent No. 4,411,890; U.S. Patent No. 5,206,235; U.S. Patent No. 5,283,241; U.S. Patent No. 5,284,841; U.S. Patent No. 5,310,737; U.S. Patent No. 5,317,017; U.S. Patent No. 5,374,721; U.S. Patent No. 5,430,144; U.S. Patent No. 5,434,261; U.S. Patent No. 5,438,136; EPO Patent Pub. No. 0,144,230; EPO Patent Pub. No. 0,513,974; PCT Patent Pub. No. WO 94/07486; PCT Patent Pub. No. WO 94/08583; PCT Patent Pub. No. WO 94/11012; PCT Patent Pub. No. WO 94/13696; PCT Patent Pub. No. WO 94/19367; PCT Patent Pub. No. WO 95/03289; PCT Patent Pub. No. WO 95/03290; PCT Patent Pub. No. WO 95/09633; PCT Patent Pub. No. WO 95/11029; PCT Patent Pub. No. WO 95/12598; PCT Patent Pub. No. WO 95/13069; PCT Patent Pub. No.
31 WO 95/14666; PCT Patent Pub. No. WO 95/16675; PCT Patent Pub. No. WO 95/16692; PCT Patent Pub. No. WO 95/17422; PCT Patent Pub. No. WO 95/17423; Science. 260. 1640-1643 (June 11, 1993); Ann. Rep. Med. Chem.. 28, 177-186 (1993); Bioorg. Med. Chem. Ltrs.. 4(22), 2709-2714 (1994); and Proc. Natl. Acad. Sci. USA 92, 7001-7005 (July 1995).
Representative preferred growth hormone secretagoues employed in the present combination include the following:
1) N-[l(R)-[(l,2-Dihydro-l-methanesulfonylspiro[3H-indole-3,4'- piperidin]-l'-yl)carbonyl]-2-(lH-indol-3-yl)ethyl]-2-amino-2-methyl- propanamide;
2) N-[l(R)-[(l,2-Dihydro-l-methanecarbonylspiro[3H-indole-3,4'- piperidin]-l'-yl)carbonyl]-2-(lH-indol-3-yl)ethyl]-2-amino-2-methyl- propanamide;
3) N-[l(R)-[(l,2-Dihydro-l-benzenesulfonylspiro[3H-indole-3,4'- piperidin]-l'-yl)carbonyl]-2-(lH-indol-3-yl)ethyl]-2-amino-2-methyl- propanamide;
4) N-[l(R)-[(3,4-Dihydro-spiro[2H-l-benzopyran-2,4'-piperidin]-l'-yl) carbonyl]-2-(lH-indol-3-yl)ethyl]-2-amino-2-methylpropanamide;
5) N-[l(R)-[(2-Acetyl-l,2,3,4-tetrahydrospiro[isoquinolin-4,4'-piperidin]- l'-yl)carbonyl]-2-(indol-3-yl)ethyl]-2-amino-2-methyl-propanamide;
6) N-[l(R)-[(l,2-Dihydro-l-methanesulfonylspiro[3H-indole-3,4'- piperidin]-l'-yl)carbonyl]-2-(phenylmethyloxy)ethyl]-2-amino-2- methylpropanamide ;
7) N-[l(R)-[(l,2-Dihydro-l-methanesulfonylspiro[3H-indole-3,4'- piperidin]-l'-yl)carbonyl]-2-(phenylmethyloxy)ethyl]-2-amino-2- methylpropanamide methanesulfonate;
32 8) N- [1(R)- [( 1 ,2-Dihydro- 1-methanesulfonylspiro [3H-indole-3,4'- piperidin]-l,-yl)carbonyl]-2-(2',6'-difluorophenylmethyloxy)ethyl]-2- amino-2-methylpropanamide;
9) N-[l(R)-[(l,2-Dihydro-l-methanesulfonyl-5-fluorospiro[3H-indole-3,4' piperidin]-l'-yl)carbonyl]-2-(phenylmethyloxy)ethyl]-2-amino-2- methylpropanamide;
10) N-[l(S)-[(l,2-Dihydro-l-methanesulfonylspiro[3H-indole-3,4'- piperidin]-l'-yl) carbonyl]-2-(phenylmethylthio)ethyl]-2-amino-2- methylpropanamide;
11) N-[l(R)-[(l,2-Dihydro-l-methanesulfonylspiro[3H-indole-3,4'- piperidin]-l'-yl)carbonyl]-3-phenylpropyl]-2-amino-2-methyl- propanamide;
12) N-[l(R)-[(l,2-Dihydro-l-methanesulfonylspiro[3H-indole-3,4*- piperidin] - 1 '-yl)carbonyl] -3-cyclohexylpropyl] -2-amino-2-methyl- propanamide;
13) N-[l(R)-[(l,2-Dihydro-l-methanesulfonylspiro[3H-indole-3,4'- piperidin]-l'-yl)carbonyl]-4-phenylbutyl]-2-amino-2-methyl- propanamide;
14) N-[l(R)-[(l,2-Dihydro-l-methanesulfonylspiro[3H-indole-3,4'- piperidin]-l'-yl)carbonyl]-2-(5-fluoro-lH-indol-3-yl)ethyl]-2-amino-2- methylpropanamide;
15) N-[l(R)-[(l,2-Dihydro-l-methanesulfonyl-5-fluorospiro[3H-indole- 3,4'-piperidin]-l'-yl)carbonyl]-2-(5-fluoro-lH-indol-3-yl)ethyl]-2-amino-2- methylpropanamide;
- 33 - 16) N-[l(R)-[(l,2-Dihydro-l-(2-ethoxycarbonyl)methylsulfonylspiro-[3H- indole-3,4'-piperidin]-l'-yl)carbonyl]-2-(lH-indol-3-yl)ethyl]-2-amino-2- methylpropanamide;
17) N-[l(R)-[(l,2-Dihydro-l,l-dioxospiro[3H-benzothiophene-3,4'- piperidin]-l'-yl)carbonyl]-2-(phenylmethyloxy)ethyl]-2-amino-2- methylpropanamide;
and pharmaceutically acceptable salts thereof. The compounds of the invention may also be used in combination with bisphosphonates (bisphosphonic acids) and other agents, such as growth hormone secretagogues, for the treatment and the prevention of disturbances of calcium, phosphate and bone metabolism, in particular, for the prevention of bone loss during therapy with the GnRH antagonist , and in combination with estrogens, progesterones and or androgens for the prevention or treatment of bone loss or hypogonadal symptoms such as hot flashes during therapy with the GnRH antagonist.
Bisphosphonates (bisphosphonic acids) are known to inhibit bone resorption and are useful for the treatment of bone lithiasis as disclosed in U.S. Patent 4,621,077 to Rosini, et al.
The literature discloses a variety of bisphosphonic acids which are useful in the treatment and prevention of diseases involving bone resorption. Representative examples may be found in the following: U.S. Patent No. 3,251,907; U.S. Patent No. 3,422,137; U.S.
Patent No. 3,584,125; U.S. Patent No. 3,940,436; U.S. Patent No. 3,944,599;
U.S. Patent No. 3,962,432; U.S. Patent No. 4,054,598; U.S. Patent No.
4,267,108; U.S. Patent No. 4,327,039; U.S. Patent No. 4,407,761; U.S.
Patent No. 4,578,376; U.S. Patent No. 4,621,077; U.S. Patent No. 4,624,947; U.S. Patent No. 4,746,654; U.S. Patent No. 4,761,406; U.S. Patent No.
4,922,007; U.S. Patent No. 4,942,157; U.S. Patent No. 5,227,506; U.S.
Patent No. 5,270,365; EPO Patent Pub. No. 0,252,504; and J. Org. Chem. ,
36, 3843 (1971).
34 - The preparation of bisphosphonic acids and halo- bisphosphonic acids is well known in the art. Representative examples may be found in the above mentioned references which disclose the compounds as being useful for the treatment of disturbances of calcium or phosphate metabolism, in particular, as inhibitors of bone resorption. Preferred bisphosphonates are selected from the group of the following compounds: alendronic acid, etidrononic acid, clodronic acid, pamidronic acid, tiludronic acid, risedronic acid, 6-amino-l- hydroxy-hexylidene-bisphosphonic acid, and 1-hydroxy- 3(methylpentylamino)-propylidene-bisphosphonic acid; or any pharmaceutically acceptable salt thereof. A particularly preferred bisphosphonate is alendronic acid (alendronate), or a pharmaceutically acceptable salt thereof. An especially preferred bisphosphonate is alendronate sodium, including alendronate sodium trihydrate. Alendronate sodium has received regulatory approval for marketing in the United States under the trademark FOSAMAX®.
