CA2575232C - 5-substituted-2-phenylamino-benzamide as mek inhibitor - Google Patents

5-substituted-2-phenylamino-benzamide as mek inhibitor Download PDF

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CA2575232C
CA2575232C CA2575232A CA2575232A CA2575232C CA 2575232 C CA2575232 C CA 2575232C CA 2575232 A CA2575232 A CA 2575232A CA 2575232 A CA2575232 A CA 2575232A CA 2575232 C CA2575232 C CA 2575232C
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hydroxy
ethoxy
difluoro
fluoro
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CA2575232A1 (en
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Yoshiaki Isshiki
Yasunori Kohchi
Eisaku Mizuguchi
Hitoshi Iikura
Yasuaki Matsubara
Shinji Tsujii
Nobuo Shimma
Masanori Miwa
Satoshi Aida
Masami Kohchi
Takeshi Murata
Kosuke Aso
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Chugai Pharmaceutical Co Ltd
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Abstract

An objective of the present invention is to provide compounds that exhibit strong MEK-inhibiting activity and are stable in vivo and soluble in water, which can be used as preventive or therapeutic agents for proliferative diseases.
The compounds of the present invention and pharmaceutically acceptable salts thereof are represented by the following formula (1):

(see formula 1) [where R1, R2, R3, R4, and X are the same as defined in the present patent application].

Description

DESCRIPTION

Technical Field The present invention relates to novel compounds having MEK inhibitory activity and pharmaceutically acceptable salts thereof, intermediates for synthesis of the compounds, and pharmaceutical compositions comprising the compounds or pharmaceutically acceptable salts thereof.
The compounds of the present invention can be used as MEK inhibitors. The compounds can be used to treat proliferative diseases, for example, cancers, psoriasis, restenosis, autoimmune diseases, and atherosclerosis, and other diseases such as sequelae of heart failure, heterograft rejection, osteoarthritis, chronic rheumatoid arthritis, asthma, cystic fibrosis, hepatomegalia, cardiac hypertrophy, Alzheimer's disease, diabetes, septic shock, and HIV
infection.
Background Art Cell survival is regulated by various extracellular signals, for example, growth factors, cytokines, and extracellular matrices (ECM), via cell surface receptors.
Two major signal transduction pathways regulate the process of signal transduction from the cell surface to the nucleus. One is the Ras signaling pathway, and the other is the P13K (Phosphatidylinositol 3 kinase) pathway. The P13K pathway is either activated via cell surface receptors or indirectly by Ras. The present invention focuses on the Ras signaling pathway.
The MAPK (mitogen-activated protein kinase) cascade which comprises three kinases, namely, Raf, MEK (MAPK or ERK kinase), and ERK (extracellular stimulus regulated kinase), is a key component of the Ras signaling pathway. The cascade starts with the activation of Ras and in response to extracellular signals, plays an important role in regulating cell proliferation, differentiation, and transformation (Person, G, F. Robinson, T. Beers Gibson, B. Xu, M.
Karandikar, K. Berman, and M. H. Cobb. Endocrine Rev., 22, 153-183 (2001);
Bryan A. Ballif and John Blenis, Cell Growth & Differentiation, 12, 397-408 (2001); Cobb MH, Prog. Biophys.
Mol. Biol., 71 479-500 (1999); Lewis TS, Shapiro PS and Ahn NG Adv. Cancer Res., 74 49-139 (1998); Kolch W, Biochem. J., 351, 289-305 (2000); Judith S Sebolt-Leopold, Oncogene, 19, 6594-6599 (2000); Roman Herrera and Judith S. Sebolt-Leopold, Treds in Molecular Medicine, 8, S27-S31 (2002)).
Ras activation is regulated through the interplay between GTP-exchange factors (GEFs) and GTPase-activating proteins (GAPs) (Giorgio Scita, Pierluigi Tenca, Emanuela Frittoli Arianna Tocchetti, Metello Innocenti, Giuseppina Giardina and Pier Paolo Di Fiore, EMBO
Journal. 19, 2393-2398 (2000)). GEFs activate Ras through the formation of Ras-GTP complex, and GAPs inactivate Ras through the formation of Ras-GDP complex. Ras activation results from growth factor-mediated extracellular signals to cell surface receptors or from Ras mutations.
Ras mutations are found in many human cancer cells. It is known that such Ras mutations result in sustained Ras activation (GTP complex) and play key roles in the proliferation of human cancer cells.
Activated Ras interacts with Raf-1, a serine/threonine protein kinase, to activate Raf-l (Daum G; Eisenmann-Tappe I, Fries HW, Troppmair J and Rapp UR, Trends Biochem.
Sci., 19, 474-480 (1994); Stokoe D, Macdonald SG; Cadwallader K, Symons M and Hacock JF, Science, 264, 1463-1467 (1994)).
Activated Raf-l then phosphorylates and activates MEK1 and MEK2. MEK is phosphorylated on two serine residues (Ser218 and Ser222) (Dent P, Haser W, Haystead TA, Vincent LA, Roberts TM and Sturgill TW, Science, 257, 1404-1407 (1992); Crews CM, Alessandrini A and Erikson RL, Science, 258, 478-480 (1992); Her JH, Lakhani S, Zu K, Vila J, Dent P, Sturgill TW and Weber MJ, Biochem. J., 296, 25-31 (1993); Alessi, D.
R., Y. Saito, D. G.
Campgell, P. Cohen, G. Sithanandam, U. Rapp, A. Ashworth, C. J. Marshall, and S. Cowley.
Trends Biochem. Sci. 21 373-372 (1994); Zheng, C. F., and K. L. Guan. J. Biol.
Chem. 268, 23933-23939 (1993)).
MEK is a dual-specificity kinase. Activated MEK phosphorylates ERK1 and ERK2 on tyrosine (185) and threonine (183) residues (Anderson NG; Maller JL, Tonks NK
and Sturgill TW, Nature, 343, 651-653 (1990); Seger R and Krebs EG; FASEG J, 9 716-735 (1995)).
The MEK-mediated ERK phosphorylation results in not only ERK activation but also translocation of ERK to the nucleus.
Activated ERK (MAPK) activates various substrates, for example, transcription factors in the cytoplasm and nucleus, and the result is that the activation leads to cellular changes (proliferation, differentiation, and transformation) depending on the extracellular signal.
MEK has a strict substrate specificity. ERK1 and ERK2 are the only substrates of MEK phosphorylation that have been identified (Seger R, Alin N( Posada J, Munar ES, Jensen AM, Cooper JA, Cobb MH and Kregs EG; J. Biol. Chem., 267, 14373-14381 (1992)).
Strict substrate specificity (limited substrates: ERKI and 2) and dual specificity (phosphorylation on both tyrosine and threonine), which are unique properties of MEK bur rarely found in other kinases, are suggested to play a central role in the MEK
integration of signals in the MAPK pathway.
Constitutive activation of the MEK/MAPK pathway is shown to be associated with the neoplastic phenotypes of a relatively large number of cancer cell types (Hoshino R, Chatani Y, Yamori T, Tsuruo T, Oka H, Yoshida 0, Shimada Y, Ari-I S, Wada H, Fujimoto J, Kohno M, oncogene, 18, 813 (1999); Kim SC, Hahn JS, Min YH, Yoo NC, Ko YW, Lee WJ, Blood, 93, 3893 (1999); Morgan MA, Dolp 0, Reuter CW, Blood, 97, 1823 (2001)).
In addition, constitutive activation of MEK has been reported to result in cellular alteration (transformation or canceration) (Cowley S, Paterson H, Kemp P and Marshall CJ, Cell, 77, 841-852 (1994); Mansour SJ, Matten WT, Hermann AS, Candia JM, Rong S, Fukasawa K, Vande Woude GF and Ahn NG; Science, 265, 966-970 (1994)).
Furthermore, studies of MEK inhibitors (PD98059 and others) have revealed that MEK
inhibition not only results in impaired cell proliferation, but also has impact on various cellular events, including cell differentiation, apoptosis, and angiogenesis (Dudley DT, Pang L, Decker SJ, Bridges AJ and Saltiel AR, Proc. Natl. Acad. Sci. USA, 92, 7686-7689 (1995); Alessi DR, CuendaA, Cohen P, Dudley DT and Saltiel AR, J. Biol. Chem., 270, 27489-27494 (1995); Pages G; Lenorman D, L'Allemain G; Chambard JC, Meloche S and Puyssegur J, Proc.
Natl. Acad. Sci.
USA., 90, 8319-8323 (1993); Pang L, Sawada T, Decker SJ and Saltiel AR., J.
Biol. Chem., 270, 13585-13588 (1995); Finalay D, Healy V, Furlong F, O'Connell FC, Keon NK and Martin F, Cell Death Differ. 7, 303-313 (2000); Holmstrom TH, Tran SE, Johnson VL, Alin NG;
Chow SC and Eriksson JE, Mol. Cell. Biol., 19, 5991-6002 (1999); Elliceiri BP, Klemke R, Stromblad S and Cherexh DA, J. Cell Biol., 141, 1255-1263 (1998); Milanini J, Vinals F, Pouyssegur J and Pages G; J. Biol. Chem., 273, 18165-18172 (1998)).
The above-described findings suggest that MEK, one of the major mediators in the MAPK cascade, can serves as a potential target for therapeutic agents used in treating diseases caused by aberrant cell proliferation.
There are many previously reported MEK inhibitors including, for example, compounds having the backbone structure of a 2-phenylaminobenzoic acid or a derivative thereof, and which comprise various types of substituents at different positions (US Patent No.
6251943; US Patent No. 6310060; US Patent No. 6506798; International Publication WO 98/37881; WO
99/01421;
WO 99/01426; WO 00/35435; WO 00/35436; WO 00/37141; WO 00/40235; WO 00/40237;
WO
00/41505; WO 00/41994; WO 00/42002; WO 00/42003; WO 00/42022; WO 00/42029; WO
00/64856; WO 01/05390; WO 01/05391; WO 01/05392; WO 01/05393; WO 01/68619; WO
02/06213; WO 02/18319; WO 03/062189; WO 03/062191; WO 03/077855; WO 03/077914;
WO
04/056789; and Japanese Patent Application Kokai Publication No. (JP-A) 2001-(unexamined published Japanese patent application)). The previously reported compounds also include N-alkoxy-2-phenylamino-benzamide derivatives which have an alkoxy residue as the substituent on the amide nitrogen atom. Furthermore, the reported compounds also include compounds which comprise as a substituent, a halogen atom, a carbamoyl group, a sulfamoyl group, or such, at position 5 of the benzamide ring (International Publication WO 98/37881; WO
99/01426; WO 00/42003; WO 01/68619; and WO 02/06213).
Meanwhile, the anti-cancer effect of compounds comprising the feature of an MEK
inhibitor, as reported, has been drawing attention. Such compounds include, for example, compound CI-1040 described below (in Example 95 of WO 99/01426). The result of a phase I
clinical trial of compound CI-1040 was reported in the American Society of Clinical Oncology Annual Meeting in 2002 (American Society of Clinical Oncology Annual Meeting in 2002 (Abstract Nos. 320 and 321; May, 18-21, 2002)). However, various problems have been pointed out, for example, rapid hydrolysis and inactivation of the compound in vivo; high lipid solubility and low water solubility; and a wide interpatient variability in pharmacokinetic parameters. The clinical trial for CI-1040 was thus terminated. At present, PD0325901 (WO
02/06213) is currently at the stage of a phase II clinical trial in U.S.

HN O
H
N
F
F

Meanwhile, there are reports on methods of preventing or treating rheumatoid arthritis or osteoarthritis using compounds having MEK-inhibiting activity (International Publication WO
00/35436; WO 01/68619; and JP-A 2001-55376).

Disclosure of the Invention An objective of the present invention is to provide preventive or therapeutic agents for proliferative diseases, that have excellent safety, exhibit strong MEK
inhibitory effect, and are stable in vivo and soluble in water.
Through various intensive studies, the present inventors discovered that N-alkoxy-2-phenylamino-benzamide derivatives which comprise a substituent at position 5 of the ring have an unexpectedly strong MEK inhibitory effect and high water solubility, and are highly stable in vivo. In addition, the inventors discovered that the compounds of the present invention have effects of suppressing tumor growth and of suppressing the onset of arthritis, and that they could serve as preventive or therapeutic agents for cancers and arthritis with improved biological utility, thereby completing the present invention.
Specifically, the present invention includes:

[1] a compound represented by the following formula (1), or a pharmaceutically acceptable salt thereof, R4b F t~) wherein R1 represents a halogen atom, an alkenyl group, or an alkynyl group;
R2 represents a halogen atom or an alkyl group; the alkyl group may be substituted by a hydroxyl group;
R3 represents a hydrogen atom or a halogen atom;
R4 represents a hydrogen atom, an alkyl group, an alkenyl group, or an alkynyl group; the alkyl group, the alkenyl group, and the alkynyl group may have one to three substituents selected from the group consisting of -ORa, -NRaRb, -NRaCORb, a heterocyclic group, and a heteroaryl group; the heterocyclic group and the heteroaryl group may have one to three substituents selected from the group consisting of a C1_5 alkyl group, -ORa, and -NRaRb;
X represents a group represented by the following formula (i);

0--Y-Z-W (i ) wherein Y represents -0-, -NR8O-, -ONR8-, -NR8CO-, or -NR8SO2-;
Z represents an C1.8 alkylene chain which may be substituted by one to three groups represented by W';
where R8 represents a hydrogen atom, an alkyl group, -ORa, or -COR9; and the alkyl group may be substituted by a halogen atom, -ORa, or -NRaRb;
R9 represents a hydrogen atom, an alkyl group, or -ORa; and the alkyl group may be substituted by a halogen atom, -ORa, or -NRaRb;
R8 and R9 may be linked to the alkylene chain of Z or form a heterocyclic group through a linkage to the substituent represented by Ra or Rb of W) or alternatively, X represents a group represented by the following formula (ii):
OvY
N, e Y2 (ii) wherein Y1 and Y2, which may be the same or different, each represent a single bond, -CO-, -COO-, -0-, -OCO-, -NRa-, or -S02-;
Z' represents a C1_5 chain which maybe substituted by one to three groups represented by W');
in the above formulae (i) and (ii), W and W', which may be the same or different, each represent a C1.5 alkyl group, a halogen atom, an oxo group, -ORa, -COORa, -COOCORa, -CO-halogen atom, -OCORa, -CONRaRb, -SRa, -SORa, -SO2Ra, -NRaRb, -NRaCORb, -NRaSO2Rb, -SO2NRaRb, a heterocyclic group, or a heteroaryl group; the heterocyclic group and the heteroaryl group may have a substituent selected from the group consisting of a C1_5 alkyl group, -ORa, and -NRaRb; the alkyl group may be substituted by a hydroxyl group, a C1_5 alkoxy group, or an amino group;
the above substituents except the oxo group and the halogen may be linked to each other to form a cycloalkyl group or a heterocyclic group; the cycloalkyl group or the heterocyclic group may have a substituent selected from the group consisting of, -ORa, -NRaRb, and a C1_5 alkyl group that may be substituted with -ORa;
Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1_5 alkyl group; the alkyl group may be substituted by one to three groups selected from the group consisting of a hydroxyl group, a C1_5 alkoxy group, and an amino group;
provided that, when X is the group represented by the above formula (i) and Y
is not -0-, W may be a hydrogen atom;
Herein, the symbol "=" used in the formulae such as (i), (ii), (iii), and (iv) means the site of bonding.
[2] the compound according to [1], or a pharmaceutically acceptable salt thereof, wherein X represents the group -Y-Z-W of the formula (i) and Z represents a C1.5 alkylene chain, wherein the alkylene chain may have one to three substituents selected from the group consisting of a C1.5 alkyl group, a halogen atom, -ORa, -NRaRb, and an oxo group; the above substituents except the oxo group and the halogen atom may be linked to each other to form a cycloalkyl group or a heterocyclic group;
the cycloalkyl group orthe heterocyclic group may have a substituent selected from the group consisting of -ORa, -NRaRb, and a C1_5 alkyl group that may be substituted with -ORa;
Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1_5 alkyl group; and the alkyl group may be substituted by a hydroxyl group, a C1_5 alkoxy group, or an amino group;
[3] the compound according to [1] or [2], or a pharmaceutically acceptable salt thereof, wherein X represents the group -Y-Z-W of the formula (i), wherein the alkylene chain of Z is any one of the groups represented by the following formulae:
-CH2-, -(CH2)2-, -(CH2)3-, -(CH2)4-, -CH2CH(Me)-, -CH2C(Me)2-, -C(Me)2CH2-, -(CH2)2CH(Me)-, -(CH2)2C(Me)2-, -CH(Me)(CH2) 2-, -C(Me)2(CH2)2-, -CH2CH(Me)CH2-, -CH2C(Me)2CH2-, -CH2C(CH2CH2)CH2-, -CO-, -CH2CO-, -COCH2-, -(CH2)2CO-, -CO(CH2)2-, -CHOH-, -CH2CH(OH)-, -CH(OH)CH2-, -CH2CH(OH)CH2-, -CH(OH)CH2CH2-, and -CH2CH2CH(OH)-;

[4] the compound according to any one of [1] to [3], or a pharmaceutically acceptable salt thereof, wherein X represents -Y-Z-W of the formula (i), wherein R8 represents a hydrogen atom, a hydroxyl group, a C1.5 alkyl group, or -COR9;
R9 represents a hydrogen atom, a hydroxyl group, a C1_5 alkyl group, or a C1_5 alkoxy group;
the alkyl group and the alkoxy group represented byR8 and R9 may be substituted by one to three hydroxyl groups at arbitrary positions of the hydrocarbon moiety;

[5] the compound according to anyone of [1] to [4], or a pharmaceutically acceptable salt thereof, wherein X represents -Y-Z-W of the formula (i), wherein R8 represents a hydrogen atom, a hydroxyl group, a methyl group, an ethyl group, an n-propyl group, an i-propyl group, an n-butyl group, an i-butyl group, a t-butyl group, a sec-butyl group, a 1,1-dimethylpropyl group, a 2,2-dimethylpropyl group, a 1,2-dimethylpropyl group, a pentyl group, a formyl group, an acetyl group, a 2-methoxyacetyl group, a 2-ethoxyacetyl group, a 2-hydroxyacetyl group, a propionyl group, a 2-methylpropionyl group, a 2-methoxypropionyl group, a 2-ethoxypropionyl group, a 2-hydroxypropionyl group, a 3-methoxypropionyl group, a 3-ethoxypropionyl group, a 3-hydroxypropionyl group, a methoxy group, an ethoxy group, an n-propyloxy group, an i-propyloxy group, a hydroxymethyl group, or a 2-hydroxyethyl group;
[6] the compound according to any one of [1] to [5], or a pharmaceutically acceptable salt thereof, wherein X represents -Y-Z-W of the formula (i), wherein Y
represents -0-, -NHO-, -N(COCH3)0-, -N(COCH2OH)O-, -N(COCH2CH3)O-, -N(COCH(OH)CH3)0-, -N(COCH2CH2OH)O-, -N(COCH(OH)CH20H)O-, -N(COCH2CH2CH3)0-, -N(COCH2CH2CH2OH)O-, -N(COCH(OH)CH2CH3)O-, -N(COCH2CH(OH)CH3)0-, -NHCO-, or -NHSO2-;

[7] the compound according to [1], or a pharmaceutically acceptable salt thereof, wherein X represents a group represented by the formula (ii) and X is any one of the groups represented by the following formulae:

O
ZI ~Z O Z' O
O ---PZ.
N, N S." 0 0-- e - j = N,S02 0Y0"1 OYNR\ OYQ-) O\~
Zl ( f eN\_Z
6N0 O J 0N~~ 6N, wherein Z' represents a C1.5 alkylene chain which may be substituted by one to three groups represented by W';
W' represents a C1-5 alkyl group, a halogen atom, an oxo group, -ORa, -CONRaRb, -SRa, -SORa, -SO2Ra, -NRaRb, -NRaCORb, -NRaSO2Rb, -SO2NRaRb, a heterocyclic group, or a heteroaryl group;
the heterocyclic group and the heteroaryl group may have substituents selected from the group consisting of a C1_5 alkyl group, -ORa, and -NRaRb; the alkyl group may be substituted by a hydroxyl group, a C1_5 alkoxy group, or an amino group;
the above substituents except the oxo group and the halogen may be linked to each other to form a cycloalkyl group or a heterocyclic group; the cycloalkyl group or the heterocyclic group may have a substituent selected from the group consisting of -ORa, -NRaRb, and a C1_5 alkyl group that may be substituted with -ORa;
Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1_5 alkyl group; and the alkyl group may be substituted by a hydroxyl group, a Cl_s alkoxy group, or an amino group;
[8] the compound according to any one of [1] or [7], or a pharmaceutically acceptable salt thereof, wherein X represents the group represented by the formula (ii), wherein W' represents any one of the groups represented by the formulae:
-Me, -Et, -n-Pr, -i-Pr, -CH2OH, -CH2CH2OH, -CH(OH)CH3, -OH, -OMe, -OEt, -OCH2OH, -O(CH2)20H, -O(i-Pr), -O(n-Pr), -CONH2, -CONHMe, -CONHEt, -CONH(n-Pr), -CONH(i-Pr), -CONMe2, -CON(Et)Me, -SO2Me, -SOMe, -SMe, -NH2, -NHMe, -NHCH2OH, -NH(CH2)20H, -N(Me)CH2CH2OH, -NHEt, -NMe2, -N(Et)Me, -NHCOMe, -NMeCOMe, -NHCOEt, -NHCO(n-Pr), and -NHCO(i-Pr);

[9] the compound according to anyone of [1], [7], and [8], or a pharmaceutically acceptable salt thereof, wherein X represents the group represented by the formula (ii), wherein the alkylene chain of Z' is any one of the groups represented by the following formulae:
-CH2-, -(CH2) 2-, -(CH2)3-, -(CH2)4-, -CH2CH(Me)-, -CH2C(Me)2-, -C(Me)2CH2-, -(CH2)2CH(Me)-, -(CH2)2C(Me)2-, -CH(Me)(CH2)2-, -C(Me)2(CH2)2-, -CH2CH(Me)CH2-, -CH2C(Me)2CH2-, -CHOH-, -CH2CH(OH)-, -CH(OH)CH2-, -CH2CH(OH)CH2-, -CH(OH)CH2CH2-, -CH2CH2CH(OH)-, -CO-, -CH2CO-, -COCH2-, -(CH2) 2CO-, -CO(CH2)2-, and -CH2CH(OH)CH2-;
[10] the compound according to any one of [1], [7], [8], and [9], or a pharmaceutically acceptable salt thereof, wherein X represents the group represented by the formula (ii) and X is any one of the groups represented by the following formulae:

,,,N? ,,NQ rN rN~

rN O r ~ N O rN~ rN O
o o rN NRa NRa N O N O N N
Y or, N.( 0 r o r wherein the alkylene chain may be substituted at arbitrary positions by one to three substituents selected from the group consisting of a C1_5 alkyl group, a halogen atom, -ORa, -NRaRb, and an oxo group; Ra and Rb, which may be the same or different, each represent a hydrogen atom or a Ci_5 alkyl group; the alkyl group may be substituted by a hydroxyl group, a C1_5 alkoxy group, or an amino group; Ra represents a hydrogen atom or a C1_5 alkyl group; and the alkyl group may be substituted by a hydroxyl group, a C1_5 alkoxy group, or an amino group;
[11] the compound according to [1], or a pharmaceutically acceptable salt thereof, 5 wherein X represents the group represented by the following formula (iii) or (iv):

O (CH2)n'-H
1 (CH2)n Y
N N
f `O (111 or or, `0-(CH2)n H (IV ) wherein n represents an integer ranging from 1 to 5 and n' represents an integer ranging 10 from 0 to 5; the repeated units represented by -(CH2)n- or -(CH2)n'- in the formulae may be substituted at arbitrary positions in the hydrocarbon moiety by one to three substituents selected from the group consisting of a C1_5 alkyl group, a halogen atom, -ORa, -NRaRb, and an oxo group; Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1_5 alkyl group; and the alkyl group may be substituted by a hydroxyl group, a C1_5 alkoxy group, or an amino group;
[12] the compound according to [1], or a pharmaceutically acceptable salt thereof, wherein X represents a group selected from the group consisting of a 2-hydroxyethoxy group, a 3-hydroxy-2-dimethylpropoxy group, a 3-hydroxypropoxy group, a 2-carbamoylethoxy group, a 2-methylcarbamoylethoxy group, a 2-methanesulfonyl-ethoxy group, a 2-acetylamino-ethoxy group, a 2-hydroxyethoxyamino group, a 3-hydroxypropionyl amino group, a 2-hydroxyethanesulfonamide group, a 1-hydroxymethyl-cyclopropylmethoxy group, a 2,3-dihydroxy-propoxy group, a 1H-imidazol-2-ylmethoxy group, a 2-methylcarbamoyl-ethoxyamino group, a 2-acetylamino-ethoxyamino group, a 2-methanesulfonyl-ethoxyamino group, a 1 H-imidazol-2-ylmethoxyamino group, a 3-hydroxypropoxyamino group, a 2-(2-hydroxyethoxy)-ethoxy group, a 2-methylaminoethoxy group, a 2-(2-hydroxyethylamino)-ethoxy group, a 2-morpholin-4-yl-ethoxy group, a 2-(4-hydroxy-piperidin-1-yl)-ethoxy group, a 2-methylamino-ethoxyamino group, a 2,3-dihydroxy-propoxyamino group, a formyl-methoxyamino group, an acetyl-methoxyamino group, a methoxy-propionylamino group, an isobutyryl-methoxy-amino group, a (2-hydroxy-acetyl)-methoxyamino group, a methoxy-(2-methoxy-acetyl)-amino group, an acetyl-ethoxy-amino group, an ethoxy-propionyl-amino group, an acetyl-isopropoxy-amino group, an acetylhydroxyamino group, an acetoxy-acetyl-amino group, an acetyl-(2-hydroxy-ethoxy)-amino group, an acetyl-(3-hydroxy-propoxy)-amino group, an acetyl-(2-hydroxy-2-methyl-propoxy)-amino group, an acetyl-(2-acetylamino-ethoxy)-amino group, an acetyl-(2-propionylamino-ethoxy)-amino group, an acetyl-(2-isobutyrylamino-ethoxy)-amino group, an acetyl-(2-methylsulfanyl-ethoxy)-amino group, an acetyl-(3-methylsulfanyl-propoxy)-amino group, a 2-hydroxy-1,1-dimethyl-ethoxy group, a methylcarbamoylmethoxyamino group, an ethylcarbamoylmethoxyamino group, a propylcarbamoylmethoxyamino group, an isopropylcarbamoyl-methoxyamino group, a dimethylcarbamoylmethoxyamino group, a 2-ethylcarbamoyl-ethoxyamino group, a 2-propylcarbamoyl-ethoxyamino group, a 2-isopropylcarbamoyl-ethoxyamino group, a 3-methylcarbamoyl-propoxyamino group, a 2-methoxycarbonyl-ethoxyamino group, a methoxyamino group, a methoxy-methyl-amino group, an ethoxyamino group, an isopropoxyamino group, a 2-hydroxy-2-methyl-propoxyamino group, a 2-methylsulfanyl-ethoxyamino group, a 2-methanesulfinyl-ethoxyamino group, a 3-methylsulfanyl-propoxyamino group, a 3-methanesulfinyl-propoxyamino group, a 2-propionylamino-ethoxyamino group, a 2-isobutyrylamino-ethoxyamino group, a 2-hydroxy-acetylamino group, and an acetyl-(2-hydroxy-ethyl)-amino group;
[13] the compound according to [1], or a pharmaceutically acceptable salt thereof, wherein X represents a group selected from the group consisting of a 3-oxo-[1,2]oxazinan-2-yl group, a 3-oxo-isoxazolidin-2-yl group, a 4,4-dimethyl-3-oxo-isoxazolidin-2-yl group, a 4-hydroxy-3-oxo-[1,2]oxazinan-2-yl group, a 3-oxo-[ 1,4,2]dioxazinan-2-yl group, a 2-oxo-pyrrolidin-1-yl group, a 2-oxo-piperidin-l-yl group, a 2-oxo-oxazolidin-3-yl group, a 2-oxo-tetrahydro-pyrimidin-1-yl group, and a 2,3-dioxo-morpholin-4-yl group;
[14] the compound according to anyone of [1] to [13], or a pharmaceutically acceptable salt thereof, wherein Rl represents an iodine atom, a bromine atom, a vinyl group, or an ethynyl group;
[15] the compound according to anyone of [1] to [14], or a pharmaceutically acceptable salt thereof, wherein Rl represents an iodine atom or an ethynyl group;
[16] the compound according to anyone of [1] to [15], or a pharmaceutically acceptable salt thereof, wherein R2 represents a chlorine atom, a fluorine atom, a methyl group, or a hydroxymethyl group;
[17] the compound according to anyone of [1] to [16], or a pharmaceutically acceptable salt thereof, wherein R2 represents a fluorine atom;
[18] the compound according to anyone of [1] to [17], or a pharmaceutically acceptable salt thereof, wherein R3 represents a fluorine atom;
[19] the compound according to any one of [1] to [18], or a pharmaceutically acceptable salt thereof, wherein R4 represents a CI-5 alkyl group substituted by one to three hydroxyl groups;
[20] the compound according to any one of [1] to [19], or a pharmaceutically acceptable salt thereof, wherein R4 represents a group selected from the group consisting of the groups represented by the following formulae:

HO~~ HO HO

OH OH
HO
HO HO
HO OH
[21] the compound according to [1], or a pharmaceutically acceptable salt thereof, wherein Ra and Rb, which may be the same or different, each represent a group selected from the group consisting of a hydrogen atom, a methyl group, an ethyl group, an n-propyl group, an i-propyl group, an n-butyl group, an i-butyl group, a t-butyl group, a sec-butyl group, a 1, 1 -dimethylpropyl group, a 2,2-dimethylpropyl group, a 1,2-dimethylpropyl group, a pentyl group, a hydroxymethyl group, a 1- hydroxyethyl group, a 1-hydroxy-1-methylethyl group, a 2-hydroxy-l-methylethyl group, a 2-hydroxy- 1, 1 -dimethylethyl group, a 2-hydroxyethyl group, a 1-hydroxypropyl group, a 2-hydroxypropyl group, and a 3-hydroxypropyl group;
[22] the compound according to [1] to [6], or a pharmaceutically acceptable salt thereof, wherein X represents -Y-Z-W of the formula (i), wherein W and W', which may be the same or different, each represent a group selected from the group consisting of -OH, -OMe, -OEt, OCH2OH, -O(CH2)20H, -O(i-Pr), -O(n-Pr), -000H, -COOMe, -COOEt, -COOCOMe, -0001, -CONH2, -CONHMe, -CONHEt, -CONH(n-Pr), -CONH(i-Pr), -CONMe2, -CON(Et)Me, -SO2Me, -SOMe, -SMe, -NH2, -NHMe, -NHCH2OH, -NH(CH2)20H, -N(Me)CH2CH2OH, -NHEt, -NMe2, -N(Et)Me, -NHCOMe, -NMeCOMe, -NHCOEt, -NHCO(n-Pr), and -NHCO(i-Pr); and W may be a hydrogen atom when Y is not -0-;
[23] the compound according to [1], or a pharmaceutically acceptable salt thereof, wherein the compound represented by the above formula (1) is any one selected from the group consisting of.
(1) B-1 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(2-hydroxy-ethoxymethy 1)-benzamide, (2) B-2 2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)-5-(2-hydroxy-ethoxyme thyl)-benzamide, (3) B-3 N-(2,3-dihydroxy-propoxy)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-(2-hydroxy-ethoxy methyl)-benzamide, (4) B-4 2-(2-chloro-4-iodo-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)-5-(2-hydroxy-ethoxymeth yl)-benzamide, (5) B-5 3,4-difluoro-2-(2-fluoro-4-vinyl-phenylamino)-N-(2-hydroxy-ethoxy)-5-(2-hydroxy-ethoxymeth yl)-benzamide, (6) B-6 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5 -(3 -hydroxypropoxymeth yl)-benzamide, (7) B-7 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-(3-hydroxy-2,2-dimethyl-propoxymethyl)-N-(2-hydroxy-ethoxy)-benzamide, (8) B-8 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(1-hydroxymethyl-cyclo propylmethoxymethyl)-benzamide, (9) B-9 5-(2,3-dihydroxy-propoxymethyl)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benzamide, (10) B-10 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(2-methylcarbamoyl-eth oxymethyl)-benzamide, (11) B-11 5-(2-acetylamino-ethoxymethyl)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-et hoxy)-benzamide, (12) B-12 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(2-methanesulfonyl-etho xymethyl)-benzamide, (13) B-13 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(1 H-imidazol-2-yl methoxymethyl)-benzamide, (14) B-14 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5 - [2-(2-hydroxy-ethoxy)-et hoxymethyl]-benzamide, (15) B-15 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(2-methylamino-ethoxy methyl)-benzamide, (16) B-16 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[2-(2-hydroxy-ethylamin o)-ethoxymethyl]-benzamide, (17) B-17 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(2-morpholin-4-yl-ethox ymethyl)-benzamide, (18) B-18 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[2-(4-hydroxy-piperidin-1-yl)-ethoxymethyl]-benzamide, and (19) B-19 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-(2-hydroxy- l , l -dimethyl-ethoxymethyl)-N-(2-h ydroxy-ethoxy)-benzamide;
[24] the compound according to [1], or a pharmaceutically acceptable salt thereof, wherein the compound represented by the above formula (1) is any one selected from the group consisting of (1) C-1 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-hydroxy-ethoxyamin o)-methyl]-benzamide, (2) C-2 2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)-5-[(2-hydroxy-ethoxya mino)-methyl]-benzamide, (3) C-3 N-(2,3 -dihydroxy-propoxy)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5- [(2-hydroxy-ethoxy amino)-methyl]-benzamide, 5 (4) C-4 2-(2-chloro-4-iodo-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)-5-[(2-hydroxy-ethoxyamin o)-methyl] -benzamide, (5) C-5 3,4-difluoro-2-(2-fluoro-4-vinyl-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-hydroxy-ethoxyami 10 no)-methyl]-benzamide, (6) C-6 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-methylcarbamoyl-eth oxyamino)-methyl]-benzamide, (7) C-7 15 5-[(2-acetylamino-ethoxyamino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hy droxy-ethoxy)-benzamide, (8) C-8 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-methanesulfonyl-eth oxyamino)-methyl] -benzamide, (9) C-9 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(1 H-imidazol-2-ylmeth oxyamino)-methyl]-benzamide, (10) C-10 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(3-hydroxy-propoxyami no)-methyl]-benzamide, (11) C-11.
3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-methylamino-ethoxy amino)-methyl]-benzamide, (12) C-12 5-[(2,3-dihydroxy-propoxyamino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-h ydroxy-ethoxy)-benzamide, (13) C-13 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(methylcarbamoylmetho xyamino-methyl)-benzamide, (14) C-14 5-(ethylcarbamoylmethoxyamino-methyl)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-h ydroxy-ethoxy)-benzamide, (15) C-15 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(propylcarbamoylmetho xyamino-methyl)-benzamide, (16) C-16 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(isopropylcarbamoyl-m ethoxyamino)-methyl] -benzamide, (17) C-17 5-(dimethylcarbamoylmethoxyamino-methyl)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-( 2-hydroxy-ethoxy)-benzamide, (18) C-18 5-[(2-ethylcarbamoyl-ethoxyamino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2 -hydroxy-ethoxy)-benzamide, (19) C-19 5-[(2-propylcarbamoyl-ethoxyamino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-( 2-hydroxy-ethoxy)-benzamide, (20) C-20 5-[(2-isopropylcarbamoyl-ethoxyamino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benzamide, (21) C-21 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5- [(3 -methylcarbamoyl-pr opoxyamino)-methyl]-benzamide, (22) C-22 3-[N- [2,3-difluoro-4-(2-fluoro-4-iodo-phenylamino)-5-(2-hydroxyethoxycarbamoyl)benzyl] amin ooxy]propionic acid methyl ester, (24) C-24 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(methoxyamino-methyl)-benzamide, (25) C-25 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(methoxy-methyl-amino )-methyl] -benzamide, (26) C-26 5-(ethoxyamino-methyl)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-b enzamide, (27) C-27 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(isopropoxyamino-meth yl)-benzam.ide, (28) C-28 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)5-[(2-hydroxy-2-methyl-pro poxyamino)-methyl]-benzamide, (29) C-29 2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)5-[(2-hydroxy-2-methyl-propoxyamino)-methyl]-benzamide, (30) C-30 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-methylsulfanyl-ethox yamino)-methyl]-benzamide, (31) C-31 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-methanesulfinyi-etho xyamino)-methyl]-benzamide, (32) C-32 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5,-[(3-methylsulfanyl-propo xyamino)-methyl]-benzamide, (33) C-33 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(3-methanesulfinyl-prop oxyamino)-methyl]-benzamide, (34) C-34 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-- [(2-propionylamino-eth oxyamino)-methyl]-benzamide, and (35) C-35 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-isobutyrylamino-etho xyamino)-methyl]-benzamide;

[25] the compound according to [1], or a pharmaceutically acceptable salt thereof, wherein the compound represented by the above formula (1) is any one selected from the group consisting of:
(1) E-1 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(3-hydroxy-propionyla mino)-methyl]-benzamide (2) E-2 2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)-5-[(3-hydroxy-propiony lamino)-methyl]-benzamide (3) E-3 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-[(2-hydroxy-ethanesulfonylamino)-methyl]-N-( 2-hydroxy-ethoxy)-benzamide, (4) E-4 2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-5-[(2-hydroxy-ethanesulfonylamino)-methyl]-N-(2-hydroxy-ethoxy)-benzamide, (5) E-5 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-[(2-hydroxy-acetylamino)-methyl]-N-(2-hydrox y-ethoxy)-benzamide, and (6) E-6 5- { [acetyl-(2-hydroxy-ethyl)-amino]-methyl} -3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-( 2-hydroxy-ethoxy)-benzamide;

[26] the compound according to [1], or a pharmaceutically acceptable salt thereof, wherein the compound represented by the above formula (1) is any one selected from the group consisting of:
(1) F-1 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-[(formyl-methoxy-amino)-methyl]-N-(2-hydrox y-ethoxy)-benzamide, (2) F-2 5-[acetyl-methoxy-amino-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benzamide, (3) F-3 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(methoxy-propionyl-am ino)-methyl]-benzamide, (4) F-4 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(isobutyryl-methoxy-am ino)-methyl]-benzamide, (5) F-5 3 ,4-difluoro-2 -(2 -fluoro-4-iodo-phenylamino)- 5 - { [(2-hydroxy-acetyl)-methoxy-amino] -methyl } -N-(2-hydroxy-ethoxy)-benzamide, (6) F-6 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5- { f methoxy-(2-methoxy-a cetyl)-amino] -methyl } -benzamide, (7) F-7 5-[(acetyl-methoxy-amino)-methyl]-2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydr oxy-ethoxy)-benzamide, (8) F-8 2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)-5-[(methoxy-propionyl-amino)-methyl]-benzamide, (9) F-9 2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)-5-[(isobutyryl-methoxy-amino)-methyl] -benzamide, (10) F-10 5-[(acetyl-ethoxy-amino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-e thoxy)-benzamide, (11) F-11 5-[(ethoxy-propionyl-amino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydro xy-ethoxy)-benzamide, (12) F-12 5-[(acetyl-isopropoxy-amino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydro xy-ethoxy)-benzamide, (13) F-13 5-[(acetyl-hydroxy-amino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy -ethoxy)-benzamide, (14) F-14 5-[(acetoxy-acetyl-amino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-ben zam i de, (15) F-15 5- { [acetyl-(2-hydroxy-ethoxy)-amino] -methyl } -3 ,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N
-(2-hydroxy-ethoxy)-benzamide, (16) F-16 5-{ [acetyl-(3-hydroxy-propoxy)-amino]-methyl}-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benzamide, (17) F-17 5-{ [acetyl-(2-hydroxy-2-methyl-propoxy)-amino]-methyl} -3,4-difluoro-2-(2-fluoro-4-iodo-phen ylamino)-N-(2-hydroxy-ethoxy)-benzamide, (18) F-18 5- { [acetyl-(2-acetylamino-ethoxy)-amino] -methyl } -3 ,4-difluoro-2-(2-fluoro-4-iodo-phenylamino )-N-(2-hydroxy-ethoxy)-benzamide, (19) F-19 5- { [acetyl-(2-propionylamino-ethoxy)-amino]-methyl} -3,4-difluoro-2-(2-fluoro-4-iodo-phenyla mino)-N-(2-hydroxy-ethoxy)-benzamide, (20) F-20 5- { [acetyl-(2-isobutyrylamino-ethoxy)-amino] -methyl } -3,4-difluoro-2-(2-fluoro-4-iodo-phenyla mino)-N-(2-hydroxy-ethoxy)-benzamide, (21) F-21 5 5-{ [acetyl-(2-methylsulfanyl-ethoxy)-amino]-methyl} -3,4-difluoro-2-(2-fluoro-4-iodo-phenylam ino)-N-(2-hydroxy-ethoxy)-benzamide, (22) F-22 5- { [acetyl-(3-methylsulfanyl-propoxy)-amino]-methyl } -3,4-difluoro-2-(2-fluoro-4-iodo-phenyla mino)-N-(2-hydroxy-ethoxy)-benzamide, 10 (23) F-23 5-[(acetyl-ethoxy-amino)-methyl]-2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydrox y-ethoxy)-benzamide, (24) F-24 5- [(ethoxy-propionyl-amino)-methyl]-2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hy 15 droxy-ethoxy)-benzamide, (25) F-25 5- { [acetyl-(2-hydroxy-ethoxy)-amino]-methyl} -2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluor o-N-(2-hydroxy-ethoxy)-benzamide, and (26) F-26 20 5-{[acetyl-(2-hydroxy-2-methyl-propoxy)-amino]-methyl}-2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)-benzamide;
[27] the compound according to [1], or a pharmaceutically acceptable salt thereof, wherein the compound represented by the above formula (1) is any one selected from the group consisting of:
(1) G-1 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(3-oxo-[
1,2]oxazinan-2-ylmethyl)-benzamide, (2) G-2 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(3-oxo-isoxazolidin-2-y1 methyl)-benzamide, (3) G-3 5 -(4,4-dimethyl-3 -oxo-isoxazolidin-2-ylmethyl)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benzamide, (4) G-4 2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)-5-(3-oxo-[ 1,2] oxazinan-2-ylmethyl)-benzamide, (5) G-5 2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)-5-(3-oxo-isoxazolidin-2 -ylmethyl)-benzamide, (6) G-6 N-(2,3-dihydroxy-propoxy)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-(3-oxo-[ 1,2]oxazin an-2-ylmethyl)-benzamide, (7) G-7 N-(2,3 -dihydroxy-propoxy)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-(3-oxo-isoxazolidin -2-ylmethyl)-benzamide, and (8) G-8 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(4-hydroxy-3-oxo-[ 1,2]o xazinan-2-ylmethyl)-benzamide;

[28] the compound according to [1], or a pharmaceutically acceptable salt thereof, wherein the compound represented by the above formula (1) is any one selected from the group consisting of:
(1) H-1 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(3-oxo-[
1,4,2]dioxazinan -2-ylmethyl)-benzamide, (2) H-2 2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)-5-(3-oxo-[ 1,4,2]dioxazi nan-2-ylmethyl)-benzamide, (3) H-3 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(2-oxo-pyrrolidin-1-ylm ethyl)-benzamide, (4) H-4 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(2-oxo-piperidin-1-ylmet hyl)-benzamide, (5) H-5 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(2-oxo-oxazolidin-3-ylm ethyl)-benzamide, (6) H-6 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(2-oxo-tetrahydro-pyrimi din- l-ylmethyl)-benzamide, and (7) H-7 5-(2,3-dioxo-morpholin-4-ylmethyl)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydrox y-ethoxy)-benzamide;

[29] a synthetic intermediate (E) of the compound represented by the formula (1) according to [1], wherein the intermediate is represented by the fallowing formula (6):

HO O

N

I I /

UO F
(6) wherein R1 represents a halogen atom, an alkenyl group, or an alkynyl group;
R2 represents a halogen atom or an alkyl group; the alkyl group may be substituted by a hydroxyl group;
R3 represents a hydrogen atom or a halogen atom;
in the above formula (6), the group represented by the following formula (a):

U__r*
LO
(a) represents a 3- to 10-membered heterocyclic group that may have one to three substituents selected from the group consisting of a C1_5 alkyl group, a halogen atom, -ORa, -NRaRb, and an oxo group;
the above substituents except the oxo group and the halogen atom may be linked to each other to form a cycloalkyl group or a heterocyclic group; the cycloalkyl group or the heterocyclic group may have a substituent selected from the group consisting of -ORa, NRaRb, and a C1_5 alkyl group that may be substituted with -ORa;
Ra and Rb, which may be the same or different, each represent a hydrogen atom or a CI-5 alkyl group; the alkyl group may be substituted by a hydroxyl group, a C1_5 alkoxy group, or an amino group;
U represents -0-, -CONRd-, -S-, -SO-, -SO2-, -NRd-, -NRdCO-, -NRdSO2-, -SO2NRd-, a divalent heterocyclic group, or a divalent heteroaryl group; Rd represents a hydrogen atom or a C1_5 alkyl group; the alkyl group may be substituted by a hydroxyl group, a C1_5 alkoxy group, or an amino group;
R1, R2, R3, and U may have protecting group(s) required for the synthesis;

[30] the synthetic intermediate (E) according to [29], wherein R1 represents an iodine atom, a bromine atom, an ethynyl group, or a vinyl group;
R2 represents a chlorine atom or a fluorine atom;
R3 represents a fluorine atom; and U represents -0-;

[31] the synthetic intermediate (E) according to [29], wherein the heterocyclic group represented by the formula (a) is a [1,3]dioxoran-2-yl group or a [1,3]dioxan-2-yl group, which may be substituted by a hydroxyl group or a C1_5 alkyl group;

[32] a synthetic intermediate (F) of the compound represented by the formula (1) according to [11, wherein the intermediate is represented by the following formula (7):

R4'O

HN O
H Rz N

UO F
(7) wherein R1 represents a halogen atom, an alkenyl group, or an alkynyl group;
R2 represents a halogen atom or an alkyl group; the alkyl group may be substituted by a hydroxyl group;
R3 represents a hydrogen atom or a halogen atom;
R4 represents a hydrogen atom, an alkyl group, an alkenyl group, or an alkynyl group; the alkyl group, the alkenyl group, and the alkynyl group may have one to three substituents selected from the group consisting of -ORa, -NRaRb, -NRaCORb, a heterocyclic group, and a heteroaryl group; the heterocyclic group and the heteroaryl group may have one to three substituents selected from the group consisting of a C1.5 alkyl group, -ORa, and -NRaRb; Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1_5 alkyl group; the alkyl group may be substituted by a hydroxyl group, a C1_5 alkoxy group, or an amino group;

in the above formula (7), the group represented by the following formula (a):
U~
UO
(a) represents a 3- to 10-membered heterocyclic group that may have one to three substituents selected from the group consisting of a C1_5 alkyl group, a halogen atom, -ORa, -NRaRb, and an oxo group;
the above substituents except the oxo group and the halogen atom may be linked to each other to form a cycloalkyl group or a heterocyclic group; the cycloalkyl group or the heterocyclic group may have a substituent selected from the group consisting of -ORa, NRaRb, and a C1_5 alkyl group that may be substituted with -ORa;
Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1_5 alkyl group; and the alkyl group may be substituted by a hydroxyl group, a C1_5 alkoxy group, or an amino group;
U represents -0-, -CONRd-, -S-, -SO-, -SO2-, -NRd-, -NRdCO-, -NRdSO2-, -SO2NRd-, a divalent heterocyclic group, or a divalent heteroaryl group; Rd represents a hydrogen atom or a C1_5 alkyl group; the alkyl group may be substituted by a hydroxyl group, a C1_5 alkoxy group, or an amino group;
R1, R2, R3, and U may have protecting group(s) required for the synthesis;

[33] the synthetic intermediate (F) according to [32], wherein R1 represents an iodine atom, a bromine atom, an ethynyl group, or a vinyl group;
R2 represents a chlorine atom or a fluorine atom;
R3 represents a fluorine atom;
R4 represents a hydroxy alkyl group, in whichthe hydroxy moiety may be protected; and U represents -0-;

[34] the synthetic intermediate (F) according to [32], wherein the heterocyclic group represented by the formula (a) is a [1,3]dioxolan-2-yl group or a [1,3]dioxan-2-yl group, which may be substituted by a hydroxyl group or a C1.5 alkyl group;
[35] a synthetic intermediate (I) of the compound represented by the formula (1) according to [1], wherein the intermediate is represented by the following formula (10):

HO O

' H
N
~Z~ ry \ I I ~
W O. R3 R1 F (10) wherein R1 represents a halogen atom, an alkenyl group, or an alkynyl group;
R2 represents a halogen atom or an alkyl group; the alkyl group may be substituted by a hydroxyl 5 group;
R3 represents a hydrogen atom or a halogen atom;
Z represents a C1_8 alkylene chain which may be substituted by one to three groups represented by W' W or W', which may be the same or different, each represent a hydrogen atom, a C1_5 alkyl group, 10 a halogen atom, an oxo group, -ORa, -COORa, -COOCORa, -CO-[halogen atom], -OCORa, -CONRaRb, -SRa, -SORa, -SO2Ra, -NRaRb, -NRaCORb, -NRaSO2Rb, -SO2NRaRb, a heterocyclic group, or a heteroaryl group;
the heterocyclic group and the heteroaryl group may have a substituent selected from the group consisting of a C1_5 alkyl group, -ORa, and -NRaRb; the alkyl group may be substituited by a 15 hydroxyl group, a C1.5 alkoxy group, or an amino group;
the above substituents except the oxo group and the halogen atom may be linked to each other to form a cycloalkyl group or a heterocyclic group; the cycloalkyl group or the heterocyclic group may have a substituent selected from the group consisting of -ORa, -NRaRb, and a C1_5 alkyl group that may be substituted with -ORa;
20 Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1_5 alkyl group; and the alkyl group may be substituted a hydroxyl group, a C1_5 alkoxy group, or an amino group; and R1, R2, R3, Z, W and W' may have protecting group(s) required for the synthesis;

25 [36] the synthetic intermediate according to [35], which is a synthetic intermediate (K) represented by the following formula (12):

HO O

H
N
Q Z' N

O F (12) wherein R1 represents a halogen atom, an alkenyl group, or an alkynyl group;
R2 represents a halogen atom or an alkyl group; the alkyl group may be substituted by a hydroxyl group;
R3 represents a hydrogen atom or a halogen atom;
Z' represents a C1.5 alkylene chain that may be substituted by one to three groups represented by W';

W' represents any one of the groups represented by the formulae:
-OH, -OMe, -OEt, -OCH2OH, -O(CH2)20H, -O(i-Pr), -O(n-Pr), -CONH2, -CONHMe, -CONHEt, -CONH(n-Pr), -CONH(i-Pr), -CONMe2, -CON(Et)Me, -SO2Me, -SOMe, -SMe, -NH2, -NHMe, -NHCH2OH, -NH(CH2)20H, -N(Me)CH2CH2OH, -NHEt, -NMe2, -N(Et)Me, -NHCOMe, -NMeCOMe, -NHCOEt, -NHCO(n-Pr), and -NHCO(i-Pr);
Q represents -ORc, -OCORc, -NRcRd, or a halogen atom; Rc and Rd, which may be the same or different, each represent a hydrogen atom or a C1_5 alkyl group;
R1, R2, and R3 are defined herein above; and R1, R2, R3, Z', Q and W' may have protecting group(s) required for the synthesis;

[37] the synthetic intermediate according to [35] or [36], wherein R1 represents an iodine atom, a bromine atom, an ethynyl group, or a vinyl group;
R2 represents a chlorine atom or a fluorine atom; and R3 represents a fluorine atom;

[38] a synthetic intermediate (L) of the compound represented by the formula (1) the according to [1], wherein the intermediate is represented the following formula (13):

R4, 0 HN O

H
N
Q Z' N

O F (13) wherein R1 represents a halogen atom, an alkenyl group, or an alkynyl group;
R2 represents a halogen atom or an alkyl group; the alkyl group may be substituted by a hydroxyl group;
R3 represents a hydrogen atom or a halogen atom;
R4 represents a hydrogen atom, an alkyl group, an alkenyl group, or an alkynyl group; the alkyl group, the alkenyl group, and the alkynyl group may have one to three substituents selected from the group consisting of -ORa, -NRaRb, -NRaCORb, a heterocyclic group, and a heteroaryl group; the heterocyclic group and the heteroaryl group may have one to three substituents selected from the group consisting of a C1_5 alkyl group, -ORa, and -NRaRb; Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1_5 alkyl group; the alkyl group may be substituted by a hydroxyl group, a C1_5 alkoxy group, or an amino group;
Z' represents a C1_5 alkylene chain that may have one to three groups represented by W';
W' represents the group represented by any one of the groups represented by the following formulae:
-OH, -OMe, -OEt, -OCH2OH, -O(CH2)20H, -O(i-Pr), -O(n-Pr), -CONH2, -CONHMe, -CONHEt, -CONH(n-Pr), -CONH(i-Pr), -CONMe2, -CON(Et)Me, -SO2Me, -SOMe, -SMe, -NH2, -NHMe, -NHCH2OH, -NH(CH2)20H, -N(Me)CH2CH2OH, -NHEt, -NMe2, -N(Et)Me, -NHCOMe, -NMeCOMe, -NHCOEt, -NHCO(n-Pr), and -NHCO(i-Pr);
Q represents -ORc, -OCORc, -NRcRd, or a halogen atom; Rc and Rd, which may be the same or different, each represent a hydrogen atom or a C1_5 alkyl group; and R1, R2, R3, R4, Z', Q, and W' may have protecting group(s) required for the synthesis];
[39] the synthetic intermediate (L) according to [38], wherein R1 represents an iodine atom, a bromine atom, an ethynyl group, or a vinyl group;
R2 represents a chlorine atom or a fluorine atom;
R3 represents a fluorine atom; and R4 represents a hydroxy alkyl group, in which the hydroxy alkyl moiety may be protected;

[40] a method for producing any one of the compounds (M), (N), (M'), and (N'), wherein the method comprises reacting a reducing agent, in a solvent at neutral pH or in the presence of an acid, with a synthetic intermediate (E) represented by the following formula (6) or a synthetic intermediate (F) represented by the following formula (7):
R4'0 i HO O H HN O

U R3 Ri U R3 R~
UO F O F

wherein R1 represents a halogen atom, an alkenyl group, or an alkynyl group;
R2 represents a halogen atom or an alkyl group; the alkyl group may be substituted by a hydroxyl group;
R3 represents a hydrogen atom or a halogen atom;
R4 represents a hydrogen atom, an alkyl group, an alkenyl group, or an alkynyl group;
the alkyl group, the alkenyl group, and the alkynyl group may have one to three substituents selected from the group consisting of -ORa, -NRaRb, -NRaCORb, a heterocyclic group, and a heteroaryl group; the heterocyclic group and the heteroaryl group may have one to three substituents selected from the group consisting of a C1_5 alkyl group, -ORa, and -NRaRb;
Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1.5 alkyl group; and the alkyl group may be substituted by a hydroxyl group, a C1_5 alkoxy group, or an amino group;
in the formulae (6) and (7), the group represented by the following formula (a):
U-111~6 UO
(a) represents a 3- to 10-membered heterocyclic group that may have one to three substituents selected from the group consisting of a C1_5 alkyl group, a halogen atom, -ORa, -NRaRb, and an oxo group;
the above substituents except the oxo group and the halogen atom may be linked to each other to form a cycloalkyl group or a heterocyclic group; the cycloalkyl group or the heterocyclic group may have a substituent selected from the group consisting of -ORa, -NRaRb, and a C1_5 alkyl group that may be substituted with -ORa;
Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1_5 alkyl group; and the alkyl group may be substituted by a hydroxyl group, a C1_5 alkoxy group, or an amino group;
U represents -0-, -CONRd-, -S-, -SO-, -SO2-, -NRd-, -NRdCO-, -NRdSO2-, -SO2NRd-, a divalent heterocyclic group, or a divalent heteroaryl group; Rd represents a hydrogen atom or a C1_5 alkyl group; the alkyl group may be substituted by a hydroxyl group, a C1_5 alkoxy group, or an amino group; and R1, R2, R3, and U may have protecting group(s) required for the synthesis to thereby obtain the compounds (M), (N), (M'), and (N') represented by the formulae (14), (15), (14'), and (15'), respectively:

R4,, 0 HO O HN O

H
N \

HOIIZI'U R3 / R1 HO~Z'U R3 / R1 F (14) F (15) R4'_0 HO O HN O

H_U'Z1O R 6 R H_U,Z10 / R a R

F (14') F (15) wherein R1, R2, R3, R4, and U are defined herein above in formulae (6) and (7);
Z corresponds to the alkylene chain constituting the ring in the above formula (a); Z represents a C1_8 alkylene chain, which may be substituted by one to three groups represented by W'; W' represents any one of substituents selected from the group consisting of a C1_5 alkyl group, a halogen atom, -ORa, -NRaRb, and an oxo group; the above substituents except the oxo group and the halogen atom may be linked to each other to form a cycloalkyl group or a heterocyclic group;
Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1_5 alkyl 5 group; the alkyl group may be substituted by a hydroxyl group, a C1_5 alkoxy group, or an amino group;

[41] a method for producing compound (I) or compound (J), wherein the method comprises reacting a reducing agent, in a solvent at neutral pH or in the presence of an acid, with 10 a synthetic intermediate (G) of the compound represented by the formula (1) according to [1], wherein (G) is represented by the following formula (8):
HO O

H
N
lZ" N I I /
W Or R3 R1 F (8) wherein R1 represents a halogen atom, an alkenyl group, or an alkynyl group;
R2 represents a halogen atom or an alkyl group; the alkyl group may be substituted by a hydroxyl group;
R3 represents a hydrogen atom or a halogen atom;
Z represents a C1-8 alkylene chain that may have one to three groups represented by W';
W or W', which may be the same or different, each represent a hydrogen atom, a alkyl group, a halogen atom, an oxo group, -ORa, -COORa, -COOCORa, -CO-[halogen atom], -OCORa, -CONRaRb, -SRa, -SORa, -SO2Ra, -NRaRb, -NRaCORb, -NRaSO2Rb, -SO2NRaRb, a heterocyclic group, or a heteroaryl group;
the heterocyclic group and the heteroaryl group may have a substituent selected from the group consisting of a C1_5 alkyl group, -ORa, and -NRaRb; the alkyl group may be substituted by a hydroxyl group, a C1_5 alkoxy group, or an amino group;
the above substituents except the oxo group and the halogen may be linked to each other to form a cycloalkyl group or a heterocyclic group; the cycloalkyl group or the heterocyclic group may have a substituent selected from the group consisting of -ORa, -NRaRb, and a C1_5 alkyl group that may be substituted with -ORa;
Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1_5 alkyl group; the alkyl group may be substituted by a hydroxyl group, a C1_5 alkoxy group, or an amino group; and R1, R2, R3, Z, W, and W' may have protecting group(s) required for the synthesis, or a synthetic intermediate (H) of the compound represented by the formula (1) according to [1], wherein (H) is represented by the following formula (9):

R4~, 0 I
HN O

H
N
"Z" N \ I I /
W O''j R3 R1 F (9) wherein R1 represents a halogen atom, an alkenyl group, or an alkynyl group;
R2 represents a halogen atom or an alkyl group; the alkyl group may be substituted by a hydroxyl group;
R3 represents a hydrogen atom or a halogen atom;
R4 represents a hydrogen atom, an alkyl group, an alkenyl group, or an alkynyl group;
the alkyl group, the alkenyl group, and the alkynyl group may have one to three substituents selected from the group consisting of -ORa, -NRaRb, -NRaCORb, a heterocyclic group, and a heteroaryl group; the heterocyclic group and the heteroaryl group may have one to three substituents selected from the group consisting of a C1_5 alkyl group, -ORa, and -NRaRb;
Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1.5 alkyl group; and the alkyl group may be substituted by a hydroxyl group, a C1_s alkoxy group, or an amino group;
Z represents a Cl_8 alkylene chain that may be substituted by one to three groups represented by W';
W or W', which may be the same or different, each represent a hydrogen atom, a C1_5 alkyl group, a halogen atom, an oxo group, -ORa, -COORa, -COOCORa, -CO-[halogen atom], -OCORa, -CONRaRb, -SRa, -SORa, -SO2Ra, -NRaRb, -NRaCORb, -NRaSO2Rb, -SO2NRaRb, a heterocyclic group, or a heteroaryl group;
the heterocyclic group and the heteroaryl group may have a substituent selected from the group consisting of a C1.5 alkyl group, -ORa, and -NRaRb; the alkyl group may be substituted by a hydroxyl group, a C1.5 alkoxy group, or an amino group;
the above substituents except the oxo group and the halogen atom may be linked to each other to form a cycloalkyl group or a heterocyclic group; the cycloalkyl group or the heterocyclic group may have a substituent selected from the group consisting of -ORa, -NRaRb, and a C1.5 alkyl group that may be substituted with -ORa;
Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1_5 alkyl group; and the alkyl group may be substituted by a hydroxyl group, a C1_5 alkoxy group, or an amino group;
R1, R2, R3, Z, W, and W' may have protecting group(s) required for the synthesis, to thereby obtain compound (I) represented by the following formula (10):

HH
'ZI
W O~N \ R3 R1 F (10) or compound (J) represented by the following formula (11):
R4.0 HN O

IZ-IN
W O \ I R3 I R1 F (11) in the formulae (10) and (11), R1, R2, R3, R4, Z, W, and W' are defined herein above in formulae (8) and (9);

[42] a method for producing compound (0) or compound (P), wherein the method comprises allowing a synthetic intermediate (K) or (L) represented by the following formula (13) to intramolecularly cyclize at neutral pH or in the presence of an acid or a base in a solvent that optionally contains a peptide condensing agent, wherein the synthetic intermediates (K) and (L) are represented by the following formulae (12) and (13), respectively:

HO O

H
N
Q Z
Y 'IN I

0 F (12) R4,0 HN O

H
N
Q Z' N I I /

O F (13) n the above formulae (12) and (13), R1 represents a halogen atom, an alkenyl group, or an alkynyl group;
R2 represents a halogen atom or an alkyl group; the alkyl group may be substituted by a hydroxyl group;
R3 represents a hydrogen atom or a halogen atom;
R4 represents a hydrogen atom, an alkyl group, an alkenyl group, or an alkynyl group;
the alkyl group, the alkenyl group, and the alkynyl group may have one to three substituents selected from the group consisting of -ORa, -NRaRb, -NRaCORb, a heterocyclic group, and a heteroaryl group; the heterocyclic group and the heteroaryl group may have one to three substituents selected from the group consisting of a C1_5 alkyl group, -ORa, and -NRaRb;
Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1.5 alkyl group; and the alkyl group may be substituted by a hydroxyl group, a C1_5 alkoxy group, or an amino group;
Z' represents a C1_Salkylene chain that may be substituted by one to three groups represented by W';
Wrepresents any one of the groups of -OH, -OMe, -OEt, -OCH2OH, -O(CH2)2OH, -O(i-Pr), -O(n-Pr), -CONH2, -CONHMe, -CONHEt, -CONH(n-Pr), -CONH(i-Pr), -CONMe2, -CON(Et)Me, -S02Me, -SOMe, -SMe, -NH2, -NHMe, -NHCH2OH, -NH(CH2)20H, -N(Me)CH2CH 2OH, -NHEt, -NMe2, -N(Et)Me, -NHCOMe, -NMeCOMe, -NHCOEt, -NHCO(n-Pr), and -NHCO(i-Pr);
Q represents -ORc, -OCORc, -NRcRd, or a halogen atom; Rc and Rd, which may be the same or different, each represent a hydrogen atom or a C1.5 alkyl group;
R1, R2, R3, R4, Z', W', and Q may have protecting group(s) required for the synthesis, to thereby obtain compound (0) represented by the following formula (16):

HO O

H
e 0 N
Z',N
O \ R3 R1 F (16) or compound (P) represented by the following formula (17):

R4~
HN O

H
'O N
Z-" N

F (17) in the formula (16) and (17), R1, R2, R3, R4, and Z' are defined herein above in formulae (12) and (13);
[43] a method for producing compound (S) or compound (T), wherein the method comprises reacting, in the presence of a base or an acid, or at neutral pH, in a solvent that optionally contains a condensing agent, the synthetic intermediate (I) of the compound represented by the formula (1) according to [1], the intermediate being represented by the following formula (10):

HO O

H
N
H
VN,Z,0 R3 R1 F (10) or the synthetic intermediate _(J) of the compound represented by the formula (1) according to [1], the intermediate being represented by the following formula (11):

R4, 0 H
N
Z' N \ I /
V1r~ O R3 R1 F (11) in the formulae (10) and (11), R1 represents a halogen atom, an alkenyl group, or an alkynyl group;
R2 represents a halogen atom or an alkyl group; the alkyl group may be substituted by a 10 hydroxyl group;
R3 represents a hydrogen atom or a halogen atom;
R4 represents a hydrogen atom, an alkyl group, an alkenyl group, or an alkynyl group;
the alkyl group, the alkenyl group, and the alkynyl group may have one to three substituents selected from the group consisting of -ORa, -NRaRb, -NRaCORb, a 15 heterocyclic group, and a heteroaryl group; the heterocyclic group and the heteroaryl group may have one to three substituents selected from the group consisting of a C1.5 alkyl group, -ORa, and -NRaRb; Ra and Rb, which may be the same or different, each represent a hydrogen atom or a CI-5 alkyl group; the alkyl group may be substituted by a hydroxyl group, a C1_s alkoxy group, or an amino group;
20 Z represents a C1_8 alkylene chain that may be substituted by one to three groups represented by W';
W or W', which may be the same or different, each represent a hydrogen atom, a C1_5 alkyl group, a halogen atom, an oxo group, -ORa, -COORa, -COOCORa, -CO-[halogen atom], -OCORa, -CONRaRb, -SRa, -SORa, -SO2Ra, -NRaRb, -NRaCORb, -NRaSO2Rb, 25 -SO2NRaRb, a heterocyclic group, or a heteroaryl group;
the heterocyclic group and the heteroaryl group may have a substituent selected from the group consisting of a C1_5 alkyl group, -ORa, and -NRaRb; the alkyl group may be substituted by a hydroxyl group, a C1.5 alkoxy group, or an amino group;
the above substituents except the oxo group and the halogen may be linked to each other to form a cycloalkyl group or a heterocyclic group; the cycloalkyl group or the heterocyclic group may have a substituent selected from the group consisting of -ORa, -NRaRb, and a C1_5 alkyl group that may be substituted with -ORa;
Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1.5 alkyl group; the alkyl group may be substituted by a hydroxyl group, a C1_5 alkoxy group, or an amino group;
R1, R2, R3, R4, Z, W, and W' may have protecting group(s) required for the synthesis with a carboxylic acid derivative represented by the following formula:

wherein R9 represents a hydrogen atom, an alkyl group, or -ORa; the alkyl group may be substituted by a halogen atom, -ORa, or -NRaRb;
Q represents -ORc, -OCORc, -NRcRd, or a halogen atom; Rc and Rd, which may be the same or different, each represent a hydrogen atom or a C1.5 alkyl group;
Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1.5 alkyl group; and the alkyl group may be substituted by a hydroxyl group, a C1_5 alkoxy group, or an amino group;
R9 and Q may have protecting group(s) required for the synthesis, to thereby obtain compound (S) represented by the following formula (18):
HO O

Zl~
VV-' OWN R3 R1 F (1 8) or compound (T) represented by the following formula (19):
R4,O
I
HN O

H

Z'N W O R3 R1 F (1 9) in the formulae (18) and (19), R1, R2, R3, R4, Z, and W are defined herein above in formulae (10) and (11); and R9 is the carboxylic acid derivative defined herein above;
[44] a pharmaceutical composition comprising as an active ingredient the compound according to any one of [1] to [28] or a pharmaceutically acceptable salt thereof;

[45] an MEK inhibitor comprising as an active ingredient the compound according to any one of [1] to [28] or a pharmaceutically acceptable salt thereof;

[46] a preventive or therapeutic agent for a proliferative disease, which comprises as an active ingredient the compound according to any one of [1] to [28] or a pharmaceutically acceptable salt thereof;
[47] the preventive or therapeutic agent for a proliferative disease according to [46], wherein the proliferative disease is a cancer;

[48] the preventive or therapeutic agent for a proliferative disease according to [47], wherein the cancer is a cancer depending on the Ras-MAPK signaling pathway;

[49] the preventive or therapeutic agent for a proliferative disease according to [47] or [48], wherein the cancer is breast, lung, colorectal, prostate, liver, ovarian, uterine, or pancreatic cancer;
[50] a method for preventing or treating a proliferative disease, wherein the methodcomprises administering a pharmaceutically effective dose of a composition that comprises as an active ingredient the compound according to any one of [1] to [28] or a pharmaceutically acceptable salt thereof to a patient who needs prevention or treatment for the proliferative disease;
[51] the method according to [50], wherein the proliferative disease is a cancer;
[52] the method according to [50], wherein the cancer is a cancer depending on the Ras-MAPK signaling pathway;

[53] the method according to [51] or [52], wherein the cancer is breast, lung, colorectal, prostate, liver, ovarian, uterine, or pancreatic cancer;

[54] the method according to any one of [50] to [53], wherein the method further comprises radiotherapy, another chemotherapy, or administration of an angiogenesis inhibitor;
[55] use of the compound according to any one of [1] to [28] or a pharmaceutically acceptable salt thereof in the production of a preventive or therapeutic agent for a disease to which MEK inhibition is effective;

[56] a preventive or therapeutic agent for a joint disorder with inflammation, wherein the agent comprises as an active ingredient the compound according to any one of [1] to [28] or a pharmaceutically acceptable salt thereof;
[57] the preventive or therapeutic agent for a joint disorder with inflammation according to [56], wherein the joint disorder with inflammation is osteoarthritis or rheumatoid arthritis;

[58] a method for preventing or treating osteoarthritis or rheumatoid arthritis, wherein the method comprises administering a pharmaceutically effective dose of a composition that comprises as an active ingredient the compound according to any one of [1] to [28] or a pharmaceutically acceptable salt thereof to a patient who needs prevention or treatment for osteoarthritis or rheumatoid arthritis.
The present inventors synthesized the above-described N-alkoxy-2-phenylaminobenzamide derivatives for the first time. The inventors found that the compounds have an unexpectedly strong MEK inhibitory effect regardless of the substituent in position 5. In addition, the inventors found that the compounds of the present invention have a superior effect with respect to tumor growth suppression activity, as well as a superior effect towards inflammation-related joint disorders.
Interestingly, the compounds of the present invention were found to have superior effects in addition to the MEK inhibitory activity. Specifically, the compounds of the present invention were found to be highly stable in hepatic microsomes, as compared with other N-alkoxy-2-phenylamino-benzamide derivatives. Furthermore, the compounds were found to be more soluble in water in comparison with conventional compounds.
The Cmax and AUC values, and the half-life for the above-described compounds of the present invention are expected to be higher than those of conventional compounds.
Furthermore, the compounds of the present invention are expected to have good in vivo absorption, and low interpatient variability in the PK parameters. The active forms can exist at high concentrations in blood for a long period of time. Thus compared with the conventional compounds, sufficient levels of the active forms of the compounds of the present invention are exposed to the target molecule (i.e., MEK) as. The increased efficacy and the less frequent administration as resulted are expected to reduce the burden of patient.
Herein, the "alkyl group" refers to a monovalent group derived from an aliphatic hydrocarbon by removal of an arbitrary hydrogen atom, and comprises the subgroup structure of a hydrocarbyl group or a hydrocarbon containing hydrogen and carbon atoms, but has no hetero atoms or unsaturated carbon-carbon bonds in the backbone. The alkyl group includes groups comprising a linear or branched structure. The alkyl group is preferably an alkyl group comprising one to eight carbon atoms (hereinafter "C1_8" indicates that the number of carbon atoms in the range of one to eight), and more preferably a C1_5 alkyl group.
Specifically, the alkyl group includes a methyl group, an ethyl group, an isopropyl group, a butyl group, an n-butyl group, a sec-butyl group, an isobutyl group, a t-butyl group, a pentyl group, an isopentyl group, a 2,3-dimethylpropyl group, a hexyl group, a 2,3-dimethyihexyl group, a 1,1-dimethylpentyl group, a heptyl group, and an octyl group.
Herein, the "alkenyl group" refers to a monovalent group having at least one double bond (two adjacent SP2 carbon atoms). Depending on the configurations of the double bond and the substituent (if exists), the geometry around the double bond can be of the entgegen (E) or zusammen (Z) (trans or cis) configuration. The alkenyl group may be linear or branched, and preferably includes C2.8 alkenyl groups, more preferably C2.5 alkenyl groups.
Specifically, such alkenyl groups include, for example, a vinyl group, an ally group, a 1-propenyl group, a 2-propenyl group, a 1-butenyl group, a 2-butenyl group (including cis and trans forms), a 3-butenyl group, a pentenyl group, and a hexenyl group.
Herein, the "alkynyl group" refers to a monovalent group having at least one triple bond (two adjacent SP carbon atoms). The alkynyl group may be linear or branched, and preferably includes C2.8 alkynyl groups, more preferably C2_5 alkynyl groups.
Specifically, the alkynyl group includes, for example, an ethynyl group, a 1-propynyl group, a propargyl group, a 3-butynyl group, a pentynyl group, a hexynyl group, a 3-phenyl-2-propynyl group, a 3-(2'-fluorophenyl)-2-propynyl group, a 2-hydroxy-2-propynyl group, a 3-(3-fluorophenyl)-2-propynyl group, and a 3-methyl-(5-phenyl)-4-pentynyl group.
The alkenyl group and the alkynyl group may each have one or more double bonds or 5 triple bonds. They may also have double bonds and triple bonds at the same time.
Herein, the "cycloalkyl group" refers to a cyclic aliphatic hydrocarbon group comprising a ring. The cycloalkyl group preferably includes C3_8 cycloalkyl groups.
Specifically, the cycloalkyl group includes, for example, a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, and a cyclooctyl group.
10 Herein, the "alkylene chain" or "alkylene group" refer to a divalent group represented by -(CH2)n-. The alkylene chain preferably includes C1_8 alkylene chains (n =
1-8), more preferably C1_5 alkylene chains (n = 1-5), preferably C1_3 alkylene chains (n = 1-3), in particular.
Herein, the "aryl group" refers to a monovalent aromatic hydrocarbon ring. The aryl group preferably includes C6-lo aryl groups. Specifically, the aryl group includes, for example, 15 a phenyl group, a 1-naphthyl group, and a 2-naphthyl group.
Herein, the "hetero atom" refers to a sulfur atom, an oxygen atom, or a nitrogen atom.
Herein, the "heteroaryl group" refers to an aromatic ring group containing one or more of the hetero atoms that constitute the ring. The heteroaryl group may be partially saturated.
The heteroaryl group may be a heteroaryl group in which the ring may be a monocyclic or 20 bicyclic group obtained through condensation with a benzene ring or a monocyclic heteroaryl ring. The number of atoms constituting the ring preferably ranges from 5 to 10 (C5_10 heteroaryl groups).
Specifically, the heteroaryl group includes, for example, a furyl group, a thienyl group, a pyrrolyl group, an imidazolyl group, a pyrazolyl group, a thiazolyl group, an isothiazolyl group, 25 an oxazolyl group, an isooxazolyl group, an oxadiazolyl group, a thiadiazolyl group, a triazolyl group, a tetrazolyl group, a pyridyl group, a pyrimidyl group, a pyridazinyl group, a pyrazinyl group, a triazinyl group, a benzofuranyl group, a benzothienyl group, a benzothiadiazolyl group, a benzothiazolyl group, a benzooxazolyl group, a benzooxadiazolyl group, a benzoimidazolyl group, an indolyl group, an isoindolyl group, an indazolyl group, a quinolyl group, an 30 isoquinolyl group, a cinnolinyl group, a quinazolinyl group, a quinoxalinyl group, a benzodioxolyl group, an indolidinyl group, and an imidazopyridyl group.
Herein, the "heterocyclic group" refers to a non-aromatic monovalent ring, in which the number of atoms constituting the ring preferably ranges from 3 to 8 (C3_8 heterocyclic group), and wherein the ring contains one to three hetero atoms and may have double bonds.
35 Specifically, the heterocyclic group includes, for example, a morpholino group, a thiomorpholino group, a piperidin-l-yl group, a 4-substituted piperidin-l-yl group, a piperazin-l-yl group, a 4-substituted piperazin-l-yl group, a pyrrolidin-l-yl group, a pyrrolinyl group, an imidazolidinyl group, an imidazolinyl group, a pyrazolidinyl group, a pyrazolinyl group, a [1,3]dioxolan-2-yl group, and a [1,3]dioxan-2-yl group. Among these, groups that can be used preferably are: a morpholino group, a thiomorpholino group, a piperidin-l-yl group, a 4-substituted piperidin-1-yl group, a piperazin-l-yl group, a 4-substituted piperazin-l-yl group, a [1,3]dioxolan-2-yl group, and a [1,3]dioxan-2-yl group.
Herein, the "halogen atom" refers to a fluorine atom, a chlorine atom, a bromine atom, or an iodine atom.
Herein, the "alkoxy group" refers to an oxy group to which the above-defined "alkyl group" has been linked. The alkoxy group preferably includes C1_8 alkoxy groups, and more preferably C1_5 alkoxy groups. Specifically, the alkoxy group includes, for example, a methoxy group, an ethoxy group, a 1-propoxy group, a 2-propoxy group, an n-butoxy group, an i-butoxy group, a sec-butoxy group, a t-butoxy group, a 1-pentyloxy group, a 2-pentyloxy group, a 3-pentyloxy group, a 2-methyl-l-butyloxy group, a 3-methy-l-butyloxy group, a 2-methyl-2-butyloxy group, a 3-methy-2-butyloxy group, a 2,2-dimethyl-l-propyloxy group, a 1-hexyloxy group, a 2-hexyloxy group, a 3-hexyloxy group, a 2-methyl-l-pentyloxy group, a 3-methyl-l-pentyloxy group, a 4-methyl-l-pentyloxy group, a 2-methyl-2-pentyloxy group, a 3-methyl-2-pentyloxy group, a 4-methyl-2-pentyloxy group, a 2-methyl-3-pentyloxy group, a 3-methyl-3-pentyloxy group, a 2,3-dimethyl-l-butyloxy group, a 3,3-dimethyl-l-butyloxy group, a 2,2-dimethyl-l-butyloxy group, a 2-ethyl-1-butyloxy group, a 3,3-dimethyl-2-butyloxy group, a 2,3-dimethyl-2-butyloxy group, and a 1-methyl cyclopropyl methoxy group.
Herein, the "amino group" refers to a monovalent group that has a nitrogen atom with two hydrogen atoms (represented by -NH2).
Herein, the "cycloalkylalkyl group" refers to a group derived from the above-defined "alkyl group" by substitution of the above-defined "cycloalkyl group" at an arbitrary position of the alkyl group. The cycloalkylalkyl group preferably includes C3_8 cycloalkyl C1-4 alkyl groups. Specifically, the cycloalkylalkyl group includes, for example, a cyclopropylmethyl group, a cyclopropylethyl group, a cyclopentylmethyl group, a cyclopentylethyl group, a cyclohexylmethyl group, and a cyclohexylethyl group.
Herein, the "cycloalkylalkenyl group" refers to a group derived from the above-defined "alkenyl group" by substitution of the above-defined "cycloalkyl group" at an arbitrary position of the alkenyl group. The cycloalkylalkenyl group preferably includes C3_8 cycloalkyl C24 alkenyl groups.
Herein, the "cycloalkylalkynyl group" refers to a group derived from the above-defined "alkynyl group" by substitution of the above-defined "cycloalkyl group" at an arbitrary position of the alkynyl group. The cycloalkylalkynyl group preferably includes C3_8 cycloalkyl C2-a alkynyl groups.
Herein, the "arylalkyl group" refers to a group derived from the above-defined "alkyl group" by substitution of the above-defined "aryl group" at an arbitrary position of the aryl group. The arylalkyl group preferably includes C6_10 aryl C1.1 alkyl groups.
Specifically, the arylalkyl group includes, for example, a benzyl group, a phenethyl group, and a 3-phenyl-l-propyl group.
Herein, the "arylalkenyl group" refers to a group derived from the above-defined "alkenyl group" by substitution of the above-defined "aryl group" at an arbitrary position of the alkenyl group. The arylalkenyl group preferably includes C6_10 aryl C2_4 alkenyl groups.
Herein, the "arylalkynyl group" refers to a group derived from the above-defined "alkynyl group" by substitution of the above-defined "aryl group" at an arbitrary position of the alkynyl group. The arylalkynyl group preferably includes C6_10 aryl C2_4 alkynyl groups.
Herein, the "heteroarylalkyl group" refers to a group derived from the above-defined "alkyl group" by substitution of the above-defined "heteroaryl group" at an arbitrary position of the alkyl group. The heteroarylalkyl group preferably includes C5_10 heteroaryl C1-4 alkyl groups.
Specifically, the heteroarylalkyl group includes, for example, a pyridyl-4-ylmethyl group, an oxazolyl-2-ylmethyl group, a 2-(pyridyl-4-yl)ethyl group, and a 2-(oxazolyl-2-yl)ethyl group.
Herein, the "heteroarylalkenyl group" refers to a group derived from the above-defined "alkenyl group" by substitution of the above-defined "heteroaryl group" at an arbitrary position of the alkenyl group. The heteroarylalkenyl group preferably includes C5_10 heteroaryl C24 alkenyl groups.
Herein, the "heteroarylalkynyl group" refers to a group derived from the above-defined "alkynyl group" by substitution of the above-defined "heteroaryl group" at an arbitrary position of the alkynyl group. The heteroarylalkynyl group preferably includes Cs_10 heteroaryl C24 alkynyl groups.
Herein, the "heterocyclic alkyl group" refers to a group derived from the above-defined "alkyl group" by substitution of the above-defined "heterocyclic group" at an arbitrary position of the alkyl group. The heterocyclic alkyl group preferably includes C3_8 heterocyclic CI-C4 alkyl groups. Specifically, the heterocyclic alkyl group includes, for example, a morpholin-4-yl-methyl group, a 2-(morpholin-4-yl)ethyl group, a 4-hydroxy-piperidin-l-yl-methyl group, a 2-(4-hydroxy-piperidin-l-yl)ethyl group, a 4-methyl-piperazin-l-yl-methyl group, and a 2-(4-methyl-piperazin-l-yl)ethyl group.
Herein, the "heterocyclic alkenyl group" refers to a group derived from the above-defined "alkenyl group" by substitution of the above-defined "heterocyclic group" at an arbitrary position of the alkenyl group. The heterocyclic alkenyl group preferably includes C3_8 heterocyclic C24 alkenyl groups.
Herein, the "heterocyclic alkynyl group" refers to a group derived from the above-defined "alkynyl group" by substitution of the above-defined "heterocyclic group" at an arbitrary position of the alkynyl group. The heterocyclic alkynyl group preferably includes C3_8 heterocyclic C24 alkynyl groups.
Herein, the "hydroxyalkyl group" refers to a group derived from the above-defined "alkyl group" by substitution of a hydroxyl group at an arbitrary position of the alkyl group.
The hydroxyalkyl group preferably includes hydroxy C1-4 alkyl groups.
Herein, the "dihydroxyalkyl group" refers to a group derived from the above-defined "alkyl group" by substitution of hydroxyl groups at two arbitrary positions of the alkyl group.
The dihydroxyalkyl group preferably includes dihydoroxy C1-4 alkyl groups.
Herein, the "alkyloxyalkyl group" refers to a group derived from the above-defined "hydroxyalkyl group" by substitution of a hydroxyl group in the above-defined "alkyl group".
The alkyloxyalkyl group preferably includes C1_8 alkyloxy C1-4 alkyl groups.
Herein, the "hydroxyalkyloxyalkyl group" refers to a group derived from the above-defined "alkyloxyalkyl group" by substitution of a hydroxyl group at an arbitrary position in the terminal alkyl group. The hydroxyalkyloxyalkyl group preferably includes hydroxy CI-8 alkyloxy C14 alkyl groups.
Herein, the "aminoalkyl group" refers to a group derived from the above-defined "alkyl group" by substitution of an amino group (H2N-) at an arbitrary position of the alkyl group.
The aminoalkyl group preferably includes amino C14 alkyl groups.
Herein, the "alkylaminoalkyl group" refers to a group derived from the above-defined "aminoalkyl group" by substitution of the above-defined "alkyl group" at one or two arbitrary positions in the amino group. The alkylaminoalkyl group preferably includes C1_8 alkylamino C1-4 alkyl groups. When two hydrogen atoms are replaced with alkyl groups, the alkyl groups may be the same or different.
Herein, the "hydroxyalkylaminoalkyl group" refers to a group derived from the above-defined "alkylaminoalkyl group" by substitution of a hydroxyl group at an arbitrary position in the terminal alkyl group. The hydroxyalkylaminoalkyl group preferably includes hydroxy C1_8 alkylamino C1-4 alkyl groups.
Herein, the "iminoalkyl group" refers to a group derived from the above-defined "alkyl group" obtained by substitution of an imino group (=NH) at an arbitrary position of the alkyl group. The iminoalkyl group preferably includes imino C14 alkyl groups.
Herein, the "hydroxyiminoalkyl group" refers to a group derived from the above-defined "iminoalkyl group" by substituting the hydrogen atom in the imino group with a hydroxyl group. The hydroxyiminoalkyl group preferably includes hydroxyimino C1.4 alkyl groups.
Herein, the "alkoxyiminoalkyl group" refers to a group derived from the above-defined "hydroxyiminoalkyl group" by substituting a hydrogen atom of the hydroxyl group with the above-defined "alkyl group". The alkoxyiminoalkyl group preferably includes C1_8 alkyloxyimino C1.4 alkyl groups.
The compounds of the present invention include the free forms and the pharmaceutically acceptable salts of the compounds. Such "salts" are not limited to any particular salts, as long as they are pharmaceutically acceptable salts derived from the compound represented by formula (1) of the present invention (herein sometimes also referred to as "compound I"). The salts include, for example, acid salts formed by reacting compound I of the present invention with an acid, and base salts formed by reacting compound I of the present invention with a base.
Preferred acids for use in preparing the pharmaceutically acceptable acid salts of compound I of the present invention are acids that form non-toxic acid salts of compound I of the present invention. The acid salts include, for example, hydrochloride, hydrobromate, hydroiodide, nitrate, sulfate, bisulfate, phosphate, acid phosphate, acetate, lactate, citrate, acid citrate, tartrate, bitartrate, succinate, maleate, fumarate, gluconate, saccharate, benzoate, methanesulfonate, ethanesulfonate, benzenesulfonate, p-toluenesulfonate, and 1,1'-methylene-bis-(2-hydroxy-3-naphtoic acid) salt.
Preferred bases for use in preparing pharmaceutically acceptable base salts of compound I of the present invention are bases that form non-toxic base salts of compound I of the present invention. The base salts include, for example, alkali metal salts such as sodium salt and potassium salt, alkali earth metal salts such as calcium salt and magnesium salt, ammonium salts, water-soluble amine addition salts such as the N-methyl glucamine salt, lower-alkanol ammonium salts, and pharmaceutically acceptable salts derived from other organic amines bases.
Compound I of the present invention may contain absorbed water or forms hydrates when it is allowed to stand in the atmosphere and to absorb moisture. Such salts are also included in the salts of compound I of the present invention.
Furthermore, compound I of the present invention may absorb solvents to form solvates.
Such salts are also included in the salts of compound I of the present invention.
Herein, "MEK" (MAPK/ERK/Kinase; MAPK is the abbreviation for mitogen-activated protein kinase, and ERK is the abbreviation for extracellular signal-regulated kinase) refers to the dual-specificity kinase that is associated with the MAP kinase and the ERK
kinase. "MEK
inhibition" refers to the MEK-mediated competition, inhibition, or cancellation of a cascade or of the activities of proteins produced in the cascade. Accordingly, the inhibition includes the competition, inhibition, or cancellation of the activities of the MAP/ERK
kinase or of the activities of the genes encoding the MAP/ERK kinase. Herein, the "Ras-"K
signaling pathway" is defined as the sequential pathway of Ras -> Raf -> MEK -> ERK, and is one of the pathways that transmit growth signals from various growth factor receptors on the cell 5 membrane to the nucleus through the cytoplasm. The phrase "cancer depending on the Ras-"K signaling pathway" refers to a cancer that proliferates mainly depending on the Ras-MAPK signaling pathway. In other words, the phrase means a cancer whose growth or survival is reduced by blocking or inhibiting the Ras-MAPK signaling pathway.
Herein, the "proliferative disease" refers to a disorder caused by deficiencies in the 10 cellular signal transduction system or the signal transduction mechanism of a certain protein.
The proliferative disease includes, for example, cancers, psoriasis, restenosis, autoimmune diseases, and atherosclerosis.
Herein, the "inflammation-related joint disorders" specifically refers to diseases such as osteoarthritis, rheumatoid arthritis, reactive arthritis, viral arthritis, purulent arthritis, and 15 tuberculous arthritis. The inflammation-related joint disorders also include arthralgia caused by these diseases (for example, knee joint pain caused by rheumatoid arthritis).
Herein, the "preventive or therapeutic agent for an inflammation-related joint disorder"
includes not only therapeutic agents for the above-described joint diseases, but also preventive agents for the diseases, agents for use in suppressing the advancement of the diseases (to prevent aggravation 20 or to maintain current conditions), and such.
In the present invention, there is no limitation on the type of "protecting group", as long as it is a group commonly used to protect an ethynyl group, a hydroxyl group, or an amino group.
An ethynyl protecting group includes, for example, silyl groups such as a trimethylsilyl 25 group, a triethylsilyl group, an isopropyldimethylsilyl group, a t-butyldimethylsilyl group, a methyldiisopropylsilyl group, a methyl-t-butylsilyl group, a triisopropylsilyl group, a diphenylmethylsilyl group, a diphenylbutylsilyl group, a diphenylisopropylsilyl group, and a phenyldiisopropylsilyl group. Among them, a trimethylsilyl group or such is preferred.
A hydroxyl protecting group includes, for example, alkylsilyl groups such as a 30 trimethylsilyl group, a triethylsilyl group, an isopropyldimethylsilyl group, a t-butyldimethylsilyl group, a methyldiisopropylsilyl group, a methyldi-t-butylsilyl group, a triisopropylsilyl group, a diphenylmethylsilyl group, a diphenylbutylsilyl group, a diphenylisopropylsilyl group, and a phenyldiisopropylsilyl group; C1_6 alkylcarbonyl groups such as an acetyl group and a propionyl group; phenylcarbonyl group; C1_6 alkyloxycarbonyl groups such as a methoxycarbonyl group, 35 an ethoxycarbonyl group, and a t-butoxycarbonyl group; a vinyl group; a tetrahydrofuranyl group; alkoxymethyl groups such as a methoxymethyl group and an ethoxymethyl group;