Additionally, a compound of the present invention may be co-administered with a 5α-reductase 2 inhibitor, such as finasteride or epristeride; a 5α-reductase 1 inhibitor such as 4,7β-dimethyl-4-aza-5α- cholestan-3-one, 3-oxo-4-aza-4,7β-dimethyl-16β-(4-chlorophenoxy)-5α- androstane, and 3-oxo-4-aza-4,7β-dimethyl-16β-(phenoxy)-5α-androstane as disclosed in WO 93/23420 and WO 95/11254; dual inhibitors of 5α- reductase 1 and 5α-reductase 2 such as 3-oxo-4-aza-17β-(2,5- trifluoromethylphenyl-carbamoyl)-5α-androstane as disclosed in WO 95/07927; antiandrogens such as flutamide, casodex and cyproterone acetate, and alpha-1 blockers such as prazosin, terazosin, doxazosin, tamsulosin, and alfuzosin.
Further, a compound of the present invention may be used in combination with growth hormone, growth hormone releasing hormone or growth hormone secretagogues, to delay puberty in growth hormone deficient children, which will allow them to continue to gain height before fusion of the epiphyses and cessation of growth at puberty. Further, a compound of the present invention may be
- 35 used in combination or co-administered with a compound having luteinizing hormone releasing activity such as a peptide or natural hormone or analog thereof. Such peptide compounds include leuprorelin, gonadorelin, buserelin, triptorelin, goserelin, nafarelin, histrelin, deslorelin, meterlin and recirelin.
For combination treatment with more than one active agent, where the active agents are in separate dosage formulations, the active agents may be administered separately or in conjunction. In addition, the administration of one element may be prior to, concurrent to, or subsequent to the administration of the other agent.
The pharmaceutical compositions containing the active ingredient may be in a form suitable for oral use, for example, as tablets, troches, lozenges, aqueous or oily suspensions, dispersible powders or granules, emulsions, hard or soft capsules, or syrups or elixirs. Compositions intended for oral use may be prepared according to any method known to the art for the manufacture of pharmaceutical compositions 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 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 technique described in the U.S. Patent 4,256,108; 4,166,452; and 4,265,874 to form osmotic therapeutic tablets for control release.
- 36 Formulations for oral use may also be presented as hard gelatin capsules wherein the active ingredient is mixed with an inert solid diluent, for example, calcium carbonate, calcium phosphate or kaolin, or as 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 contain the active material in admixture with excipients suitable for the manufacture of aqueous suspensions. Such excipients are suspending agents, for example sodium carboxymethyl-cellulose, methylcellulose, hydroxy-propylmethy- cellulose, sodium alginate, polyvinyl-pyrrolidone, gum tragacanth and gum acacia; dispersing or wetting agents may be a naturally-occurring phosphatide, for example 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 heptadecaethylene-oxycetanol, 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 acids and hexitol anhydrides, for example polyethylene sorbitan monooleate. The aqueous suspensions may also contain one or more preservatives, for example ethyl, or n-propyl, p-hydroxybenzoate, one or more coloring agents, one or more flavoring agents, and one or more sweetening agents, such as sucrose, saccharin or aspartame. 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 mineral oil such as liquid paraffin. The oily suspensions may contain a thickening agent, for example beeswax, hard paraffin or cetyl alcohol. 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
37 - ingredient 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 invention may also be in the form of an 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 liquid paraffin or mixtures of these. Suitable emulsifying agents may be naturally-occurring phosphatides, for example soy beans, lecithin, and esters or partial esters derived from fatty acids and hexitol anhydrides, for example sorbitan monooleate, and condensation products of the said partial esters with ethylene oxide, for example polyoxyethylene sorbitan monooleate. The emulsions may also contain sweetening and flavouring 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 injectable aqueous or oleagenous suspension. This suspension may be formulated according to the known art using those suitable dispersing or wetting agents and suspending agents which have been mentioned 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-butane diol. 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 conventionally employed as a solvent or suspending medium. For this purpose any bland fixed oil may be employed including synthetic mono- or diglycerides. In addition, fatty acids such as oleic acid find use in the preparation of injectables. Compounds of Formula I may also be administered in the form of a suppositories for rectal administration of the drug. These compositions can be prepared by mixing the drug with a suitable non-
38 irritating excipient which is solid at ordinary temperatures but liquid at the rectal temperature and will therefore melt in the rectum to release the drug. Such materials are cocoa butter and polyethylene glycols. For topical use, creams, ointments, jellies, solutions or suspensions, etc., containing the compound of Formula I are employed. (For purposes of this application, topical application shall include mouth washes and gargles.)
The compounds for the present invention can be administered in intranasal form via topical use of suitable intranasal vehicles, or via transdermal routes, using those forms of transdermal skin patches well known to those of ordinary skill in the art. To be administered in the form of a transdermal delivery system, the dosage administration will, of course, be continuous rather than intermittent throughout the dosage regimen. Compounds of the present invention may also be delivered as a suppository employing bases such as cocoa butter, glycerinated gelatin, hydrogenated vegetable oils, mixtures of polyethylene glycols of various molecular weights and fatty acid esters of polyethylene glycol.
The dosage regimen utilizing the compounds of the present invention is selected in accordance with a variety of factors including type, species, age, weight, sex and medical condition of the patient; the severity of the condition to be treated; the route of administration; the renal and hepatic function of the patient; and the particular compound thereof employed. A physician or veterinarian of ordinary skill can readily determine and prescribe the effective amount of the drug required to prevent, counter, arrest or reverse the progress of the condition. Optimal precision in achieving concentration of drug within the range that yields efficacy without toxicity requires a regimen based on the kinetics of the drug's availability to target sites. This involves a consideration of the distribution, equilibrium, and elimination of a drug. Preferably, doses of the compound of structural formula I useful in the method of the present invention range from 0.01 to 1000 mg per adult human per day. Most preferably, dosages range from 0.1 to 500 mg/day. For
39 oral administration, the compositions are preferably provided in the form of tablets containing 0.01 to 1000 milligrams of the active ingredient, particularly 0.01, 0.05, 0.1, 0.5, 1.0, 2.5, 5.0, 10.0, 15.0, 25.0, 50.0, 100 and 500 milligrams of the active ingredient for the symptomatic adjustment of the dosage to the patient to be treated. An effective amount of the drug is ordinarily supplied at a dosage level of from about 0.0002 mg/kg to about 50 mg/kg of body weight per day. The range is more particularly from about 0.001 mg/kg to 1 mg/kg of body weight per day. Advantageously, the active agent of the present invention may be administered in a single daily dose, or the total daily dosage may be administered in dividend doses of two, three or four times daily.
The amount of active ingredient that may be combined with the carrier materials to produce a single dosage form will vary depending upon the host treated and the particular mode of administration.
It will be understood, however, that the specific dose level for any particular patient will depend upon a variety of factors including the age, body weight, general health, sex, diet, time of administration, route of administration, rate of excretion, drug combination and the severity of the particular disease undergoing therapy.
The following examples illustrate the preparation of some of the compounds of the invention and are not to be construed as limiting the invention disclosed herein.
EXAMPLE 1
- 40 -
Figure imgf000043_0001
(g)-l-(iV.N-Diisobutylamino)-2-f2-(3.5-dimethylphenyl)- 3-ri-methyl-2-(imidazo[4.5-b1pyridin-6-yl)ethyn-lH-pyrrolo [2.3-61-pyridin-5-yl}-2-methylpropan-l-one
Step 1A: Methyl (S)-2-[3-(2-benzyloxy-l-methylethyl)-2-triethylsilyl- lH-pyrrolor2.3-b1pyridin-5-yll-2-methylpropanoate
A vigorously stirred suspension of methyl 2-(6-amino-5- iodopyridin-3-yl)-2-methylpropanoate (4.61 g, 14.4 mmol), (<S)-(4- benzyloxy-3-methylbut-l-ynyl)triethylsilane (4.98 g, 17.3 mmol),
Pd(dppf)Cl2»CH2Cl2 (0.59 g, 0.72 mmol) LiCl (0.61 g, 14.4 mmol), Na2CO3 (3.82 g, 36.0 mmol) and ΛT^/V-dimethylformamide (60 mL) was degassed via three vacuum/nitrogen ingress cycles and the resulting mixture was heated at approximately 90°C overnight. After cooling to ambient temperature, the reaction mixture was diluted with ethyl acetate and filtered through celite® washing copiously with ethyl acetate. The filtrate was poured into water and extracted with ethyl acetate (x3). The combined organic extract was washed with brine, dried (MgSO4) and concentrated in vacuo. The residue was purified by flash chromatography on silica gel (gradient elution; 20-25% ethyl acetate/hexanes as eluent) to give the title compound as a viscous pale yellow oil (6.11 g, 95%).