alkoxylated alkoxymethyl groups such as a 2-methoxyethoxymethyl group;
alkoxyethyl groups such as a 1-ethoxyethyl group; a benzyloxymethyl group; substituted benzyl groups such as a benzyl group, a 4-methylbenzyl group, a 4-methoxybenzyl group, and an o-nitrobenzyl group;
and formyl groups. Among these, an alkylsilyl group is preferred, and a t-butyldimethylsilyl group or such is more preferred.
Protecting groups that are used to protect an amino group include, for example, a methoxycarbonyl group; substituted Cl-C6 alkyl-oxycarbonyl groups such as a cyclopropyl methoxycarbonyl group, a 2,2,2-trichloroethoxycarbonyl group, a 2-iodoethoxycarbonyl group, a 2-trimethylsilylethoxycarbonyl group, a 2-methylthioethoxycarbonyl group, a 2-methylsulfonylethoxycarbonyl group, an isobutyloxy carbonyl group, a t-butoxycarbonyl group (BOC group); C1-C6 alkenyl-oxycarbonyl groups such as a vinyloxycarbonyl group and an allyloxycarbonyl group; a benzyloxycarbonyl group (CBZ group); substituted benzyl-oxycarbonyl groups such as a p-methoxybenzyloxy carbonyl group, a 2,4-dichlorobenzyloxy carbonyl group, and a p-cyanobenzyloxy carbonyl group;
formyl groups;
acetyl groups; substituted C1-C6 alkyl-carbonyl groups such as a dichloroacetyl group, a trichloroacetyl group, and a trifluoroacetyl group; phthalimide groups (name provided as the protected functional group); benzyl groups; and substituted benzyl groups such as a 3,4-dimethoxybenzyl group. Among these, an alkyl-oxycarbonyl group is preferred, and the t-butoxycarbonyl (BOC) group and such are more preferred.
Compound I of the present invention represented by the above formula (1) preferably includes compounds comprising the following:
(1) Rl is preferably an iodine atom, a bromine atom, a vinyl group, or an ethynyl group, and more preferably an iodine atom or an ethynyl group.
(2) R2 is preferably a chlorine atom, a fluorine atom, a methyl group, or a hydroxymethyl group, more preferably a fluorine atom or a chlorine atom, and particularly preferably a fluorine atom.
(3) R3 is preferably a hydrogen atom or a fluorine atom, and more preferably a fluorine atom.
(4) R4 is preferably an alkyl group that has one to three substituents selected from the group consisting of -ORa, -NRaRb, -NRaCORb, a heterocyclic group, and a heteroaryl group.
Ra and Rb can each represent a hydrogen atom or an alkyl group. The alkyl group may have preferably a hydroxyl group, an alkoxy group, or an amino group as a substituent.
The heterocyclic group and the heteroaryl group may have one to three substituents selected from the group consisting of an alkyl group, -ORa, and -NRaRb. The alkyl group may have a hydroxyl group, an alkoxy group, or an amino group as a substituent.
The substituent is preferably an alkyl group or -ORa, more preferably a methyl group, a hydroxyethyl group, or -OH (hydroxyl group).
More preferably, R4 is an alkyl group that has one to three substituents selected from the group consisting of -ORa, -NRaRb, and -NRaCORb.
Still more preferably, R4 is an alkyl group that has one to three -ORa, and particularly preferably an alkyl group that has one to three -OH (hydroxyl group). The alkyl group is preferably a C1-C8 alkyl group, more preferably a Cl-C5 alkyl group, and particularly preferably a C 1-C3 alkyl group.
Preferably, Ra and Rb can each represent a hydrogen atom or a C1-C5 alkyl group, and more preferably a hydrogen atom.
The R4 includes, for example, a hydroxyalkyl group, a dihydroxyalkyl group, a hydroxyalkyloxyalkyl group, a hydroxyalkylaminoalkyl group, an acylaminoalkyl group, a heteroarylalkyl group, a heterocyclic alkyl group, and a heterocyclic alkyl group containing hydroxy groups.
More preferably, R4 represents a 2-hydroxyethyl group, a 3-hydroxypropyl group, a 2,3-dihydroxypropyl group, a 2-hydroxy-l-(hydroxymethyl)ethyl group, a 2-hydroxypropyl group, a 2-methyl-2-hydroxypropyl group, a 1-methyl-2-hydroxyethyl group, a 2-(2-hydroxyethoxy)ethyl group, a 2-(2-hydroxyethylamino)ethyl group, a 2-(morpholin-4-yl)ethyl group, a 2-(4-methylpiperazin-l-yl)ethyl group, a 2-(4-hydroxypiperidin-1-yl)ethyl group, a pyridylmethyl group, an imidazol-2-ylmethyl group, and a 2-acetylaminoethyl group.
Still more preferably, R4 represents a 2-hydroxyethyl group, a 3-hydroxypropyl group, a 2,3-dihydroxypropyl group, a 2-hydroxy-1-(hydroxymethyl)ethyl group, a 2-hydroxypropyl group, a 2-methyl-2-hydroxypropyl group, a 1-methyl-2-hydroxyethyl group, and a 2-(2-hydroxyethoxy)ethyl group. Among these, the 2-hydroxyethyl group, 3-hydroxypropyl group, 2,3-dihydroxypropyl group, and 2-hydroxy-1-(hydroxymethyl)ethyl group shown below are preferred.

HO,,,- HO HO
OH OH
HO

HO HO
HO
D--~ OH

Among these, the particularly preferred R4 includes a 2-hydroxyethyl group and a 2,3-dihydroxypropyl group.
In the embodiments of the present invention, the above-defined R1, R2, R3, and R4 can be combined appropriately. For example, the specific combinations that are preferred are as follows:
Rl represents an iodine atom, a bromine atom, a vinyl group, or an ethynyl group;
R2 represents a chlorine atom, a fluorine atom, a methyl group, or a hydroxymethyl group;
R3 represents a fluorine atom; and R4 represents an alkyl group that is substituted by one to three hydroxyl groups; or alternatively R1 represents an iodine atom or an ethynyl group;
R2 represents a fluorine atom;
R3 represents a fluorine atom; and R4 represents a group selected from the following groups:
HOB - HO HO

OH OH
HO

HO HO
HO OH
(5) the above-defined X represents the group represented by formula (i) or formula (ii) below:

O1Y~' ~Y-Z-W N
(i) \Y2 (ii ) In formula (i), Y represents -0-, -NR8O-, -ONR8-, -NR8CO-, or -NR8S02- (unless otherwise indicated, these substituents have Z bonded to their right-hand side);
Z represents a C1_8 alkylene chain which may be substituted by one to three groups represented by W';
R8 represents a hydrogen atom, an alkyl group, -ORa, or -COR9; and the alkyl group may have a halogen atom, -ORa, or -NRaRb as a substituent;
R9 represents a hydrogen atom, an alkyl group, or -ORa; and the alkyl group may have a halogen atom, -ORa, or -NRaRb as a substituent;

R8 and R9 may be linked to the alkylene chain of Z, or form a heterocyclic group through a linkage to the substituent represented by Ra or Rb in W.
In formula (ii), Y1 and Y2, which may be the same or different, each represent a single bond, -CO-, -COO-, -0-, -OCO-, -NRa-, or -S02-;
Z' represents a CI_8 alkylene chain which may be substituted by one to three groups represented by W'.
In formulae (i) and (ii) above, W and W', which may be the same or different, each represent a C1_5 alkyl group, a halogen atom, an oxo group, -ORa, -COORa, -COOCORa, -CO-[halogen atom], -OCORa, -CONRaRb, -SRa, -SORa, -SO2Ra, -NRaRb, -NRaCORb, -NRaSO2Rb, -SO2NRaRb, a heterocyclic group, or a heteroaryl group. The heterocyclic group and the heteroaryl group may have a substituent selected from the group consisting of a C1_5 alkyl group, -ORa, and -NRaRb; and the alkyl group may have a hydroxyl group, a C1_5 alkoxy group, or an amino group as a substituent.
The above-mentioned substituents, except the oxo group and the halogen atom, may be linked to each other to form a cycloalkyl group or a heterocyclic group. The cycloalkyl group or heterocyclic group may have a substituent selected from the group consisting of a C1_5 alkyl group which may be substituted with -ORa, -ORa, and -NRaRb.
When X is the group represented by the above formula (i) and Y is not -0-, W
may be a hydrogen atom.
Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1_5 alkyl group; and the alkyl group may have one to three substituents selected from hydroxyl groups, C1.5 alkoxy groups, and amino groups.
Herein, the above-defined Ra and Rb, which may be the same or different, preferably each represent a group selected from the group consisting of. a hydrogen atom, a methyl group, an ethyl group, an n-propyl group, an i-propyl group, an n-butyl group, an i-butyl group, a t-butyl group, a sec-butyl group, a 1, 1 -dimethylpropyl group, a 2,2-dimethylpropyl group, a 1,2-dimethylpropyl group, a pentyl group, a hydroxymethyl group, a 1-hydroxyethyl group, a 1-hydroxy- l -methylethyl group, a 2-hydroxy- l -methylethyl group, a 2-hydroxy- 1, 1 -dimethylethyl group, a 2-hydroxyethyl group, a 1-hydroxypropyl group, a 2-hydroxypropyl group, and a 3-hydroxypropyl group.
A preferred embodiment of the group represented by formula (i) above is as follows:
(i-1) In the above-defined X, the R8 in Y preferably represents a hydrogen atom, a hydroxyl group, a C1_5 alkyl group, or -COR9, and more preferably, a hydrogen atom, a hydroxyl group, a methyl group, an ethyl group, an n-propyl group, an i-propyl group, an n-butyl group, a sec-butyl group, an i-butyl group, a t-butyl group, a 1, 1 -dimethylpropyl group, a 2,2-dimethylpropyl group, a 1,2-dimethylpropyl group, a pentyl group, or -COR9.

In this case, R9 preferably represents a hydrogen atom, a hydroxyl group, a C1_5 alkyl group, or a C1_5 alkoxy group, and more preferably, a hydrogen atom, a methyl group, an ethyl group, an n-propyl group, an i-propyl group, an n-butyl group, a sec-butyl group, a t-butyl group, a 2,2-dimethylpropyl group, a 1,2-dimethylpropyl group, a pentyl group, a methoxy group, an 5 ethoxy group, an n-propoxy group, an i-propoxy group, an n-butoxy group, an i-butoxy group, a sec-butoxy group, an i-butyl group, a t-butoxy group, a 1, 1 -dimethylpropyl group, a 2,2-dimethylpropoxy group, a 1,2-dimethylpropoxy group, or a pentyloxy group.
The alkyl group and the alkoxy group represented by R8 and R9 may contain substitutions of one to three hydroxyl groups at arbitrary positions of the hydrocarbon moiety.
10 Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1_5 alkyl group; and the alkyl group may have a hydroxyl group, a C1.5 alkoxy group, or an amino group as a substituent.
(i-2) More preferably, the R8 in Y represents a hydrogen atom, a hydroxyl group, a methyl group, an ethyl group, an n-propyl group, an i-propyl group, an n-butyl group, an i-butyl 15 group, a t-butyl group, a sec-butyl group, a 1, 1 -dimethylpropyl group, a 2,2-dimethylpropyl group, a 1,2-dimethylpropyl group, a pentyl group, a formyl group, an acetyl group, a 2-methoxyacetyl group, a 2-ethoxyacetyl group, a 2-hydroxyacetyl group, a propionyl group, a 2-methylpropionyl group, a 2-methoxypropionyl group, a 2-ethoxypropionyl group, a 2-hydroxypropionyl group, a 3-methoxypropionyl group, a 3-ethoxypropionyl group, a 20 3-hydroxypropionyl group, a methoxy group, an ethoxy group, an n-propyloxy group, an i-propyloxy group, a hydroxymethyl group, or a 2-hydroxyethyl group.
(i-3) More preferably, the Y in the above-defined X represents -0-, -NHO-, -N(COCH3)0-, -N(COCH2OH)O-, -N(COCH2CH3)O-, -N(COCH(OH)CH3)0-, -N(COCH2CH2OH)O-, -N(COCH(OH)CH2OH)O-, -N(COCH2CH2CH3)0-, 25 -N(COCH2CH2CH2OH)O-, -N(COCH(OH)CH2CH3)0-, -N(COCH2CH(OH)CH3)Q-, -NHCO-, or -NHSO2-.
(i-4) More preferably, the above-defined W and W', which may be the same or different, each represent -OH, -OMe, -OEt, -OCH2OH, -O(CH2)20H, -O(i-Pr), -O(n-Pr), -COOH, -COOMe, -COOEt, -COOCOMe, -0001, -CONH2, -CONHMe, -CONHEt, -CONH(n-Pr), 30 -CONH(i-Pr), -CONMe2, -CON(Et)Me, -SO2Me, -SOMe, -SMe, -NH2, -NHMe, -NHCH2OH, -NH(CH2)20H, -N(Me)CH2CH 2OH, -NH Et, -NMe2, -N(Et)Me, -NHCOMe, -NMeCOMe, -NHCOEt, -NHCO(n-Pr), or -NHCO(i-Pr); and when Y is not -0-, W may be a hydrogen atom.
(i-5) In formula (i) above, the alkylene chain of Z in the above X preferably represents an alkylene chain having one to five carbon atoms.
35 The alkylene chain may have one to three substituents selected from the group consisting of: a C1_5 alkyl group, a halogen atom, -ORa, -NRaRb, and an oxo group, and the above substituents except the oxo group and the halogen atom may be linked to each other to form a cycloalkyl group or a heterocyclic group. The cycloalkyl group and the heterocyclic group may have a substituent selected from the group consisting of a C1_5 alkyl group, which may be substituted with -ORa, -ORa, and -NRaRb.
Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1.5 alkyl group; and the alkyl group may have a hydroxyl group, a C1_5 alkoxy group, or an amino group as a substituent.
(i-6) In the above-defined W or W', Ra and Rb may be the same or different, preferably each representing a hydrogen atom or a C1_5 alkyl group; and the alkyl group may have a hydroxyl group or a C1.5 alkoxy group.
(i-7) More preferably, in the X of formula (i) above, the alkylene chain of Z
is any one of the groups represented by the following formulae:
-CH2-, -(CH2)2-, -(CH2)3-, -(CH2)4-, -CH2CH(Me)-, -CH2C(Me)2-, -C(Me)2CH2-, -(CH2)2CH(Me)-, -(CH2)2C(Me)2-, -CH(Me)(CH2)2-, -C(Me)2(CH2)2-, -CH2CH(Me)CH2-, -CH2C(Me)2CH2-, -CH2C(CH2CH2)CH2- (where C(CH2CH2) represents a divalent cyclopropane ring), -CO-, -CH2CO-, -COCH2-, -(CH2)2CO-, -CO(CH2)2-, -CHOH-, -CH2CH(OH)-, -CH(OH)CH2-, -CH2CH(OH)CH2-, -CH(OH)CH2CH2-, and -CH2CH2CH(OH)-.
A preferred embodiment of the group represented by the above formula (ii) is as follows:
(ii-1) The above-defined X is preferably any one of the groups represented by the following formulae:

O O\_`7j / \j' O O
~Z' I z' Z, N, N, ~ N J 01' S
* S02 O r 0~ Z O\/NRa O~ 0_0 I ~ '( 1 N, 0-) ~NZ' -N } N,,_ Z) [wherein, Z' preferably represents a C1_5 alkylene chain which may be substituted by one to three groups represented by W';
Wrepresents a C1_5 alkyl group, a halogen atom, an oxo group, -ORa, -CONRaRb, -SRa, -SORa, -SO2Ra, -NRaRb, -NRaCORb, -NRaSO2Rb, -SO2NRaRb, a heterocyclic group, or a heteroaryl group; the heterocyclic group and the heteroaryl group may have a substituent selected from the group consisting of a C1_5 alkyl group, -ORa, and -NRaRb; the alkyl group may have a hydroxyl group, a C1.5 alkoxy group, or an amino group as a substituent;

the above substituents except the oxo group and the halogen atom may be linked to each other to form a cycloalkyl group or a heterocyclic group; the cycloalkyl group or the heterocyclic group may have a substituent selected from the group consisting of. a C1.5 alkyl group which may be substituted with -ORa, -ORa, and -NRaRb;
Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1_5 alkyl group; and the alkyl group may have a hydroxyl group, a C1_5 alkoxy group, or an amino group as a substituent].
(ii-2) More preferably, the above-defined Z' represents a C1_3 alkylene chain which may be substituted by one to three groups represented by W'.
W' represents a C1_3 alkyl group, an oxo group, -ORa, -CONRaRb, -SRa, -SORa, -SO2Ra, -NRaRb, -NRaCORb, -NRaSO2Rb, -SO2NRaRb, a heterocyclic group, or a heteroaryl group; the heterocyclic group and the heteroaryl group may have a substituent selected from the group consisting of: a C1_5 alkyl group, -ORa, and -NRaRb; and the alkyl group may have a hydroxyl group, a C1_5 alkoxy group, or an amino group as a substituent.
Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1.5 alkyl group; and the alkyl group may have a hydroxyl group, a C1.5 alkoxy group, or an amino group as a substituent.
(ii-3) Furthermore, W' which may substitute for the arbitrary positions in the alkylene chain of the above-defined Z' represents any one of the groups represented by the following formulae:
-Me, -Et, -n-Pr, -i-Pr, -CH2OH, -CH2CH2OH, -CH(OH)CH3, -OH, -OMe, -OEt, -OCH2OH, -O(CH2)20H, -O(i-Pr), -O(n-Pr), -000H, -COOMe, -COOEt, -CONH2, -CONHMe, -CONHEt, -CONH(n-Pr), -CONH(i-Pr), -CONMe2, -CON(Et)Me, -SO2Me, -SOMe, -SMe, -NH2, -NHMe, NHCH2OH, -NH(CH2)20H, -N(Me)CH2CH2OH, -NHEt, -NMe2, -N(Et)Me, -NHCOMe, -NMeCOMe, -NHCOEt, -NHCO(n-Pr), and -NHCO(i-Pr).
(ii-4) Furthermore, W' which may substitute for the arbitrary positions in the alkylene chain of the above-defined Z' represents any one of the groups represented by the following formulae:
-Me, -Et, -n-Pr, -i-Pr, -CH2OH, -CH2CH2OH, -CH(OH)CH3, -OH, -OMe, -OEt, -OCH2OH, -O(CH2)20H, -O(i-Pr), -O(n-Pr), -CONH2, -CONHMe, -CONHEt, -CONH(n-Pr), -CONH(i-Pr), -CONMe2, -CON(Et)Me, -SO2Me, -SOMe, -SMe, -NH2, -NHMe, -NHCH2OH, -NH(CH2)2OH, -N(Me)CH2CH2OH, -NHEt, -NMe2, -N(Et)Me, -NHCOMe, -NMeCOMe, -NHCOEt, -NHCO(n-Pr), and -NHCO(i-Pr).
(ii-5) In W' of the above-defined Z', Ra and Rb, which may be the same or different, preferably each represent a hydrogen atom or an alkyl group having one to five carbon atoms;
and the alkyl group may have a hydroxyl group or an alkoxy group having one to five carbon atoms.
(ii-6) The alkylene chain of Z' in the above-defined X preferably represents any one of the groups represented by the following formulae:
-CH2-, -(CH2)2-, -(CH2)3-, -(CH2)4-, -CH2CH(Me)-, -CH2C(Me)2-, -C(Me)2CH2-, -(CH2)2CH(Me)-, -(CH2)2C(Me)2-, -CH(Me)(CH2)2-, -C(Me)2(CH2)2-, -CH2CH(Me)CH2-, -CH2C(Me)2CH2-, -CHOH-, -CH2CH(OH)-, -CH(OH)CH2-, -CH2CH(OH)CH2-, -CH(OH)CH2CH2-, -CH2CH2CH(OH)-, -CO-, -CH2CO-, -COCH2-, -(CH2)2CO-, -CO(CH2)2-, and -CH2CH(OH)CH2-.
X represented by the above formula (i) or (ii) is more preferably groups represented by formula (iv) or (iii) below:

O (CH2)n''-H
I (CH2)n N,O J (Iii) or WI N`O_(CH2)n-H (iv) [wherein, n represents an integer of 1 to 5, and n' represents an integer of 0 to 5; the repeating units represented by -(CH2)n- or -(CH2)n'- may be substituted at arbitrary positions by one to three substituents selected from the group consisting of. a C1_5 alkyl group, a halogen atom, -ORa, -NRaRb, and an oxo group; Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1_5 alkyl group; and the alkyl group may have a hydroxyl group, a C1_5 alkoxy group, or an amino group as a substituent].
In another preferred embodiment, X-CH2-* in the compound of the present invention represented by formula (1) includes compounds comprising the structure shown below as a substructure. In the formula, * represents linkage at position 5 of the parent benzamide ring.

<0 More specifically, X represented by the above formula (i) or (iv) includes the following groups:
a 2-hydroxyethoxy group, a 3-hydroxy-2-dimethylpropoxy group, a 3-hydroxypropoxy group, a 2-carbamoylethoxy group, a 2-methylcarbamoylethoxy group, a 2-methanesulfonyl-ethoxy group, a 2-acetylamino-ethoxy group, a 2-hydroxyethoxy-amino group, a 3-hydroxypropionylamino group, a 2-hydroxyethanesulfonamide group, a 1-hydroxymethyl-cyclopropylmethoxy group, a 2,3-dihydroxy-propoxy group, a 1 H-imidazol-2-ylmethoxy group, a 2-methylcarbamoyl-ethoxyamino group, a 2-acetylamino-ethoxyamino group, a 2-methanesulfonyl-ethoxyamino group, a 1H-imidazol-2-ylmethoxyamino group, a 3-hydroxypropoxyamino group, a 2-(2-hydroxy-ethoxy)-ethoxy group, a 2-methylamino-ethoxy group, a 2-(2-hydroxy-ethylamino)-ethoxy group, a 2-morpholin-4-yl-ethoxy group, a 2-(4-hydroxy-piperidin-l-yl)-ethoxy group, a 2-methylamino-ethoxyamino group, a 2,3-dihydroxy-propoxyamino group;
a formyl-methoxyamino group, an acetyl-methoxyamino group, a methoxy-propionylamino group, an isobutyryl-methoxy-amino group, a (2-hydroxy-acetyl)-methoxyamino group, a methoxy-(2-methoxy-acetyl)-amino group, an acetyl-ethoxy-amino group, an ethoxy-propionyl-amino group, an acetyl-isopropoxy-amino group, an acetyl-hydroxy-amino group, an acetoxy-acetyl-amino group, an acetyl-(2-hydroxy-ethoxy)-amino group, an acetyl-(3-hydroxy-propoxy)-amino group, an acetyl-(2-hydroxy-2-methyl-propoxy)-amino group, an acetyl-(2-acetylamino-ethoxy)-amino group, an acetyl-(2-propionyl-amino-ethoxy)-amino group, an acetyl-(2-isobutyrylamino-ethoxy)-amino group, an acetyl-(2-methylsulfanyl-ethoxy)-amino group, an acetyl-(3-methylsulfanyl-propoxy)-amino group;
a 2-hydroxy- 1, 1 -dimethyl-ethoxy group;
a methylcarbamoylmethoxyamino group, an ethylcarbamoylmethoxyamino group, a propylcarbamoylmethoxyamino group, an isopropylcarbamoyl-methoxyamino group, a dimethylcarbamoylmethoxyamino group, a 2-ethylcarbamoyl-ethoxyamino group, a 2-propylcarbamoyl-ethoxyamino group, a 2-isopropylcarbamoyl-ethoxyamino group, a 3-methylcarbamoyl-propoxyamino group, a 2-methoxycarbonyl-ethoxyamino group, a methoxyamino group, a methoxy-methyl-amino group, an ethoxyamino group, an isopropoxyamino group, a 2-hydroxy-2-methyl-propoxyamino group, a 2-methylsulfanyl-ethoxyamino group, a 2-methanesulfmyl-ethoxyamino group, a 3-methylsulfanyl-propoxyamino group, a 3-methanesulfmyl-propoxyamino group, a 2-propionylamino-ethoxyamino group, a 2-isobutyrylamino-ethoxyamino group;
a 2-hydroxy-acetylamino group, and an acetyl-(2-hydroxy-ethyl)-amino group.
More specifically, X represented by the above formula (ii) or (iii) preferably includes the following groups:

O
fN ~N rN 01' N

N O N~ N O
or oO -t =r o r ~

~NRa NRa or, rO eN W ;~O

[wherein, the alkylene chain may be substituted at arbitrary positions by 'one to three substituents selected from the group consisting of. a C1_5 alkyl group, a halogen atom, -ORa, -NRaRb, and an oxo group; Ra and Rb, which may be the same or different, each represent a hydrogen atom or a 5 C1_5 alkyl group; and the alkyl group may have a hydroxyl group, a C1.5 alkoxy group, or an amino group as a substituent; Ra represents a hydrogen atom or a C1_5 alkyl group; and the alkyl group may have a hydroxyl group, a C1_5 alkoxy group, or an amino group as a substituent.
More specifically, X represented by the above formula (ii) or (iii) includes the following groups:
10 a 3-oxo-[1,2]oxazinan-2-yl group, a 3-oxo-isoxazolidin-2-yl group, a 4,4-dimethyl-3-oxo-isoxazolidin-2-yl group, a 4-hydroxy-3-oxo-[1,2]oxazinan-2-yl group, a 3-oxo-[1,4,2]dioxazinan-2-yl group, a 2-oxo-pyrrolidin-1-yl group, a 2-oxo-piperidin-1-yl group, a 2-oxo-oxazolidin-3-ylmethyl group, a 2-oxo-tetrahydro-pyrimidin-1-yl group, and a 2,3-dioxo-morpholin-4-yl group.
15 From the preferred embodiments (1)-(5) described above, the preferred embodiments of R1 to R4, and X can be selected at one's discretion, and combined into compounds of the present invention.
More specifically, compound I of the present invention represented by formula (1) includes, for example, those described below, but is not limited thereto.
R4~, O
I
HN O

X \ I I /

F (1) In the Table, compound names are also shown together with their compound numbers.
[Table 1]

Compound No. Structure Compound name 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(2-hydroxy-ethoxym ethyl)-benzamide Fq^/ ~ I F I / 1 2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)-5-(2-hydroxy-ethoxymethyl)-benzamide B-2 pF

CH F N-(2,3-dihydroxy-propoxy)-3,4-difluoro-2-(2-fluoro-4-iodo-4'ja ~~ I
phenylamino)-5-{2-hydroxy-ethoxymethyl)-benzamide lo.^Y
o a 2-(2-chloro-4-iodo-phenylamino)-3,4-difluoro-N-(2-hydro xy-ethoxy)-5-(2-hydroxy-etho xym ethyl)-benzamide F /

F 3,4-difluoro-2-(2-fluoro-4-vinyl-phenylamino)-N-(2-hydroxy-ethoxy)-5-(2-hydroxy-etho xymethyl)-benzamide ro^J

F
3.4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5- (3-hydroxypropoxymethyl)-benzamide F
/

~~Q o F 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-(3-hydroxy-2,2-dim ethyl-propoxymethyl)-N-(2-hydroxy-ethoxy)-~p benzamide -v v ~ F / 1 p F 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(1-hydroxymethyl-F , cyclopropylmethoxymethyl)-benzamide 1~.^Q
F d,I-5-(2,3-dihydroxy-propoxymethyl)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-/ benzamide b~4 F 3,4-difluoro-2-(2-Fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(2-methylcarbamoyl-ethoxymethyl)-F benzamide 5-(2-acetyla m ino-etho xymethyl)-3,4-d iuoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benzamide 4 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(2-metha n e su lfo nyl-ethoxymethyl)-~S~ 1 benzamide OS O

3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-o hydroxy-ethoxy)-5-(1 H-imidazol-2-yl methoxymethyl)-benzamide 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[2-(2-hydroxy-ethoxy)-ethoxymethyl]-benzamide ~v\4 0 3,4-difluoro-2--(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(2-m ethylam ino-ethoxym ethyl)-benzamide p~Q 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[2-(2-hydroxy-ethylamino)-" -^ F ethoxymethyl]-benzamide 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydro xy-ethoxy)-5-(2-morpholin-4-yl-etho xymethyl)-' benzamide 3,4-difluoro-2-(2-filuoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[2-(4-hydroxy-piperidin-1 -yl)-ethoxymethyl]-benzam ide 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-(2-hydroxy-1, 1 -dimethyl-ethoxymethyl)-N-(2-hydroxy-ethoxy)-HO benzamide Compound No. Structure Compound name ro~4 0 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-F hydroxy-ethoxy)-5-[(2-hydroxy-ethoxyamino)-methyl]-'~~ benzamide o F 2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)-5-[(2-hydroxy-ethoxya m ino)-m ethyl]-benzamide HK N-(2,3-dihydroxy-propoxy)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-[(2-hydroxy-ethoxyamino)-methyl]-benzamide 2-(2-chloro-4-iodo-phenylamino)-3,4-difluoro-N-(2-hydroxy-eth oxy)-5-[(2-hydroxy-ethoxyamino)-m ethyl]-benzamide 3,4-difluoro-2-(2-fluoro-4-vinyl-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-hydroxy-ethoxyam ino)-methyl]-benzamide I 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-methylcarbamoyl-ethoxyamino)-methyl]-benzamide 5-[(2-acetylamino-ethoxyamino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benzamide 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-methanesulfonyi-ethoxyamino)-~o- methyl]-benzamide 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(1 H-imidazol-2-ylmethoxyamino)-methyl]-benzamide 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(3-hydroxy-propoxyamino)-methyl]-F benzamide 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-methylamino-ethoxyamino)-methyl]-benzamide ro~P 5-[(2,3-dihydroxy-propoxyamino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-`~ benzamide On F

ND_~=o o F 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-H H hydroxy-ethoxy)-5-(methylcarbamoylmethoxyamino-methyl)-benzamide Ho HN ~" 5-(ethylcarbamoylmethoxyamino-methyl)-3,4-difluoro-2-(2-- fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-0 benzamide ff o HN-0H 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2--H-6-9 N-O hydroxy-ethoxy)-5-(propylcarbamoylmethoxyamino-methyl)-F benzamide F

HD,--O 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-H-+r hydroxy-ethoxy)-5-[(isopropylcarbamoyl-methoxyamino)-methyl]-benzamide 5-(dimethylcarbamoylmethoxyamino-methyl)-3,4-difluoro-2-~ H (2-fuoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-~ F 6, benzamide F 5-[(2-ethylcarbamoyl-ethoxyamino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-F benzamide o w~O o F 5-[(2-propylcarbamoyl-ethoxyamino)-methyl]-3,4-difluoro-~ 2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benzamide o ''~a F 5-[(2-isopropylcarbamoyl-ethoxyamino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-F ethoxy)-benzamide o 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2--^p hydroxy-ethoxy)-5-[(3-methylcarbamoyl-propoxyamino)-F methyl]-benzamide HD-~, 0 o F 3-[N-[2,3-difluoro-4-(2-fluoro-4-iodo-phenylamino)-5-(2-" hydroxyethoxycarbamoy1)benzyI]aminooxy]prop o H ~ ionic acid methyl ester HD''~4 F 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-hydroxyam inomethyl-N-(2-hydroxy-ethoxy)-benzamide HD=~'o ~ F 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(methoxyamino-methyl)-benzamide F

F 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-H
hydroxy-ethoxy)-5-[(methoxy-methyl-amino)-methyl]-F , benzamide W-fo F 5-(ethoxyamino-methyl)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benzamide Ho-o H F 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-~
hydroxy-ethoxy)-5-(isopropoxyamino-methyl)-benzamide ro~Q
H F 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-N 1 hydroxy-ethoxy)5-[(2-hydroxy-2-methyl-propoxyamino)--+~~0o F (- 7 methyl]-benzamide 2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)5-[(2-hydroxy-2-methyl-pro poxyam ino)-NOx`~ F methyi]-benzamide 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N- (2-hydroxy-ethoxy)-5-[(2-methylsulfanyl-ethoxyam ino)--'S`^o' F u methyl]-benzamide Ho/-p off F 3,4-difluoro-2--(2- luoro-4-iodo-phenylamino)-N--(2-9 H hydroxy-ethoxy)-5-[(2-methanesulfinyl-ethoxyamino)-'S.-o F F I methyl]-benzamide o F 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydro xy-etho xy)-5-[(3-methyl sufanyl-propo xyam ino)-~s~~o' F I methyl]-benzamide HO_--,?
HN 0 H 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(3-methanesulfinyl-propoxyamino)-s0 '" methyl]-benzamide o F 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hyd roxy-etho xy)-5-[(2-p ropoio nyla mino-etho xyam ino)-lr F Z~l methyl]-benzamide F -Jy'-'-O- methyl]-benzamide Compound No. Structure Compound name MD~/~o F 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(3-hydroxy-propionylamino)-m ethyl]-l benzamide E-1 o F

~~4 0 2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy -5-[(3-hydroxy-propionylamino)-methyl]-benzamide H;~ F 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-[(2-hydroxy-ethanesulfonylamino)-methyl]-N-(2-hydroxy-w~s, I F I ethoxy)-benzamide 0_0 F

F 2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-5-[(2-hydroxy-ethanesulfonylamino)-methyl]-N-(2-hydroxy-F ethoxy)-benzamide o o HO,_,.
"' F 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-[(2-H hydroxy-acetylamino)-methyl]-N-(2-hydroxy-ethoxy)-HO.YH I F I benzamide E-5 o F

H F 5-{[acetyl-(2-hydroxy-ethyl)-amino]-methyl}-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-F benzamide Compound No. Structure Compound name 3,4-diuoro-2-(2-fluoro-4-iodo-phenylamino)-5-[(formyF
F v _1 methoxy-amino)-methyl]-N-(2-hydroxy-ethoxy)-benzamide F

1O~`o HN O F 5-[acetyl-methoxy-amino-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benzamide F

HO=^4 o H F 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-0 hydroxy-ethoxy)-5-[(methoxy-propionyl-amino)-methyl]-F I benzamide HN-0 1, 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-0 ff hydroxy-ethoxy)-5-[(isobutyryl-methoxy-amino)-methyl]-~" benzamide HD'"4 o 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-([(2-hydroxy-acetyl)-methoxy-amino]-methyl}-N-(2-hydroxy-~'Y F ~`I ethoxy)-benzamide 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-4[methoxy-(2-methoxy-acetyl)-amino]-`o'Y methyl}-benzamide o F 5-[(acetyl-methoxy-amino)-methyl]-2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)-benzamide F

o 2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-W, 1 hydroxy-etho xy)-5-[(methoxy-prop ionyl-amino)-methyl]-benzamide iO~4 0 2-(4-ethynyl-2-=fluoro-phenylamino)-3,4-difluoro-N-(2-I hydroxy-ethoxy)-5-[(isobutyryl-methoxy-amino)-methyl]-o FF benzamide F 5-[(acetyl-ethoxy-amino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benzamide O F

5-[(ethoxy-propionyl-amino)-methyl]-3.4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benzamide F
Ho,-~o o F 5-[(acetyl-isopropoxy-amino)-methyl]-3,4-difluoro-2-(2-~ fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benzamide o F

w -o 5-[(acetyl-hydroxy-amino)-methyl]-3,4-difluoro-2-(2-oõ fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)--y F benzamide : o F 5-[(acetoxy-acetyl-amino)-methyl]-3,4-difluoro-2-(2-x4 " fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-F benzamide F-14 Vo F

fO~4 o F 5-{[acetyl-(2-hydroxy-ethoxy)-amino]-methyl}-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benzamide 5-{[acetyH3-hydroxy-propoxy)-amino]-methyl}-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N(2-hydroxy-F ethoxy)-benzamide 5-[[acetyl-(2-hydroxy-2-methyl-propoxy)-amino]-methyl}-F
p 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benzamide 0 5-([acetyl-(2-acetylamino-ethoxy)-amino]-methyl}-3,4-Y~=Y difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-0 F ethoxy)-benzamide F 5-([acetyl-(2-propionylamino-ethoxy)-amino]-methyl}-3,4-'Yk4 difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-6" ethoxy)-benzamide HD,~- 5-([acetyl-(2-isobutyrylamino-ethoxy)-amino]-methyl}-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-yt ethoxy)-benzamide 5-([acetyK2-methylsulfanyl-ethoxy)-amino]-methyl}-3,4-.S.~o difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-F ethoxy)-benzamide F 5-([acetyl-(3-methylsulfanyl-propoxy)-amino]-methyl}-3,4-- ~ difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-F ethoxy)-benzamide 5-[(acetyl-ethoxy-amino)-methyl]-2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)-benzamide 1 x'4 F 5-[(ethoxy-propionyl-amino)-methyl]-2-(4-ethynyl-2-'1O fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)-~Y F benzamide 5-([acetyl-(2-hydroxy-ethoxy)-amino]-methyl}-2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-F ethoxy)-benzamide F 5-([acetyl-(2-hydroxy-2-methyl-propoxy)-amino]-methyl}-HO~Q 2-(4-ethynyl-2--fluoro-phenylamino)-3,4-difluoro-N-(2-F hydroxy-ethoxy)-benzamide Compound No_ Structure Compound name o 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-o hydroxy-ethoxy)-5-(3-oxo-[1,2]oxazinan-2-ylmethyl)-f I benzamide O F

HO,-o' F 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(3-oxo-isoxazolidin-2-ylmethyl)-0 F benzamide ~~q o F 5-(4,4-dimethyl-3-oxo-isoxazolidin-2-ylmethyl)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-F ethoxy)-benzamide G-3 o F

o F 2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-~9 F hydroxy-ethoxy)-5-(3-oxo-[1,2]oxazinan-2-ylmethyl)-F benzamide ~~q o 2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)-5-(3-oxo-isoxazolidin-2-ylmethyl)-~" benzamide HOF N-(2,3-dihydroxy-propoxy)-3,4-difluoro-2-(2-fluoro-4-iodo-o phenylamino)-5-(3-oxo-[1,2]oxazinan-2-ylmethyl)-F benzamide HOB ' 9 N-(2,3-dihydroxy-propoxy)-3,4-difluoro-2-(2-luoro-4-iodo-\/Q`,o H phenylamino)-5-(3-oxo-isoxazolidin-2-ylmethyl)-benzamide HO~~q o F 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-q hydroxy-ethoxy)-5-(4-hydroxy-3-oxo-[1,2]oxazinan-2-Ho~" ylmethyl)-benzamide Compound No. Structure Compound name HO`~~D
Ft F 3,4-difluoro-2--(2-fluoro-4-iodo-phenylamino)-N-(2-~4 hydroxy-ethoxy)-5-(3-oxo-[1,4,2]dioxazinan-2-ylmethyl)-F benzamide H-1 o F
HO,_,--o 1 F 2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-~. hydroxy-ethoxy)-5-(3-oxo-[1,4,2]dioxazinan-2-ylmethyl)-o~i+ i F \ benzamide 3, 4-d iflu oro-2-(2-fl u o ro-4-io do-phenylamino)-N-(2-hydroxy-ethoxy)-5-(2-oxo-pyrrolidin-l-ylmethyl)-benzamide F

O F
3,4-d ifluoro-2-(2-fluoro-4-io do-phenylamino)-N-(2-1 -- -- hydroxy-ethoxy)-5-(2-oxo-piperidin-l-ylmethyl)-benzamide F
H-4 o F
Ho'-~o F 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(2-oxo-oxazolidin-3-ylmethyl)-F - benzamide o F 3,4-difluoro-2-(2-fuoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(2-oxo-tetrahydro-pyrimidin-1-- 1 = F 1 - ylmethyl)-benzamide HO'-'~o F 5-(2,3-dioxo-morpholin-4-ylmethyl)-3,4-difluoro-2-(2-o-) ~ fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-oy F benzamide Compound I of the present invention preferably includes, Exemplary Compound NOs.
B-1, B-2, B-6, B-9, B-12, C-1, C-2, C-6, C-7, C-8, C-10, C-13, C-24, C-28, C-29, C-31, C-34, C-35, F-1, F-2, F-3, F-4, F-5, F-6, F-7, F-8, F-9, G-1, G-2, G-3, G-4, and G-5, more preferably Exemplary Compound NOs. B-1, B-2, B-9, B-12, C-1, C-6, C-7, C-8, C-10, C-13, C-24, C-28, C-31, C-35, F-1, F-2, F-3, F-4, F-5, F-6, F-7, F-8, F-9, G-1, G-2, G-3, G-4, and G-5, particularly preferably Exemplary Compound NOs. B-1, C-1, C-10, C-13, F-1, F-2, F-5, G-1, G-2, G-3, G-4, and G-5.
Synthetic intermediates are used to produce compound. I. For example, synthetic intermediates A, B, C, D, E, F, G, H, I, J, K, and L represented by the following formulae (2) to (13) can be preferably used, but they are not limited thereto.

Synthetic intermediate (A) Synthetic intermediate (A) represented by formula (2):
HO O

\

R3 F (2) wherein, R1, R2, and R3 are the same as R1, R2, and R3 in the above formula (1). Preferred embodiments thereof are the same. These may comprise protecting group(s) required for the synthesis.
For example, as preferred embodiments, R1 is an iodine atom, a bromine atom, an ethynyl group, a vinyl group, or a carbamoyl group, R2 is a chlorine atom or a fluorine atom, and R3 is a fluorine atom.
The compounds represented by the formula (2) include, for example, 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-vinyl-benzoic acid (R1=I, R2=F, R3=F).
Synthetic intermediate (B) Synthetic intermediate (B) represented by formula (3):
R4,, 0 HN O

/ a \

F (3) wherein, R1, R2, R3, and R4 are the same as R1, R2, R3, and R4 in the above formula (1).
Preferred embodiments thereof are the same. These may comprise protecting group(s) required for the synthesis.
For example, as preferred embodiments of intermediate (B), R1 is an iodine atom, a bromine atom, an ethynyl group, or a vinyl group, R2 is a chlorine atom or a fluorine atom, R3 is a fluorine atom, and R4 is a hydroxyalkyl group.
The compounds represented by the formula (3) include, for example, N-[2-tert-butyl-dimethyl-silanyloxy)-ethoxy]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-vi nyl-benzamide (R1=I, R2=F, R3=F, R4=2-t-butyl-dimethyl-silanyloxyethyl).

Synthetic intermediate (C) Synthetic intermediate (C) represented by formula (4):

H
N

F (4) wherein, R1, R2, and R3 are the same as R1, R2, and R3 in the above formula (1). Preferred embodiments thereof are the same. These may comprise protecting group(s) required for the synthesis.
For example, as preferred embodiments, R1 is an iodine atom, a bromine atom, an ethynyl group, or a vinyl group, R2 is a chlorine atom or a fluorine atom, and R3 is a fluorine atom.
The compounds represented by the formula (4) include, for example, 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-formyl-benzoic acid (R1=I, R2=F, R3=F).
Synthetic intermediate (D) Synthetic intermediate (D) represented by formula (5):
R4~

'L

F (5) wherein, R1, R2, R3, and R4 are the same as R1, R2, R3, and R4 in the above formula (1).
Preferred embodiments thereof are the same. These may comprise protecting group(s) required for the synthesis.
For example, as preferred embodiments, R1 is an iodine atom, a bromine atom, an ethynyl group, or a vinyl group, R2 is a chlorine atom or a fluorine atom, R3 is a fluorine atom, and R4 is a hydroxyalkyl group.
The compounds represented by the formula (5) include, for example, 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-formyl-N-(2-hydroxy-ethoxy)-benzamide (R1=I, R2=F, R3=F, R4=2-hydroxyethyl).

Synthetic intermediate (E) 5 Synthetic intermediate (E) represented by formula (6):
HO O

N
I I ~

UO F
(6) wherein, R1, R2, and R3 are the same as R1, R2, and R3 in the above formula (1). Preferred embodiments thereof are the same. R1, R2, R3, and U may comprise protecting group(s) required for the synthesis.
10 For example, R1 is preferably an iodine atom, a bromine atom, an ethynyl group, or a vinyl group; R2 is preferably a chlorine atom or a fluorine atom; and R3 is preferably a fluorine atom.
In the above formula (6), a group represented by formula (a):
U

LO (a) 15 indicates a 3 to 10-membered heterocyclic group which may have one to three substituents selected from the group consisting of a C1_5 alkyl group, a halogen atom, an oxo group, -ORa, -COORa, -COOCORa, -CO-[halogen atom], -OCORa, -CONRaRb, -SRa, -SORa, -SO2Ra, -NRaRb, -NRaCORb, -NRaSO2Rb, -SO2NRaRb, a heterocyclic group, and a heteroaryl group.
The heterocyclic group and the heteroaryl group in the (a) may have a substituent 20 selected from the group consisting of a C1_5 alkyl group, -ORa, and -NRaRb The alkyl group may be substituted by a hydroxyl group, a C1_5 alkoxy group, or an amino group. The above substituents except the oxo group and the halogen atom may be linked to each other to form a cycloalkyl group or a heterocyclic group; the cycloalkyl group or the heterocyclic group may have a substituent selected from the group consisting of -ORa, -NRaRb, and a C1_5 alkyl group 25 which may be substituted with -ORa.
Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1.5 alkyl group; the alkyl group may be substituted by one to three groups selected from a hydroxyl group, a C1_5 alkoxy group, and an amino group.

The group represented by the above (a) more preferably indicates a 3 to 10-membered heterocyclic group which may have one to three substituents selected from the group consisting of a C1.5 alkyl group, a halogen atom, -ORa, -NRaRb, and an oxo group, and still more preferably indicates a 3 to 10-membered heterocyclic group which may be substituted by one to three hydroxyl groups or C1.5 alkyl groups. The above substituents except the above oxo group and halogen atom may be linked to each other to form a cycloalkyl group or a heterocyclic group; the cycloalkyl group or the heterocyclic group may have a substituent selected from the group consisting of -ORa, -NRaRb, and a C1_5 alkyl group which may be substituted with -ORa.
Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1_5 alkyl group; the alkyl group may be substituted by a hydroxyl group, a C1_5 alkoxy group, or an amino group-U represents -0-, -CONRd-, -5-, -SO-, -SO2-, -NRd-, -NRdCO-, -NRdSO2-, -SO2NRd-, a bivalent heterocyclic group, or a bivalent heteroaryl group. Rd represents a hydrogen atom or a C1_5 alkyl group; the alkyl group may be substituted by a hydroxyl group, a C1_5 alkoxy group, or an amino group.
The above U is preferably -0-, -CONRd-, -SO2-, -NRdCO-, a heterocyclic group, or a heteroaryl group, and more preferably -0-, -CONRd-, -SO2-, -NRdCO-, or a heteroaryl group.
Rb is preferably a hydrogen atom, a methyl group or an ethyl group.
The above U is more preferably -0-, -CONH-, -SO2-, -NHCO-, a bivalent imidazolyl group, and particularly preferably -0-.
Alternatively, the (a) is preferably a 5- or 6-membered heterocyclic group which may be substituted by one to three hydroxyl groups or C1.5 alkyl groups, and more preferably a [1,3]dioxolan-2-yl group or a [1,3]dioxan-2-yl group which may be substituted by one to three hydroxyl groups or C1_5 alkyl groups.
More specifically, preferred embodiments include the case where the R1 is an iodine atom, a bromine atom, an ethynyl group, or a vinyl group; the R2 is a chlorine atom or a fluorine atom; the R3 is a fluorine atom; and the U is -0-.
The compounds represented by the formula (6) include, for example, 5-[1,3]dioxolan-2-yl-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-benzoic acid (R1=I, R2=F, R3=F, U=-O- ((a) is a [1,3]dioxolan-2-yl group)).

Synthetic intermediate (F) Synthetic intermediate (F) represented by formula (7):

R4,0 I
HN O
H Rp N

1J R3 R, UO F
(7) wherein, R1, R2, R3, and R4 are the same as R1, R2, R3, and R4 in the above formula (1).
Preferred embodiments thereof are the same. These may comprise protecting group(s) required for the synthesis.
For example, as preferred embodiments, RI is preferably an iodine atom, a bromine atom, an ethynyl group, or a vinyl group, R2 is preferably a chlorine atom or a fluorine atom, R3 is preferably a fluorine atom, and R4 is preferably a hydroxyalkyl group.
In the above formula (7), a group represented by formula (a):
U -T`-*

LO (a) indicates a 3 to 10-membered heterocyclic group which may have one to three substituents selected from the group consisting of a C1_5 alkyl group, a halogen atom, an oxo group, -ORa, -COORa, -COOCORa, -CO-[halogen atom], -OCORa, -CONRaRb, -SRa, -SORa, -SO2Ra, -NRaRb, -NRaCORb, -NRaSO2Rb, -SO2NRaRb, a heterocyclic group, and a heteroaryl group.
The heterocyclic group and the heteroaryl group in the (a) may have a substituent selected from the group consisting of a C1_5 alkyl group, -ORa, and -NRaRb.
The alkyl group may be substituted by a hydroxyl group, a C1_5 alkoxy group, or an amino group. The above substituents except the oxo group and the halogen atom may be linked to each other to form a cycloalkyl group or a heterocyclic group; the cycloalkyl group or the heterocyclic group may have a substituent selected from the group consisting of -ORa, -NRaRb, and a C1_5 alkyl group which may be substituted with -ORa.
Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1_5 alkyl group; the alkyl group may be substituted by one to three groups selected from a hydroxyl group, a CI-5 alkoxy group, and an amino group.
The group represented by the above (a) more preferably indicates a 3 to 10-membered heterocyclic group which may have one to three substituents selected from the group consisting of a C1_5 alkyl group, a halogen atom, -ORa, -NRaRb, and an oxo group, and still more preferably indicates a 3 to 10-membered heterocyclic group which may be substituted by one to three hydroxyl groups or C1.5 alkyl groups. The above substituents except the above oxo group and halogen atom may be linked to each other to form a cycloalkyl group or a heterocyclic group; the cycloalkyl group or the heterocyclic group may have a substituent selected from the group consisting of -ORa, -NRaRb, and a C1_5 alkyl group which may be substituted with -ORa.
Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1_5 alkyl group; the alkyl group may be substituted by a hydroxyl group, a C1.5 alkoxy group, and an amino group.
U represents -0-, -CONRd-, -S-, -SO-, -SO2-, -NRd-, -NRdCO-, -NRdSO2-, -SO2NRd-, a bivalent heterocyclic group or a bivalent heteroaryl group. Rd and Re which may be the same or different, each represent a hydrogen atom or a C1_5 alkyl group; the alkyl group may be substituted a hydroxyl group, a C1_5 alkoxy group, or an amino group. U may comprise protecting group(s) required for the synthesis.
The above U is preferably -0-, -CONRd-, -SO2-, -NRdCO-, the heterocyclic group or the heteroaryl group, and more preferably -0-, -CONRd-, -SO2-, -NRdCO-, or the heteroaryl group. Rd is preferably a hydrogen atom, a methyl group or an ethyl group.
The above U is still more preferably -0-, -CONH-, -SO2-, -NHCO-, a bivalent imidazolyl group, and particularly preferably -0-.
Alternatively, the (a) is preferably a 5- or 6-membered heterocyclic group which may be substituted by one to three hydroxyl groups or C1.5 alkyl groups.
The (a) is more preferably a 5- or 6-membered ring which may be substituted by one to three hydroxyl groups or C1_5 alkyl groups, and U is -0-. Still more preferably, the (a) is a [1,3]dioxolan-2-yl group or a [1,3]dioxan-2-yl group which may be substituted by one to three hydroxyl groups or C1.5 alkyl groups.
More specifically, preferred embodiments include the case where the R1 is an iodine atom, a bromine atom, an ethynyl group, or a vinyl group; the R2 is a chlorine atom or a fluorine atom; the R3 is a fluorine atom; R4 is a hydroxyalkyl group; and the U is -0-.
The compounds represented by the formula (7) include, for example, 5-[ 1,3]dioxolane-2-yl-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-bent amide (R1=I, R2=F, R3=F, F4=2-hydroxyethyl, U=-O- ((a) is a [1,3]dioxolan-2-yl group)).
Synthetic intermediate (G) Synthetic intermediate (G) represented by formula (8):

WZ"Or I R3 R1 F (8) wherein R1 represents a halogen atom, an alkenyl group, or an alkynyl group;
R2 represents a halogen atom or an alkyl group; the alkyl group may be substituted by a hydroxyl group; and R3 represents a hydrogen atom or a halogen atom.
Z represents an alkylene chain having one to eight carbon atoms, which may be substituted by one to three groups represented by W'];
W and W', which may be the same or different, each represent a Ci_5 alkyl group, a halogen atom, an oxo group, -ORa, -COORa, -COOCORa, -CO-[halogen atom], -OCORa, -CONRaRb, -SRa, -SORa, -SO2Ra, -NRaRb, -NRaCORb, -NRaSO2Rb, -SO2NRaRb, a heterocyclic group, or a heteroaryl group. The heterocyclic group and the heteroaryl group may have a substituent selected from the group consisting of a C1_5 alkyl group, -ORa, and -NRaRb.
The alkyl group may be substituted by a hydroxyl group, a C1_5 alkoxy group or an amino group.
The above substituents except the oxo group and the halogen atom may be linked to each other to form a cycloalkyl group or a heterocyclic group; the cycloalkyl group or the heterocyclic group may have a substituent selected from the group consisting of -ORa, -NRaRb, and a C1.5 alkyl group which may be substituted with -ORa;
Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1_5 alkyl group; the alkyl group may be substituted by one to three groups selected from a hydroxyl group, a C1.5 alkoxy group, and an amino group.
Furthermore, the preferred embodiments of W or W are the same as the above.
The above R1, R2, R3, Z, W, and Wmay comprise protecting group(s) required for the synthesis.
The R1 is preferably an iodine atom, a bromine atom, an ethynyl group, or a vinyl group, the R2 is preferably a chlorine atom or a fluorine atom, and the R3 is preferably a fluorine atom.
Synthetic intermediate (H) Synthetic intermediate (H) represented by formula (9):

R4,, 0 HN O

' Z"11 N

F (9) wherein R1 represents a halogen atom, an alkenyl group, or an alkynyl group;
R2 represents a halogen atom or an alkyl group; the alkyl group may be substituted by a hydroxyl 5 group;
R3 represents a hydrogen atom or a halogen atom; and R4 represents a hydrogen atom, an alkyl group, an alkenyl group, or an alkynyl group. The alkyl group, the alkenyl group, and the alkynyl group may have one to three substituents selected from the group consisting of -ORa, -NRaRb, -NRaCORb, a heterocyclic group, and a heteroaryl 10 group. The heterocyclic group and the heteroaryl group may have one to three substituents selected from the group consisting C1_5 alkyl groups, -ORa, and -NRaRb.
Ra and Rb, which may be the same or different, each represent a hydrogen atoms or a C1_5 alkyl group; the alkyl group may be substituted by a hydroxyl group, a C1_5 alkoxy group, or an amino group.
15 Z represents an alkylene chain having one to eight carbon atoms, which may be substituted by one to three groups reprenseted by W'.
W and W', which may be the same or different, each represent a C1_5 alkyl group, a halogen atom, an oxo group, -ORa, -COORa, -COOCORa, -CO-[halogen atom], -OCORa, -CONRaRb, -SRa, -SORa, -SO2Ra, -NRaRb, -NRaCORb, -NRaSO2Rb, -SO2NRaRb, a 20 heterocyclic group, or a heteroaryl group. The heterocyclic group and the heteroaryl group may have substituents selected from the group consisting of a C1.5 alkyl group, -ORa, and -NRaRb.
The alkyl group may be susbstituted by a hydroxyl group, a C1_5 alkoxy group, or an amino group.
The above substituents except the oxo group and the halogen atom may be linked to 25 each other to form a cycloalkyl group or a heterocyclic group; the cycloalkyl group or the heterocyclic group may have a substituent selected from the group consisting of -ORa, -NRaRb, and a C1_5 alkyl group which may be substituted with -ORa.
Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1_5 alkyl group; the alkyl group may be substituted by one to three groups selected from a 30 hydroxyl group, a C1.5 alkoxy group, and an amino group.

Furthermore, the preferred embodiments of W or W' are the same as the above.
The above R1, R2, R3, Z, W, and W' may comprise protecting group(s) required for the synthesis.
The R1 is preferably an iodine atom, a bromine atom, an ethynyl group, or a vinyl group, the R2 is preferably a chlorine atom or a fluorine atom, the R3 is preferably a fluorine atom, and the R4 is preferably a hydroxyalkyl group. The hydroxyalkyl group may be protected.

Synthetic intermediate (I) Synthetic intermediate (I) represented by formula (10):
HO O

M :6, W Z~O~a \ R3 R1 F (10) wherein R1 represents a halogen atom, an alkenyl group, or an alkynyl group;
R2 represents a halogen atom or an alkyl group; the alkyl group may have a hydroxyl group as a substituent; and R3 represents a hydrogen atom or a halogen atom.
Z represents an alkylene chain having one to eight carbon atoms, which may be substituted by one to three groups represented by W'.
W and W', which may be the same or different, each represent a C1.5 alkyl group, a halogen atom, an oxo group, -ORa, -COORa, -COOCORa, -CO-[halogen atom], -OCORa, -CONRaRb, -SRa, -SORa, -SO2Ra, -NRaRb, -NRaCORb, -NRaSO2Rb, -SO2NRaRb, a heterocyclic group, or a heteroaryl group. The heterocyclic group and the heteroaryl group may have substituents selected from the group consisting of a C1_5 alkyl group, -ORa, and -NRaRb.
The alkyl group may be substituted by a hydroxyl group, a C1_5 alkoxy group, or an amino group.
The above substituents except the oxo group and the halogen atom may be linked to each other to form a cycloalkyl group or a heterocyclic group; the cycloalkyl group or the heterocyclic group may have a substituent selected from the group consisting of -ORa, -NRaRb, and a C1_5 alkyl group which may be substituted with -ORa.
Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1_5 alkyl group; the alkyl group may be substituted by one to three groups selected from a hydroxyl group, a C1.5 alkoxy group, and an amino group.
Furthermore, the preferred embodiments of W or W are the same as the above.

The above R1, R2, R3, Z, W, and W' may comprise protecting group(s) required for the synthesis.
The R1 is preferably an iodine atom, a bromine atom, an ethynyl group, or a vinyl group, the R2 is preferably a chlorine atom or a fluorine atom, and the R3 is preferably a fluorine atom.
Synthetic intermediate (J) Synthetic intermediate (J) represented by formula (11).
R4,?

HN O

I a HH I
W.'Z"OWN \ R3 R1 F (11) wherein R1 represents a halogen atom, an alkenyl group, or an alkynyl group;
R2 represents a halogen atom or an alkyl group; the alkyl group may have a hydroxyl group as a substituent;
R3 represents a hydrogen atom or a halogen atom; and R4 represents a hydrogen atom, an alkyl group, an alkenyl group, or an alkynyl group. The alkyl group, the alkenyl group, and the alkynyl group may have one to three substituents selected from the group consisting of -ORa, -NRaRb, -NRaCORb, a heterocyclic group, and a heteroaryl group. The heterocyclic group and the heteroaryl group may have one to three substituents selected from the group consisting of a C1_5 alkyl group, -ORa, and -NRaRb. Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1_5 alkyl group; the alkyl group may be substituted by a hydroxyl group, a C1_5 alkoxy group, or an amino group.
Z represents an alkylene chain having one to eight carbon atoms, which may be substituted by one to three groups represented by W.
W and W', which may be the same or different, each represent a C1_5 alkyl group, a halogen atom, an oxo group, -ORa, -COORa, -COOCORa, -CO-[halogen atom], -OCORa, -CONRaRb, -SRa, -SORa, -SO2Ra, -NRaRb, -NRaCORb, -NRaSO2Rb, -SO2NRaRb, a heterocyclic group, or a heteroaryl group. The heterocyclic group and the heteroaryl group may have substituents selected from the group consisting of a C1_5 alkyl group, -ORa, and -NRaRb.
The alkyl group may be substituted by a hydroxyl group, a C1_5 alkoxy group, or an amino group as substituents.

The above substituents except the oxo group and the halogen atom may be linked to each other to form a cycloalkyl group or a heterocyclic group. The cycloalkyl group or the heterocyclic group may have a substituent selected from the group consisting of -ORa, -NRaRb, and a C1_5 alkyl group which may be substituted with -ORa.
Ra and Rb, which may be the same or different, each represent a hydrogen atom or a CI-5 alkyl group; the alkyl group may be substituted by one to three groups selected from a hydroxyl group, a C1_5 alkoxy group, and an amino group.
Furthermore, the preferred embodiments of W or W are the same as the above.
The above RI, R2, R3, R4, Z, W, and W' may comprise protecting group(s) required for the synthesis.
The RI is preferably an iodine atom, a bromine atom, an ethynyl group, or a vinyl group, the R2 is preferably a chlorine atom or a fluorine atom, the R3 is preferably a fluorine atom, and the R4 is preferably a hydroxyalkyl group. The hydroxyalkyl group may be protected.

esthetic intermediate (K) Synthetic intermediate (K) represented by formula (12):
HO O

H
N
Q Z A
Y -- O \ R3 R1 O F (12) wherein RI represents a halogen atom, an alkenyl group, or an alkynyl group;
R2 represents a halogen atom or an alkyl group; the alkyl group may have a hydroxyl group as a substituent;
R3 represents a hydrogen atom or a halogen atom; and Q is -ORc, -OCORc, -NRcRd, or a halogen atom, Re and Rd are the same or different, and each represent a hydrogen atom or an alkyl group.
Z' represents an alkylene chain having one to five carbon atoms, which may be substituted by one to three groups represented by W.
W' preferably represents a C1_5 alkyl group, a halogen atom, an oxo group, -ORa, -COORa, -COOCORa, -CO-[halogen atom], -OCORa, -CONRaRb, -SRa, -SORa, -SO2Ra, -NRaRb, -NRaCORb, -NRaSO2Rb, -SO2NRaRb, a heterocyclic group, or a heteroaryl group.
The heterocyclic group and the heteroaryl group may have substituents selected from the group consisting of a CI-5 alkyl group, -ORa, and -NRaRb. The alkyl group may have a hydroxyl group, a C1_5 alkoxy group, or an amino group as substituents. The above substituents except the oxo group and the halogen atom may be linked to each other to form a cycloalkyl group or a heterocyclic group. The cycloalkyl group or the heterocyclic group may have a substituent selected from the group consisting of -ORa, -NRaRb, and a C1_5 alkyl group which may be substituted with -ORa.
Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1_5 alkyl group; the alkyl group may be substituted by one to three groups selected from a hydroxyl group, a Ci_5 alkoxy group, and an amino group.
W is more preferably a group represented by the following formulae, -OH, -OMe, -OEt, -OCH2OH, -O(CH2) 20H, -O(i-Pr), -O(n-Pr), -CONH2, -CONHMe, -CONHEt, -CONH(n-Pr), -CONH(i-Pr), -CONMe2, -CON(Et)Me, -SO2Me, -SOMe, -SMe, -NH2, -NHMe, -NH CH2OH, -NH (CH2) 20H, -N(Me)CH2 CH 20H, -NH Et, -NMe2, -N(Et)Me, -NHCOMe, -NMeCOMe, -NHCOEt, -NHCO(n-Pr), or -NHCO(i-Pr).
Furthermore, the preferred embodiments of W' are the same as the above.
The above R1, R2, R3, Z', Q, and Wmay comprise protecting group(s) required for the synthesis.
The Ri is preferably an iodine atom, a bromine atom, an ethynyl group, or a vinyl group, the R2 is preferably a chlorine atom or a fluorine atom, and the R3 is preferably a fluorine atom.
Synthetic intermediate (L) Synthetic intermediate (L) represented by formula (13):
R4.0 HN O

H
N
Q Z' ,N I I /

O F (13) wherein Ri represents a halogen atom, an alkenyl group, or an alkynyl group;
R2 represents a halogen atom or an alkyl group; the alkyl group may have a hydroxyl group as a substituent;
R3 represents a hydrogen atom or a halogen atom; and R4 represents a hydrogen atom, an alkyl group, an alkenyl group, or an alkynyl group. The alkyl group, the alkenyl group; and the alkynyl group may have one to three substituents selected from the group consisting of -ORa, -NRaRb, -NRaCORb, a heterocyclic group, and a heteroaryl group. The heterocyclic group and the heteroaryl group may have one to three substituents selected from the group consisting of a C1-5 alkyl group, -ORa, and -NRaRb. Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1_5 alkyl group; the alkyl group may be substituted by a hydroxyl group, a Cl_5 alkoxy group, and an amino group.
5 Z' represents an alkylene chain having one to five carbon atoms, which may be substituted by one to three groups represented by W'.
W' preferably represents a C1_5 alkyl group, a halogen atom, an oxo group, -ORa, -COORa, -COOCORa, -CO-[halogen atom], -OCORa, -CONRaRb, -SRa, -SORa, -SO2Ra, -NRaRb, -NRaCORb, -NRaSO2Rb, -SO2NRaRb, a heterocyclic group, or a heteroaryl group.
10 The heterocyclic group and the heteroaryl group may have substituents selected from the group consisting of a C1_5 alkyl group, -ORa, and -NRaRb. The alkyl group may be substituted by a hydroxyl group, a C1.5 alkoxy group, or an amino group. The above substituents except the oxo group and the halogen atom may be linked to each other to form a cycloalkyl group or a heterocyclic group; the cycloalkyl group or the heterocyclic group may have a substituent 15 selected from the group consisting of-ORa, -NRaRb, and a C1.5 alkyl group which may be substituted with -ORa.
Ra and Rb, which may be the same or different, each represent a hydrogen atom or a Cl_5 alkyl group; the alkyl group may be substituted by one to three groups selected from a hydroxyl group, a Cl_5 alkoxy group, and an amino group.
20 W' is more preferably a group represented by the following formulae, -OH, -OMe, -OEt, -OCH2OH, -O(CH2) 2OH, -O(i-Pr), -O(n-Pr), -CONH2, -CONHMe, -CONHEt, -CONH(n-Pr), -CONH(i-Pr), -CONMe2, -CON(Et)Me, -SO2Me, -SOMe, -SMe, -NH2, -NHMe, -NH CH2OH, -NH (CH2) 20H, -N(Me)CH2 CH 20H, -NH Et, -NMe2, -N(Et)Me, -NHCOMe, -NMeCOMe, -NHCOEt, -NHCO(n-Pr), or -NHCO(i-Pr).
25 Furthermore, the preferred embodiments of W' are the same as the above.
Q is -ORc, -OCORc, -NRcRd, or a halogen atom, Rc and Rd are the same or different, and represent a hydrogen atom or a C1_5 alkyl group.
The above R1, R2, R3, R4, Z', W', and Q may comprise protecting group(s) required for the synthesis.
30 The R1 is preferably an iodine atom, a bromine atom, an ethynyl group, or a vinyl group, the R2 is preferably a chlorine atom or a fluorine atom, the R3 is preferably a fluorine atom, the R4 is preferably a hydroxyalkyl group, and the hydroxyalkyl group may be protected.
Methods for producing compound (1) according to the present invention using these synthetic intermediates of compound (1) include the following methods (1) to (4).
(1) Production method when Z is -Y-Z-W

This method comprises reacting synthetic intermediate (E) represented by the above formula (6) with a reducing agent in a solvent at a neutral pH or in the presence of an acid, to thereby obtain compound (M) or (M') represented by formula (14) or (14') respectively.
Alternatively, this method comprises reacting the synthetic intermediate (F) represented by the above formula (7) with a reducing agent in a solvent at a neutral pH or in the presence of an acid, to thereby obtain compound (N) or (N) represented by formula (15) or (15') respectively.
R4,, 0 I
HO O HN O

HOZU R3 R1 HO~Z'U R3 R1 F (14) F (15) R4,, 0 HO O H RZ HN O

N I ~ ~ \ N
H'Ul~Z7O R3 R, H'U'Z~O R3 R, F (14') F (15') In the formulae (14), (14'), (15), and (15'), R1, R2, R3, R4, and U each are the same as those in the formulae (6) and (7). In the formulae (14), (14'), (15), and (15'), Z corresponds to the cyclized alkylene chain in the above (a), and the Z represents an alkylene chain having one to eight carbon atoms, which may be substituted by one to three groups represented by W'.
W' preferably includes a group selected from the group consisting of a C1.5 alkyl group, a halogen atom, an oxo group, -ORa, -COORa, -COOCORa, -CO-[halogen atom], -OCORa, -CONRaRb, -SRa, -SORa, -SO2Ra, -NRaRb, -NRaCORb, -NRaSO2Rb, -SO2NRaRb, a heterocyclic group, and a heteroaryl group.
The heterocyclic group and the heteroaryl group in the (a) may have substituents selected from the group consisting of a C1_5 alkyl group, -ORa, and -NRaRb.
The alkyl group may have a hydroxyl group, a C1_5 alkoxy group, or an amino group as a substituent. The above substituents except the oxo group and the halogen atom may be linked to each other to form a cycloalkyl group or a heterocyclic group; the cycloalkyl group or the heterocyclic group may have a substituent selected from the group consisting of -ORa, -NRaRb, and a C1_5 alkyl group which may be substituted with -ORa.
The above W' includes more preferably a group selected from the group consisting of a C1_5 alkyl group, a halogen atom, -ORa, -NRaRb, and an oxo group, and still more preferably a hydroxyl group or a C1_5 alkyl group. The above substituents except the oxo group and the halogen atom may be linked to each other to form a cycloalkyl group or a heterocyclic group; the cycloalkyl group or the heterocyclic group may have a substituent selected from the group consisting of -ORa, -NRaRb, and a C1_5 alkyl group which may be substituted with -ORa.
Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1.5 alkyl group; the alkyl group may be substituted by one to three groups selected from a hydroxyl group, a C1.5 alkoxy group, and an amino group.
The above solvent includes methanol, ethanol, diethyl ether, tetrahydrofuran, toluene, methylene chloride, and acetonitrile.
The above reducing agent includes sodium boron hydride, sodium borocyanohydride, triethylsilane, trimethylsilane, lithium aluminum hydride, diisopropyl aluminum hydride, borane-pyridine complex, decaborane, diborane, borane-dimethylsulfide complex, borane-THF
complex, hydrogen, zinc boron hydride, samarium (II) iodide, and tributyltin hydride.
Preferable examples include, diisopropyl aluminum hydride, sodium boron hydride, and triethylsilane.
The above acid includes acetic acid, hydrochloric acid, trifluoroacetic acid, trifluoroboron-diethyl ether complex, trimethylsilyl triflate, BiC13, A1C13, titanium tetrachloride, and trimethylsilyl chloride.
The above reaction can be performed typically at about -78 C to about 120 C
for about one hour to about 2 days.