Step IB: Methyl (S)-2-[3-(2-benzyloxy-l-methylethyl)-2-iodo-lH- pyrrolo [2.3-61 pyridin-5-yll -2-methylpropanoate
- 41 A solution of iodine monochloride (2.83 g, 17.4 mmol) in MeOH (25 mL) was added over approximately 0.5 h via pressure equalizing addition funnel to a vigorously stirred mixture of methyl (5')-2-[3-(2-benzyloxy-l-methylethyl)-2-triethylsilyl-lH-pyrrolo[2,3- b]pyridin-5-yl]-2-methylpropanoate (6.00 g, 13.4 mmol) and silver tetrafluoroborate (3.39 g, 17.4 mmol) in MeOH/THF (1:2; 75 mL) at 0°C. After an additional 0.5h, the reaction was quenched with 1M Na2S2O3, warmed to room temperature and filtered through celite® washing copiously with ethyl acetate. The filtrate was concentrated under reduced pressure, poured into 1M Na2S2O3 and extracted with ethyl acetate (x3). The combined organic extract was washed with brine, dried (MgSO4) and concentrated in vacuo. The residue was purified by flash chromatography on silica gel (25% ethyl acetate/hexanes as eluent) to give the title compound as a colourless solid (5.54 g, 84%).
Step IC: Methyl (S)-2-[3-(2-benzyloxy-l-methylethyl)-2-(3,5-dimethyl- phenyl)-lH-pyrrolor2.3-fclpyridin-5-yl1-2-methylpropanoate A vigorously stirred suspension of methyl (S)-2-[3-(2- benzyloxy-l-methylethyl)-2-iodo-lH-pyrrolo[2,3-6]pyridin-5-yl]-2- methylpropanoate (4.00 g, 8.12 mmol), 2,5-dimethylphenylboronic acid (1.83 g, 12.2 mmol) and Pd(dppf)Cl2*CΗ2Cl2 (0.33 g, 0.406 mmol) in toluene/MeOH (5:2; 140 mL) was degassed via three vacuum/nitrogen ingress cycles and the resulting mixture was heated to approximately 80°C. 1M Na2CO3 (20.3 mL, 20.3 mmol) was added dropwise via syringe and the resulting mixture maintained at reflux overnight. After cooling to ambient temperature, the reaction mixture was diluted with ethyl acetate and filtered through celite® washing copiously with ethyl acetate. The filtrate was poured into water and extracted with ethyl acetate (x3). The combined organic extract was washed with brine, dried (MgSO4) and concentrated in vacuo. The residue was purified by flash chromatography on silica gel (25% ethyl acetate/hexanes as eluent) to afford the title compound as a colourless foam (3.82 g, 100%).
42 - Step ID: (S)-2-[3-(2-Benzyloxy-l-methylethyl)-2-(3,5-dimethylphenyl)- lH-pyrroloF2.3-b1pyridin-5-yll-2-methylpropanoicacid A vigorously stirred suspension of methyl (S)-2-[3-(2- benzyloxy-l-methylethyl)-2-(3,5-dimethyl-phenyl)-lH-pyrrolo[2,3- 6]pyridin-5-yl]-2-methylpropanoate (3.82 g, 8.12 mmol) and 2N KOΗ (40.6 mL, 0.081 mol) in MeOΗ (40 mL) was heated at 80°C for approximately 4 h. After cooling to room temperature, the reaction mixture was acidified to pΗ 6 with 2N ΗC1 and extracted with ethyl acetate (x3). The combined organic extract was washed with brine, dried (MgSO4) and concentrated in vacuo. The crude residue was used without further purification in the subsequent reaction.
Step IE: (S -l-(N,N-Diisobutylamino)-2-[3-(2-benzyloxy-l-methyl- ethyl)-2-(3,5-dimethylphenyl)-lH-pyrrolo[2,3-&]pyridin- 5-yll-2-methylpropan-l-one
PyBOP is added to a stirred mixture of (.S)-2-[3-(2-benzyloxy- l-methylethyl)-2-(3,5-dimethylphenyl)-lH-pyrrolo[2,3-δ]pyridin-5-yl]-2- methylpropanoic acid, diisobutylamine and triethylamine in CΗ2C12 at ambient temperature. After approximately 12h, the reaction mixture is poured into water/brine (1:1) and extracted with ethyl acetate. The combined organic extract is washed with brine, dried (MgSO4) and concentrated in vacuo. The residue is purified by flash chromatography on silica gel (gradient elution; 60-75% ethyl acetate/hexanes as eluent) to give the title compound.
Step IF: (S)-l-(N^V-Diisobutylamino)-2-[3-(2-benzyloxy-l-methyl- ethyl)-2-(3,5-dimethylphenyl)-lH-l-(;ter£-butoxycarbonyl)- pyrrolo [2.3-61 pyridin-5-yll-2-methylpropan-l-one
Di~ er -butyldicarbonate is added to stirred suspension of (S)-l-(Λ"^-diisobutylamino)-2-[3-(2-benzyloxy-l-methylethyl)-2-(3,5- dimethylphenyl)-lH-pyrrolo[2,3-δ]pyridin-5-yl]-2-methylpropan-l-one, DMAP, and potassium carbonate in CH2C12 at room temperature. After approximately 3h, the reaction mixture is poured into water and extracted with ethyl acetate. The combined organic extract is washed
- 43 with brine, dried (MgSO4) and concentrated in vacuo. The residue is purified by flash chromatography on silica gel (60% ethyl acetate/hexanes as eluent) to give the title compound.
Step 1G: (S)-l-(ΛyV^Diisobutylamino)-2-[3-(2-hydroxy-l-methyl- ethyl)-2-(3,5-dimethylphenyl)-lH-l-(£er -butoxycarbonyl)- pyrrolo [2.3-61 pyridin-5-yll -2-methylpropan-l-one
A mixture of (<S)-l-(N -v'-diisobutylamino)-2-[3-(2-benzyloxy- l-methylethyl)-2-(3,5-dimethylphenyl)-lH-l-( er -butoxycarbonyl)- pyrrolo[2,3-6]pyridin-5-yl]-2-methylproρan-l-one and Pd(OH)2 (Pd-20%) in glacial acetic acid/EtOH (1:1) is hydrogenated at 50 psi for about 4 days. The resulting mixture is filtered through celite® washing copiously with EtOH, the filtrate is evaporated in vacuo and the residue purified by flash chromatography on silica gel (gradient elution; 75-90% ethyl acetate/hexanes) to give the title compound.
Step lH: (5)-l-(NrN-Diisobutylamino)-2-[3-(2-azido-l-methylethyl)-2- (3,5-dimethylphenyl)-lH-l-( er£-butoxycarbonyl)pyrrolo- r2.3-61pyridin-5-yll-2-methylpropan-l-one DEAD is added dropwise via syringe to a stirred solution of (S)-l-(NN-diisobutylamino)-2-[3-(2-hydroxy-l-methylethyl)-2-(3,5- dimethylphenyl)- IH- l-(ter£-butoxycarbonyl)pyrrolo [2,3-6] -pyridin-5-yl] - 2-methylpropan-l-one, ZnN6 #2py, PPh3 and imidazole in CΗ2C12 at approximately 0°C. The reaction mixture is allowed to warm to room temperature overnight, and is then filtered through celite® washing copiously with CH2C12. The filtrate is poured into water and extracted with CH2C12. The combined organic extract is washed with brine, dried (MgSO4) and concentrated in vacuo. The residue is purified by flash chromatography on silica gel (gradient elution; 25-40% ethyl acetate/hexanes as eluent) to give the title compound.
Step II: (S)-l-(Λ^N-Diisobutylamino)-2-[3-(2-amino-l-methyl- ethyl)-2-(3,5-dimethylphenyl)-lH-l-(ter£-butoxycarbonyl)- pyrrolo [2.3-61 pyridin-5-yll -2-methylpropan-l-one
44 A mixture of (<S)-l-(Λ V-diisobutylamino)-2-[3-(2-azido- l-methylethyl)-2-(3,5-dimethylphenyl)-lH-l-( er -butoxycarbonyl)- pyrrolo[2,3-6]pyridin-5-yl]-2-methylpropan-l-one and Pd/C (Pd-10%) in MeOΗ/EtOΗ is hydrogenated at 50 psi overnight. The resulting mixture is filtered through celite® washing copiously with EtOΗ, the filtrate is evaporated in vacuo and the residue purified by preparative thin layer chromatography on silica gel (100%ethyl acetate as eluent) to give the title compound.
Step U: (S)-l-(iV^V-Diisobutylamino)-2-[3-(2-(2,4-dinitrobenzene- sulfonylamino)-l-methylethyl)-2-(3,5-dimethylphenyl)-lH-l- ( er -butoxycarbonyl)pyrrolo[2,3-6]pyridin-5-yl]-2-methyl- propan-1-one
2,4-Dinitrobenzenesulfonyl chloride is added in one portion to a stirred solution of (SVl- Λ jN-diisobutylamino^-fS- -amino-l- methyl-ethy ^-^δ-dimethylpheny -lH-l- er^-butoxycarbonyl^^ pyrrolo [2,3-6] -pyridin-5-yl] -2-methylpropan-l-one and 2,4,6-collidine in CΗ2C12 at approximately 0°C. After 5 min., the resulting mixture is warmed to ambient temperature and aged for 2h. The reaction mixture is poured into water and extracted with ethyl acetate. The combined organic extract is washed with brine, dried (MgSO4) and concentrated in vacuo. The residue is purified by flash chromatography on silica gel (50% ethyl acetate/hexanes as eluent) to give the title compound.
Step IK: (S)-6-{2-[N-(5-[2-(N^-Diisobutylamino)-l,l-dimethyl-2- oxoethyl]-2-(3,5-dimethylphenyl)-lH-l-(^er^-butoxycarbonyl)- pyrrolo [2,3-6] pyridin-3-yl] propyl)-AT-(2,4-dinitrobenzene- sulfonyl)]aminoethyl}-3-(2-trimethylsilylethoxymethyl)-3H- imidazo[4.5-61pyridine DEAD is added dropwise via syringe to a stirred solution of (S)-l-(N' rN-diisobutylamino)-2-[3-(2-(2,4-dinitrobenzenesulfonylamino)- l-methylethyl)-2-(3,5-dimethylphenyl)-lH-l-( er£-butoxycarbonyl)- pyrrolo[2,3-6]pyridin-5-yl]-2-methylpropan-l-one, 2-[3-(2-trimethylsilyl- ethoxymethyl)-3H-imidazo[4,5-6]pyridin-6-yl]ethanol and PPh3 in
- 45 benzene at room temperature. After approximately lh, the reaction mixture is concentrated in vacuo and the residue is purified by flash chromatography on silica gel (60-80% ethyl acetate/hexanes as eluent) to give the title compound.
Step IL: (5)-6-{2- [2- [5- [2-(N,N-Diisobutylamino)- 1 , l-dimethyl-2-oxo- ethyl]-2-(3,5-dimethylphenyl)-lH-l-(ter£-butoxycarbonyl)- pyrrolo [2,3-6] pyridin-3-yl]propylamino]ethyl}-3-(2-trim ethyl - silylethoxymethyl)-3H-imidazo[4.5-61pyridine n-Propylamine is added to a stirred solution of crude
(S)-6-{2-[Λ^-(5-[2-(N^-diisobutylamino)-l,l-dimethyl-2-oxoethyl]-2-(3,5- dimethylphenyl)-lH-l-(ter -butoxycarbonyl)pyrrolo [2,3-6] pyridin-3- yl]propyl)-N-(2,4-dinitrobenzenesulfonyl)]aminoethyl}-3-(2-trimethylsilyl- ethoxymethyl)-3H-imidazo[4,5-6]pyridine in CΗ2C12 at room temperature. After approximately 20 min, the volatiles are evaporated in vacuo and the residue is purified by preparative thin layer chromatography on silica gel (100% ethyl acetate as eluent) to give the title compound.
Step 1M: (S)-l-(iV,N-Diisobutylamino)-2-{2-(3,5-dimethylphenyl)- 3-[l-methyl-2-(imidazo[4,5-6]pyridin-6-yl)ethyl]-lH- pyrrolo [2.3-61 pyridin-5-yl)-2-methylpropan-l-one
A solution of (S)-6-{2-[2-[5-[2-(N^-diisobuylamino)-l,l- dimethyl-2-oxoethyl]-2-(3,5-dimethylphenyl)-lH-l-(^er^-butoxycarbonyl)- pyrrolo[2,3-6]pyridin-3-yl]propylamino]ethyl}-3-(2-trimethylsilyl- ethoxymethyl)-3H-imidazo[4,5-6]pyridine in 2N ΗCl/EtOΗ (1:1) is aged for approximately 2h at 75°C. After cooling to room temperature, the reaction mixture is adjusted to pΗ 9 with 5N NaOΗ and extracted with ethyl acetate. The combined organic extract is washed with brine, dried (MgSO4) and concentrated in vacuo. The residue is purified by preparative thin layer chromatography on silica gel (100% ethyl acetate as eluent) to give the title compound.
PREPARATION OF SYNTHETIC INTERMEDIATES
46 Methyl 2-(6-amino-5-iodopyridin-3-yl)-2-methylpropanoate
Step A: Ethyl 2-methyl-2-(pyridin-3-yl)propanoate A solution of ethyl-3-pyridylacetate (10.0 g, 60.5 mmol) in
THF (50 mL) was added over approximately 0.5 h via pressure equalizing addition funnel to a stirred mixture of potassium hexamethyldisilazane (48.3 g, 0.242 mmol) in THF (250 mL) at -20°C. After 0.5 h, Mel was added dropwise so as to maintain the internal temperature between -15°C to -20°C. After warming to approximately 0°C over 12h, the reaction was quenched with saturated aqueous NH4C1 and concentrated under reduced pressure. The residue was partitioned between ethyl acetate and water, the organic phase separated and the aqueous phase re-extracted with ethyl acetate (x3). The combined organic extract was washed with brine, dried (MgSO4) and concentrated in vacuo. The residue was purified by flash chromatography on silica gel (30% ethyl acetate/hexanes as eluent) to give the title compound as a pale yellow oil (10.1 g, 86%).
Step B: Ethyl 2-methyl-2-(pyridin-3-yl)propanoate-N-oxide eta-chloroperoxybenzoic acid (55%; 21.3 g, 67,9 mmol) was added in one portion to a vigorously stirred emulsion of ethyl 2- methyl-2-(pyridin-3-yl)propanoate and NaHCO3 (17.5 g, 0.209 mmol) in water/chloroform (1:1; 500 mL) at ambient temperature. After approximately 12 h, the organic phase was separated and the aqueous phase extracted with chloroform (x3). The combined organic extract was washed with brine, dried (MgSO4) and concentrated in vacuo. The residue (10.9 g, 100%) was judged pure by a combination of TLC and H nmr analysis and was used without further purification in the subsequent reaction.
Step C: Ethyl 2-[6-(2,2-dimethyl-4-oxo-4H-l,3-benzoxazin-3-yl)- pyridin-3-yn-2-methylpropanoate
A solution of 4-chloro-2,2-dimethyl-2H-l,3-benzoxazine
- 47 - (10.1 g, 51.6 mmol) and ethyl 2-methyl-2-(pyridin-3-yl)propanoate- N-oxide (9.0 g, 43.0 mmol) in 1,2-dichloroethane (100 mL) was heated at approximately 90°C for 3 d. After cooling to room temperature, the solvent was evaporated under reduced pressure and the residue purified by flash chromatography on silica gel (gradient elution; 20-25% ethyl acetate/hexanes as eluent) to give the title compound as a pale yellow viscous oil (14.3 g, 90%).
Step D: 2-(6-Aminopyridin-3-yl)-2-methylpropanoic acid hydrochloride
A stirred mixture of ethyl 2-[6-(2,2-dimethyl-4-oxo-4H-l,3- benzoxazin-3-yl)-pyridin-3-yl]-2-methylpropanoate (13.3 g, 36.1 mmol) in concentrated ΗC1 (50 mL) was heated at 100°C overnight. After cooling to ambient temperature, the reaction mixture was concentrated in vacuo and the residue washed exhaustively with chloroform to give the title compound as a colourless solid (6.90 g, 88%).
Step E: Methyl 2-(6-aminopyridin-3-yl)-2-methylpropanoate
A solution of 2-(6-aminopyridin-3-yl)-2-methylpropanoic acid hydrochloride (35.0 g, 0.162 mmol) and concentrated Η2SO4 (5 mL) in MeOH (250 mL) was heated at reflux overnight. After cooling to ambient temperature, the reaction was quenched cautiously with saturated aqueous NaHCO3 and concentrated in vacuo. The residue was partitioned between ethyl acetate and water, the organic phase separated and the aqueous phase re-extracted with ethyl acetate (¥3). The combined organic extract was washed with brine, dried (MgSO4) and concentrated in vacuo. The residue (31.6 g, 100%) was judged pure by a combination of TLC and XH nmr analysis and was used without further purification in the subsequent reaction.
Step F: Methyl 2-(6-amino-5-iodopyridin-3-yl)-2-methylpropanoate
A solution of methyl 2-(6-aminopyridin-3-yl)-2-methyl- propanoate (10.0 g, 51.5 mmol) in MeOH (50 mL) was added over approximately 0.5 h via pressure equalizing addition funnel to a
48 vigorously stirred suspension of iodine (17.0 g, 67.0 mmol) and silver trifluoroacetate (14.8 g, 67.0 mmol) in MeOH (200 mL) at room temperature. After 3 h, the reaction was quenched sequentially with 1M Na2S2O3 followed by saturated aqueous NaHCO3. The resulting mixture was filtered through celite® washing copiously with ethyl acetate, the filtrate concentrated in vacuo and the residue partitioned between ethyl acetate and water. The organic phase was separated and the aqueous phase was re-extracted with ethyl acetate (¥3). The combined organic extract was washed with brine, dried (MgSO4) and concentrated in vacuo. The residue was purified by flash chromatography on silica gel (gradient elution; 35-40% ethyl acetate/hexanes as eluent) to give the title compound as an off-white solid (10.3 g, 62%).