(2) Production method when Z is -Y-Z-W (2) Compound (I) represented by the above formula (10) can be obtained by reacting synthetic intermediate (G) represented by the above formula (8) with a reducing agent in a solvent at a neutral pH or in the presence of an acid. Alternatively, compound (J) represented by the above formula (11) can be obtained by reacting synthetic intermediate (H) represented by the above formula (9) with a reducing agent in a solvent at a neutral pH or in the presence of an acid.
The above solvent include methanol, ethanol, diethyl ether, tetrahydrofuran, toluene, methylene chloride, and acetonitrile.
The above reducing agent includes sodium boron hydride, sodium boron cyanohydride, triethylsilane, trimethylsilane, lithium aluminum hydride, diisopropyl aluminum hydride, borane-pyridine complex, decaborane, diborane, borane-dimethylsulfide complex, borane-THF complex, zinc boron hydride, and tributyltin hydride. Preferably, sodium boron cyanohydride, sodium boron hydride, triethylsilane, and borane-pyridine complex can be included.
The above acid includes acetic acid, hydrochloric acid, trifluoroacetic acid, dichloroacetic acid, trifluoroboron-diethyl ether complex, trimethylsilyl triflate, A1C13, titanium tetrachloride, and trimethylsilyl chloride. Preferable examples include dichloroacetic acid, hydrochloric acid, and trifluoroacetic acid.
The above reaction can be performed typically at about -78 C to about 120 C
for about one hour to about 2 days.

(3) Production method when Z is a heterocyclic group Compound (0) represented by the following formula (16) can be obtained by intramolecularly cyclizing synthetic intermediate (K) represented by the above formula (12) in a solvent at a neutral pH, in the presence of an acid or in the presence of a base, and further in the presence of a peptide condensing agent if necessary, for example, in the case of Q=OH.
Alternatively, compound (P) represented by the following formula (17) can be obtained by intramolecularly cyclizing synthetic intermediate (L) represented by the above formula (13) in a solvent at a neutral pH, in the presence of an acid or in the presence of a base, and further in the presence of a peptide condensing agent if necessary, for example, in the case of Q=OH.

HO O

H

Z" N
:-0~ R3 R1 F (16) R4,O
I
HN O

H
flO / I N I \
Z'~O.N R3 / R1 F (17) In the above formulae (16) and (17), R1, R2, R3, R4, and Z' each are the same as those in the above formulae (12) and (13).

Preparation of compound (XXV) The above solvent includes methanol, ethanol, diethyl ether, tetrahydrofuran, toluene, methylene chloride, and acetonitrile.

The above acid includes A1Me3, acetic acid, hydrochloric acid, trifluoroacetic acid, dichloroacetic acid, trifluoroboron-diethyl ether complex, trimethylsilyl triflate, AiC13, titanium tetrachloride, and trimethylsilyl chloride.
The above base includes triethylamine, Hunig's base, DBU, sodium methylate, and potassium carbonate.
The above reaction can be performed typically at room temperature to about 80 C for about one hour to about one day.
In the case of Q=OH, compound (16) or (17) can be obtained by treating compound (12) or (13) with a condensing agent for peptide synthesis and a base in an appropriate solvent. In this case, the above solvent may be dichloromethane, THF, and dimethylformamide, and preferably dichloromethane.
The above base includes triethylamine, Hunig's base, or DBU, and preferably Hunig's base.
The above peptide condensing agent includes 1,3-dicyclohexylcarbodiimide (DCC), 2-ethoxy-l-ethoxycarbonyl-1, 2-dihydroquinoline (EEDQ), bromo-tris(pyrrolidino)-phosphonium hexafluorophosphate (PyBrOP), 1-ethyl-3-(3'-dimethylaminopropyl)carbodiimide (EDC), (benzotriazolyloxy)tripyrrolidino-phosphonium hexafluorophosphate (PyBOP), 3-hydroxy-4-oxo-3,4-dihydro-1,2,3-benzotriazine (HODhBt), and hydroxybenzotriazole (HOBt).
The above reaction can be performed typically at about 10 C to about 30 C, preferably about 22 C (room temperature) for about one hour to about 2 days, preferably about 10 hours.
(4) Production method when Z is a chain substituent having a partial structure -N(OR)CO-R' This method comprises reacting synthetic intermediate (I) represented by the above formula (10) with a carboxylate derivative (including carboxylic acid) represented by R9CO-Q in a solvent in the presence of a base or an acid or at a neutral pH, in the presence of a condensing agent if necessary to thereby obtain compound (S) represented by the following formula (18).
Alternatively, this method comprises reacting synthetic intermediate (J) represented by the above formula (11) with a carboxylate derivative (including carboxylic acid) represented by R9CO-Q in a solvent in the presence of a base or an acid or at a neutral pH, in the presence of a condensing agent if necessary, to thereby obtain compound (T) represented by the following formula (19).
R9 represents a hydrogen atom, an alkyl group, or -ORa; the alkyl group may be substituted by a halogen atom, -ORa, or -NRaRb.
Q is -ORc, -OCORc, -NRcRd, or a halogen atom, and Re and Rd are the same or different and represent a hydrogen atom or a C1_5 alkyl group.
Ra and Rb are the same or different, and represent a hydrogen atom or a C1.5 alkyl group; the alkyl group may have a hydroxyl group, a C1.5 alkoxy group, or an amino group as substituents.
R9 and Q may comprise protecting group(s) required for the synthesis.

N

F (18) R4. 0 "Z"N

5 F (19) In the formulae (18) and (19), R1, R2, R3, R4, Z, and W each are the same as those in the formulae (10) and (11), and R9 is the same as that defined for the above carboxylate derivative.
The above solvent includes dichloromethane, THF, and dimethylformamide. The above base includes triethylamine, Hunig's base, or DBU, and preferably Hunig's base.
10 The above peptide condensing agent includes 1,3-dicyclohexylcarbodiimide (DCC), 2-ethoxy-l-ethoxycarbonyl-1,2-dihydroquinoline (EEDQ), bromo-tris(pyrrolidino)-phosphonium hexafluorophosphate (PyBrOP), 1-ethyl-3-(3'-dimethylaminopropyl) carbodiimide (EDC), (benzotriazolyloxy) tripyrrolidino -phosphonium hexafluorophosphate (PyBOP), 3-hydroxy-4-oxo-3,4-dihydro-1,2,3-benzotriazine 15 (HODhBt), and hydroxybenzotriazole (HOBt). Preferable examples include the combination of 1-ethyl-3-(3'-dimethylaminopropyl)carbodiimide (EDC) with N-hydroxybenzotriazole (HOBt), and the combination of 1-ethyl-3-(3'-dimethylaminopropyl)carbodiimide (EDC) with 3-hydroxy-4-oxo-3,4-dihydro-1,2,3-benzotriazine (HODhBt).
The above reaction can be performed typically at about 0 C to about 30 C, preferably 20 about 22 C (room temperature) for about one hour to about 2 days, preferably about 10 hours.
Compound I represented by the formula (1) according to the present invention can be produced, for example in accordance with the following methods. In the following reaction processes 1 to 4 and descriptions thereof, R1 to R4, R8, R9, X, Y, Z, Z', W, Ra, Rb, and compound I

are the same as those described in the above formula (1).
Reaction process 1 HO O HO O HO O R4~, L IV R2 p Ni~ VI
Br or 1 R3 R3 \ \ ( R3 R1 F F F
!! III V
R4. R4, O R4,, HMN I XI-1 ?

M:6M IX `~
0 R31 R1 X \ I R3 IaRl F F F
VII VIII
I
Reaction process 2 X

0\ x R3 R1 R3 I r R1 F F
X XI
R4,0 R4N, NH2 \ R3 RI X \ I I

F
V F
Reaction process 3 R4~, 1 R4,, ?

R3 halo R3 RI
F F
XII Rj R1 = \ / Rk Rh RI
I-a I-b Reaction process 4 HNOIZ, O.H HO 0 R2 HO O

M"6 XIII O
I "6 I I \ R3 R7 F XIV
X
R4, NHZ
R4, R4, R4,, H~ O H==ZIO=H HN 0 O~ \ R3 6 Rl / R3 R1 H~O~Z'O 4RR1 F Z-O F
Vlll XV F I-c Reaction process 5 HO 0 R2 w z`O' H

~ X > Z N R3 6M
O~ R3 / R1 F
F XVII
X

R4~ R4~ R4, a q NN

' ( / R1 yf ~p~N~ \ I R3 I / Rt ,N
F H f0 R3 R1 Viii W OH XVill 1-d XVI
Reaction process 6 Ho 0 R2 Ho O Rz R9 0 Ho 0 R2 xx-O- R3 R1 o.N I / R' R9~0 \ I a O' R3 RI
F F F
XVII XIX xx t R4`0 I ~
R4,~ R4, R9 O OI

/ N ~ R9~ O
I
w-'-o- R3 / R1o/I I R3 6RI
F F
1-d 1-e Reaction process 7 a - a T \
O NTOWN I R3 I R1 O Ora R3 / R1 R3 / RI
p F 0 F F
XXII XXIV XXV

R4, ? VI

R4, R4,0 R4`0 H / \ 0 / a \
pR3 R1 \ ,N R3 R1 O- ~T IN 6RI

Reaction process 1 Reaction process 1 indicates a method for producing compound I represented by the formula (1). In this process, L means a leaving group, for example, fluorine, chlorine, bromine, or iodine, or an activated hydroxyl group, for example, phosphate ester and sulfonate ester.
The compound (5-iodinated or 5-brominated benzoic acid derivative) represented by the formula (II) can be easily obtained by, for example, using methods described in publicly known literature (F. Mongin, E. Marzi, and M. Schlosser, European Journal of Organic Chemistry, 2771-2777 (2001) or A. Groweiss, Organic Process Research & Development, 4, 30-33 (2000)) or similar methods thereto.

Preparation of 5-vinylbenzoic acid derivative (III) 5-Vinylbenzoic acid derivative (III) can be obtained by, for example, reacting 5-iodinated or 5-brominated benzoic acid derivative (II) with a vinylated organic metal reagent in an appropriate solvent in the presence of a transition metal catalyst.
The above solvent includes, for example, dimethylformamide, THE
(tetrahydrofuran), DMSO (dimethyl sulfoxide), isopropanol, methanol, and ethanol, and preferably, THE or isopropanol is used.
As the above transition metal catalyst, for example, palladium complex can be preferably used. As the palladium complex, for example, Pd(PPh3)4, (PhCN)2PdCI2, (MeCN)2PdC12, and (PPh3)2PdCl2 can be used.
The above vinylated organic metal reagent includes, for example, vinylated organic magnesium, vinylated organic aluminum, vinylated organic silicon, vinylated organic boron, vinylated organic zinc, and vinylated organic tin. Among them, vinyl organic tin (Stille's method) or vinyl borate (Suzuki's method) can be preferably used. If necessary, it is possible to add an appropriate base such as t-butylamine, triethylamine, or Hunig's base in the reaction system.
The reaction can be performed typically at about 15 C to about 130 C, preferably about 60 C for about four hours to about four days, preferably about 10 hours.
The reaction can be easily performed with reference to the following literature.
a) J. K. Stille, Angew. Chem., Int. Ed. Engl. 1986, 25, 508-524.
b) N. Miyaura, A. Suzuki, Chem. Rev. 1995, 95, 2457-2483 c) A. Suzuki, J. Organomet. Chem., 1999, 576, 147-168.
d) Suzuki, A, In Metal-Catalyzed Cross Coupling Reactions; Diederich, F., Stang, P. J., Eds.;
VCH: Weinheim, 1998; pp49-97.

Preparation of 2-(phenylamino)-5-vinylbenzoic acid derivative (V) 2-(Phenylamino)-5-vinylbenzoic acid derivative (V) can be synthesized by reacting aniline derivative (IV) with 5-vinylbenzoic acid derivative (III). This reaction can be performed using, for example, methods described in a patent document (WO
00/64856) and 5 literature (M. H. Chen, V. G. Beylin, E. Iakovleva, S. J. Kesten, J. Magano, D. Drieze, Synthetic Communications, 32(3), 411-417 (2002)) or similar methods thereto.
Specifically, the reaction can be performed by reacting 5-vinylbenzoic acid derivative (I11) with an equal or excessive amount of aniline derivative (IV) in a solvent in the presence of a base.
10 The above solvent includes, for example, THE and toluene, and preferably THE
The above base includes, for example, lithium diisopropylamide, lithium hexamethyldisilazide, lithium n-butyl, sodium hydride, and sodium amide, and preferably lithium isopropylamide or lithium hexamethyldisilazide.
The above reaction can be performed typically at about -78 C to about 25 C for about 15 four hours to about four days, preferably about one day.

Preparation of hydroxamic acid derivative (VII) A 2-phenylamino-5-vinylbenzoic acid derivative (V) can converted into a hydroxamic acid derivative (VII) by reacting (V) with a hydroxylamine derivative (VI) represented by 20 NH2OR4 in an appropriate solvent in the presence of a condensing agent for peptide synthesis and in the presence or the absence of a base.
The above solvent includes dichloromethane, THF, and dimethylformamide, and preferably dichloromethane.
The above base includes triethylamine, Hunig's base, or DBU
25 (1,8-diazabicyclo[5.4.0]-undecene), or DMAP (4-dimethylaminopyridine), and preferably Hunig's base.
The above peptide condensing agent include 1,3-dicyclohexylcarbodiimide (DCC), 2-ethoxy- l -ethoxycarbonyl-1,2-dihydroquinoline (EEDQ), bromo-tris(pyrrolidino)-phosphonium hexafluorophosphate (PyBrOP), 30 1-ethyl-3-(3'-dimethylaminopropyl)carbodiimide (EDC), (benzotriazolyloxy)tripyrrolidino-phosphonium hexafluorophosphate (PyBOP), 3-hydroxy-4-oxo-3,4-dihydro-1,2,3-benzotriazine (HODhBt), and hydroxybenzotriazole (HOBt).
Preferable examples include the combination of 1-ethyl-3-(3'-dimethylaminopropyl)carbodiimide (EDC) with N-hydroxybenzotriazole (HOBt), 35 and the combination of 1-ethyl-3-(3'-dimethylaminopropyl)carbodiimide (EDC) with 3-hydroxy-4-oxo-3,4-dihydro-1,2,3-benzotriazine (HODhBt).

The above reaction can be performed typically at about 10 C to about 30 C, preferably about 22 C (room temperature) for about one hour to about two days, preferably about 10 hours.
Preparation of aldehyde (VIII) A hydroxamic acid derivative (VII) can be converted into an aldehyde (VIII) by reacting (VIII) with an appropriate oxidizing agent in an appropriate solvent.
The above solvent includes THF, diethyl ether, dichloromethane, dimethylformamide, DMSO, chloroform, carbon tetrachloride, or acetonitrile, and preferably THE
and dichloromethane.
The above oxidizing agent includes ozone, osmium tetroxide-sodium metaperiodate, and ruthenium chloride-sodium metaperiodate.
The above reaction can be performed typically at about 10 C to about 30 C, preferably about 22 C (room temperature) for about two hours to about two days, preferably about 10 hours.
Preparation of compound (I) An aldehyde (VIII) can be converted into compound (I) by reacting (VIII) with compound (IX) in an appropriate solvent in the presence of an appropriate reducing agent and if necessary an appropriate acid.
The above solvent includes methanol, ethanol, diethyl ether, tetrahydrofuran, toluene, and methylene chloride.
The above reducing agent includes sodium boron hydride, sodium boron cyanohydride, triethylsilane, lithium aluminum hydride, diisopropyl aluminum hydride, borane-pyridine complex, and decaborane.
The above acid includes acetic acid, hydrochloric acid, trifluoroacetic acid, trifluoroboron-diethyl ether complex, trimethylsilyl triflate, BiCl3, trifluoromethanesulfonic acid, p-toluenesulfonic acid, and pyridinium-p-toluenesulfonic acid.
The above reaction can be performed typically at about -78 C to about 120 C
for about one hour to about two days.
The reaction can be easily performed by, for example, using methods described in the following literature or similar methods thereto.
a) Daniel Dube and Adrew A. Scholte, Tetrahedron Letters, 1999, 40, 2295-2298 b) Koich Fukase, Yoshiyuki Fukase, Masato Oikawa, Wen-Chi Liu, Yasuo, Suda, and Shoichi Kusumoto, Tetrahedron, 1998, 54, 4033-4050 c) Seung Hwan Lee, Yong Lune Park, and Cheol Min Yoon, Tetrahedron Letters, 1999, 40, d) Makoto Wada, Sonoe Nagayama, Kaori Mizurtani, Ryoichi Hiroi, and Norikazu Miyoshi, Chemistry Letters, 2002, 248-249 e) Kikkugawa, Y., Ogawa, Y., Chem. Pharm. Bull., 1979,27,2405-2410 Reaction process 2 Reaction process 2 is an example process for preparing compound I from 2-(phenylamino)-5-vinylbenzoic acid derivative (V) shown in reaction process 1 by a process other than reaction process 1.

Preparation of carbonyl (XI) 2-(Phenylamino)-5-vinylbenzoic acid derivative (V) can be converted into a carbonyl (X) in accordance with the method for converting a hydroxamic acid derivative (VII) into a carbonyl (VIII) described above.
More specifically, the conversion can be accomplished by reacting a 2-(4-iodophenylamino)-5-vinylbenzoic acid derivative (V) with an appropriate oxidizing agent in an appropriate solvent.
The appropriate solvent includes THF, diethyl ether, dichloromethane, dimethylformamide, DMSO, chloroform, carbon tetrachloride, or acetonitrile, and preferably THF and dichloromethane. The above oxidizing agent includes ozone, osmium tetroxide-sodium metaperiodate, and ruthenium chloride-sodium metaperiodate.
The above reaction can be performed typically at about 10 C to about 30 C, preferably about 22 C (room temperature) for about two hours to about two days, preferably about 10 hours.

Preparation of compound A carbonyl (X) can be converted into compound (XI) in accordance with the method for converting an aldehyde (VIII) into compound I described above.
More specifically, the conversion can be accomplished by reacting a carbonyl (X) with compound (IX) in an appropriate solvent in the presence of an appropriate reducing agent and if necessary an appropriate acid.
The above solvent includes methanol, ethanol, diethyl ether, tetrahydrofuran, toluene, and methylene chloride.
The above reducing agent includes sodium boron hydride, sodium boron cyanohydride, triethylsilane, lithium aluminum hydride, diisopropyl aluminum hydride, borane-pyridine complex, and decaborane.
The above acid includes acetic acid, hydrochloric acid, trifluoroacetic acid, trifluoroboron-diethyl ether complex, trimethylsilyl triflate, BiC13, trifluoromethanesulfonic acid, p-toluenesulfonic acid, and pyridinium-p-toluenesulfonic acid.
The above reaction can be performed typically at about -78 C to about 120 C
for about one hour to about two days.
The reaction can be easily performed by, for example, using methods described in the following literature or similar methods thereto.
a) Daniel Dube and Adrew A. Scholte, Tetrahedron Letters, 1999, 40, 2295-2298 b) Koich Fukase, Yoshiyuki Fukase, Masato Oikawa, Wen-Chi Liu, Yasuo, Suda, and Shoichi Kusumoto, Tetrahedron, 1998, 54, 4033-4050 c) Seung Hwan Lee, Yong Lune Park, and Cheol Min Yoon, Tetrahedron Letters, 1999, 40, d) Makoto Wada, Sonoe Nagayama, Kaori Mizurtani, Ryoichi Hiroi, and Norikazu Miyoshi, Chemistry Letters, 2002, 248-249 e) Kikkugawa, Y., Ogawa, Y., Chem. Pharm. Bull., 1979,27,2405-2410 Preparation of compound I (1) Compound (XI) can be converted into compound I in accordance with the method for converting a 2-(phenylamino)-5-vinylbenzoic acid derivative (V) into a hydroxamic acid derivative (VII) described above.
More specifically, compound I can be obtained by reacting compound (XI) with a hydroxylamine derivative (VI) represented by NH2OR4 in an appropriate solvent in the presence of a peptide condensing agent and in the presence or the absence of a base.
The above solvent include dichioromethane, THF, and dimethylformamide, and preferably dichloromethane.
The above base include triethylamine, Hunig's base, or DBU, and preferably Hunig's base.
The above peptide condensing agent include 1,3-dicyclohexylcarbodiimide (DCC), 2-ethoxy-l-ethoxycarbonyl-1,2-dihydroquinoline (EEDQ), bromo-tris(pyrrolidino)-phosphonium hexafluorophosphate (PyBrOP), 1-ethyl-3 -(3'-dimethylaminopropyl)carbodiimide (EDC), (benzotriazolyloxy)tripyrrolidino-phosphonium hexafluorophosphate (PyBOP), 3-hydroxy-4-oxo-3,4-dihydro-1,2,3-benzotriazine (HODhBt), and hydroxybenzotriazole (HOBt).
Preferable examples include the combination of 1-ethyl-3-(3'-dimethylaminopropyl)carbodiimide (EDC) with N-hydroxybenzotriazole (HOBt), and the combination of 1-ethyl-3-(3'-dimethylaminopropyl)carbodiimide (EDC) with 3-hydroxy-4-oxo-3,4-dihydro-1,2,3-benzotriazine (HODhBt).
The above reaction can be performed typically at about 10 C to about 30 C, preferably about 22 C (room temperature) for about one hour to about two days, preferably about 10 hours.
Reaction process 3 Reaction process 3 is an example process for preparing, from compound (XII), compounds (I-a) and (I-b), in particular among compounds I represented by the formula (1).
Compound (XII) is one of compound I where RI is a halogen atom such as iodine atom, bromine atom, or chlorine atom, and preferably iodine atom.
In compounds (I-a) and (I-b), Rl is an alkynyl group or an alkenyl group; an unsaturated bond is present between a carbon directly bound to a benzene ring containing R2 and an adjacent carbon thereto. Rh to Rk represent substituents on the carbon atoms that are connected by an unsaturated bond. Rh, Ri, Rj, Rk independently represent a hydrogen atom or a Ci_6 alkyl group.

Preparation of compound (I-a) Compound (XII) can be converted into compound (I-a) using, for example, Sonogashira method described in literature (K. Sonogashira, Y. Tohda and N. Hagihara, Tetrahedron Lett. 16, 4467-4470 (1975)). Specifically, compound (I-a) can be obtained by reacting compound (XII) with alkyne in an appropriate solvent, e.g., THF, in the presence of a catalytic amount of palladium complex, e.g., (PPh3)2PdC12, as well as a catalytic amount of a copper reagent, e.g., copper iodide, and an appropriate base, e.g., triethylamine or Hunig's base.
The above reaction can be performed typically at about 10 C to about 100 C, preferably about 40 C
to 60 C for about two hours to about two days.

Preparation of compound (I-b) (1) Compound (XII) can be converted into compound (I-b) in accordance with the method for converting a 5-iodinated, 5-brominated benzoic acid derivative (II) into a 5-vinylbenzoic acid derivative (III) shown in reaction process 1.
More specifically, compound (I-b) can be obtained by reacting compound (XII) with a vinylated organic metal reagent in an appropriate solvent in the presence of a transition metal catalyst. The above solvent includes dimethylformamide, THF, DMSO, isopropanol, methanol, and ethanol, and preferably THF or isopropanol. The above transition metal catalyst includes, for example palladium complex, and specifically Pd(PPh3)4, (PhCN)2PdC12, (MeCN)2PdC12, or (PPh3)2PdC12. The above vinylated organic metal reagent includes, for example, vinylated organic magnesium, vinylated organic aluminum, vinylated organic silicon, vinylated organic boron, vinylated organic zinc, and vinylated organic tin. Preferable examples include vinyl organic tin (Stille's method) or vinyl borate (Suzuki's method). If necessary, it is possible to add an appropriate base such as triethylamine, t-butylamine, or Hunig's base in the reaction system.
The above reaction can be performed typically at about 15 C to about 130 C, preferably about 60 C for about four hours to about four days, preferably about 10 hours.
The reaction can be easily performed with reference to the following literature:
5 a) J. K. Stille, Angew. Chem., Int. Ed. Engl. 1986, 25, 508-524.
b) N. Miyaura, A. Suzuki, Chem. Rev. 1995, 95, 2457-2483 c) A. Suzuki, J. Organomet. Chem., 1999, 576, 147-168.
d) Suzuki, A, In Metal-Catalyzed Cross Coupling Reactions; Diederich, F., Stang, P. J., Eds.;
VCH: Weinheim, 1998; pp49-97.
Preparation of compound I-b) (2) Compound (I-b) can also be obtained by reducing compound (I-a). A reducing method includes, for example, a method of hydrogenating in a solvent in the presence of Lindler catalyst.
The above solvent includes ethanol, methanol, and hexane. The reaction can be performed typically at about 10 C to about 30 C, preferably about 22 C (room temperature) for about 10 minutes to about two days.

Reaction process 4 Reaction process 4 is an example process for preparing compound I represented by the formula (1), particularly compound (I-c) having Y=O (oxygen atom) and W=OH, from compound (X) or (VIII).

Preparation of compound IV) An acetal compound (XIV) can be prepared by reacting carbonyl compound (X) with a diol (XIII) in an appropriate solvent in the presence of an acid in a catalytic amount.
The above solvent includes THF, DMF, and dichloromethane.
The above acid includes p-toluene sulfonic acid, camphor sulfonic acid, hydrochloric acid, and pyridinium-p-toluenesulfonic acid.
The reaction can be performed typically at about 10 C to about 30 C, preferably about 22 C (room temperature) for about one hour to about two days.

Preparation of compound (XV) Carboxylic acid (XIV) can be converted into hydroxamate ester (XV) in accordance with the method for converting a 2-(phenylamino)-5-vinylbenzoic acid derivative (V) into a hydroxamic acid derivative (VII) described above.
More specifically, compound (XV) can be obtained by reacting compound (XIV) with a hydroxylamine derivative (VI) represented by NH20R4 in an appropriate solvent in the presence of a peptide condensing agent and in the presence or the absence of a base.
The above solvent includes dichloromethane, THF, and dimethylformamide, and preferably dichloromethane.
The above base includes triethylamine, Hunig's base, or DBU, and preferably Hunig's base.
The above peptide condensing agent includes 1,3-dicyclohexylcarbodiimide (DCC), 2-ethoxy- l -ethoxycarbonyl-1,2-dihydroquinoline (EEDQ), bromo-tris(pyrrolidino)-phosphonium hexafluorophosphate (PyBrOP), 1-ethyl-3 -(3'-dimethylaminopropyl)carbodiimide (EDC), (benzotriazolyloxy)tripyrrolidino-phosphonium hexafluorophosphate (PyBOP), 3-hydroxy-4-oxo-3,4-dihydro-1,2,3-benzotriazine (HODhBt), and hydroxybenzotriazole (HOBt).
Preferably, the combination of 1-ethyl-3-(3'-dimethylaminopropyl)carbodiimide (EDC) with N-hydroxybenzotriazole (HOBt), and the combination of 1-ethyl-3-(3'-dimethylaminopropyl)carbodiimide (EDC) with 3-hydroxy-4-oxo-3,4-dihydro-1,2,3-benzotriazine (HODhBt) can be included.
The above reaction can be performed typically at about 10 C to about 30 C, preferably about 22 C (room temperature) for about one hour to about two days, preferably about 10 hours.
An aldehyde (VIII) can be converted into a cyclic acetal (XV) by the same method as the above method for conversion of an aldehyde (X) into a cyclic acetal (XIV).
More specifically, the conversion can be accomplished by reacting acarbonyl compound (VIII) with a diol (XIII) in an appropriate solvent in the presence of an acid in a catalytic amount.
The above solvent includes THF, DMF, and dichloromethane.
The above acid includes p-toluenesulfonic acid, camphor sulfonic acid, hydrochloric acid, and pyridinium-p-toluenesulfonic acid.
The reaction can be performed typically at about 10 C to about 30 C, preferably about 22 C (room temperature) for about one hour to about two days.

Preparation of compound I-c) A cyclic acetal (XV) can be converted into compound (I-c) by reacting a cyclic acetal (XV) with an appropriate reducing agent in an appropriate solvent and if necessary in the presence of an appropriate acid.
The above solvent includes methanol, ethanol, diethyl ether, tetrahydrofuran, toluene, methylene chloride, and acetonitrile.
The above reducing agent includes sodium boron hydride, sodium boron cyanohydride, triethylsilane, trimethylsilane, lithium aluminum hydride, diisopropyl aluminum hydride, borane-pyridine complex, decaborane, diborane, borane-dimethylsulfide complex, borane-THF
complex, hydrogen, zinc boron hydride, samarium (II) iodide, and tributyltin hydride.
Preferable examples include, diisopropyl aluminum hydride, sodium boron hydride, and triethylsilane.
The above acid includes acetic acid, hydrochloric acid, trifluoroacetic acid, trifluoroboron-diethyl ether complex, trimethylsilyl triflate, BiC13, A1C13, titanium tetrachloride, trimethylsilyl chloride, trifluoromethanesulfonic acid, p-toluenesulfonic acid, and pyridinium-p-toluenesulfonic acid.
The above reaction can be performed typically at about -78 C to about 120 C
for about one hour to about two days.
The above reaction can be performed by using methods described in the following literature or similar methods thereto.
a) E. L. Eliel, V. G. Badding, and M. N. Rerick, J. Am. Chem. Soc., 1962, 84, 2371.
b) A. R. Abdum-Nur, and C. H. Issidorides, J. Org. Chem., 1962, 27, 67.
c) L. I. Zakharkin and I. M. Khorlina, Izvest. Akad. Nauk S.S.S.R., Otd. Khim.
Nauk. 1959, 2255; Chem. Abs. 1960, 54, 10837h.
d) W. L. Howard, and J. H. Jr. Brown, J. Org. Chem., 1961, 26, 1026.
e) B. Fleming, and H. I. Bolker, Can. J. Chem. 1974, 52, 888.
f) L. I. Zakharkin, V. I. Stanko, Y. A. Chapovskii, Izvest. Akad. Nauk S.S.S.R., Otd. Khim. Nauk.
1962, 1118; Chem. Abs. 1962, 981b.
g) D. A. Hove, and A. Jordan, Tetrahedron Lett., 1978, 19, 1357.
h) T. Tsunoda, M. Suzuki, and R. Noyori, Tetrahedron Lett., 1979, 20, 4679.
i) D. N. Kursanov, Z. N. Parnes, N. M. Loim, Synthesis, 1974, 633.
j) H. Kotsuki, Y. Ushio, N. Yoshimura, and M. Ochi, J. Org. Chem., 1987, 52, 2594-2596.
k) B. Bartels, and R. Hunter, J. Org. Chem., 1993, 58, 6756-6765.
1) G. Adam, and D. Seebach, Synthesis, 1988, 5, 373-375.
m) B-Z. Zheng, M. Yamauchi, H. Dei, S-I. Kusaka, K. Matusui, and O. Yonemitsu, Tetrahedron Lett., 2000, 41, 6441-6446.
n) T. Ohta, T. Michibata, K. Yamada, R. Omori, I. Furukawa, Chem. Commun., 2003, 10, 1192-1193.
o) Org. Prep. Proc. Int. 1985, 17, 11.
Reaction process 5 Reaction process 5 is an example process for preparingcompound I represented by the formula (1), particularly compound (I-d) having Y=-NHO-, from compound (X) or compound (VIII).

Preparation of compound (XVII) An aldehyde (X) can be converted into oxime ether (XVII) by stirring an aldehyde (X) with an o-alkyl-hydroxylamine derivative (XVI) in an appropriate solvent.
The above solvent includes dichloromethane, ethanol, chloroform, THF, dimethylformamide, and diethyl ether, and preferably dichloromethane or ethanol.
Preparation of compound (XVIII) Compound (XVII) can be converted into hydroxamate ester (XVIII) in accordance with the method for converting a 2-(phenylamino)-5-vinylbenzoic acid derivative (V) into a hydroxamic acid derivative (VII) described above.
More specifically, hydroxamate ester (XVIII) can be obtained by reacting compound (XVII) with a hydroxylamine derivative (VI) represented by NH2OR4 in an appropriate solvent in the presence of a peptide condensing agent and in the presence or the absence of a base.
The above solvent includes dichloromethane, THF, and dimethylformamide, and preferably dichloromethane.
The above base includes triethylamine, Hunig's base, or DBU, and preferably Hunig's base.
The above peptide condensing agent includes 1,3-dicyclohexylcarbodiimide (DCC), 2-ethoxy- l -ethoxycarbonyl-1,2-dihydroquinoline (EEDQ), bromo-tris(pyrrolidino)-phosphonium hexafluorophosphate (PyBrOP), 1-ethyl-3-(3'-dimethylaminopropyl)carbodiimide (EDC), (benzotriazolyloxy)tripyrrolidino-phosphonium hexafluorophosphate (PyBOP), 3-hydroxy-4-oxo-3,4-dihydro-1,2,3-benzotriazine (HODhBt), and hydroxybenzotriazole (HOBt).
Preferable examples include the combination of 1-ethyl-3-(3'-dimethylaminopropyl)carbodiimide (EDC) with N-hydroxybenzotriazole (HOBt), and the combination of 1-ethyl-3-(3'-dimethylaminopropyl)carbodiimide (EDC) with 3-hydroxy-4-oxo-3,4-dihydro-1,2,3-benzotriazine (HODhBt).
The above reaction can be performed typically at about 10 C to about 30 C, preferably about 22 C (room temperature) for about one hour to about two days, preferably about 10 hours.
Compound (XVIII) can also be prepared from the aldehyde (VIII). Specifically, compound (XVIII) can be obtained by stirring an aldehyde (VIII) with an o-alkyl-hydroxylamine derivative (XVI) in an appropriate solvent.
The above solvent includes dichloromethane, ethanol, chloroform, THF, dimethylformamide, and diethyl ether, and preferably dichloromethane or ethanol.

Preparation of compound (I-d) Oxime ether (XVIII) can be converted into compound (I-d) by reacting oxime ether (XVIII) with an appropriate reducing agent in an appropriate solvent and if necessary in the presence of an appropriate acid.
The above solvent includes methanol, ethanol, diethyl ether, tetrahydrofuran, toluene, methylene chloride, and acetonitrile.
The above reducing agent includes sodium boron hydride, sodium boron cyanohydride, triethylsilane, trimethylsilane, lithium aluminum hydride, diisopropyl aluminum hydride, borane-pyridine complex, decaborane, diborane, borane-dimethylsulfide complex, borane-THF
complex, zinc boron hydride, and tributyltin hydride. Preferable examples include sodium boron cyanohydride, sodium boron hydride, triethylsilane, and borane-pyridine complex.
The above acid includes acetic acid, hydrochloric acid, trifluoroacetic acid, dichloroacetic acid, trifluoroboron-diethyl ether complex, trimethylsilyl triflate; A1C13, titanium tetrachloride, and trimethylsilyl chloride. Preferable examples include dichloroacetic acid, hydrochloric acid, trifluoroacetic acid, trifluoromethanesulfonic acid, p-toluenesulfonic acid, and pyridinium-p-toluenesulfonic acid.
The above reaction can be performed typically at about -78 C to about 120 C
for about one hour to about two days.
The reaction can be performed by using methods described in the following literature or similar methods thereto.
a) M. Kawase, and Y. Kikugawa, J. Chem. Soc. Perkin Trans. 1, 1979, 643 -645.
b) B. Hegedues, and A. F. Krasso, Helv. Chim. Acta, 1970, 53, 959-963.
c) R. F. Borch, et al, J. Am. Chem. Soc., 1971, 93, 2897-2904.
d) D D. Sternbach, W. C. L. Jamison, Tetrahedron Lett., 1981, 22, 3331-3334.
e) M. Ueda, H. Miyabe, M. Namba, T. Nakabayashi, and T. Naito, Tetrahedron Lett., 2002, 43, 4369-4372.
f) M. Gustafsson, R. Olsson, C-M. Andersson, Tetrahedron Lett., 2001, 42, 133-136.
g) M. Fujita, H. Oishi, T. Hiyama, Chem. Lett., 1986, 837-838.
h) R. Camehn, K. Rehse, Arch. Pharma. (Weinheim Ger.), 2000, 333, 130-134.
Reaction process 6 Reaction process 6 is an example process for preparing compound I represented by the formula (1), particularly compound (I-e) having Y=-NR8O- and R=C(=O)R9, from compound (I-d) or compound (XVII).
Preparation of compound (I-e) from compound (I-d) Compound (I-e) can be prepared from compound (I-d)by making carboxylic acid (XXI) represented by R9-COOH into an active ester with an appropriate peptide condensing agent in an appropriate solvent, and reacting the ester with compound (I-d) in the presence or the absence of an appropriate base.
The above solvent includes dichloromethane, THF, and dimethylformamide.
The above base includes triethylamie, Hunig's base, or DBU, and preferably Hunig's base.
The above peptide condensing agent includes 1,3-dicyclohexylcarbodiimide (DCC), 2-ethoxy- l -ethoxycarbonyl-1,2-dihydroquinoline (EEDQ), bromo-tris(pyrrolidino)-phosphonium hexafluorophosphate (PyBrOP), 1-ethyl-3-(3'-dimethylaminopropyl)carbodiimide (EDC), (benzotriazolyloxy)tripyrrolidino-phosphonium hexafluorophosphate (PyBOP), 3-hydroxy-4-oxo-3,4-dihydro-1,2,3-benzotriazine (HODhBt), and hydroxybenzotriazole (HOBt).
Preferable examples include the combination of 1 -ethyl-3 -(3'-dimethylaminopropyl)carbodiimide (EDC) with N-hydroxybenzotriazole (HOBt), and the combination of 1-ethyl-3-(3'-dimethylaminopropyl)carbodiimide (EDC) with 3-hydroxy-4-oxo-3,4-dihydro-1,2,3-benzotriazine (HODhBt).
The above reaction can be performed typically at about 0 C to about 30 C, preferably about 22 C (room temperature) for about one hour to about two days, preferably about 10 hours.
Compound (I-e) can be prepared from compound (XVII).

Preparation of compound . ) Oxime ether (XVII) can be converted into a reduced compound (XIX) thereof in accordance with the method for converting a oxime (XVIII) into compound (I-d) described above.
Specifically, the conversion can be accomplished by reacting oxime ether (XVII) with an appropriate reducing agent in an appropriate solvent and if necessary in the presence of an appropriate acid.
The above solvent includes methanol, ethanol, diethyl ether, tetrahydrofuran, toluene, methylene chloride, and acetonitrile.
The above reducing agent includes sodium boron hydride, sodium boron cyanohydride, triethylsilane, trimethylsilane, lithium aluminum hydride, diisopropyl aluminum hydride, borane-pyridine complex, decaborane, diborane, borane-dimethylsulfide complex, borane-THF
complex, zinc boron hydride, and tributyltin hydride. Preferable examples include sodium boron cyanohydride, sodium boron hydride, triethylsilane, and borane-pyridine complex.
The above acid includes acetic acid, hydrochloric acid, trifluoroacetic acid, dichloroacetic acid, trifluoroboron-diethyl ether complex, trimethylsilyl triflate, AICl3, titanium tetrachloride, and trimethylsilyl chloride. Preferable examples include dichloroacetic acid, hydrochloric acid, trifluoroacetic acid, trifluoromethanesulfonic acid, p-toluenesulfonic acid, and pyridinium-p-toluenesulfonic acid.
The above reaction can be performed typically at about -78 C to about 120 C
for about one hour to about five days.