(»Sr)-(4-Benzyloxy-3-methylbut-l-ynyl)triethylsilane
Step AA: Methyl (.S)-3-benzyloxy-2-methylpropanoate
An oven dried 1 L single-necked round bottom flask was equipped with a magnetic stir bar and then charged sequentially with 15.948 g (0.135 mol) of (i?)-(-)-methyl-3-hydroxy-2-methylpropanoate, carbon tetrachloride (150 mL), cyclohexane (300 mL), and 35.796 g (0.142 mol) of benzyl 2,2,2-trichloroacetimidate. Trifluoromethanesulfonic acid (0.8 mL; 9.0 mmol) was added to the solution and the resulting mixture was stirred for 16 h at room temperature under an N2 atmosphere. The reaction mixture was then filtered and the filtrate concentrated in vacuo. The residue was redissolved in 150 mL EtOAc and extracted with saturated aqueous NaHCO3 (1x100 mL). The organic layer was washed with saturated NaCl, dried (MgSO4), filtered and evaporated. The residual oil was purified on a silica gel flash chromatography column eluted with 10% EtOAc-hexane. The purified fractions were combined and evaporated in vacuo to afford 20.787 (74%) of the title compound as a colorless oil. MS (Cl): m/e = 209 (M+l).
Step BB: CS)-3-Benzyloxy-2-methylpropan-l-ol
- 49 An oven dried three-necked 2 L round bottom flask was equipped with a mechanical stirrer, a reflux condenser and a 500 mL constant pressure addition funnel. The flask was charged with a solution of 62.252 g (0.299 mol) of methyl (S)-3-benzyloxy-2- methylpropanoate in 600 mL of anhydrous THF, and a 1.0 M solution of lithium aluminum hydride (300 mL; 0.3 mol) was transferred into the dropping funnel via a cannula. Stirring was started and the lithium aluminum hydride solution was added over 45 minutes to the reaction under an N2 atmosphere while the temperature of the reaction mixture was maintained between 25-30°C using an external ice-water bath. After the addition was complete, the reaction was stirred an additional 6 h at room temperature at which point TLC analysis (20% EtOAc-hexane) indicated complete reaction. The reaction mixture was then cooled with an external ice-water bath and quenched by serial addition of 11.4 mL water, 11.4 mL of 15% aqueous NaOH, and 34.2 mL water. The reaction mixture was then filtered, the solids were washed with EtOAc, the filtrate and washings were combined and evaporated in vacuo. The residue was redissolved in EtOAc, washed with 10% aqueous NaHSO4, saturated NaCl, dried (MgSO4), filtered and evaporated. The residue was purified by Kugelrohr distillation to afford 47.67 g (89%) of the title compound as a colorless oil. MS (Cl): m/e = 181 (M+l).
Step CC: GS)-3-Benzyloxy-2-methylpropanal An oven dried three-necked 2 L round bottom flask was equipped with a mechanical stirrer, a thermometer, an N2 inlet, and a septum. The flask was charged with 24.050 g (0.189 mol) of oxalyl chloride and 425 mL CH2C12. The reaction mixture was stirred under an N2 atmosphere and cooled to -78°C with an external dry ice-acetone bath. A solution of methyl sulfoxide (29.607 g; 0.379 mol) in 85 mL CH2C12 was then added over 5 min to the reaction mixture via cannula. After the adition, the reaction was stirred an additional 5 min and then a solution of 31.048 g (0.172 mol) of GS)-3-benzyloxy-2-methylpropan-l-ol in 170 mL CH2C12 was added via cannula. When the second addition was
50 completed the reaction mixture was stirred for 15 min at -78°C then 111.32 g (0.861 mol) of ΛT,N-diisopropylethylanιine was added via syringe. The reaction mixture was stirred an addition 15 min at -78°C, the cooling bath was removed and the reaction was allowed to warm. When the internal temperature had reached -15°C, 350 mL of a 10% aqueous NaHSO4 solution was slowly added and the mixture was transferred to a separatory funnel. The organic layer was separated, washed with aqueous NaHSO4 (2x250 mL), saturated NaCl, dried (MgSO4), filtered and evaporated. The residue was used immediately in the next step without further purification.
Step DD: CS -4-Benzyloxy-l,l-dibromo-3-methylbutene
An oven dried three-necked 2 L round bottom flask was equipped with a mechanical stirrer, a thermometer, an N2 inlet, and a septum. The flask was charged with 180.71 g (0.689 mol) of triphenylphosphine and 925 mL of CH2C12. The reaction mixture was stirred under an N2 atmosphere and cooled to 0-5°C with an external ice- water bath. The septum was then removed and 114.25 g (0.344 mol) of carbon tetrabromide was added in portions through the open neck of the flask at a rate that maintained the temperature of the reaction mixture below 20°C. After the addition was complete the reaction was stirred for 1 h and then a solution of the CS)-3-benzyloxy-2-methylpropanal from the previous step dissolved in 150 mL of CH2C12 was added via cannula over a 5 min period. The reaction mixture was stirred under N2 for an additional 1 h and allowed to warm to room temperature. A separate 10 L three-necked round bottom flask was equipped with a mechanical stirrer and charged with 4 L of hexane. The stirrer was started and the crude reaction mixture was introduced as a slow stream which resulted in formation of a granular precipitate. After the transfer was complete the reaction mixture was filtered and the solids were carefully washed with hexane. The filtrate was evaporated in vacuo and additional solids were deposited. The residue was resuspended in hexane, filtered and the filtrate reevaporated. The resulting oil was purified by Kugelrohr
51 distillation to afford 46.54 g (81% for two steps) of the title compound as a colorless oil.
Step EE: GS0-(4-benzyloxy-3-methylbut-l-ynyl)triethylsilane An oven dried 100 mL single-necked round bottom flask was equipped with a magnetic stir bar and a septum then charged with 5.171 g (15.5 mmol) of (S)-4-benzyloxy-l,l-dibromo-3-methylbutene and 20 mL of anhydrous THF. The reaction mixture was stirred at -78°C under an N2 atmosphere and 12.4 mL of a 2.5 M solution of rc-butyllithium (31.0 mmol) was added dropwise via syringe over 15 min. The reaction mixture was stirred at -78°C for an additional 1 h, then quenched with 10% aqueous NaHSO4 and extracted into EtOAc. The organic layer was washed with water (3x25 mL), sturated NaCl, then dried (MgSO4), filtered, and evaporated. The residue was purified by Kugelrohr distillation to afford 3.999 g (90%) of the title compound as a colorless oil.
2-r3-(2-Trimethylsilylethoxymethyl) -3H-imidazof4.5-61pyridin-6-yl1-ethanol
Step AAA: 2-Amino-5-bromo-3-nitropyridine
Sulfuric acid (290 mL) was cooled to 0 °C, followed by the slow addition of 2-amino-5-bromopyridine (50 g, 289 mmol). Nitric acid (15 mL) was added dropwise over 30 min with the aid of a pressure- equalized dropping funnel. After 90 min at 0 °C, the reaction mixture was heated to 75 °C for 2 h. After cooling to ambient temperature, the reaction mixture was poured into 1500 mL of ice-water and neutralized to pΗ 8 with 50% NaOΗ (w/w). The precipitate formed was collected on a fritted funnel, washed with 1000 mL cold water, and dried in vacuo , which provided 39.7 g of the title compound (63% yield).
Step BBB: 5-Bromo-2.3-diaminopyridine
2-Amino-5-bromo-3-nitropyridine (3.5 g, 16.1 mmol) was combined with FeCl3 »20 (0.217 g, 0.8 mmol) and activated charcoal (1.6 g) to which dry methanol (160 mL) was added. The mixture was
52 heated to 70 °C for 10 min, cooled to ambient temperature followed by the dropwise addition of hydrazine (2.57 g, 80.3 mmol) over 5 min. Heating was resumed and the reaction was maintained at 70 °C for 2 h. After cooling to ambient temperature, the reaction contents were filtered through a pad of celite®, eluted with methanol followed by removal of the solvent in vacuo. The residue was dissolved in ethyl acetate and washed with H2O, brine, dried (Na2SO4), filtered, concentrated in vacuo, and the crude reside was purified by flash chromatography on silica gel using a gradient elution (10, 20, 40, 60, and 80% ethyl acetate/hexanes). According to this procedure, 2.8 g (93% yield) of the title compound was obtained.
Step CCC: 5-Bromoimidazopyridine
5-Bromo-2,3-diaminopyridine (4.87 g, 26 mmol) was dissolved in triethyl orthoformate (150 mL) and 3 drops of concentrated hydrochloric acid followed by heating to reflux for 50 h. After cooling to ambient temperature, the reaction mixture was poured into hexanes and the precipitate formed was collected by filtration. The solids were diluted with H2O and basified to pH 10 with 1.25 N NaOH. The aqueous layer was extracted three times with ethyl acetate The combined organic extracts were washed with brine, dried (Na2SO4), filtered and concentrated in vacuo. The crude residue was purified by silica gel chromatography using 95:5 CH2C12-(10% NH4OH-MeOH) as the eluent. Following this protocol, 3.1 g (60% yield) of the title compound was obtained.
Step DDD: 6-Bromo-3-(2-trimethysilylethoxymethyl) -3H-imidazo
T4.5-61 -pyridine
5-Bromoimidazopyridine (3.0 g, 15.1 mmol) was dissolved in dry N, N- dimethylformamide (50 mL) and cooled to 0 °C, at which time a 60% oil dispersion of NaΗ (0.667 g, 16.7 mmol) was added in portions over 10 min. After 15 min at 0 °C, the reaction was allowed to warm to ambient temperature for an additional 90 min. To the homogeneous solution was added dropwise 2-(trimethylsilyl)ethoxymethyl chloride
53 - (SEM-C1, 3.03 g, 18.2 mmol). The reaction was maintained at ambient temperature for 40 h, at which time the mixture was poured into ice- water. The aqueous layer was extracted with diethyl ether 3 times, and the combined organic extracts were washed with brine, dried (MgSO4), filtered, and concentrated to dryness in vacuo. The crude residue was loaded onto a silica-gel column and eluted with ethyl acetate/ hexane (20, 30, to 40 %). According to this procedure, 2.55 g (52% yield) of the title compound was obtained.
Step EEE: 6-Ethenyl-3-(2-trimethysilylethoxymethyl)-3H-imidazo-
[4.5-61 -pyridine
To a solution of 6-bromo-3-(2-trimethysilylethoxymethyl) - 3H-imidazo- [4,5-6] -pyridine (1.3 g, 4 mmol) and bis(triphenylphosphine)- palladium (II) chloride in DMF (12 mL) was added tributylvinyl tin (2.14 g, 6.7 mmol). The reaction vessel was evacuated-purged (N2) several times followed by heating to 95 °C for 15 h. After cooling, the crude reaction mixture was filtered through a pad of celite® and eluted with ethyl ether. The ethereal mixture was washed several times with saturated KF, brine, dried (Na2SO4), filtered and concentrated in vacuo. The crude residue was purified by flash chromatography on silica gel using a gradient elution of ethyl acetate/hexanes ( 10, 20, 30 to 40%) which provided 1.06 g of the title compound (97% yield).
Step FFF: 6-(2-Bromo-l-hydroxyethyl)-3-(2-trimethysilyl- ethoxymethyP- 3H-imidazo [4.5-61 -pyridine
To a soution of 6-ethenyl-3-(2-trimethysilylethoxymethyl) - 3H-imidazo- [4,5-6] -pyridine (1.06 g, 3.8 mmol) in DMSO-Η2O (18.0 mIJ2.0 mL) was added ΛLbromosuccinimide (1.37 g, 7.7 mmol) slowly over 5 min. The reaction was maintained at ambient temperature for 30 min at which time the reaction mixture was partitioned between ethyl acetate-H2O. After separation of the layers, the aqueous layer was extracted three times with ethyl acetate. The combined extracts were washed with brine, dried (Na2SO4), filtered and concentrated in vacuo. The crude residue was used without further purification.
54 Step GGG: 6-Oxiranyl-3-(2-trimethylsilylethoxymethyl)-3H-imidazo-
[4.5-61 pyridine
The crude 6-(2-bromo-l-hydroxyethyl)-3-(2-trimethysilyl- ethoxymethyl) -3H-imidazo [4,5-6] -pyridine (1.42 g, 3.8 mmol) was dissolved in (5:1) TΗF- -butanol (20 mL) to which potassium -butoxide (0.85 g, 7.6 mmol) was added in several portions over 5 min. After 90 min at ambient temperature, the reaction mixture was partitioned between ethyl acetate-H2O. After separation of the layers, the aqueous layer was extracted three times with ethyl acetate. The combined extracts were washed with brine, dried (Na2SO4), filtered and concentrated in vacuo. The crude residue (918 mg) was used without purification.
Step HHH: 2-[3-(2-Trimethylsilylethoxymethyl)-3H-imidazo-
[4.5-61 pyridin-6-yll -ethanol
6-Oxiranyl-3-(2-trimethylsilylethoxymethyl)-3H-imidazo- [4,5-6] pyridine (918 mg, 3.15 mmol) was combined with 10% Pd/C (400 mg) and ammonium formate (993 mg, 15.75 mmol) and the mixture was suspended in methanol (25 mL). The reaction mixture was heated to 70°C for 2.5 h. After cooling to ambient temperature, the mixture was filtered through celite®, eluted with methanol, concentrated in vacuo. The crude residue was purified by flash chromatography on silica gel using 75% ethyl acetate/hexanes then 95:5 CΗ2Cl2/MeOΗ as the eluents, which provided 480 mg of the title compound (43% yield for 3 steps).
Following procedures similar to those described above, the following compounds are prepared:
- 55 HaC^CHa CH3
Figure imgf000058_0001
- . RT
H,C^ CH3
Figure imgf000058_0002
Ex. # -(A)-Rι
1A
^ V^ ^N Me
IB
Figure imgf000058_0003
H
- 56 -

Claims

WHAT IS CLAIMED IS:
A compound of the formula
10 * Nk-(A)-R! RlOa
Figure imgf000059_0001
(I)
wherein
A is Cχ-C6 alkyl, substituted Cχ-C6 alkyl, C3-C7 cycloalkyl, substituted C3-C7 cycloalkyl, C3-C6 alkenyl, substituted
C3-C6 alkenyl, C3-C6 alkynyl, substituted C3-C6 alkynyl,
C1-C6 alkoxy, or C0-C5 alkyl-S(O)n-Co-C5 alkyl, C0-C5 alkyl-
O-C0-C5 alkyl, C0-C5 alkyl-NRi8-Co-C5 alkyl where Rl8 and the C0-C5 alkyl can be joined to form a ring, \ ^N-(CH2)p-
R!6 , or a single bond,
R╬╕ is hydrogen, C1-C6 alkyl, substituted Cl-C╬▓ alkyl, wherein the substituents are as defined below; aryl, substituted aryl, aralkyl or substituted aralkyl, wherein the substituents are as defined for R3, R4 and R5. Rl is
57 - 1
^N ^N
R
T . I II"13 ΓÇóΓûá"13 13 *> N
R
R14 R15 14 R 15 R14 R 15
N. ,Z. N Γûá^r
N ^R
II "^ l|R"13 -NRl3
N
R14 R R14 Ri5 R14 R 15
13
R 14"
(T
N N- II "^ I|R"13
Figure imgf000060_0001
r~Ri3 J -N 15
RuV" R 15 R╬╣ " R 13
R R ┬╗╬╣1.4╬╣\^ Zv
N N
II
-R-|3 ΓûáR 13 N
N^> N N^
R R13
15 15
Z Z.
N
"^ I]R "13
Figure imgf000060_0002
^ "R"13
Figure imgf000060_0003
R 13
^┬╗A' ΓûáN
^R ^'Ri Ri4 N R 15 R N R1£
^1R
II N^ ^f ^ ΓÇö R N^ " h 13
Figure imgf000060_0004
N y \-
" -T R13 R,< N R 15 K14 Rl5
R14\N.
N II l| R"13 ϋ-Rι 3
Figure imgf000060_0005
-N Y
N'
"14 R 15 Rύ N' R13 R 15
R14\N. .Z. R Λ,4 Λ Z^ _NΪI_D R •ΛΛ,/4yw Z^ II
N^VΓÇö * Nc^y 13 N^ V N
R 15 R R
15 13
- 58 - 231
N. N ISL
"^ r i^ N
I ^R M3 R 13 y V N y v- - -R 13 R, N R 15 R R 15 R, N R 15
N. ^N
N> .Z. r^ f r N
II - R 13
7 N
N' R15 R R 15 ^R14
Rl4 R 13
,N.