Preparation of compound (XX) An alkoxyamine (XIX) can be converted into an amide (XX) in accordance with the method for converting compound (I-d) into compound (I-e) described above.
More specifically, the preparation can be performed by making carboxylic acid (XXI) represented by R9-COOH into an active ester with an appropriate peptide condensing agent in an appropriate solvent, and reacting the ester with the amine (XIX) in the presence or the absence of an appropriate base.
The above solvent includes dichloromethane, THF, and dimethylformamide.
The above base includes triethylamine, Hunig's base, or DBU, and preferably Hunig's base.
The above peptide condensing agent includes 1,3-dicyclohexylcarbodiimide (DCC), 2-ethoxy- l -ethoxycarbonyl-1,2-dihydroquinoline (EEDQ), bromo-tris(pyrrolidino)-phosphonium hexafluorophosphate (PyBrOP), 1-ethyl-3-(3'-dimethylaminopropyl)carbodiimide (EDC), (benzotriazolyloxy)tripyrrolidino-phosphonium hexafluorophosphate (PyBOP), 3-hydroxy-4-oxo-3,4-dihydro-1,2,3-benzotriazine (HODhBt), and hydroxybenzotriazole (HOBt).
Preferable examples include the combination of 1-ethyl-3-(3'-dimethylaminopropyl)carbodiimide (EDC) with N-hydroxybenzotriazole (HOBt), and the combination of 1-ethyl-3-(3'-dimethylaminopropyl)carbodiimide (EDC) with 3-hydroxy-4-oxo-3,4-dihydro-1,2,3-benzotriazine (HODhBt).
The above reaction can be performed typically at about 0 C to about 30 C, preferably about 22 C (room temperature) for about one hour to about two days, preferably about 10 hours.
Preparation of compound (I-e) A carboxylic acid (XX) can be converted into a desired compound (I-e) in accordance with the method for converting a 2-(phenylamino)-5-vinylbenzoic acid derivative (V) into a hydroxamic acid derivative (VII) described above.
More specifically, compound (I-e) can be obtained by reacting compound (XX) with a hydroxylamine derivative (VI) represented by NH2OR4 in an appropriate solvent in the presence of a peptide condensing agent and in the presence or the absence of a base.
The above solvent includes dichloromethane, THF, and dimethylformamide, and preferably dichloromethane.
The above base includes triethylamine, Hunig's base, or DBU, and preferably Hunig's base.
The above peptide condensing agent includes 1,3-dicyclohexylcarbodiimide (DCC), 2-ethoxy-l-ethoxycarbonyl-1, 2-dihydroquinoline (EEDQ), bromo-tris(pyrrolidino)-phosphonium hexafluorophosphate (PyBrOP), 1-ethyl-3-(3'-dimethylaminopropyl)carbodiimide (EDC), (benzotriazolyloxy)tripyrrolidino-phosphonium hexafluorophosphate (PyBOP), 3 -hydroxy-4-oxo-3,4-dihydro - 1,2,3 -benzotriazine (HODhBt), and hydroxybenzotriazole (HOBt).
Preferable examples include the combination of 1-ethyl-3-(3'-dimethylaminopropyl)carbodiimide (EDC) with N-hydroxybenzotriazole (HOBt), and the combination of 1-ethyl-3-(3'-dimethylaminopropyl)carbodiimide (EDC) with 3 -hydroxy-4-oxo-3,4-dihydro-1,2,3 -benzotriazine (HODhBt).
The above reaction can be performed typically at about 10 C to about 30 C, preferably about 22 C (room temperature) for about one hour to about two days, preferably about 10 hours.
Reaction process 7 Reaction process 7 shows a method of synthesizing compound I represented by the formula (1), particularly compound (I-g) where X is particularly represented by the following formula.

Z~ O
O

The preparation can be performed by using compounds (XXII) and (XVIII) where W
is represented by C(=O)Q in an oxime ether represented by (XVII) or (XVIII) in reaction process 5.
Here, Q represents -ORc, -OCORc, -NRcRd, or a halogen atom; Rc and Rd, which may be the same or different, each represent a hydrogen atom or a C1_5 alkyl group.

Preparation of compound (XXIV) A carboxylic acid-oxime (XXII) can be converted into carboxylic acid-alkoxyamine (XXIV) in accordance with the method for converting an oxime (XVIII) into compound (I-d) described above.
More specifically, the conversion can be accomplished by reacting oxime ether (XVII) with an appropriate reducing agent in an appropriate solvent and if necessary in the presence of an appropriate acid.
The above solvent includes methanol, ethanol, diethyl ether, tetrahydrofuran, toluene, methylene chloride, and acetonitrile.
The above reducing agent includes sodium boron hydride, sodium boron cyanohydride, triethylsilane, trimethylsilane, lithium aluminum hydride, diisopropyl aluminum hydride, borane-pyridine complex, decaborane, diborane, borane-dimethylsulfide complex, borane-THF
complex, zinc boron hydride, and tributyltin hydride. Preferable examples include sodium boron cyanohydride, sodium boron hydride, triethylsilane, and borane-pyridine complex.
The above acid includes acetic acid, hydrochloric acid, trifluoroacetic acid, dichloroacetic acid, trifluoroboron-diethyl ether complex, trimethylsilyl triflate, A1C13, titanium tetrachloride, trimethylsilyl chloride, trifluoromethanesulfonic acid, p-toluenesulfonic acid, and pyridinium-p-toluenesulfonic acid. Preferable examples include dichloroacetic acid, hydrochloric acid, and trifluoroacetic acid.
The above reaction can be performed typically at about -78 C to about 120 C
for about one hour to about five days.

Preparation of compound ) Alkoxyamine (XXIV) can be converted into a cyclized compound (XXV) by stirring in an appropriate solvent at a neutral pH or in the presence of an appropriate acid or an appropriate base at an appropriate temperature.
In some cases, during the preparation of alkoxyamine (XXIV), cyclization can be accomplished only by heating the reaction system.
The above solvent includes methanol, ethanol, diethyl ether, tetrahydrofuran, toluene, methylene chloride, and acetonitrile.
The above acid includes A1Me3, acetic acid, hydrochloric acid, trifluoroacetic acid, dichloroacetic acid, trifluoroboron-diethyl ether complex, trimethylsilyl triflate, A1C13, titanium tetrachloride, trimethylsilyl chloride, trifluoromethanesulfonic acid, p-toluenesulfonic acid, and pyridinium-p-toluenesulfonic acid.
The above base includes triethylamine, Hunig's base, DBU, sodium methylate, and potassium carbonate.
The above reaction can be performed typically at room temperature to about 80 C for about one hour to about one day.

Preparation of compound (I-g) Compound (XXV) can be converted into compound (I-g) in accordance with the method for converting a 2-(phenylamino)-5-vinylbenzoic acid derivative (V) into a hydroxamic acid derivative (VII) described above.
More specifically, compound (I-g) can be obtained by reacting compound (XXV) with a hydroxylamine derivative (VI) represented by NHZOR4 in an appropriate solvent in the presence of a peptide condensing agent and in the presence or the absence of a base.
The above solvent includes dichloromethane, THF, and dimethylformamide, and preferably dichloromethane.
The above base includes triethylamine, Hunig's base, or DBU, and preferably Hunig's base.
The above peptide condensing agent includes 1,3-dicyclohexylcarbodiimide (DCC), 2-ethoxy-l-ethoxycarbonyl-1,2-dihydroquinoline (EEDQ), bromo-tris(pyrrolidino)-phosphonium hexafluorophosphate (PyBrOP), 1-ethyl-3 -(3'-dimethylaminopropyl)carbodiimide (EDC), (benzotriazolyloxy)tripyrrolidino-phosphonium hexafluorophosphate (PyBOP), 3-hydroxy-4-oxo-3,4-dihydro-1,2,3-benzotriazine (HODhBt), and hydroxybenzotriazole (HOBt).
Preferable examples include the combination of 1-ethyl-3-(3'-dimethylaminopropyl)carbodiimide (EDC) with N-hydroxybenzotriazole (HOBt), and the combination of 1-ethyl-3-(3'-dimethylaminopropyl)carbodiimide (EDC) with 3-hydroxy-4-oxo-3,4-dihydro-1,2,3-benzotriazine (HODhBt).
The above reaction can be performed typically at about 10 C to about 30 C, preferably about 22 C (room temperature) for about one hour to about two days, preferably about 10 hours.
Compound (I-g) can also be obtained, by the same conversion method, from oxime (XXIII) to which hydroxamic acid ester has been already introduced.
Preparation of compound (XXVI) Reduction of oxime (XXIII) can be performed in accordance with the method for converting oxime (XVIII) into compound (I-d) described above.
More specifically, the conversion can be accomplished by reacting oxime ether (XVII) with an appropriate reducing agent in an appropriate solvent and if necessary an appropriate acid.
The above solvent includes methanol, ethanol, diethyl ether, tetrahydrofuran, toluene, methylene chloride, and acetonitrile.
The above reducing agent includes sodium boron hydride, sodium boron cyanohydride, triethylsilane, trimethylsilane, lithium aluminum hydride, diisopropyl aluminum hydride, borane-pyridine complex, decaborane, diborane, borane-dimethylsulfide complex, borane-THF
complex, hydrogenated zinc boron, and tributyltin hydride. Preferable examples include sodium boron cyanohydride, sodium boron hydride, triethylsilane, and borane-pyridine complex .
The above acid includes acetic acid, hydrochloric acid, trifluoroacetic acid, dichloroacetic acid, trifluoroboron-diethyl ether complex, trimethylsilyl triflate, AiC13, titanium tetrachloride, trimethylsilyl chloride, trifluoromethanesulfonic acid, p-toluenesulfonic acid, and pyridinium-p-toluenesulfonic acid. Preferable examples include dichloroacetic acid, hydrochloric acid, and trifluoroacetic acid.
The above reaction can be performed typically at about -78 C to about 120 C
for about one hour to about five days.

Preparation of compound (I-g) A cyclized compound (XXVI) can be converted into compound (I-g) in accordance with the method for converting alkoxyamine (XXIV) into a cyclized compound (XXV) described above.
More specifically, the conversion can be accomplished by stirring in an appropriate solvent at a neutral pH or in the presence of an appropriate acid or an appropriate base at an appropriate temperature.
In some cases, during the preparation of alkoxyamine (=V), cyclization can be accomplished only by heating the reaction system. The cyclization can also be accomplished in the presence of an acid catalyst without the addition of a condensing agent when Q is OH in the above alkoxyamine (XXVI).
The above solvent includes methanol, ethanol, diethyl ether, tetrahydrofuran, toluene, methylene chloride, and acetonitrile.
The above acid includes A1Me3, acetic acid, hydrochloric acid, trifluoroacetic acid, dichloroacetic acid, trifluoroboron-diethyl ether complex, trimethylsilyl triflate, A1C13, titanium tetrachloride, trimethylsilyl chloride, trifluoromethanesulfonic acid, p-toluenesulfonic acid, and pyridinium-p-toluenesulfonic acid.
The above base includes triethylamine, Hunig's base, DBU, sodium methylate, and potassium carbonate.
The above reaction can be performed typically at room temperature to about 80 C for about one hour to about one day.
In particular, when Q is OH, compound (I-g) can be obtained by treating compound (XXVI) with a peptide condensing agent in the presence or the absence of a base and in an appropriate solvent.
The above solvent includes dichloromethane, THF, and dimethylformamide, and preferably dichloromethane.
The above base includes triethylamine, Hunig's base, or DBU, and preferably Hunig's base.
The above peptide condensing agent includes 1,3-dicyclohexylcarbodiimide (DCC), 2-ethoxy- l -ethoxycarbonyl-1,2-dihydroquinoline (EEDQ), bromo-tris(pyrrolidino)-phosphonium hexafluorophosphate (PyBrOP), 1 -ethyl-3-(3'-dimethylaminopropyl)carbodiimide (EDC), (benzotriazolyloxy)tripyrrolidino-phosphonium hexafluorophosphate (PyBOP), 3-hydroxy-4-oxo-3,4-dihydro-1,2,3-benzotriazine (HODhBt), and hydroxybenzotriazole (HOBt).
Preferable examples include the combination of 1-ethyl -3-(3'-dimethylaminopropyl)carbodiimide (EDC) with N-hydroxybenzotriazole (HOBt), and the combination of 1-ethyl-3-(3'-dimethylaminopropyl)carbodiimide (EDC) with 3 -hydroxy-4-oxo-3,4-dihydro-1,2,3 -benzotriazine (HODhBt).
The above reaction can be performed typically at about 10 C to about 30 C, preferably about 22 C (room temperature) for about one hour to about two days, preferably about 10 hours.
As in the above, examples of methods for producing compound I according to the present invention have been described. Isolation and purification of desired compounds shown in reaction processes 1 to 7 above can be performed by applying standard chemical manipulations such as extraction, concentration, evaporation, crystallization, filtration, recrystallization, and various chromatographic operations.
The compounds of the present invention and pharmaceutically acceptable salts thereof include all stereoisomers of compound I represented by the formula (1) (e.g., enantiomers, diastereomers (including cis and trans geometric isomers)), racemic bodies of the above isomers and mixtures thereof. Particularly, in the present invention, compound I
includes stereoisomers.
The compounds of the present invention and pharmaceutically acceptable salts thereof can be in some tautomer forms, e.g., enol and imine forms, keto and enamine forms, and mixture thereof. The tautomers are present as a mixture of a tautomer set in a solution. In a solid form, typically one tautomer is dominant. One tautomer is sometimes described, but all tautomers of the compounds of the present invention are included in the present invention.
Furthermore, the present invention includes atropisomers. The atropisomer means compound I represented by the formula (1), which can be divided into isomers whose rotation is limited.
These isomers can be isolated by standard methods utilizing physicochemical difference between the isomers. For example, a racemic compound can be made into a sterically purified isomer by a general optical resolution, e.g., the optical resolution method by leading to a diastereomer salt with an optically active acid such as tartaric acid. A
mixture of diastereomers can be separated using fractional crystallization or various chromatographic operations (e.g., thin layer chromatography, column chromatography, gas chromatography and such).

When compound I according to the present invention is obtained as a free compound, it is possible to convert it into a salt which the above compound I may form, or a hydrate or a solvate thereof in accordance with standard methods.
When compound I according to the present invention is obtained as a salt, a hydrate or a solvate of compound I, it is possible to convert it into compound I in a free form in accordance with standard methods.
Compound I of the present invention or pharmaceutically acceptable salts thereof have a strong MEK inhibitory effect, are excellent in stability in vivo and solubility in water, and are useful as preventing agents or therapeutic agents for proliferative diseases.
Compound I of the present invention or pharmaceutically acceptable salts thereof are particularly useful as preventing agents or therapeutic agents for cancers and joint disorders with inflammation.
The cancers include, for example, breast cancer, lung cancer, colorectal cancer, prostate cancer, liver cancer, ovarian cancer, uterine cancer, and pancreatic cancer.
The joint disorders with inflammation include, for example, osteoarthritis, rheumatoid arthritis, reactive arthritis, viral arthritis, purulent arthritis, and tuberculous arthritis.
Furthermore, they are useful as preventing agents or therapeutic agents (especially, therapeutic agents) for other various cancers such as brain cancer acute leukemia, stomach cancer and non-small cell lung cancer, and diseases such as psoriasis, restenosis, autoimmune diseases, and atherosclerosis, as well as sequelae of heart failure, heterograft rejection, osteoarthritis, chronic rheumatoid arthritis, asthma, cystic fibrosis, hepatomegalia, cardiac hypertrophy, Alzheimer disease, diabetes, septic shock, and HIV infection.
They are particularly useful as preventing agents or therapeutic agents (especially, therapeutic agents) for cancers depending on the Ras-MAPK signaling pathway.
Furthermore, the present invention relates to methods for preventing or treating proliferative diseases, e.g., cancers or joint diseases with inflammation.
Another embodiment of the present invention includes methods for preventing or treating solid or hematopoietic MEK-related (including Ras-related) cancers or joint diseases with inflammation. Examples of the cancers are the same as the above. Examples of the other cancer and disease are the same as the above.
These methods include a step of administering a pharmaceutically effective dose of a pharmaceutical composition comprising compound I disclosed herein or apharmaceutically acceptable salt thereof to a patient in need of such a treatment or with such a disease or condition.
When the pharmaceutical compositions of the present invention are used as an MEK
inhibitor, therapeutic agents or preventing agents for the proliferative diseases, administration methods thereof include oral, rectal, parenteral (intravenous, intramuscular, subcutaneous), intracisternal, intravaginal, intraperitoneal, intrabladder, topical (infusion, powder medicine, ointment, gel or cream) administrations and inhalation (oral or nasal spray).
Dosage forms thereof include, for example, tablets, capsules, granules, powder, pills, aqueous and non-aqueous oral solutions and suspensions, and parenteral solutions filled in containers which adapt for dispensing an individual dosage. The dosage form can also be adapted to various administration methods which comprise controlled release formulations such as subcutaneous implant.
The above formulations are produced by well-known methods using additives such as an excipient, a lubricant (coating agent), a binder, a disintegrating agent, a stabilizer, a taste masking/flavoring agent, and a diluting agent.
For example, the excipient includes lactose, crystalline cellulose, calcium hydrogenphosphate, and starches such as starch, potato starch, and corn starch.
The coating agent includes, for example, ethylcellulose, hydroxypropylcellulose, hydroxypropylmethylcellulose, shellac, talc, carnauba wax, and paraffin.
The binder includes, for example, polyvinyl pyrrolidone, macrogol, and the same compounds as in the above excipients.
The disintegrating agent includes, for example, the same compounds as in the above excipients, and chemically modified starches and celluloses such as cross carmellose sodium, sodium carboxymethylstarch, and crosslinked polyvinyl pyrrolidone.
The stabilizer includes, for example, paraoxybenzoic acid esters such as methylparaben and propylparaben; alcohols such as chlorobutanol, benzyl alcohol and phenylethyl alcohol;
benzalkonium chloride; phenols such as phenol and cresol; thimerosal;
dehydroacetic acid; and sorbic acid.
The taste masking/flavoring agent includes, for example, sweeteners, acidifiers and flavors usually used.
As solvents for producing liquid formulations, it is possible to use ethanol, phenol, chlorocresol, purified water, distilled water and such.
A surfactant or an emulsifier includes, for example, polysorbate 80, polyoxyl stearate 40, and lauromacrogol.
When the pharmaceutical compositions of the present invention are used as a MEK
inhibitor, or therapeutic agents or preventing agents for proliferative diseases, amounts of the compounds of the present invention and pharmaceutically acceptable salts thereof to be used vary depending on condition, age, body weight, relative health state, presence of other medicaments, administration method and such. For example, for a patient (warm-blooded animal, especially human), in the case of an oral agent, an effective amount is preferably 0.1 to 1000 mg, more preferably 1 to 300 mg per kg of body weight per day, and an amount to be used per day is preferably in the range of 10 to 800 mg for an adult patient with usual body weight as an active ingredient (compound I). In the case of a parenteral agent, an effective amount is preferably 0.1 to 1000 mg, and more preferably 10 to 800 mg per kg of body weight per day. It is desirable to administer this once a day or by dividing into several times a day depending on the condition.
The above pharmaceutical compositions of the present invention can be used in combination with the other radiation therapy, chemotherapy and administration of an angiogenesis inhibitor.
The compounds according to the present invention and the pharmaceutically acceptable salts thereof have a MEK inhibitory effect, a cell growth inhibitory effect, are excellent in stability in vivo and solubility in water, and are useful as preventing agents or therapeutic agents for proliferative diseases, e.g., cancers and joint diseases with inflammation.

Brief Description of the Drawing Figure 1 is a graph showing the inhibitory effect on the development of arthritis in terms of the relation between arthritis score (Y axis) and days after LPS
administration (X axis). (Test Example 6).

Best Mode for Carrying Out the Invention The present invention is illustrated in more detail below with reference to Examples.
NMR analyses were performed on JNM-EX270 (270 MHz, JEOL) or JNM-GSX400 (400 MHz, JEOL), and the NMR data are expressed as ppm (parts per million, 6) referencing the deuterium lock signal from the sample solvent.
Mass spectral data were obtained using JMS-DX303 (JEOL) or JMS-SX/SX I 02A
(JEOL), or a micromass spectrometer (Navigator, Finnigan) equipped with a gradient high performance liquid chromatography (Agilent 1100, Agilent Technologies).
Specific rotation was measured using sodium D line (589 nm) at room temperature.
Commercially available reagents were used without further purification. Room temperature represents a range from about 20 to about 25 C. All the non-aqueous reactions were carried out under a nitrogen atmosphere. Concentration or evaporation of the solvent under reduced pressure was done using a rotary evaporator.
In the preparation of a compound, functional groups were protected with protecting groups as needed, and after having prepared the target molecule, the protecting groups were removed. The selection of the protecting groups and the procedures for protection and deprotection were done according to the methods described in, for example, Greene and Wuts, "Protective Groups in Organic Synthesis" (2nd Ed., John Wiley & Sons, 1991).
[Example 1]
3,4-Difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(2-hydroxy-ethoxymeth yl)-benzamide (Compound B-1) HOB/~O
HN O
F
M , HO"'-~ O
F I
F

Step A
Preparation of 2,3,4-trifluoro-5-iodo-benzoic acid HO O

F
I F
F

2,3,4-Trifluoro-5-iodo-benzoic acid was prepared according to the method described in literature (F. Mongin, E. Marzi, and M. Schlosser, European Journal of Organic Chemistry, 2771-2777 (2001)).
Step B
Preparation of 2,3,4-trifluoro-5-vinyl-benzoic acid HO O

F
\ ( ~ F
F
To a solution of 2,3,4-trifluoro-5-iodo-benzoic acid (447 mg, 1.48 mmol) prepared in Step A in tetrahydrofuran (10 mL) were added tris(dibenzylideneacetone)dipalladium (45 mg, 0.05 mmol, product No. 32877-4, Aldrich), tri-2-furylphosphine (23 mg, 0.01 mmol), and vinyltributyltin (865 L, 3.0 mmol) under an argon atmosphere, and the mixture was stirred at 40 C for 3 hours.
After completion of the reaction, insoluble matter was removed through a celite column.
One mol/L sodium hydroxide solution (30 mL), and then methylene chloride were added to the reaction solution, and the layers were separated. Another 1 mol/L sodium hydroxide solution (30 mL) was added to the organic layer, and the layers were separated. One mol/L hydrochloric acid solution (60 mL) was added to acidify the resultant aqueous layer, and the aqueous layer was extracted twice with methylene chloride (50 mL). The resultant organic layer was dried over anhydrous sodium sulfate and filtered. The solvent was evaporated under reduced pressure, and the residue was washed with hexane, filtered, and dried to give 2,3,4-trifluoro-5-vinyl-benzoic acid (248.9 mg, 83% yield) as a.pale yellow solid.

'H-NMR(CDC13, 270MHz) 6(PPM): 5.54(1H, d, J=11.2Hz), 5.92(1H, d, J=17.8Hz), 6.78(1H, dd, J= 17.8, 11.2Hz), 7.95(1H, td, J=7.6, 2.6Hz) EIMS m/z 202(M+H) Step C
Preparation of 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-vinyl-benzoic acid HO O HH F

\ I ~ F I ~ I
F

To a solution of 2-fluoro-4-iodoaniline (5.056 g, 21.336 mmol) in tetrahydrofuran (anhydrous, 30 mL) was added dropwise 2.0 M lithium diisopropylamide (a solution in heptane/tetrahydrofuran/ethylbenzene, 13 mL, 26 mmol) with stirring at -78 C
under an argon atmosphere.
Afters minutes, a solution of 2,3,4-trifluoro-5-vinyl-benzoic acid (1.724 g, 8.534 mmol) prepared in Step B in tetrahydrofuran (anhydrous, 20 mL) was added dropwise to the reaction mixture. The reaction mixture was warmed gradually to room temperature, and stirred for 3 days.
One mol/L hydrochloric acid solution was added to the reaction mixture to bring pH to 3. Then, the solution was extracted with ethyl acetate. The extract was washed sequentially with water and saturated brine, and the organic layer was dried over anhydrous sodium sulfate and filtered. The solvent was evaporated under reduced pressure, and the resultant dark brown solid was triturated with methylene chloride to give 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-vinyl-benzoic acid (2.352 g, 66% yield) as a pale yellow solid.

IH-NMR(CD3OD, 270MHz) S(PPM): 5.41(1H, d, J=11.5Hz), 5.86(1H, d, J=17.2Hz), 6.76(1H, td, J=8.6, 5.6Hz), 6.79(1 H, dd, J=17.2, 11.5Hz), 7.41(1 H, m), 7.48(1 H, dd, J=10.6, 2.0Hz), 8.05(1 H, dd, 7.9, 2.0Hz) ESI(LC/MS positive mode) m/z 420 (M+H) Step D
Preparation of N-[2-(tert-butyldimethylsilanyloxy)-ethoxy]-3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-5-vin yl-benzamide HH F
/ N \
\ \ I F I
F

To a solution of 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-vinyl-benzoic acid (6.2 g, 14.8 mmol) prepared in Step C in methylene chloride (100 ml) were added O-[2-(tert-butyldimethylsilanyloxy)-ethyl]-hydroxylamine (3.40 g, 17.8 mmol), 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide hydrochloride (3.40 g, 17.8 mmol), 1-hydroxybenzotriazole monohydrate (3.0 g, 22.1 mmol), and N,N-diisopropylethylamine (5.1 ml, 29.6 mmol), and the mixture was stirred at room temperature for 20 hours.
The reaction mixture was concentrated under reduced pressure, and water (300 ml) was added thereto. The mixture was extracted with ethyl acetate (500 ml), and the organic layer was washed with saturated brine (200 ml), dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (500 g, n-hexane/ethyl acetate (20:1)) to give N-[2-(tert-butyldimethylsilanyloxy)ethoxy]-3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-5-viny lbenzamide (6.36 g, 73%) as a pale yellow solid.

1H-NMR(CD3OD, 270MHz) S(PPM) 0.07 (6H, s), 0.86 (9H, s), 3.91 (21-1, dd, J =
5.0, 4.0 Hz), 4.07(2H,dd,J=5.0,4.0Hz),5.44(1H,d,J=11.2Hz),5.81 (1H,d,J=17.5Hz),6.57(1H,td,J
= 8.9, 5.0 Hz), 6.74 (1H, dd, J = 17.8, 10.9 Hz), 7.32 (1H, br. d, J = 7.9 Hz), 7.37 - 7.42 (2H, m), 8.20 (1H, br. s), 9.38 (1H, br. s) ESI(LC/MS positive mode) m/z 593 (M+H) Step E
Preparation of N-[2-(tert-butyldimethylsilanyloxy)-ethoxy] -3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-5-for myl-benzamide iii- Q
HN O
F
a O" I F I /
F

N-[2-(Tert-butyldimethylsilanyloxy)-ethoxy]-3,4-difluoro-2-(2-fluoro-4-iodophenylami no)-5-vinyl-benzamide (27.4 g, 46.27 mmol) prepared in Step D was dissolved in a mixed solvent of tetrahydrofuran (300 ml) and water (90 ml). To this solution, an aqueous solution of osmium tetroxide (0.1 mM, 9.25 ml, 0.95 mmol) and sodium metaperiodate (38.6 g, 0.180 mol) were added at 0 C, and the mixture was stirred at room temperature for 3 hours.
Insoluble matter was removed by celite filtration, and washed with ethyl acetate. The combined filtrate and washing were washed with an aqueous solution of 0.2 M
sodium thiosulfate and saturated brine, dried over magnesium sulfate, and evaporated under reduced pressure to give a mixture (37.1 g) of N-[2-(tert-butyldimethylsilanyloxy)-ethoxy] -3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-5-for myl-benzamide and a desilylated product, 3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-5-formyl-N-(2-hydroxy-ethoxy)-benzamide (the same compound as the product in the next step). (Pure N-[2-(tert-butyldimethylsilanyloxy)-ethoxy]-3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-5-for myl-benzamide can be obtained by purification with silica gel chromatography (300 g, n-hexane/ethyl acetate (5:1)).

1H-NMR(CD3OD, 270MHz) 6(PPM) 0.11 (6H, s), 0.78 (9H, s), 3.97 (2H, dd, J =
5.1, 4.3 Hz), 4.13 (2H, dd, J = 4.6, 4.3 Hz), 6.82 (1H, td, J = 8.6, 4.1 Hz), 7.30 - 7.38 (2H, m), 7.78 (1H, dd, J
= 6.8, 2.2 Hz), 9.64 (2H, br s), 10.15 (1H, s) ESI(LC/MS positive mode) m/z 595 (M+H) Step F
Preparation of 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-formyl-N-(2-hydroxy-ethoxy)-benzamide HO,,/1,O
HN O
F
\
I I

F

N-[2-(Tert-butyldimethylsilanyloxy)-ethoxy]-3,4-difluoro-2-(2-fluoro-4-iodophenylami no)-5-formyl-benzamide (37.1 g as a crude product containing the desilylated product) prepared in Step E was dissolved in a mixed solvent of tetrahydrofuran (200 ml) and water (16 ml). To this solution, p-toluenesulfonic acid monohydrate (1.76 g, 9.25 mmol) was added, and the mixture was stirred at room temperature for 12 hours. The reaction mixture was extracted with ethyl acetate, and the organic layer was washed with saturated brine, dried over magnesium sulfate, and evaporated under reduced pressure. The resultant residue was triturated with ethyl acetate to give 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-formyl-N-(2-hydroxy-ethoxy)-benzamide (16.0 g, 72% yield in two steps) as a yellow solid.

1H-NMR(DMSO-d6 270MHz) 6(PPM) 3.17(1H, d, J=4.6Hz), 3.59(2H, t, J=4.6Hz), 3.85(2H, t, J=4.6Hz), 6.99(1H, td, J=8.9, 3.0), 7.48(1H, d=8.3Hz), 7.67(1H, d, J=10.9Hz), 7.86(1H, d, J=6.9Hz), 9.64(1H, br.s), 10.02(1H, s) ESI(LC/MS positive mode) m/z 481 (M+H) Step G
Preparation of 5-[1,3]dioxolan-2-yl-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benza mide HO,,-,,-,, o HN O
F
O F
O F
To a solution of 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-formyl-N-(2-hydroxy-ethoxy)-benzamide (15.99 g, 33.3 mmol) prepared in Step F in anhydrous THE (150 ml) were added ethylene glycol (70 ml) and p-toluenesulfonic acid monohydrate (316.6 mg, 1.66 mmol) at room temperature, and the mixture was stirred for 14 hours. Then ethylene glycol (100 ml) was added, and the reaction mixture was stirred for additional 8 hours. The reaction mixture was poured into saturated aqueous sodium bicarbonate, and extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium bicarbonate and saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure to give 5-[ 1,3 ] dioxolan-2-yl-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benza mide (21.69 g) as a crude product.
'H-NMR(CDC13, 270MHz) S(PPM) 3.76 (1H, br. s, OH), 4.044.23 (8H, m), 6.00 (1H, s), 6.60 (1 H, td, J = 8.6, 4.3 Hz), 7.3 3 (1 H, dt, J = 6.9, 1.3 Hz), 7.42 (1 H, dd, J
= 9.9, 1.7 Hz), 7.52 (1 H, br. d, J = 6.9 Hz), 8.32 (1H, br. s), 9.09 (1H, br. s) ESI(LC/MS positive mode) m/z 525 (M+H) Step H
Preparation of 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(2-hydroxy-ethoxymethy 1)-benzamide HO,,,,,,,O
I
HN O
F
~O
HO F I
F
To a solution of 5-[ 1,3]dioxolan-2-yl-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benza mide (21.69 g) obtained in Step G in anhydrous THE (100 ml) were added sodium borohydride (4.21 g, 111.4 mmol) and trifluoroacetic acid (5.08 ml, 66.8 mmol) with ice-cooling, and the mixture was stirred at room temperature overnight. The reaction mixture was poured into saturated aqueous sodium bicarbonate, and extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium bicarbonate and saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (Si02 600 g, 100% AcOEt to AcOEt/MeOH (50:1 to 20:1)) to give 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(2-hydroxy-ethoxymethy 1)-benzamide (13.9 g, 80%) as a white powder.

1H-NMR(CD3OD, 270MHz) S(PPM) 3.51 (2H, dd, J = 3.9, 3.3 Hz), 3.603.63 (4H, m), 3.86 (2H, dd, J = 4.9, 4.3 Hz), 4.52 (2H, s), 6.50 (1H, td, J = 8.6, 4.6 Hz), 7.23 (1H, ddd, J = 8.6, 2.0, 1.0 Hz), 7.33 (1 H, dd, J = 10.9, 2.0 Hz), 7.43 (1 H, dd, J = 6.9, 2.0 Hz) ESI(LC/MS positive mode) m/z 527(M+H) [Example 2]
2-(4-Ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)-5-(2-hydroxy-ethoxym ethyl)-benzamide (Compound B-2) HO~~O
HN O
F
. a ~O
HO F
F

To a solution of 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(2-hydroxy-ethoxymethy l)-benzamide (46.1 mg, 87.6 mol) obtained in Step H of Example 1 in tetrahydrofuran (anhydrous, 2.0 ml) were added trimethylsilylacetylene (48.5 L, 0.350 mmol), copper iodide (3.3 mg, 17.5 mol), (PPh3) 2PdCl2 (3.7 mg, 5.3 mol), and Hunig's base (diisopropylethylamine, 149 L, 0.876 mmol), and the mixture was stirred at 50 C for 2 hours.
The reaction mixture was concentrated under reduced pressure. 0.1 N
Hydrochloric acid was added to the resultant residue, and the mixture was extracted with ethyl acetate. The organic layer was washed with 0.1 N hydrochloric acid and brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The resultant residue was purified by silica gel column chromatography (Presep Silica Gel Type S (Wako Pure Chemical Industries), 10 g, CH2C12/MeOH (10:1)) to give 3,4-difluoro-2-(2-fluoro-4-trimethylsilanylethynyl-phenylamino)-N-(2-hydroxy-ethoxy)-5-(2-hy droxy-ethoxymethyl)-benzamide (37.6 mg, 86%).
To a solution of the resultant 3,4-difluoro-2-(2-fluoro-4-trimethylsilanylethynyl-phenylamino)-N-(2-hydroxy-ethoxy)-5-(2-hy droxy-ethoxymethyl)-benzamide (37.6 mg) in tetrahydrofuran (anhydrous, 1.0 ml) was added tetra-n-butylammonium fluoride (1 M solution in THF, 113 L, 113 mol) at room temperature, and the mixture was stirred for 3 hours. The reaction mixture was concentrated under reduced pressure. 0.1 N Hydrochloric acid was added to the resultant residue, and the mixture was extracted with ethyl acetate. The combined organic layers were washed with 0.1 N
hydrochloric acid and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The resultant residue was purified by silica gel column chromatography (Presep Silica Gel Type S (Wako Pure Chemical Industries), 10 g, CH2C12/MeOH (10:1 to 5:1)) to give 2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)-5-(2-hydroxy-ethoxyme thyl)-benzamide (21.9 mg, 68%) as a yellow powder.

1H-NMR(CD3OD, 270MHz) 6(PPM) 3.03 (1H, s), 3.66 (2H, dd, J = 4.6, 3.6 Hz), 3.75 (2H, t, J =
4.3 Hz), 3.83 (2H, t, J = 4.3 Hz), 4.04 (2H, dd, J = 4.6, 3.6 Hz), 4.58 (2H, s), 6.68 (1H, td, J = 8.3, 5.6 Hz), 7.14 (d, J = 8.6 Hz), 7.18 (dd, J = 11.2, 1.6 Hz), 7.54 (d, J = 5.3 Hz), 8.50 (1 H, br. s) ESI(LC/MS positive mode) m/z 425 (M+H) The compounds of Examples 3 and 4 below were synthesized by preparing cyclic acetal compounds using an aldehyde, 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-formyl-N-(2-hydroxy-ethoxy)-benzamide obtained in Step F of Example 1 as a starting material, and 1,3-propanediol or 2,2-dimethyl-1,3-propanediol, respectively, instead of ethylene glycol used as a reagent in Step G
of Example 1, and subjecting the acetal compounds to reducing conditions similar to those in Step H of Example 1.
[Example 3]
3,4-Difluoro-2-(2-fluoro-4-iodophenylamino)-N-(2-hydroxy-ethoxy)-5-(3 -hydroxy-propoxymeth yl)-benzamide (Compound B-6) HO,,~O
I
HN O
F
HO~,O \ F I I
F

1H-NMR(CD3OD, 270MHz) S(PPM) 1.83(2H, quin., J=6.3Hz), 3.64(4H, m), 3.68(2H, m), 3.95(2H, m), 4.57(2H, br.s), 6.59(1H, td, J=8.9, 4.6Hz), 7.34(1H, dd, J=8.6, 1.3Hz), 7.43(IH, dd, J=10.9, 2.0Hz), 7.50(1H, m) ESI(LC/MS positive mode) m/z 541(M+H) [Example 4]
3,4-Difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-(3-hydroxy-2,2-dimethyl-propoxymethyl)-N-(2 -hydroxy-ethoxy)-benzamide (Compound B-7) HO~~
O

HN O
F
HOI'i\ CO
\ F
F

1H-NMR(CD3OD, 270MHz) S(PPM) 0.90(6H, s), 3.37(2H, s), 3.70(2H, dd, J=4.9, 4.3Hz), 3.93(2H, dd, J=4.9, 4.3Hz), 4.57(2H, s), 6.60(1H, td, J=8.9, 4.6Hz), 7.34(1H, d, J=8.6Hz), 7.44(1H, dd, J=10.6, 2.0Hz), 7.47(1H, m) ESI(LC/MS positive mode) m/z 569(M+H) [Example 5]
5-(2, 3 -Dihydroxy-propoxymethyl)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)benzamide HO,,,,,,,O
I
HN O
HH F
OH
HOI
F I
F

Step A
Preparation of 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-formyl-benzoic acid HO O HH F

O I ~ I ~
F
H F

3,4-Difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-vinylbenzoic acid (200 mg, 0.477 mmol) prepared in Step C of Example 1 was dissolved in tetrahydrofuran (20 ml) and water (1 mL). To this reaction mixture, an aqueous solution of 0.1 M osmium tetroxide (1.0 mL) and sodium metaperiodate (510 mg, 2.39 mmol) were added at room temperature, and the mixture was stirred for 2 hours. Insoluble matter was removed through a celite column, and ethyl acetate extraction was performed.
The extract was washed sequentially with water and saturated brine, and the organic layer was dried over anhydrous sodium sulfate, and filtered. The solvent was evaporated under reduced pressure, and the resultant dark brown solid was triturated with methanol to give 3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-5-formyl-benzoic acid (133.6 mg, 66% yield) as a pale yellow solid.

1H-NMR(DMSO-d6, 270MHz) b(PPM) 7.11(1H, td, J=8.6, 3.6), 7.53(1H, m), 7.71(1H, dd, J=10.2,1.7Hz), 8.27(1H, dd, J=7.3,1.3Hz), 10.00(1H,s), 10.08(1H, br.s) ESI(LC/MS positive mode) m/z 422 (M+H) Step B
Preparation of 5-allyloxymethyl-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-benzoic acid HO O
F
F I
F

To bismuth (III) chloride (37 mg, 0.188 mmol) that was dried by heating under reduced pressure, methylene chloride (anhydrous, 3 ml suspension) was added under argon flow, and the mixture was stirred thoroughly. To this suspension, allyl alcohol (40 L, 0.57 mmol), triethylsilane (107 L, 0.671 mmol), and 3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-5-formyl-benzoic acid (200 mg, 0.475 mmol) prepared in Step A were added at room temperature, and the mixture was stirred for a whole day and night. After completion of the reaction, the reaction mixture was extracted with ethyl acetate.
The extract was washed sequentially with water and saturated brine, and the organic layer was dried over anhydrous sodium sulfate, and filtered. The solvent was evaporated under reduced pressure, and the resultant dark brown solid was purified with Presep (Wako Pure Chemical Industries, 10 g).
5-Allyloxymethyl-3,4-difluoro-2-(2-fluoro-4-iodophenylamino)benzoic acid (140.7 mg, 64%
yield) was obtained as a light brown solid from fractions eluted with 100%
ethyl acetate.

'H-NMR(CD3OD, 270MHz) S(PPM) 4.08(2H, m), 4.56(2H, s), 5.25(1H, d, J=10.2Hz), 5.32(1H, d, J=17.1Hz), 5.92(1H, m), 6.80(1H, m), 7.41(1H, d, J=10.2Hz), 7.48(1H, d, J=10.6Hz), 7.96(1H, m) ESI(LC/MS positive mode) m/z 464 (M+H) Step C
Preparation of 5-allyloxymethyl-N-[2-(tert-butyldimethylsilanyloxy)ethoxy]-3,4-difluoro-2-(2-fluoro-4-iodophe nylamino)-benzamide Si~O~~\O

F I
F

To a solution of 5-allyloxymethyl-3,4-difluoro-2-(2-fluoro-4-iodophenylamino)benzoic acid (140 mg, 0.302 mmol) prepared in Step B in NN-dimethylformamide (anhydrous, 4 mL) were added N-hydroxysuccinimide (41 mg, 0.363 mmol) and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (70 mg, 0.363 mmol) at room temperature under argon flow, and the mixture was stirred thoroughly.
Subsequently, O-[2-(t-butyldimethylsilanyloxy)ethyl]-hydroxyamine (86 mg, 0.453 mmol) was added thereto, and the mixture was stirred for 2 hours. After completion of the reaction, the reaction mixture was extracted with ethyl acetate.
The extract was washed sequentially with water and saturated brine, and the organic layer was dried over anhydrous sodium sulfate, and filtered. The solvent was evaporated under reduced pressure, and the resultant brown oil was purified with Mega Bond Elut silica gel (Varian, 5 g).
5-Allyloxymethyl-N-[2-(tert-butyldimethylsilanyloxy)ethoxy]-3,4-difluoro-2-(2-fluoro-4-iodoph enylamino)benzamide (35.5 mg, 18% yield) was obtained as a pale yellow oil from fractions eluted with 10% ethyl acetate/hexane.

'H-NMR(CDC13, 270MHz) S(ppm) 0.04(6H, s), 0.79(9H, s), 3.83(2H, m), 4.03(2H, m), 4.44(2H, s), 5.18(1H, d, J=11.5Hz), 5.26(1H, m), 5.87(1H, m), 6.48(1H, td, J=8.6, 4.9Hz), 7.23(1H, d, J=8.9Hz), 7.31(1H, m), 7.32(1H, m), 8.30(1H, br.s), 9.25(1H, br.s) ESI(LC/MS positive mode) m/z 637 (M+H) Step D
Preparation of 5-allyloxymethyl-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benzami de HO O

HN O

F
F

To a solution of 5-allyloxymethyl-N-[2-(tert-butyl-dimethyl-silanyloxy)-ethoxy]-3,4-difluoro-2-(2-fluoro-4-iodop henylamino)-benzamide (35.5 mg, 0.056 mmol) prepared in Step C in tetrahydrofuran (anhydrous, 4 mL) was added dropwise tetra-n-butylammonium fluoride (1 mol/L
solution in tetrahydrofuran, 0.5 mL, 0.5 mmol) at room temperature, and the mixture was stirred for 4 hours.
After completion of the reaction, the solvent was evaporated under reduced pressure, and the yellow oil was extracted with ethyl acetate. The extract was washed sequentially with water and saturated brine, and the organic layer was dried over anhydrous sodium sulfate, and filtered. The solvent was evaporated under reduced pressure, and the resultant brown oil was purified by preparative TLC (60% ethyl acetate/hexane as a developing solvent) to give 5-allyloxymethyl-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benzami de (11 mg, 38% yield) as a white solid.
'H-NMR(CD3OD, 270MHz) 6(PPM) 3.70(2H, dd, J=4.9, 4.3Hz), 3.93(2H, dd, J=4.9, 4.3Hz), 4.09(2H, dt, J=5.6, 1.3Hz), 4.57(2H, s), 5.21(1H, ddd, J=10.2, 3.0, 1.3Hz), 5.33(1H, ddd, J=17.1, 4.9, 1.6Hz), 5.96(1H, m), 6.61(1H, td, J=8.6, 4.3Hz), 7.34(1H, dt, J=8.6, 1.0Hz), 7.45(1H, dd, J=8.6, 2.0Hz), 7.46(1H, dd, J=6.9, 2.0Hz) ESI(LC/MS positive mode) m/z523 (M+H) Step E
Preparation of d,1-5-(2,3-dihydroxy-propoxymethyl)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydro xyethoxy)-benzamide HO,,-,,-,,O

HN O
F
OH
HO~~,O l F
F

To a solution of -allyloxymethyl-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-ben zam i 5 de (11 mg, 0.021 mmol) prepared in Step D in tetrahydrofuran (anhydrous, 4 mL) and water (1 mL) were added 4% osmium tetroxide solution (100 L) and 30% hydrogen peroxide solution (0.5 mL) at room temperature, and the mixture was stirred for 3 hours. After completion of the reaction, the reaction mixture was extracted with ethyl acetate.
The extract was washed sequentially with water and saturated brine, and the organic layer was dried over anhydrous sodium sulfate, and filtered. The solvent was evaporated under reduced pressure, and the resultant brown oil was purified with Mega Bond Elut silica gel (Varian, 5 g).
d,1-5-(2,3-Dihydroxy-propoxymethyl)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydro xy-ethoxy)-benzamide (6.8 mg, 58%) was obtained as a white solid from fractions eluted with 10% methanol/methylene chloride.

'H-NMR(CD3OD, 270MHz) S(PPM) 3.51-3.64(4H, m), 3.70(2H, dd, J=5.3, 4.6H-z), 3.81(1H, quin. J=5.3Hz), 3.94(2H, t, J=4.9), 4.63(2H, s), 6.61(1H, td, J=8.6, 4.6Hz), 7.35(1H, m), 7.50(1H, br.d, J=5.9Hz) ESI(LC/MS positive mode) m/z557 (M+H) [Example 6]
3,4-Difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-hydroxy-ethoxyamin o)-methyl]-benzamide (Compound C-1) HOB/\
O

HN O
F
HO,,/,,,O~a \ F / I
F
Step A
Preparation of (E)-N-[2-(t-butyl-dimethyl-silanyloxy)-ethoxy]-5={[2-(t-butyl-dimethyl-silanyloxy)-ethoxyimino ]-methyl l -3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-benzamide \1/
OI ,a I ~\O O F
I
F
F

To a solution of 3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-5-formyl-benzoic acid (130 mg, 0.309 mmol) prepared in Step A of Example 5 in methylene chloride (anhydrous, 5 mL) were added 1-hydroxybenzotriazole (42 mg, 0.309 mmol), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (177 mg, 0.926 mmol), and N,N-diisopropylethylamine (161 L, 0.926 mmol) at room temperature under argon flow, and the mixture was stirred thoroughly. Subsequently, O-[2-(t-butyl-dimethyl-silanyloxy)-ethyl]-hydroxyamine (177 mg, 0.926 mmol) was added thereto, and the mixture was stirred for 17 hours. After completion of the reaction, the reaction mixture was extracted with ethyl acetate.
The extract was washed sequentially with water and saturated brine, and the organic layer was dried over anhydrous sodium sulfate, and filtered. The solvent was evaporated under reduced pressure,- and the resultant brown oil was purified with Mega Bond Elut silica gel (Varian, 10 g).
(E)-N-[2-(t-Butyl-dimethyl-silanyloxy)-ethoxy]-5- { [2-(t-butyl-dimethyl-silanyloxy)-ethoxyimin o]-methyl}-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-benzamide (137.1 mg, 58% yield) was obtained as a pale yellow solid from fractions eluted with 10% ethyl acetate/hexane.

1H-NMR(CDC13, 270MHz) 8(PPM): 0.08(6H,s), 0.09(6H, s), 0.87(9H,s), 0.91(9H,s), 3.92(4H,m), 4.12(2H,m), 4.26(2H,m), 6.64(1H, td, J=8.6, 5.3Hz), 7.35(1H,m), 7.41(1H, dd, J=10.3, 1.711z), 7.73(1H, br.s), 8.22(1H,s), 8.78(1H,br.s), 9.43(1H, br.s) EIMS m/z 767(M+H) Step B
Preparation of (E)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-hydroxy-ethoxyi mino)-methyl]-benzamide HOB/~
HN O
F
HO,,/,, O"N F LI
F

To a solution of (E)-N-[2-(t-butyl-dimethyl-silanyloxy)-ethoxy]-5- { [2-(t-butyl-dimethyl-silanyloxy)-ethoxyimino ]-methyl}-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-benzamide (410 mg, 0.534 mmol) prepared in Step A in tetrahydrofuran (anhydrous, 20 mL) was added dropwise tetra-n-butylammonium fluoride (1 moIJL solution in tetrahydrofuran, 1.4 mL, 1.4 mmol) at room temperature, and the mixture was stirred for 4 hours.
After completion of the reaction, the solvent was evaporated under reduced pressure, and the yellow oil was extracted with ethyl acetate. The extract was washed sequentially with water and saturated brine, and the organic layer was dried over anhydrous sodium sulfate, and filtered. The solvent was evaporated under reduced pressure, and the resultant brown oil was purified with Mega Bond Elut silica gel (Varian, 5 g). The pale yellow solid obtained from fractions eluted with 100% ethyl acetate was triturated with ethyl acetate to give (E)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-hydroxy-ethoxyi mino)-methyl] -benzamide (134 mg, 47% yield) as a white solid.

'H-NMR(CD3OD, 270MHz) S(PPM): 3.72(2H, t, J=4.9Hz), 3.82(2H, t, J=4.9Hz), 3.95(2H, dd, J=4.9, 4.3Hz), 4.26(2H, dd, J=4.9, 4.6), 6.72(1H, td, J=8.6, 4.3Hz), 7.39(1H, m), 7.47(1H, dd, J=10.6, 1.6Hz), 7.81(1H, dd, J=4.9, 1.6Hz), 8.29(1H, s) ESI(LC/MS positive mode) m/z 540 (M+H) Step C
Preparation of 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-hydroxy-ethoxyamin o)-methyl]-benzamide HN O
F
HOBO~ H N I I
\ F i F

To a solution of (E)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-hydroxy-ethoxyi mino)-methyl]-benzamide (3.62 g, 6.70 mmol) obtained in Step B in methanol (100 ml) were added portionwise trifluoroacetic acid (6.5 ml) and sodium cyanoborohydride (3.78 g, 60.2 mmol) over 2 days while monitoring the progression of the reaction by TLC. The reaction mixture was poured into water, and extracted with ethyl acetate. The organic layer was washed with saturated aqueous sodium bicarbonate, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (CH2C12/MeOH (15:1)), and the resultant crude compound was crystallized from methylene chloride to give 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-hydroxy-ethoxyamin o)-methyl]-benzamide (1.66 g, 46%, as a total of first and second crystals).

1H-NMR(CD3OD, 270MHz) 6(PPM): 3.63 - 3.70 (6H, m), 3.94 (2H, dd, J = 4.9, 4.3 Hz), 4.08 (2H, s), 6.5 9 (1 H, td, J=8.6, 4.3 Hz), 7.3 4(1 H, d, J = 8.2 Hz), 7.44 (1 H, dd, J = 10.9, 2.0 Hz), 7.50 (1H, dd, J = 6.9, 2.0Hz).
ESI(LC/MS positive mode) m/z 542 (M+H) Step B' The oxime compound, (E)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-hydroxy-ethoxyi mino)-methyl]-benzamide obtained in Step B of Example 6 may be easily prepared from 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5 -formyl-N-(2-hydroxy-ethoxy)-ben zam i de obtained in Step F of Example 1 by a reaction with 2-aminooxyethanol in THE at room temperature.
Namely, 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-formyl-N-(2-hydroxy-ethoxy)-benzamide (1.37 g) and aminooxy ethanol (262 mg) were mixed in THE at room temperature for 12 hours, and then the solvent was evaporated to give 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-hydroxy-ethoxyimin o)-methyl]-benzamide.

Step C' 3,4-Difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-hydroxy-eth oxyamino)-methyl]-benzamide obtained in Step C of Example 6 may be prepared in another condition. Namely, 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-hydroxy-ethoxyimin o)-methyl]-benzamide (1.76 g, 3.27 mmol) obtained in Step B (or Step B') of Example 6 was suspended in methylene chloride, and borane-pyridine complex (1.21 g, 13.1 mmol) and dichloroacetic acid (1.69 g, 13.1 mmol) were added thereto at room temperature. The mixture was stirred for 3 hours. The solvent was evaporated, and the residue was purified by silica gel chromatography using CH2C12/MeOH as a developing solvent to give 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-hydroxy-ethoxyamin o)-methyl]-benzamide (1.40 g).

[Example 7]
3,4-Difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)5-[(3 -hydroxy-propoxyami no)-methyl]-benzamide (Compound C-10) HOB -HN O
F
F
F

Step A
Synthesis of (E)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(3 -hydroxy-propoxy imino)-methyl]-benzamide HOB -HN O
F
HO~~ON F I
F

The title compound was obtained by a procedure similar to that in Step B' of Example 6 using 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-formyl-N-(2-hydroxy-ethoxy)-benzamide obtained in Step F of Example 1 as a starting material and 3-aminooxy n-propanol as a reagent.
1H-NMR(DMSO-d6, 400MHz) S(PPM) 1.58(2H, m), 3.37(2H, t, J=6.4Hz), 3.55(4H, m), 3.81(2H, t, J=4.6Hz), 3.93(2H, d, J=5.9Hz), 4.38(1H, br), 4.71(1 H, br), 6.59(1H, m), 6.77(1 H, t, J=5.9Hz), 7.34(1H, d, J=8.8Hz), 7.48(1H, d, J=6.9Hz), 7.55(lH, dd, J=10.7Hz, 2.0Hz), 8.63(1H, br), 11.72(1 H, br) ESI(LC/MS positive mode) m/z 556 (M+H) Step B
3,4-Difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)5-[(3 -hydroxy-propoxyami no)-methyl]-benzamide (Compound C-10) HOB/~
O

HN O
F
HO O F
F
The title compound was obtained by a procedure similar to that in Step C' of Example 6 from (E)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(3-hydroxy-propoxy imino)-methyl]-benzamide obtained in Step A.

1H-NMR(DMSO-d6, 400MHz) S(PPM) 1.58(2H, m), 3.37(2H, t, J=6.4Hz), 3.55(4H, m), 3.81(2H, t, J=4.6Hz), 3.93(2H, d, J=5.9Hz), 4.38(1H, br), 4.71(1H, br), 6.59(1H, m), 6.77(1H, t, J=5.9Hz), 7.34(IH, d, J=8.8Hz), 7.48(1H, d, J=6.9Hz), 7.55(1H, dd, J=10.7Hz, 2.0Hz), 8.63(1H, br), 11.72(1H, br) ESI(LC/MS positive mode) m/z 556 (M+H) [Example 8]
3,4-Difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-hydroxy-2-methyl-p ropoxyamino)-methyl]-benzamide (Compound C-28) Step A
Preparation of 1-aminooxy-2-methyl-propan-2-ol hydrochloride O,NH2 HO
=HCI
Preparation of 1 -aminooxy-2-methyl-propan-2-ol hydrochloride was performed as described in the following literature:
Monatsh Chem Verw Teile Andere Wiss (1961) 92 p 725-739.
Step B
(E)-3,4-Difluoro-2-(2-fluoro-4-iodophenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-hydroxy-2-methy 1-propoxymlino)-methyl]-benzamide HOB -O

HN O
F
/ a HO N
/~~O F I
F
The title compound was obtained by a procedure similar to that in Step B' of Example 6 using 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-formyl-N-(2-hydroxy-ethoxy)-benzamide obtained in Step F of Example 1 as a starting material and 1-aminooxy-2-methyl-propan-2-ol hydrochloride obtained in Step A.

'H-NMR(CD3OD, 270MHz) S(PPM) 3.30(6H, s), 3.72(2H, m), 3.94(2H, m), 4.08(2H, s), 6.72(1H, m), 7.38(1H, d=8.6Hz), 7.47(1H, d, J=10.9Hz), 7.80(1H, br.d, J=5.3Hz), 8.30(1H, s) ESI(LC/MS positive mode) m/z 568 (M+H) Step C
3,4-Difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-hydroxy-2-methyl-p ropoxyamino)-methyl]-benzamide (Compound C-28) HOB/~
O

HN O
F
HO ~ry ~ O F I
F
The title compound was obtained by a procedure similar to that in Step C' of Example 6 from (E)-3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-hydroxy-2-methyl -propoxyimino)-methyl]-benzamide obtained in Step A.

'H-NMR(DMSO-d6, 400MHz) S(PPM) 1.01(6H, s), 3.55(2H, t, J=4.4Hz), 3.82(2H, t, J=4.4Hz), 3.95(2H, d, J=4.9Hz), 4.40(1H, br), 4.70(1H, br), 6.58(1H, m), 6.96(1H, t, J=4.9Hz), 7.34(1H, d, J=8.3Hz), 7.49(1H, d, J=6.8Hz), 7.55(1H, d, J=10.8Hz), 8.56(1H, br), 11.72(1H, br). The peak of a methylene group is overlapping with that of H2O peak.
ESI(LC/MS positive mode) m/z 570 (M+H) [Example 9]
3,4-Difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-methylsulfanyl-etho xyamino)-methyl]-benzamide (Compound C-30) -,--~,O
i HN O F

0 F ,I
F

Step A
Synthesis of O-(2-methylsulfanyl-ethyl)-hydroxylamine 0,NH2 O-(2-Methylsulfanyl-ethyl)-hydroxylamine (CAS No. 101512-32-7) was prepared according to the method described in the following literature:
Bull. Acad. Sci. USSR Div. Chem. Sci. (Engl. Transl.); 1967; 1743-1745.
Step B
Synthesis of (E)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-methylsulfanyl-e thyoxyimino)-methyl] -benzamide HN O F
S\'~O,N" I F
F
The title compound was obtained by a procedure similar to that in Step B' of Example 6 using 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-formyl-N-(2-hydroxy-ethoxy)-benzamide obtained in Step F of Example 1 as a starting material and O-(2-methylsulfanyl-ethyl)-hydroxylamine obtained in Step A as a reagent.
Namely, 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-formyl-N-(2-hydroxy-ethoxy)-benzamide (2.6 g, 5.415 mmol) was dissolved in a mixed solvent of methylene chloride (50 mL), THE (20 mL), and methanol (10 mL).
O-(2-Methylsulfanyl-ethyl)-hydroxylamine (924 mg, 8.621 mmol) was added thereto, and the mixture was stirred at room temperature for 3 hours.

After completion of the reaction, the solvent was evaporated under reduced pressure to give a pale yellow crude product. The residue was triturated with a proper amount of ethyl acetate:hexane (7:3) to give (E)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-methylsulfanyl-e thoxyimino)-methyl]-benzamide (1.1 g) as a white solid.

1H-NMR(CD3OD, 270MHz) S(PPM) 2.15(3H, s), 2.82(2H, dd, J=6.9, 6.6Hz), 3.72(2H, dd, J=
4.9, 4.3Hz), 3.95(2H, dd, J= 4.9, 4.3Hz), 4.34(2H, dd, J=6.9, 6.6Hz), 6.72(1H, td, J=8.6, 4.3Hz), 7.39(1H, m), 7.47(1H, dd, J=10.6, 2.0Hz), 7.81(1H, dd, J=7.3, 2.0Hz), 8.25(1H, s) ESI(LC/MS positive mode) m/z 570(M+H) Step C
3,4-Difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-methylsulfanyl-etho xyamino)-methyl]-benzamide (Compound C-30) The title compound was obtained by a procedure similar to that in Step C' of Example 6 using (E)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-methylsulfanyl-e thyoxyimino)-methyl]-benzamide obtained in Step B as a starting material.
Namely, (E)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-methylsulfanyl-e thyoxyimino)-methyl] -benzamide (104.8 mg, 0.184 mmol) was dissolved in methylene chloride (anhydrous, l0 mL). Borane-pyridine complex (140 L, 1.38 mmol) and then dichloroacetic acid (115 L, 1.38 mmol) were added thereto with cooling the reaction vessel in an ice-bath under a nitrogen atmosphere. The ice-bath was removed, and the mixture was stirred at room temperature for 17 hours. After completion of the reaction, the reaction mixture was extracted with ethyl acetate, and the organic layer was washed sequentially with water and saturated brine, dried over anhydrous Na2SO4, and concentrated under reduced pressure. The resultant yellow residue was purified by silica gel column chromatography (Mega Bond Elut, Varian, 5%
methanol/methylene chloride as an eluent). The resultant fraction was concentrated under reduced pressure and the oily residue was triturated with 5% ethyl acetate/hexane to give 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-methylsulfanyl-ethox yamino)-methyl]-benzamide (110 mg) as a white solid.

1H-NMR(CD3OD, 270MHz) 8(PPM) 2.06(3H, s), 2.62(2H, t, J=6.6Hz), 3.70(2H, m), 3.77(2H, t, J=6.6Hz), 3.94(2H, m), 4.07(2H, s), 6.56(1H, td, J=8.7, 4.8Hz), 7.32(1H, m), 7.43(IH, dd, J=10.7, 2.0Hz), 7.53(1H, dd, J=7.3, 2.0Hz) ESI(LC/MS positive mode) m/z 572(M+H) [Example 10]
3,4-Difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-methanesulfinyl-eth oxyamino)-methyl]-benzamide (Compound C-3 1) HO,,,-.O

F

To a solution of 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-methylsulfanyl-ethox yamino)-methyl]-benzamide (10 mg, 0.017 mmol) obtained in Step C of Example 9 in a mixed solvent of acetone (1.8 mL) and water (0.2 mL) was added 30% aqueous hydrogen peroxide (3 L, 0.026 mmol), and the mixture was stirred for 17 hours.
After completion of the reaction, the reaction mixture was extracted with ethyl acetate, and the organic layer was washed sequentially with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The resultant residue was purified by preparative TLC (No. 5744, Merck, 5% methanol/methylene chloride as a developing solvent) to give 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-methanesulfmyl-etho xyamino)-methyl]-benzamide (4.0 mg, 39%) as an off-white solid.
1H-NMR(CD3OD, 270MHz) S(PPM) 2.62(3H, s), 2.88(1H, m), 2.92(1H, m), 3.70(2H, m), 3.93(2H, m), 4.00(2H, m), 4.08(2H, s), 6.60(1H, td, J=8.7, 4.6Hz), 7.34(1H, m), 7.44(1H, dd, J=10.6, 2.0Hz), 7.48(1H, m) ESI(LC/MS positive mode) m/z 588(M+H) [Example 11 ]
3,4-Difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-methanesulfonyl-eth oxyamino)-methyl]-benzamide (Compound C-8) HN O
F
O O
/SAO-a F II
F
To a solution of 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-methanesulfmyl-etho xyamino)-methyl]-benzamide (10 mg, 0.017 mmol) obtained in Example 10 in a mixed solvent of methanol (1.8 mL) and water (0.2 mL) was added sodium metaperiodate (6 mg, 0.026 mmol) at room temperature, and the mixture was stirred for 17 hours. After completion of the reaction, the reaction mixture was extracted with ethyl acetate, and the organic layer was washed sequentially with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The resultant residue was purified by preparative TLC
(No. 5744, Merck, 5% methanol/methylene chloride as a developing solvent) to give 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-methanesulfonyl-eth oxyamino)-methyl]-benzamide (1.3 mg, 13%) as an off-white solid.

1H-NMR(CD3OD, 270MHz) 8(PPM) 2.94(3H, s), 3.26(2H, partial hidden), 3.71(214, dd, J=4.9, 4.3Hz), 3.93(2H, dd, J=4.9, 4.3Hz), 4.04(2H, dd, J=5.7, 5.4Hz), 4.10(2H, s), 6.61(1H, td, J=8.7, 4.6Hz), 7.33(1H, m), 7.43(1H, dd, J=10.7, 1.811z), 7.50(1H, m) ESI(LC/MS positive mode) m/z 604(M+H) [Example 12]
3,4-Difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(3 -methylsulfanyl-prop oxyamino)-methyl]-benzamide (Compound C-32) Step A
Preparation of 2-(3-methylsulfanyl-propoxy)-isoindole-1,3-dione O

SO

3-Methylsulfanyl-propan-l-ol (4.133 g, 38.92 mmol) was dissolved in THE
(anhydrous, 100 mL). To this solution, triphenylphosphine (10.2 g, 38.92 mmol) and N-hydroxyphthalimide (6.4 mg, 38.92 mmol) were added and dissolved with stirring.
Diisopropyl azodicarboxylate (8.5 mL, 42.812 mmol) was added dropwise thereto with cooling the reaction vessel in an ice-bath under nitrogen atmosphere. The reaction mixture was warmed to room temperature, and stirred for 5 hours. After completion of the reaction, the reaction mixture was concentrated under reduced pressure, and triturated with diethyl ether:hexane (1:1, about 100 ml) to precipitate triphenylphosphine oxide as a white solid, which was filtered off.
The filtrate was concentrated under reduced pressure to give a yellow oily residue. The resultant yellow oil was purified by silica gel flash chromatography (BW300, Fuji Silysia Chemical, 20% ethyl acetate/hexane as an eluent) to give 2-(3-methylsulfanyl-propoxy)-isoindole-1,3-dione (6.4 g, 65%).

1H-NMR(CDC13, 270MHz) S(PPM) 2.04(2H, m), 2.15(3H, s), 2.78(2H, m), 4.33(2H, dd, J=6.3, 6.1Hz), 7.72-7.88(4H, m) ESI(LC/MS positive mode) m/z 252(M+H) Step B
Synthesis of O-(3-methylsulfanyl-propyl)-hydroxylamine S,,~O,NH2 2-(3-Methylsulfanyl-propoxy)-isoindole-1,3-dione (6.4 g, 25.5 mmol) obtained in Step A was dissolved in methylene chloride (anhydrous, 50 mL). To this solution, methylhydrazine (1.5 mL, 28 mmol) was added dropwise, and the mixture was stirred for 1 hour.
The precipitated white solid was filtered off, and the filtrate was concentrated under reduced pressure.
The yellow oily residue was extracted with ethyl acetate, and the organic layer was washed sequentially with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The resultant yellow oily residue was purified by vacuum distillation (1 mmHg, 57 C) to give O-(3-methylsulfanyl-propyl)-hydroxylamine (3.15 g, 68%) as a colorless oil.
1H-NMR(CDC13, 270MHz) S(PPM) 1.88(2H, m), 2.11(3H, s), 2.55(2H, dd, J=7.6, 7.lHz), 3.75(2H, dd, J=6.3, 6.1Hz), 5.37(2H, br.s) ESI(LC/MS positive mode) m/z 122(M+H) Step C

Synthesis of (E)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5 -[(3 -methylsulfanyl-p ropoxyimino)-methyl] -benzamide HO

HN O
F
H
N
.'N~ F
The title compound was obtained by a procedure similar to that in Step B of Example 9 using 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-formyl-N-(2-hydroxy-ethoxy)-benzamide obtained in Step F of Example 1 as a starting material and O-(3-methylsulfanyl-propyl)-hydroxylamine obtained in Step B as a reagent.
Namely, 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-formyl-N-(2-hydroxy-ethoxy)-benzamide (76 mg, 0.158 mmol) was dissolved in a mixed solvent of methylene chloride (5 mL) and methanol (1 mL). O-(3-Methylsulfanyl-propyl)-hydroxylamine (100 L) was added thereto, and the mixture was stirred at room temperature for 3 hours. After completion of the reaction, the solvent was evaporated under reduced pressure to give a pale yellow crude product. The residue was triturated with a proper amount of ethyl acetate:hexane (1:9) to give (E)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(3-methylsulfanyl-p ropoxyimino)-methyl]-benzamide (88.8 mg, 96%) as a white solid.

1H-NMR(CDCl3, 270MHz) S(PPM) 2.03(2H, m), 2.13(3H, s), 2.63(2H, dd, J=7.3, 7.IHz), 3.79(2H, m), 4.30(2H, t, J=6.3Hz), 6.66(1H, td, J=8.6, 4.5Hz), 7.35(1H, m), 7.42(1H, dd, J=10.2, 1.8Hz), 7.77(1H, dd, J=6.8, 2.0Hz), 8.21(1H, s), 8.60(1H, br.s), 9.15(1H, br.s) ESI(LC/MS positive mode) m/z584(M+H) Step D
Synthesis of 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(3-methylsulfanyl-prop oxyamino)-methyl]-benzamide (Compound C-32) HO,_,,--,0 HN O
F
H
N
H
S,N F
F

The title compound was obtained by a procedure similar to that in Step C of Example 9.
Namely, (E)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(3-methylsulfanyl-p ropoxyimino)-methyl]-benzamide was reduced with borane-pyridine complex in the presence of dichloroacetic acid to give 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(3-methylsulfanyl-prop oxyamino)-methyl]-benzamide (26.54 mg, 79%).
1H-NMR(CD3OD, 270MHz) 8(PPM) 1.78(2H, m), 2.03(3H, s), 2.47(2H, dd, J=7.4, 7.1Hz), 3.70(2H, t, J=6.1Hz), 3.71(2H, m), 3.92(2H, m), 4.06(2H, s), 6.59(l H, td, J=8.7, 4.3Hz), 7.34(1H, dd, J=8.4, 1.1Hz), 7.44(1H, dd, J=10.7, 1.811z), 7.49(1H, m) ESI(LC/MS positive mode) m/z586(M+H) [Example 13]
3,4-D iuoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(3 -methanesulfinyl-pro poxyamino)-methyl]-benzamide (Compound C-33) HO,,~ O

HN O
H F
(rac) N I \
H
sON F
o F
O
The title compound was obtained by a procedure similar to that in Example 10 using 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(3-methylsulfanyl-prop oxyamino)-methyl]-benzamide obtained in Example 12 as a starting material.
Namely, 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(3-methylsulfanyl-prop oxyamino)-methyl]-benzamide was treated with 30% aqueous hydrogen peroxide in aqueous acetone to synthesize 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(3 -methanesulfmyl-prop oxyamino)-methyl]-benzamide (6.34 mg, 62%).

1H-NMR(CD3OD, 270MHz) S(PPM) 1.96(2H, m), 2.64(3H, s), 2.83(2H, m), 3.71(2H, m), 3.75(2H, dd, J=6.1, 5.9Hz), 3.92(2H, dd, J=4.9, 4.3Hz), 6.59(IH, td J=8.7, 4.3Hz), 7.34(1H, br,d, J=8.6Hz), 7.44(1H, dd, J=10.7, 2.0 Hz), 7.49(1H, dd, J=7.3, 1.8Hz) ESI(LC/MS positive mode) m/z602(M+H) [Example 14]
3,4-Difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-hydroxyaminomethyl-N-(2-hydroxy-ethoxy)-be nzamide (Compound C-23) Step A
Synthesis of (E)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5 -(hydroxyimino-meth yl)-benzamide O

HN O
H

N
HORN.. F
F

The title compound was obtained by a procedure similar to that in Step B of Example 9 using 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-formyl-N-(2-hydroxy-ethoxy)-benzamide obtained in Step F of Example 1 as a starting material and N-hydroxyamine hydrochloride (commercially available) as a reagent. 111.7 mg (100%).

1H-NMR(CD3OD, 270MHz) S(PPM) 3.71 (2H, dd, J = 4.9, 4.3 Hz), 3.93 (2H, dd, J =
4.6, 4.3 Hz), 6.70 (1 H, td, J = 8.6, 4.3 Hz), 7.3 8 (1 H, dt, J = 8.3 , 1.3 Hz), 7.46 (1 H, dd, J = 10.9, 2.O Hz), 7.80 (1H, br. d, J = 5.9 Hz), 8.21 (1H, s) ESI(LC/MS positive mode) m/z 496 (M+H) Step B
Synthesis of 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-hydroxyaminomethyl-N-(2-hydroxy-ethoxy)-be nzamide (Compound C-23) HO,,,~O

HN O
F
H
N
H
HO'N F / I
F

The title compound was obtained by a procedure similar to that in Step C of Example 9.
Namely, (E)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(hydroxyimino-meth yl)-benzamide was reduced with borane-pyridine complex in the presence of dichloroacetic acid to give 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-hydroxyaminomethyl-N-(2-hydroxy-ethoxy)-be nzamide (28.14 mg, 81%).
1H-NMR(CD3OD, 270MHz) 5(PPM) 3.71(2H, dd, J=4.8, 4.4Hz), 3.94(2H, dd, J=4.8, 4.lHz), 4.08(2H, s), 6.60(1H, td, J=8.7, 4.5Hz), 7.35(1H, br.d, J=8.6Hz), 7.44(1H, dd, J=10.6, 1.8Hz), 7.52(1 H, br.d, J=7.4Hz) ESI(LC/MS positive mode) m/z 498 (M+H) [Example 15]
3,4-Difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(methoxyamino-methyl) -benzamide (Compound C-24) Step A
Synthesis of (E)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5 -(methoxyimino-meth yl)-benzamide HO

HN O
F
H
N N j F
O
F
The title compound was obtained by a procedure similar to that in Step B of Example 9 using 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-formyl-N-(2-hydroxy-ethoxy)-benzamide obtained in Step F of Example 1 as a starting material and N-methoxyamine hydrochloride (commercially available) as a reagent. 128 mg (99%).

1H-NMR(CD3OD, 270MHz) 8(PPM) 3.72(2H, dd, J=4.8, 4.6Hz), 3.95(2H, dd, J=4.8, 4.6Hz), 3.98(3H, s), 6.71(1H, td, J=8.7, 4.5Hz), 7.41(1H, m), 7.47(1H, dd, J=10.6, 2.011z), 7.81(1H, dd, J=7.4, 2.1 Hz), 8.22(1 H, s) ESI(LC/MS positive mode) m/z 510(M+H) Step B
Synthesis of 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(methoxyamino-methyl)-benzamide (Compound C-24) HO

HN O
F
H
~O I \ N I \
HN / I
F

The title compound was obtained by a procedure similar to that in Step C of Example 9.
Namely, (E)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(methoxyimino-meth yl)-benzamide was reduced with borane-pyridine complex in the presence of dichloroacetic acid to give 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(methoxyamino-methyl)-benzamide (28.14 mg, 81%).

1H-NMR(CD3OD, 270MHz) 8(PPM) 3.50(3H, s), 3.70(2H, m), 3.93(2H, m), 4.08(2H, s), 6.59(1H, td, J=8.9, 4.2Hz), 7.34(1H, m), 7.44(1H, dd, J=10.6, 1.811z), 7.48(1H, br.s) ESI(LC/MS positive mode) m/z 512(M+H) [Example 16]
3,4-Difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5- [(methoxy-methyl-amin o)-methyl]-benzamide (Compound C-25) HO

HN O
H
I
O N
N F
F

To a solution of 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-formyl-N-(2-hydroxy-ethoxy)-benzamide (56.2 mg, 0.117 mmol) in tetrahydrofuran (anhydrous) were added 0,N-dimethyl-hydroxylamine hydrochloride (commercially available, 34 mg, 0.351 mmol) and sodium cyanoborohydride (34 mg, 0.541 mmol) under nitrogen atmosphere, and the mixture was stirred at room temperature for 3 hours. After completion of the reaction, the reaction mixture was extracted with ethyl acetate, and the organic layer was washed sequentially with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The resultant residue was purified by silica gel flash chromatography (Mega Bond Elut, Varian, 5%
methanol/methylene chloride as an eluent) to give 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(methoxy-methyl-amino )-methyl]-benzamide (9.72 mg, 17%) as a white solid.
IH-NMR(CD3OD, 270MHz) 8(PPM) 2.63(3H, s), 3.37(3H, s), 3.71(2H, dd, J=4.9, 4.3Hz), 3.85(2H, s), 3.94(2H, dd, J=4.8, 4.5Hz), 6.59(IH, td, J=8.9, 4.611z), 7.34(1H, m), 7.44(1H, dd, J=10.6, 1.8Hz), 7.47(1H, dd, J=8.7, 2.0Hz) ESI(LC/MS positive mode) m/z 526(M+H) [Example 17]
5-(Ethoxyamino-methyl)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-b enzamide (Compound C-26) Step A
Synthesis of (E)-5-(ethoxyimino-methyl)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy )-benzamide O
HN O
F
H
N
N I
0~ F
F

The title compound was obtained by a procedure similar to that in Step B of Example 9 using 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-formyl-N-(2-hydroxy-ethoxy)-benzamide obtained in Step F of Example 1 as a starting material and N-ethoxyamine hydrochloride (commercially available) as a reagent.

1H-NMR(CD3OD, 270MHz) S(PPM) 1.31(3H, t, J=7.OHz), 3.72(2H, m), 3.94(2H, m), 4.23(2H, q, J=7.OHz), 6.70(1H, m), 7.39(1H, br.d, J=8.4Hz), 7.47(1H, dd, J=10.7, 2.0Hz), 7.80(1H, m), 8.22(1H, s) ESI(LC/MS positive mode) m/z 524(M+H) Step B
Synthesis of 5-(ethoxyamino-methyl)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-b enzamide (Compound C-26) HO~~

F
H
N
H
OIN F I
F

The title compound was obtained by a procedure similar to that in Step C of Example 9.
Namely, (E)-5-(ethoxyimino-methyl)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy )-benzamide was reduced with borane-pyridine complex in the presence of dichloroacetic acid to give 5-(ethoxyamino-methyl)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2=hydroxy-ethoxy)-b enzamide (97.7 mg, 80% in 2 steps).

1H-NMR(DMSO-d6, 270MHz) 6(PPM) 1.03(3H, t, J=6.9Hz), 3.55(2H, m), 3.57(2H, q, J=6.9Hz), 3.83(2H, m), 3.99(2H, m), 4.71(1H, br.s), 6.60(1H, m), 7.39(1H, d, J=8.7Hz), 7.47(1H, d, J=6.6Hz), 7.57(1H, dd, J=10.9, 1.8Hz), 8.50(1H, br.s), 11.80(1H, br.s) ESI(LC/MS positive mode) m/z 526(M+H) [Example 18]
3,4-Difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(isopropoxyamino-meth yl)-benzamide (Compound C-27) Step A
Synthesis of (E)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(isopropoxyimino-m ethyl)-benzamide HOB -O
I
HN O
F
H
N
O N F
F

The title compound was obtained by a procedure similar to that in Step B of Example 9 using 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-formyl-N-(2-hydroxy-ethoxy)-benzamide obtained in Step F of Example 1 as a starting material and O-isopropylhydroxylamine hydrochloride (commercially available) as a reagent.

1H-NMR(DMSO-d6, 270MHz) 6(PPM) 1.27 (6H, d, J = 6.3 Hz), 3.57 (2H, br. q, J =
4.3 Hz), 3.84 (2H, t, J = 4.6 Hz), 4.44 (1 H, qui, J = 6.3 Hz) 4.73 (1 H, br. t, J =
5.6 Hz), 6.80 (1 H, td, J =
9.2,4.3 Hz), 7.40 (IH, br. d, J = 7.9 Hz), 7.61 (1H,dd,J=10.9,2.0Hz),7.69(1H,br.d,J=6.9 Hz), 8.22 (1 H, s), 8.84 (1H, br. s, NH), 11.98 (1 H, br. s, NH).
ESI(LC/MS positive mode) m/z 538 (M+H) Step B
Synthesis of 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(isopropoxyamino-meth yl)-benzamide (Compound C-27) O

HN O
F
H
N
)", N
O F I
F

The title compound was obtained by a procedure similar to that in Step C of Example 9.
Namely, (E)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(isopropoxyimino-m ethyl)-benzamide was reduced with borane-pyridine complex in the presence of dichloroacetic acid to give 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(isopropoxyamino-meth yl)-benzamide (65.0 mg, 89% in 2 steps).
1H-NMR(DMSO-d6, 270MHz) S(PPM) 1.02 (6H, d, J = 6.2 Hz), 3.56 (2H, br. t, J =
4.9 Hz), 3.67 (1 H, qui, J = 6.2 Hz), 3.83 (2H, br. t, J = 4.9 Hz), 3.92 (2H, br. d, J = ca 5 Hz), 4.72 (1 H, br. s), 6.59(1H,td,J=8.9,4.1 Hz), 7.36 (1H, br. d, J = 8.1 Hz),7.48(1H,br.d,J=7.0Hz),7.57(1H, dd, J = 10.8, 1.9 Hz), 8.57 (1H, br. s).
ESI(LC/MS positive mode) m/z 540(M+H) [Example 19]
3,4-Difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(methylcarbamoylmetho xyamino-methyl)-benzamide (Compound C-13) Step A
Synthesis of (1,3-dioxo-1,3-dihydro-isoindol-2-yloxy)-acetic acid methyl ester O

N
O

The title compound was prepared according to the method described in the following literature:
Sheppard, andrew et al.; J. Chem. Soc. Perkin Trans 1; 1990; 2519-2525.

Step B
Synthesis of 2-aminooxy-N-methyl-acetamide O
To a solution of (1,3-dioxo-1,3-dihydro-isoindol-2-yloxy)-acetic acid methyl ester (120.9 g, 0.51 mol) obtained in Step A in methanol (300 ml) was added methylamine (40%
solution in methanol, 1.0 L) at room temperature, and stirred at 60 C over night. The reaction mixture was concentrated under reduced pressure, and methylene chloride was added to the resultant residue to precipitate a solid, which was filtered and washed with methylene chloride.
The combined filtrate and washing were concentrated under reduced pressure.
The residue was purified by silica gel column chromatography (1.4 kg, CH2C12/MeOH (30:1 to 10:1)) to give 2-aminooxy-N-methyl-acetamide (50.3 g, 94%) as a colorless syrup.