N^ M N
<JR13
^jRl3
R
Rl5 R
Figure imgf000061_0001
15 N "Ri4
14
R .N N. M
^ l3
N; - R╬╣:
Figure imgf000061_0002
R14 R 15 R14
Rl5 M l5^ -N
\ v/v^ ΓÇö iR13
^ -iR 13
R14 N' R14
Figure imgf000061_0004
Rl5 R 15- ,N
^R13
R 13 N .N
N ^ R14 R14
Figure imgf000061_0003
^. Rl3
Figure imgf000061_0005
R-I4
- 59 - r^^i . A ?' % N R N
14
*14
r^N"N^Ri3
" 14 ^ ^ R13 s V\/\ ^\ \ \/┬╗ N^ R1 1ST "N^^ .Rnui3 y R "^14 " 14
R 13
N^N- R13 ^ -N-N 13
N
Figure imgf000062_0001
Ri4 R-I4 RH N
r^N' R 13
^ r^r 13
N^. ,
N
R 14 R14
R14
NΛ N- R13
1 % A\
Figure imgf000062_0002
R R
Figure imgf000062_0003
R:
14
13 N R13
14 R H 14
the nitrogen atoms contained in the Ri heteroaromatic rings may exist either as drawn or, when chemically allowed, in their oxidized (N→O) state; R2 is hydrogen, Cl-Cβ alkyl, substituted Ci-Cβ alkyl, aralkyl, substituted aralkyl, aryl, substituted aryl, alkyl -ORn,
Ci-C6(NRnRi2), Ci-C6(CONRnRi2) or C(NRnRi2)NH; R2 and A taken together form a ring of 5-7 atoms; R3, R4 and R5 are independently hydrogen, Cl-C╬▓ alkyl, substituted
C1-C6 alkyl, C2-C6 alkenyl, substituted C2-C6 alkenyl, CN,
60 nitro, C1-C3 perfluoroalkyl, C1-C3 perfluoroalkoxy, aryl, substituted aryl, aralkyl, substituted aralkyl, RχιO(CH2)p-, RllC(O)O(CH2)p-, RnOC(0)(CH2)p-, -(CH2)pS(O)nRl7, -(CH2)pC(O)NRnRi2 or halogen; wherein R17 is hydrogen, C1-C6 alkyl, C1-C3 perfluoroalkyl, aryl or substituted aryl;
R3 and R4 taken together form a carbocyclic ring of 3-7 carbon atoms or a heterocyclic ring containing 1-3 heteroatoms selected from
N, O and S; R╬▓ is hydrogen, C^-CQ alkyl, substituted Cl-C╬▓ alkyl, aryl, substituted aryl, C1-C3 perfluoroalkyl, CN, NO2, halogen,
RllO(CH2)p-, NRι2C(O)Rii, NRi2C(O)NRnRi2 or SOnRli; R7 is hydrogen, Cχ-C6 alkyl, or substituted C1-C6 alkyl, unless X is hydrogen or halogen, then R7 is absent; R8 is hydrogen, C(O)OR9, C(O)NRnRi2, NR11R12, C(O)Rn, NRi2C(O)Rn, NRi2C(O)NRnRi2, NRi2S(O)2Rll,
NR╬╣2S(O)2NR╬╣╬╣Ri2, OC(O)Rn, OC(O)NRuR╬╣2, ORn, SOnRll, S(O)nNRnRi2, C1-C6 alkyl or substituted Ci-C╬▓ alkyl, unless X is hydrogen or halogen, then R8 is absent; or R7 and R╬┤ taken together form a carbocyclic ring of 3-7 atoms; R9 and Rga are independently hydrogen, C1-C6 alkyl, substituted C1-C6 alkyl; aryl or substituted aryl, aralkyl or substituted aralkyl when mΓëáO; or
O
R9 and Rga taken together form a carbocyclic ring of 3-7 atoms or when mΓëáO; R9 and A taken together form a heterocyclic ring containing 3-7 carbon atoms and one or more heteroatoms when mΓëáO; or RlO and RlOa are independently hydrogen, C1-C6 alkyl, substituted C1-C6 alkyl, aryl, substituted aryl, aralkyl or substituted aralkyl; or
O Rio and RlOa taken together form a carbocyclic ring of 3-7 atoms or ;
61 R9 and RlO taken together form a carbocyclic ring of 3-7 carbon atoms or a heterocyclic ring containing one or more heteroatoms when mΓëáO; or
R9 and R2 taken together form a heterocyclic ring containing 3-7 carbon atoms and one or more heteroatoms when mΓëáO; or
RlO and R2 taken together form a heterocyclic ring containing 3-7 carbon atoms and one or more heteroatoms; RlO and A taken together form a heterocyclic ring containing 3-7 carbon atoms and one or more heteroatoms; or Rll and R12 are independently hydrogen , Ci-C╬▓ alkyl, substituted C1-C6 alkyl, aryl, substituted aryl, aralkyl, substituted aralkyl, a carbocyclic ring of 3-7 atoms or a substituted carbocyclic ring containing 3-7 atoms; Rll and R12 taken together can form an optionally substituted ring of 3-7 atoms;
Rl3 is hydrogen, OH, NR7R8, NRnSO2(Ci-C6 alkyl),
NRnS╬╕2(substituted Ci-C╬▓ alkyl), NRnSO2(aryl), NRnSO2(substituted aryl), NRnSO2(Ci-C3 perfluoroalkyl); S╬╕2NRn(Ci-C6 alkyl), SO2NRn(substituted Ci-C╬▓ alkyl), S╬╕2NRn(aryl), SO2NRn(substituted aryl), SO2NRn(Ci-C3 perfluoroalkyl); SO2NRn(C(O)Ci-C6 alkyl); SO2NRn(C(O)- substituted C1-C6 alkyl); SO2NRn(C(O)-aryl); SO2NRn(C(O)-substituted aryl); S(O)n(C╬╣-C6 alkyl); S(O)n ( substituted Ci-C╬▓ alkyl), S(O)n(aryl), S(O)n(substituted aryl), C1-C3 perfluoroalkyl, C1-C3 perfluoroalkoxy, C1-C6 alkoxy, substituted C1-C6 alkoxy, COOH, halogen, NO2 or
CN; Rl4 and R15 are independently hydrogen, C1-C6 alkyl, substituted C1-C6 alkyl, C2-C6 alkenyl, substituted C2-C6 alkenyl, CN, nitro, C1-C3 perfluoroalkyl, C1-C3 perfluoroalkoxy, aryl, substituted aryl, aralkyl, substituted aralkyl, RnO(CH2)p-, RllC(O)O(CH2)p-, RnOC(O)(CH2)p-, -(CH2)pS(O)nRl7, -(CH2)pC(O)NRnRi2 or halogen; wherein R17 is hydrogen, C1-C6 alkyl, C1-C3 perfluoroalkyl, aryl or substituted aryl;
62 Rl6 is hydrogen, Ci-C╬▓ alkyl, substituted Ci-C╬▓ alkyl, or
N(RnRi2); Rl8 is hydrogen, C1-C6 alkyl, substituted C1-C6 alkyl, C(O)ORg,
C(0)NRnRi2, C(O)Rn, S(O)nRn; Rl9 is either the definition of R13 or R14;
X is hydrogen, halogen, N, O, S(O)n, C(O), (CRnRi2)p; C2-C6 alkenyl, substituted C2-C6 alkenyl,C2-C╬▓ alkynyl, or substituted C2-C6 alkynyl; when X is hydrogen or halogen, R7 and R╬┤ are absent; when X is O, S(O)n, C(O), or CR11R12 only R7 or Rs is possible.
Z is O, S, or NR11; m is 0-3; n is 0-2; p is 0-4; and the alkyl, alkenyl and alkynyl substituents are selected from
C1-C6 alkyl, C3-C7 cycloalkyl, aryl, substituted aryl, aralkyl, substituted aralkyl, hydroxy, oxo, cyano, C1-C6 alkoxy, fluoro, C(O)ORll> aryl C1-C3 alkoxy, substituted aryl C1-C3 alkoxy, and the aryl substituents are as defined for R3, R4 and R5;
or a pharmaceutically acceptable addition salt and/or hydrate thereof, or where applicable, a geometric or optical isomer or racemic mixture thereof.
2. The compound according to Claim 1 of the formula
H3C CH3 PH3
,NHΓÇö (A)ΓÇö Ri
Figure imgf000065_0001
CH3
Figure imgf000065_0002
63 or a pharmaceutically acceptable addition salt and/or hydrate thereof, or where applicable, a geometric or optical isomer or racemic mixture thereof, wherein A and Ri are as indicated in the following table:
-(A)-Ri
^
)
^.
N' N H
^
^. >
N
Me
Figure imgf000066_0001
3. A pharmaceutical composition which comprises an effective amount of a compound as defined in Claim 1 and a pharmaceutically acceptable carrier therefor.
4. A method for antagonizing gonadotropin-releasing hormone in a subject in need thereof which comprises administering to said subject an effective amount of a compound as defined in Claim 1 to a subject suffering from a gonadotropin-releasing hormone derived disorder.
5. A method according to Claim 4 wherein the gonadotropin-releasing hormone derived disorder is a sex-hormone related condition.
6. A method according to Claim 4 wherein the gonadotropin-releasing hormone derived disorder is a sex hormone dependent cancer, benign prostatic hypertropy or myoma of the uterus.
- 64
7. A method according to Claim 6 wherein the sex hormone dependent cancer is selected from the group consisting of prostatic cancer, uterine cancer, breast cancer and pituitary gonadotrophe adenomas.
8. A method according to Claim 5 wherein the sex hormone related condition is selected from the group consisting of endometriosis, polycystic ovarian disease, uterine fibroids and precocious puberty.
9. A method for preventing pregnancy in a subject in need thereof which comprises administering an effective amount of a compound as defined in Claim 1.
10. A method for treating lupus erythematosis in a subject in need thereof which comprises administering to said subject an effective amount of a compound as defined in Claim 1.
11. A method for treating irritable bowel syndrome in a subject in need thereof which comprises administering to said subject an effective amount of a compound as defined in Claim 1.
12. A method for treating premenstrual syndrome in a subject in need thereof which comprises administering to said subject an effective amount of a compound as defined in Claim 1.
13. A method for treating hirsutism in a subject in need thereof which comprises administering to said subject an effective amount of a compound as defined in Claim 1.
14. A method for treating short stature or a growth hormone deficiency in a subject in need thereof which comprises administering to said subject an effective amount of a compound which
65 stimulates the endogenous production or release of growth hormone and an effective amount of a compound as defined in Claim 1.
15. A method for treating sleep disorders in a subject in need thereof which comprises administering to said subject an effective amount of a compound as defined in Claim 1.
16. The method of Claim 15 wherein the sleep disorder is sleep apnea.
17. A mammographic method in which the image on the mammographic film has enhanced readability relative to a mammogram effected in the absence of the method, which comprises administering to a premenopausal woman an effective amount of a compound as defined in Claim 1.
18. A pharmaceutical composition which comprises an inert carrier and an effective amount of a compound which stimulates the endogenous production or release of growth hormone in combination with a compound as defined in Claim 1.
19. A pharmaceutical composition made by combining the compound of Claim 1 and a pharmaceutically acceptable carrier therefor.
20. A process for making a pharmaceutical composition comprising combining a compound of Claim 1 and a pharmaceutically acceptable carrier.
21. Pharmaceutical therapy comprising co- administration of a compound having luteinizing hormone releasing hormone activity with a compound of Claim 1.
- 66
22. The therapy of Claim 21 wherein the compound having luteinizing hormone releasing hormone activity is a peptide compound.
23. The therapy of Claim 22 wherein the peptide compound is a natural hormone or an analog thereof.
24. The therapy of Claim 22 wherein the peptide compound is a compound selected from the group consisting of leuprorelin, gonadorelin, buserelin, triptorelin, goserelin, nafarelin, histrelin, deslorelin, meterelin and recirelin.
25. Pharmaceutical combination therapy comprising a compound having luteinizing hormone releasing hormone activity in combination with a compound of Claim 1.
26. The therapy of Claim 25 wherein the compound having luteinizing hormone releasing hormone activity is a peptide compound.
27. The therapy of Claim 26 wherein the peptide compound is a natural hormone or an analog thereof.
28. The therapy of Claim 26 wherein the peptide compound is a compound selected from the group consisting of leuprorelin, gonadorelin, buserelin, triptorelin, goserelin, nafarelin, histrelin, deslorelin, meterelin and recirelin.
67 -
PCT/US1999/006713 1998-04-02 1999-03-29 Antagonists of gonadotropin releasing hormone WO1999051231A1 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
JP2000542002A JP2002510628A (en) 1998-04-02 1999-03-29 Gonadotropin-releasing hormone antagonist
AU31178/99A AU3117899A (en) 1998-04-02 1999-03-29 Antagonists of gonadotropin releasing hormone
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US7256188B2 (en) 2001-05-14 2007-08-14 Astrazeneca Ab 3-aminoalkyl-2-aryl-indole derivatives and their use as GnRH antagonists
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US8017781B2 (en) 2005-11-15 2011-09-13 Vertex Pharmaceuticals Incorporated Azaindazoles useful as inhibitors of kinases
US8865735B2 (en) 2011-02-21 2014-10-21 Hoffman-La Roche Inc. Solid forms of a pharmaceutically active substance
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US9150570B2 (en) 2012-05-31 2015-10-06 Plexxikon Inc. Synthesis of heterocyclic compounds
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US9447089B2 (en) 2009-04-03 2016-09-20 Plexxikon Inc. Compositions and uses thereof
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US7227020B2 (en) 1999-12-24 2007-06-05 Aventis Pharma Limited Azaindoles
US6770643B2 (en) 1999-12-24 2004-08-03 Aventis Pharma Limited Azaindoles
US7306922B2 (en) 2000-09-15 2007-12-11 Astrazeneca Ab Human and rat PGC-3, PPAR-gamma coactivations and splice variants thereof
US6809098B2 (en) 2001-02-20 2004-10-26 Astrazeneca Ab Compounds
US7256188B2 (en) 2001-05-14 2007-08-14 Astrazeneca Ab 3-aminoalkyl-2-aryl-indole derivatives and their use as GnRH antagonists
US6897207B2 (en) 2001-06-21 2005-05-24 Aventis Pharmaceuticals Inc. Azaindoles
US7943616B2 (en) 2001-06-21 2011-05-17 Aventis Pharmaceuticals Inc. Azaindoles for inhibiting aurora2 and other kinases
US7547722B2 (en) 2002-08-21 2009-06-16 Astrazeneca Ab Chemical compounds
US7253290B2 (en) 2002-08-21 2007-08-07 Astrazeneca Ab Pyrazole derivatives as GnRH inhibitors
US7317010B2 (en) 2002-08-21 2008-01-08 Astrazeneca Ab Thieno-pyrrole compounds as antagonists of gonadotropin releasing hormone
US7268158B2 (en) 2002-08-21 2007-09-11 Astrazeneca Ab 6H-THIENO [2,3-b]pyrrole derivatives as antagonists of gonadotropin releasing hormone (GnRH)
US7449489B2 (en) 2002-08-21 2008-11-11 Astrazeneca Ab Indolylalkylamino-methylidenecarbamate derivatives useful as GnRH antagonists
US7132442B2 (en) 2002-08-21 2006-11-07 Astrazeneca Ab 6H-thieno[2, 3-b]pyrrole derivatives as antagonists of gonadotropin releasing hormone (GnRH)
US7514570B2 (en) 2002-08-21 2009-04-07 Astrazeneca Ab Derivatives of 3-hydroxy-4-(cyclyl-alkylaminoalkyl)-5-phenyl-1h-pyrazole as antagonists of the gonadotropin releasing hormone (GnRH) for use in the treatment of sex hormone related conditions, such as prostatic of uterine cancer
US7504509B2 (en) 2003-12-19 2009-03-17 Plexxikon, Inc. Compounds and methods for development of Ret modulators
US7498342B2 (en) 2004-06-17 2009-03-03 Plexxikon, Inc. Compounds modulating c-kit activity
US8067456B2 (en) 2004-07-14 2011-11-29 Aeterna Zentaris Gmbh Tetrahydrocarbazole derivatives having improved biological action and improved solubility as ligands of G-protein coupled receptors (GPCPs)
EP1995238A2 (en) 2004-07-14 2008-11-26 AEterna Zentaris GmbH Novel tetrahydrocarbazole derivatives with improved biological action and improved solubility as ligands for g-protein coupled receptors (GPCRS)
US7375127B2 (en) 2004-07-14 2008-05-20 Ae Zentaris Gmbh Tetrahydrocarbazole derivatives having improved biological action and improved solubility as ligands of G-protein coupled receptors (GPCRs)
US8445681B2 (en) 2005-11-15 2013-05-21 Vertex Pharmaceuticals Incorporated Azaindazoles useful as inhibitors of kinases
US8017781B2 (en) 2005-11-15 2011-09-13 Vertex Pharmaceuticals Incorporated Azaindazoles useful as inhibitors of kinases
US9169250B2 (en) 2006-11-22 2015-10-27 Plexxikon Inc. Compounds modulating c-fms and/or c-kit activity and uses therefor
US9487515B2 (en) 2006-11-22 2016-11-08 Plexxikon Inc. Compounds modulating c-fms and/or c-kit activity and uses therefor
US9469640B2 (en) 2007-07-17 2016-10-18 Plexxikon Inc. Compounds and methods for kinase modulation, and indications therefor
US9844539B2 (en) 2007-07-17 2017-12-19 Plexxikon Inc. Compounds and methods for kinase modulation, and indications therefor
US10426760B2 (en) 2007-07-17 2019-10-01 Plexxikon Inc. Compounds and methods for kinase modulation, and indications therefor
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US9447089B2 (en) 2009-04-03 2016-09-20 Plexxikon Inc. Compositions and uses thereof
US9663517B2 (en) 2009-04-03 2017-05-30 Plexxikon Inc. Compositions and uses thereof
US9096593B2 (en) 2009-11-06 2015-08-04 Plexxikon Inc. Compounds and methods for kinase modulation, and indications therefor
US9624213B2 (en) 2011-02-07 2017-04-18 Plexxikon Inc. Compounds and methods for kinase modulation, and indications therefor
US8865735B2 (en) 2011-02-21 2014-10-21 Hoffman-La Roche Inc. Solid forms of a pharmaceutically active substance
US9150570B2 (en) 2012-05-31 2015-10-06 Plexxikon Inc. Synthesis of heterocyclic compounds
US9695169B2 (en) 2012-05-31 2017-07-04 Plexxikon Inc. Synthesis of heterocyclic compounds

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