1H-NMR(CDC13, 270MHz) 6(PPM) 2.88 (3H, d, J = 5.0 Hz), 4.17 (21-1, s), 5.69 (2H, br. s).
Step C
Synthesis of (E)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[methylcarbamoylm ethoxyimino-methyl]-benzamide HOB~ O
i HN O
F

/a)r*'~oN F I
O F

To a solution of 2-aminooxy-N-methyl-acetamide (1.71 g, 16.4 mmol) obtained in Step B in a mixed solvent of methylene chloride (50 ml) and THE (25 ml) was added 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-formyl-N-(2-hydroxy-ethoxy)-benzamide (3.94 g, 8.20 mmol) obtained in Step F of Example 1 at room temperature, and the mixture was stirred for 15 hours. The reaction mixture was concentrated under reduced pressure, and methylene chloride (40 ml) was added to the resultant residue to precipitate a solid, which was filtered and washed with methylene chloride. The resultant solid was dried under reduced pressure to give (E)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5 -[methylcarbamoylm ethoxyimino-methyl]-benzamide (3.57 g, 77%) as a white solid.

'H-NMR(DMSO-d6, 270MHz) 8(PPM) 2.63 (3H, d, J = 4.6 Hz), 3.56 (2H, t, J = 4.6 Hz), 3.83 (2H, t, J = 4.3 Hz), 4.5 7 (2H, s), 4.73 (1 H, br. s), 6.82 (1 H, td, J = 8.9, 4.0 Hz), 7.41 (1 H, br. d, J
= 8.6 Hz), 7.61 (111, dd, J = 10.9, 2.0 Hz), 7.69 (1 H, br. d, J = 6.3 Hz), 7.87 (1 H, br q, J = 4.6 Hz), 8.40 (1H, s), 8.92 (111, br. s), 12.01 (1H, br. s).
ESI(LC/MS positive mode) m/z 567 (M+H) Step D
3,4-Difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(methylcarbamoylmetho xyamino-methyl)-benzamide (Compound C-13 ) HO -HN O
F
N"
HH ~ ~
~N OW H N F I
O F
To a solution of (E)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[methylcarbamoylm ethoxyimino-methyl]-benzamide (69.8 mg, 0.12 mmol) obtained in Step C in methylene chloride (15 ml) were added borane-pyridine complex (199 l, 1.92 mmol) and dichloroacetic acid (162 l, 1.92 mmol) at room temperature, and the mixture was stirred for 3.5 days.
Additional borane-pyridine complex (199 RI, 1.92 mmol) and dichloroacetic acid (162 l, 1.92 mmol) were added, and the mixture was stirred for 1 day. The reaction mixture was diluted with methylene chloride (20 ml), and washed with saturated brine (2x 20 ml). The organic layer was dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The resultant residue was purified by preparative TLC (EtOAc/MeOH (9:1)) to give 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(methylcarbamoylmetho xyamino-methyl)-benzamide (36.9 mg, 53%) as a colorless oil.

'H-NMR(CD3OD, 270MHz) 8(PPM) 2.77 (3H, s), 3.68-3.76 (2H, m), 3.92-3.98 (2H, m), 4.09 (2H, s), 4.13 (2H, s), 6.61 (1 H, dt, J = 4.3, 8.6 Hz), 7.34 (1 H, ddd, J =
1.2, 1.9, 8.6 Hz), 7.45 (1 H, dd, J = 1.9, 10.8 Hz), 7.50 (1H, dd, J = 1.9, 7.3 Hz).
ESI(LC/MS positive mode) m/z 569 (M+H) [Example 20]
5-(Ethylcarbamoylmethoxyamino-methyl)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-h ydroxy-ethoxy)-benzamide (Compound C-14) Step A
Synthesis of 2-aminooxy-N-ethyl-acetamide \/M ONH2 O
To a suspension of (1,3-dioxo-1,3-dihydro-isoindol-2-yloxy)-acetic acid methyl ester (996 mg, 4.23 mmol) obtained in Step A of Example 19 in THE (5 mL) was added ethylamine (2.0 M solution in THF, 25 ml) at room temperature, and the mixture was stirred at 60 C for 18 hours. The reaction mixture was concentrated under reduced pressure, and methylene chloride was added to the resultant residue to precipitate a solid, which was filtered and washed with methylene chloride. The combined filtrate and washing were concentrated under reduced pressure. The residue was purified by silica gel column chromatography (40 g, CH2C12/MeOH
(30:1 to 20:1)) to give 2-aminooxy-N-ethyl-acetamide (160 mg, 32%) as a colorless syrup.
'H-NMR(CD3OD, 270MHz) S(PPM) 1.14 (3H, t, J = 7.3 Hz), 3.27 (2H, q, J = 7.3 Hz), 4.07 (2H, s).
Step B
Synthesis of (E)-5-(ethylcarbamoylmethoxyimino-methyl)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-( 2-hydroxy-ethoxy)-ben za m i de Ho""'-' HV o HH F
N

o F

Using 2-aminooxy-N-ethyl-acetamide obtained in Step A, synthesis was performed according to the procedure described in Step C of Example 19 to give (E)-5-(ethylcarbamoylmethoxyimino-methyl)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-( 2-hydroxy-ethoxy)-benzamide.

'H-NMR(DMSO-d6, 270MHz) S(PPM) 1.03 (3H, t, J = 7.3 Hz), 3.14 (2H, quint., J =
7.3 Hz), 3.56 (2H, br), 3.83 (2H, br), 4.55 (2H, s), 4.72 (1H, br), 6.82 (1H, dt, J =
3.8, 8.9 Hz), 7.40 (1H, br.d,J=8.9Hz),7.61(1H,dd,J=1.6,10.8Hz),7.67(1H,br.d,J=5.1Hz),7.92(1H,t,J=5.7 Hz), 8.40 (1H, s), 8.92 (1H, br), 11.98 (1H, br).
ESI(LC/MS positive mode) m/z 581 (M+H) Step C
Synthesis of 5-(ethylcarbamoylmethoxyamino-methyl)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-h ydroxy-ethoxy)-benzamide (Compound C-14) HOB/moo I
HN O
F
\/a Ora F , O F
Using (E)-5-(ethylcarbamoylmethoxyimino-methyl)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-( 2-hydroxy-ethoxy)-benzamide obtained in Step B, synthesis was performed according to the procedure described in Step D of Example 19 to give 5-(ethylcarbamoylmethoxyamino-methyl)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-h ydroxy-ethoxy)-benzamide.

'H-NMR(CD3OD, 270MHz) S(PPM) 1.14 (3H, t, J = 7.3 Hz), 3.26 (2H, q, J = 7.3 Hz), 3.68-3.76 (2H, m), 3.91-3.99 (2H, m), 4.09 (2H, s), 4.13 (2H, s), 6.61 (1 H, dt, J =
4.6, 8.6 Hz), 7.35 (1 H, ddd, J = 1.1, 1.9, 8.6 Hz), 7.45 (IH, dd, J = 1.9, 10.8 Hz), 7.50 (1H, dd, J =
1.9, 7.2 Hz).
ESI(LC/MS positive mode) m/z 583 (M+H) [Example 21]
3,4-Difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(propylcarbamoylmetho xyamino-methyl)-benzamide (Compound C-15) Step A

Synthesis of 2-aminooxy-N-propyl-acetamide O

Using (1,3-dioxo-1,3-dihydro-isoindol-2-yloxy)-acetic acid methyl ester obtained in Step A of Example 19 and n-propylamine as an amine, synthesis was performed according to the procedure described in Step A of Example 20 to give 2-aminooxy-N-propyl-acetamide.
'H-NMR(CD3OD, 270MHz) 8(PPM) 0.93 (3H, t, J = 7.3 Hz), 1.54 (2H, hextet, J =
7.3 Hz),3.21 (2H, t, J = 7.3 Hz), 4.07 (2H, s).
Step B
Synthesis of (E)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(propylcarbamoylme thoxyimino-methyl)-benzamide HO,,-,,,,O
I
HN O
HH F
/ N \
I
0.1 F

F
Using 2-aminooxy-N-propyl-acetamide obtained in Step A, synthesis was performed according to the procedure described in Step C of Example 19 to give (E)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(propylcarbamoylme thoxyimino-methyl)-benzamide.

'H-NMR(DMSO-d6, 270MHz) 8(PPM) 0.82 (3H, t, J = 7.3 Hz), 1.43 (2H, hextet, J =
7.3 Hz), 3.07 (2H, q, J = 7.3 Hz), 3.51-3.62 (2H, m), 3.76-3.90 (2H, m), 4.56(2H, s), 4.72 (111, br), 6.82 (1 H, dt, J = 4.1, 8.6 Hz), 7.40 (1 H, dd, J = 0.8, 8.6 Hz), 7.61 (111, dd, J
= 1.6, 10.8 Hz), 7.62-7.71 (111, m), 7.90 (1 H, br. t, J = 5.7 Hz), 8.40 (111, s), 8.92 (1 H, br), 11.98 (1 H, br).
ESI(LC/MS positive mode) m/z 595 (M+H) Step C
Synthesis of 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(propylcarbamoylmetho xyamino-methyl)-benzamide (Compound C-15) HOB/~

i HN O
F
HH HH , a O-N F ' O

Using (E)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(propyicarbamoylme thoxyimino-methyl)-benzamide obtained in Step B, synthesis was performed according to the procedure described in Step D of Example 19 to give 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(propylcarbamoylmetho xyamino-methyl)-benzamide.

1H-NMR(CD3OD, 270MHz) 8(PPM) 0.93 (3H, t, J = 7.3 Hz), 1.54 (2H, hextet, J =
7.3 Hz), 3.19 (2H, q, J = 7.3 Hz), 3.68-3.76 (2H, m), 3.91-3.99 (2H, m), 4.09 (2H, s), 4.14 (2H, s), 6.61 (1H, dt, J = 4.3, 8.6 Hz), 7.35 (1H, ddd, J = 1.1, 1.9, 8.6 Hz), 7.46 (1H, dd, J = 1.9, 10.8 Hz), 7.50 (1H, dd, J = 1.9, 7.2 Hz).
ESI(LC/MS positive mode) m/z 597 (M+H) [Example 22]
3,4-Difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(isopropylcarbamoyl-m ethoxyamino)-methyl]-benzamide (Compound C-16) Step A
Synthesis of 2-aminooxy-N-isopropyl-acetamide a Y~~- oNH2 Using (1,3-dioxo-1,3-dihydro-isoindol-2-yloxy)-acetic acid methyl ester obtained in Step A of Example 19 and isopropylamine as an amine, synthesis was performed according to the procedure described in Step A of Example 20 to give 2-aminooxy-N-isopropyl-acetamide.

1H-NMR(CD3OD, 270MHz) 8(PPM) 1.17 (6H, d, J = 6.5 Hz), 3.98-4.12 (1H, m), 4.05 (2H, s).
Step B
Synthesis of (E)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(isopropylcarbamoy 1-methoxyimino)-methyl] -benzamide HO,-,,-~, Q

HN O
F
M
o N F I/ 1 Using 2-aminooxy-N-isopropyl-acetamide obtained in Step A, synthesis was performed according to the procedure described in Step C of Example 19 to give (E)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5 -[(isopropylcarbamoy 1-methoxyimino)-methyl]-benzamide.

1H-NMR(DMSO-d6, 270MHz) 8(PPM) 1.08 (3H x 2, d, J = 6.8 Hz), 3.57 (2H, br), 3.83 (2H, br), 3.85-4.02 (1H, m), 4.54(2H, s), 4.72 (1H, br), 6.82 (1H, dt, J = 4.1, 8.6 Hz), 7.41 (1H, br. d, J =
8.6 Hz), 7.61 (1 H, dd, J = 1.6, 10.8 Hz), 7.62-7.76 (1 H, m), 7.90 (1 H, br.
t, J = 5.7 Hz), 8.40 (1 H, s), 8.88 (1H, br), 11.98 (1H, br).
ESI(LC/MS positive mode) m/z 595 (M+H) Step C
Synthesis of 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(isopropylcarbamoyl-m ethoxyamino)-methyl]-benzamide (Compound C-16) HO,,~~O
I
HN O
F
a , o,aF~,I
F
Using (E)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(isopropylcarbamoy 1-methoxyimino)-methyl]-benzamide obtained in Step B, synthesis was performed according to the procedure described in Step D of Example 19 to give 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(isopropylcarbamoyl-m ethoxyamino)-methyl]-benzamide.

iH-NMR(CD3OD, 270MHz) S(PPM) 1.16 (3H x 2, d, J = 6.8 Hz), 3.72 (2H, t, J =
4.6 Hz), 3.95 (2H, t, J = 4.6 Hz), 3.96-4.12 (1 H, m), 4.07 (2H, s), 4.13 (2H, s), 6.61 (1 H, dt, J = 4.6, 8.6 Hz), 7.32-7.38 (1H, m), 7.46 (1 H, dd, J = 1.9, 10.8 Hz), 7.51 (IH, dd, J = 1.9, 7.0 Hz).
ESI(LC/MS positive mode) m/z 597 (M+H) [Example 23]
5-(Dimethylcarbamoylmethoxyamino-methyl)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benzamide (Compound C-17) Step A
Synthesis of 2-aminooxy-N,N-dimethyl-acetamide NHZ

O

To a solution of (1,3-dioxo-1,3-dihydro-isoindol-2-yloxy)-acetic acid methyl ester (992 mg, 4.22 mmol) obtained in Step A of Example 19 in methanol (4 ml) was added dimethylamine (2.0 M solution in methanol, 10 ml), and the mixture was stirred at 60 C for 16 hours. After cooling down to room temperature, the reaction mixture was concentrated under reduced pressure. The resultant residue was dissolved in methanol (7 ml), and methylhydrazine (0.27 ml, 6.74 mmol) was added thereto. The mixture was stirred at 60 C for 15 hours. After cooling down to room temperature, the reaction mixture was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (40 g, CH2C12/MeOH
(40:1 to 30:1)) to give 2-aminooxy-N,N-dimethyl-acetamide (125 mg, 25%) as a colorless syrup.
'H-NMR(CD3OD, 270MHz) S(PPM) 2.94 (3H, s), 2.97 (3H, s),4.37 (2H, s).
Step B
(E)-5-(Dimethylcarbamoylmethoxyimino-methyl)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino) -N-(2-hydroxy-ethoxy)-benzamide HOB~

HN O
F
0,N I F
O F

Using 2-aminooxy-N,N-dimethyl-acetamide obtained in Step A, synthesis was performed according to the procedure described in Step C of Example 19 to give (E)-5-(dimethylcarbamoylmethoxyimino-methyl)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benzamide.

1H-NMR(DMSO-d6, 270MHz) S(PPM) 1.08 (6H, d, J = 6.8 Hz), 3.57 (2H, br), 3.83 (2H, br), 3.85-4.02 (1 H, m), 4.54 (2H, s), 4.72 (1 H, br), 6.81 (1 H, dt, J = 4.1, 8.6 Hz), 7.40 (1 H, dd, J =
1.1, 8.6 Hz), 7.61 (11-1, dd, J =1.9, 10.8 Hz), 7.63-7.76 (1H, m), 8.36 (1H, s), 8.88 (1H, br), 11.96 (1H, br).
ESI(LC/MS positive mode) m/z 581 (M+H) Step C
Synthesis of 5-(dimethylcarbamoylmethoxyamino-methyl)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-( 2-hydroxy-ethoxy)-benzamide (Compound C-17) HO,-~~,O
I
HN O
F
I I

F I
O F

Using (E)-5-(dimethylcarbamoylmethoxyimino-methyl)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benzamide obtained in Step B, synthesis was performed according to the procedure described in Step D of Example 19 to give 5-(dimethylcarbamoylmethoxyamino-methyl)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-( 2-hydroxy-ethoxy)-benzamide.

1H-NMR(CD3OD, 270MHz) 6(PPM) 2.93 (3H, s), 2.96 (3H, s), 3.73 (2H, t, J = 4.6 Hz), 3.97 (2H, t, J = 4.6 Hz), 4.13 (2H, s), 4.3 8 (2H, s), 6.61 (1 H, dt, J = 4.6, 8.6 Hz), 7.31-7.3 8 (1 H, m), 7.44 (1 H, dd, J = 1.9, 10.5 Hz), 7.54 (1 H, dd, J = 1.9, 7.3 Hz).
ESI(LC/MS positive mode) m/z 583 (M+H) [Example 24]
5-[(2-ethylcarbamoyl-ethoxyamino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2 -hydroxy-ethoxy)-benzamide (Compound C-18) Step A
Synthesis of N-(2-ethylcarbamoyl-ethoxy)-acetimidic acid ethyl ester '----~N 0 N-H
To a known compound, 3 -(1 -ethoxyethylideneaminooxy)-propanoic acid methyl ester (CAS No. 97164-30-2, 300 mg, 1.5 85 mmol) was added a 2 M solution of methylamine in methanol (7 ml), and the mixture was stirred at 60 C for 13 hours. The reaction mixture was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography to give N-(2-ethylcarbamoyl-ethoxy)-acetimidic acid ethyl ester (182 mg, 57%
yield).

'H-NMR(CDCl3, 400MHz) 6(PPM) 1.13(3H, t, J=7.1Hz), 1.27(3H, t, J=7.3Hz), 1.92(3H, s), 2.53(2H, t, J=5.9Hz), 3.26-3.33(2H, m), 4.00(2H, q, J=7.3Hz), 4.15(2H, t, J=5.9Hz), 5.93(1H, br.s) Step B
Synthesis of (E)-5-[(2-ethylcarbamoyl-ethoxyimino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benzamide HO0,~~O,N O F

o ,a b N O-NF I
H F

To N-(2-ethylcarbamoyl-ethoxy)-acetimidic acid ethyl ester (180 mg, 0.890 mmol) obtained in Step A was added 2 M hydrochloric acid (2 ml), and the mixture was stirred at room temperature for 30 minutes. The reaction mixture was concentrated to give a crude product of 3-aminooxy-N-ethyl-propionamide hydrochloride as a residue. To this residue, a mixed solvent of tetrahydrofuran/methanol (3:1, 20 ml) and 3,4-difluoro-2-(2-fluoro-4-iodophenylamino-5-formyl-N-(2-hydroxy-ethoxy)-benzamide (500 mg, 1.078 mmol) obtained in Step F of Example 1 were added, and the mixture was stirred for 1 hour. The reaction mixture was poured into purified water, and the resultant mixture was extracted with ethyl acetate. The combined organic layers were dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography to give (E)-5-[(2-ethylcarbamoyl-ethoxyimino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benzamide (200 mg, 31 % yield).
ESI(LC/MS positive mode) m/z 595 (M+H) Step C
Synthesis of 5-[(2-ethylcarbamoyl-ethoxyamino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2 -hydroxy-ethoxy)-benzamide H ~ 6 N F I
H F
To (E)-5-[(2-ethylcarbamoyl-ethoxyimino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benzamide (40 mg, 0.067 mmol) obtained in Step B was added dichloromethane (2 ml). The mixture was stirred at room temperature, and borane-pyridine complex (40 l) and dichloroacetic acid (40 l) were added thereto. After stirring for 1 hour, the reaction mixture was poured into purified water, and the resultant mixture was extracted with dichloromethane. The combined organic layers were dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography to give 5- [(2-ethylcarbamoyl-ethoxyamino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2 -hydroxy-ethoxy)-benzamide (C-18, 29 mg, 75% yield).

1H-NMR(CD3OD, 400MHz) 8(PPM) 1.07(3H, t, J=7.2Hz), 2.37(2H, t, J=6.2Hz), 3.16(2H, q, J=7.2Hz), 3.71(2H, t, J=4.4Hz), 3.86(2H, t, J=6.2Hz), 3.95(2H, t, J=4.4Hz), 4.04(2H, s), 6.60(1H, ddd, J=8.8, 8.8, 4.4Hz), 7.33(1H, br.d, J=8.3Hz), 7.42-7.45(2H, m) ESI(LC/MS positive mode) m/z 597 (M+H) [Example 25]
5-[(2-Propylcarbamoyl-ethoxyamino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benzamide (Compound C-19) Step A
Synthesis of N-(2-propylcarbamoyl-ethoxy)-acetimidic acid ethyl ester H

To a known compound, 3-(1-ethoxy-ethylideneaminooxy)-propanoic acid methyl ester (CAS No. 97164-30-2, 300 mg, 1.585 mmol) were added methanol (3 ml) and n-propylamine (1.3 ml), and the mixture was stirred at 55 C for 15 hours. The reaction mixture was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography to give N-(2-propylcarbamoyl-ethoxy)-acetimidic acid ethyl ester (296 mg, 86% yield).

1H-NMR(CDC13, 400MHz) 8(PPM) 0.92(3H, t, J=7.4Hz), 1.26(3H, t, J=6.8Hz), 1.47-1.56(2H, m), 1.93(3H, s), 2.55(2H, t, J=6.OHz), 3.22(2H, dt, J=6.8, 6.8Hz), 4.01(2H, q, J=6.8Hz), 4.16(2H, t, J=6.OHz), 5.83(111, br.s) ESI(LC/MS positive mode) m/z 217 (M+H) Step B
Synthesis of (E)-5-[(2-propylcarbamoyl-ethoxyimino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino) -N-(2-hydroxy-ethoxy)-benzamide N O'er I F
H F

Using N-(2-propylcarbamoyl-ethoxy)-acetimidic acid ethyl ester obtained in Step A, synthesis was performed according to the procedure described in Step B of Example 24 to give (E)-5-[(2-propylcarbamoyl-ethoxyimino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino) -N-(2-hydroxy-ethoxy)-benzamide.

'H-NMR(CD3OD, 400MHz) S(PPM) 0.89(3H, t, J=7.3Hz), 1.46-1.52(2H, m), 2.59(2H, t, J=6.4Hz), 3.13(2H, t, J=7.lHz), 3.72(2H, t, J=4.6Hz), 3.95(2H, t, J=4.6Hz), 4.43(2H, t, J=6.4Hz), 6.71(1H, ddd, J=8.8, 8.8, 4.4Hz), 7.37-7.39(1H, m), 7.46(1H, dd, J=10.7, 2.0Hz), 7.81(1H, br.d, J=5.9Hz), 8.22(1 H, s) ESI(LC/MS positive mode) m/z 609 (M+H) Step C
Synthesis of 5-[(2-propylcarbamoyl-ethoxyamino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-( 2-hydroxy-ethoxy)-benzamide (Compound C-19) HO,_,-~,O,mN 0 F

0 H M"6 N O-N F I
H F
Using (E)-5-[(2-propylcarbamoyl-ethoxyimino)-methyl] -3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino) -N-(2-hydroxy-ethoxy)-benzamide obtained in Step B, synthesis was performed according to the procedure described in Step C of Example 24 to give 5- [(2-propylcarbamoyl-ethoxyamino)-methyl] -3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-( 2-hydroxy-ethoxy)-benzamide (Compound C-19).

'H-NMR(CD3OD, 400MHz) S(PPM) 0.87(3H, t, J=7.6Hz), 1.39-1.50(2H, m), 2.38(2H, t, J=6.iHz), 3.09(2H, t, J=7.OHz), 3.71(2H, t, J=4.6Hz), 3.86(2H, t, J=6.1Hz), 3.95(2H, t, J=4.6Hz), 4.04(2H, s), 6.59(1H, ddd, J=8.8, 8.8, 4.4Hz), 7.32-7.35(1H, m), 7.42-7.45(2H, m) ESI(LC/MS positive mode) m/z 611 (M+H) [Example 26]
5-[(2-Isopropylcarbamoyl-ethoxyamino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benzamide (Compound C-20) Step A
Synthesis of N-(2-isopropylcarbamoyl-ethoxy)-acetimidic acid ethyl ester N 'J~~ 0 -N
H
To a known compound, 3-(1-ethoxy-ethylideneaminooxy)-propanoic acid methyl ester (CAS No. 97164-30-2, 300 mg, 1.585 mmol) were added methanol (3 ml) and isopropylamine (1.4 ml), and the mixture was stirred at 55 C for 14 hours. Additional isopropylamine (1.0 ml) was added, and the mixture was stirred for 3 hours using a focused microwave synthesis system (Discover TM, CEM) at 100 W. The reaction mixture was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography to give N-(2-isopropylcarbamoyl-ethoxy)-acetimidic acid ethyl ester (46 mg, 13%
yield).
'H-NMR(CDC13, 400MHz) 8(PPM) 1.12(6H, d, J=7.3Hz), 1.28(3H, t, J=7.lHz), 1.91(3H, s), 2.50(2H, t, J=5.9), 4.00(2H, q, J=7.1Hz), 4.06-4.11(1H, m), 4.15(2H, t, J=5.9Hz), 5.72(1H, br.s) Step B
Synthesis of (E)-5-[(2-isopropylcarbamoyl-ethoxyimino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylami no)-N-(2-hydroxy-ethoxy)-benzamide HO0_,--,O,HN O F
0 H I i "~N)O-N~ i F
H F

Using N-(2-isopropylcarbamoyl-ethoxy)-acetimidic acid ethyl ester obtained in Step A, synthesis was performed according to the procedure described in Step B of Example 24 to give (E)-5-[(2-isopropylcarbamoyl-ethoxyimino)-methyl] -3,4-difluoro-2-(2-fluoro-4-iodo-phenylami no)-N-(2-hydroxy-ethoxy)-benzamide.

1H-NMR(CD3OD, 400MHz) 8(PPM) 1.02(6H, d, J=6.4Hz), 2.47(2H, t, J=6.4Hz), 3.63(2H, t, J=4.6Hz), 3.84-3.89(3H, m), 4.34(2H, t, J=6.4Hz), 6.62(1H, ddd, J=8.8, 8.8, 4.4Hz), 7.29(1H, br.d, J=8.8Hz), 7.37(1H, dd, J=10.3, 2.0Hz), 7.72(1H, br.d, J=6.8Hz), 8.13(1H, s) ESI(LC/MS positive mode) m/z 609 (M+H) Step C
Synthesis of 5- [(2-isopropylcarbamoyl-ethoxyamino)-methyl] -3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benzamide (Compound C-20) HO~-,O,HHN O F
o H

~Nlk~O-N F
H F
Using (E)-5-[(2-isopropylcarbamoyl-ethoxyimino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylami no)-N-(2-hydroxy-ethoxy)-benzamide obtained in Step B, synthesis was performed according to the procedure described in Step C of Example 24 to give 5-[(2-isopropylcarbamoyl-ethoxyamino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benzamide (Compound C-20).

1H-NMR(CD3OD, 400MHz) S(PPM) 0.99(6H, d, J=6.4Hz), 2.27(2H, t, J=6.1Hz), 3.62(2H, t, J=4.6Hz), 3.76(2H, t, J=6.1Hz), 3.80-3.87(3H, m), 3.95(2H, s), 6.50(1H, ddd, J=8.8, 8.8, 4.4Hz), 7.24(1H,br.d, J=8.8Hz), 7.33-7.36(2H, m) ESI(LC/MS positive mode) m/z 611 (M+H) [Example 27]
3,4-Difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-methylcarbamoyl-et hoxyamino)-methyl]-benzamide (Compound C-6) Step A
Synthesis of N-(2-methylcarbamoyl-ethoxy)-acetimidic acid ethyl ester H

To a solution of a known compound, 3-(1-ethoxyethylideneaminooxy)-propanoic acid methyl ester (CAS No. 97164-30-2, 41.3 g, 0.218 mol) in methanol (150 ml) was added methylamine (40% solution in methanol, 200 ml) at room temperature, and the mixture was stirred at 60 C for 12 hours. The reaction mixture was concentrated under reduced pressure to give N-(2-methylcarbamoyl-ethoxy)-acetimidic acid ethyl ester (41.0 g, 100%).
1H-NMR(CDC13, 400MHz) 8(PPM) 1.28(3H, t, J=7.lHz), 1.92(3H, s), 2.56(2H, t, J=5.9Hz), 2.81(3H, d, J=4.9Hz), 4.00(2H, q, J=7.1Hz), 4.15(2H, t, J=5.9Hz), 6.00(1H, br.s) Step B
Synthesis of 3-aminooxy-N-methyl-propionamide O

H

N-(2-Methylcarbamoyl-ethoxy)-acetimidic acid ethyl ester (41.0 g, 0.218 mol) obtained in Step A was dissolved in methanol (210 mL), and the solution was cooled to 0 C. To this solution, conc. hydrochloric acid (28 mL) was added dropwise over 30 minutes, and the mixture was stirred at room temperature for 30 minutes. The reaction mixture was cooled again, to which 28% aqueous ammonia (42 mL) was added portionwise, and then concentrated under reduced pressure. To the resultant residue, acetonitrile was added, and insoluble matter was filtered off. The filtrate was concentrated under reduced pressure to give 3-aminooxy-N-methyl-propionamide (25.8 g, 99%).

1H-NMR(CDC13, 400MHz) S(PPM) 2.43(2H, t, J=6.4Hz), 2.70(3H, s), 3.85(2H, t, J=6.4Hz) Step C
Synthesis of (E)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5 -[(2-methylcarbamoyl -ethoxyimino)-methyl]-benzamide H
HO- / N O F
O H
N
O I \ ~ \
--N" v _O F I
H

Using 3-aminooxy-N-methyl-propionamide obtained in Step B, synthesis was performed according to the procedure described in Step C of Example 19 to give 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-methylcarbamoyl-eth oxyimino)-methyl]-benzamide as a white solid.

1H-NMR(CD3OD, 270MHz) S(PPM) 2.59(2H, t, J=5.9Hz), 2.72(3H, s), 3.72(2H, m), 3.95(2H, m), 4.43(2H, t, J=5.9Hz), 6.72(1H, dt, J=8.9, 4.3Hz), 7.39(1H, m), 7.47(1H, dd, J=10.9, 2.0Hz), 7.80(1H, dd, J=6.9, 2.0Hz), 8.23(1H, s) ESI(LC/MS positive mode) m/z 581 (M+H) Step D
Synthesis of 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-methylcarbamoyl-eth oxyamino)-methyl]-benzamide (Compound C-6) HOB/~
HN O
F
o a \
M- ~\0 ~ F LL 1 Using 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-methylcarbamoyl-eth oxyimino)-methyl]-benzamide obtained in Step C, synthesis was performed according to the procedure described in Step C of Example 24 to give 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-methylcarbamoyl-eth oxyamino)-methyl]-benzamide (Compound C-6).

1H-NMR(CD3OD, 270MHz) 8(PPM) 2.32-2.41(2H, m), 2.69(3H, s), 3.71(2H, t, J=4.6Hz), 3.85(2H, t, J=5.9Hz), 3.89-3.96(2H, m), 4.04(2H, s), 6.54-6.64(1H, m), 7.34(1H, br.d, J=9.9Hz), 7.43(2H, dd, J=10.6, 1.9Hz) ESI(LC/MS positive mode) m/z 583 (M+H) [Example 28]
3,4-Difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(3 -methylcarbamoyl-pr opoxyamino)-methyl]-benzamide (Compound C-21) Step A
Synthesis of 4-(1,3-dioxo-1,3-dihydro-isoindol-2-yloxy)-butyric acid ethyl ester OWN

To a solution of 4-bromo-n-butyric acid ethyl ester (1.2 g, 6.13 mmol) in dimethylformamide (9 ml) were added N-hydroxyphthalimide (1.5 g, 9.19 mmol) and Hunig base (N,N-diisopropylethylamine, 2.13 mL) at room temperature, and the mixture was stirred at 80 C over night. The reaction mixture was poured into saturated aqueous ammonium chloride, and the resultant mixture was extracted with ethyl acetate (3x 40 ml). The combined organic layers were washed with saturated brine (2x 30 ml), dried over Na2SO4, and concentrated under reduced pressure. The resultant residue was purified by silica gel column chromatography (100 g, n-hexane/ethyl acetate (2:1)) to give 4-(1,3-dioxo-1,3-dihydro-isoindol-2-yloxy)-butyric acid ethyl ester (1.47 g, 100%).

'H-NMR(CDC13, 270MHz) 5(PPM) 1.28 (3H, t, J = 6.9 Hz), 2.11 (2H, q, J = 6.9 Hz), 2.64 (2H, t, J = 7.3 Hz), 4.17 (2H, q, J = 7.3 Hz), 4.27 (2H, t, J = 6.3 Hz), 7.72-7.79 (211, m), 7.81-7.89 (2H, m).
Step B
Synthesis of 4-aminooxy-N-methyl-butylamide H

O

To a solution of 4-(1,3-dioxo-1,3-dihydro-isoindol-2-yloxy)-butyric acid ethyl ester (997.5 mg, 4.59 mmol) obtained in Step A in methanol (4 mL) was added methylamine (40%
solution in methanol, 10 ml, 98.0 mmol), and the mixture was stirred at 60 C
overnight. The reaction mixture was concentrated under reduced pressure, and methylene chloride was added to the resultant residue to precipitate a solid, which was filtered and washed with methylene chloride. The combined filtrate and washing were concentrated under reduced pressure. The residue was purified by silica gel column chromatography (30 g, CH2CI2/MeOH
(8:1)) to give 4-aminooxy-N-methyl-butylamide (467.3 mg, 77%) as a colorless syrup.

1H-NMR(CDC13, 27OMHz) S(PPM) 1.94 (2H, q, J = 6.3 Hz), 2.25 (2H, t, J = 6.9 Hz), 2.81 (3H, d, J = 4.6 Hz), 3.70 (t, J = 5.9 Hz).

Step C
Synthesis of (E)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(3 -methylcarbamoyl -propoxyimino)-methyl]-benzamide HO - 0.N O F
H
,,N 0-N, I F I

To 4-aminooxy-N-methyl-butylamide (1.79 g, 13.54 mmol) obtained in Step B were added a mixed solvent of tetrahydrofuran/methanol (3:1, 100 ml) and 3,4-difluoro-2-(2-fluoro-4-iodophenylamino-5-formyl-N-(2-hydroxy-ethoxy)-benzamide (5.00 g, 10.41 mmol) obtained in Step F of Example 1, and the mixture was stirred for 13 hours. The reaction mixture was concentrated under reduced pressure to an extent where a little solvent remained, and acetonitrile was added thereto to precipitate the product. This precipitate was filtered, washed with acetonitrile, and dried under reduced pressure to give (E)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(3-methylcarbamoyl -propoxyimino)-methyl]-benzamide (4.93 g, 79% yield).

1H-NMR(DMSO-d6, 270MHz) S(PPM) 1.88 (2H, qui, J = 7.6 Hz), 2.17 (2H, t, J =
6.9 Hz), 2.56 (3H,d,J=4.6Hz),3.57(2H,br.q,J=4.6Hz),3.83(2H,t,J=4.6Hz),4.14(2H, t, J = 6.3 Hz), 4.73 (1 H, t, J = 5.6 Hz, OH), 6.80 (1 H, td, J = 8.9, 4.0 Hz), 7.40 (1 H, br.
d, J = 8.6 Hz), 7.61 (1H, dd, J = 10.9, 2.0 Hz), 7.68 (1H, br. d, J = 5.6 Hz), 7.77 (1H, br q, J = 4.6 Hz, NH), 8.26 (1H, s), 8.87 (1H, br. s, NH), 11.99 (1H, br. s, NH).
ESI(LC/MS positive mode) m/z 595 (M+H) Step D
Synthesis of 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(3 -methylcarbamoyl-pr opoxyamino)-methyl]-benzamide (Compound C-21) HO,_,,-0O,N O F
H
~N)f"-,O-N I F

To (E)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(3 -methylcarbamoyl -propoxyimino)-methyl]-benzamide (50 mg, 0.084 mmol) obtained in Step C was added dichloromethane (6 ml). The mixture was stirred at room temperature, and borane-pyridine complex (67 l, 0.673 mmol) and dichloroacetic acid (55 l, 0.673 mmol) were added thereto.
After stirring for 14 hours, the reaction mixture was diluted with ethyl acetate, and washed with purified water and saturated aqueous sodium chloride. The organic layer was dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography to give 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(3-methylcarbamoyl-pr opoxyamino)-methyl]-benzamide (Compound C-21, 32 mg, 65% yield).

'H-NMR(CD3OD, 400MHz) 8(PPM) 1.72-1.84(2H, m), 2.18(2H, t, J=7.3Hz), 2.67(3H, s), 3.63(2H, t, J=6.4Hz), 3.70(2H, t, J=4.4Hz), 3.94(2H, t, J=4.4Hz), 4.05(2H, s), 6.58(1H, ddd, J=8.8, 8.8, 4.4Hz), 7.32-7.35(1H, m), 7.43(1H, dd, J=10.5, 1.7Hz), 6.84(1H, br.d, J=6.8Hz) ESI(LC/MS positive mode) m/z 597 (M+H) [Example 29]
5-[(2-Acetylamino-ethoxyamino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-h ydroxy-ethoxy)-benzamide (Compound C-7) Step A

Synthesis of 2-aminooxy-ethyl-carbamic acid t-butyl ester )ONH2 O

The title compound was synthesized according to the methods described in J.
Med.
Chem., 1999, 42, 2007 and W002/06213.

Step B
(E)- {2-[2,3-difluoro-4-(2-fluoro-4-iodo-phenylamino)-5-(2-hydroxy-ethoxycarbamoyl)-benzylid eneaminooxy]-ethyl}-carbamic acid tert-butyl ester HO~~
HN O
F
a , O
F
I/
Y I
O F

Using 2-aminooxy-ethyl-carbamic acid t-butyl ester obtained in Step A, synthesis was performed according to the procedure described in Step C of Example 19 to give (E)- { 2- [2, 3 -difluoro-4-(2-fluoro-4-io do-phenylamino)-5-(2-hydroxy-ethoxycarbamoyl)-benzylid eneaminooxy] -ethyl} -carbamic acid tert-butyl ester.

IH-NMR(DMSO-d6, 270MHz) S(PPM) 1.38 (9H, s), 3.26 (2H, t, J = 5.9 Hz), 3.56 (2H, t, J = 4.3 Hz), 3.83 (2H, t, J = 4.3 Hz), 4.36 (2H, t, J = 5.9 Hz), 4.72 (1H, s), 6.79 (114, m), 6.95 (1H, m), 7.38 (1H, d, J = 8.9 Hz), 7.60 (1H, d, J = 10.6 Hz), 7.69 (1H, d, J = 6.3 Hz), 8.27(1H, s), 8.86 (0.5H, br.s), 11.98 (0.5H, br.s) ESI(LC/MS positive mode) m/z 639 (M+H) Step C
Synthesis of (E)-5-[(2-amino-ethoxyimino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydr oxy-ethoxy)-benzamide HO -HN O
F
H2N,/~O~N~ F

F
To a solution of { 2- [2, 3 -difluoro-4-(2-fluoro-4-iodo-phenylamino)-5 -(2-hydroxy-ethoxycarbamoyl)-benzylidenea minooxy] -ethyl} -carbamic acid tert-butyl ester (55 mg, 0.31 mmol) prepared in Step B in ethyl acetate (5 ml) was added 1 N HCl solution in ethyl acetate (1 ml), and the mixture was stirred at room temperature for 1.5 hours. After completion of the reaction, the reaction mixture was neutralized with saturated solution of sodium bicarbonate (50 ml), and extracted with ethyl acetate (3x 100 ml). The extract was washed with saturated brine, and the organic layer was dried over anhydrous sodium sulfate, and filtered. The solvent was evaporated under reduced pressure, and after washing with diethyl ether (10 ml), the residue was recrystallized from methanol to give (E)-5- [(2-amino-ethoxyimino)-methyl] -3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydr oxy-ethoxy)-benzamide (17.31 mg, 37% yield) as a pale yellow solid.
'H-NMR(DMSO-d6, 270MHz) S(PPM) 3.05 (2H, t, J = 5.6), 3.56(2H, t, J = 4.6), 3.80 (2H, t, J =
4.6), 4.28 (2H, t, J = 5.3 Hz), 6.79 (1 H, m), 7.3 8 (1 H, d, J = 9.0 Hz), 7.61 (1 H, d, J = 10.9 Hz), 8.08 (111, d, J = 7.3 Hz), 8.26 (1 H, s) ESI(LC/MS positive mode) m/z 539 (M+H) Step D
Preparation of (E)-5-[(2-acetylamino-ethoxyimino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2 -hydroxy-ethoxy)-benzamide HOB -I
HN O
F
/ a \

\O/N \ F I
O F

To a solution of (E)-5-[(2-amino-ethoxyimino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydr oxy-ethoxy)-benzamide (8.14 mg, 0.02 mmol) described in Step C in a mixed solvent of dimethylformamide (1 ml) and methanol (5 ml) was added N-methoxydiacetamide (100 mg, 0.76 mmol), and the mixture was stirred at room temperature for 14 hours.
After completion of the reaction, the solvent was evaporated under reduced pressure, and the resultant residue was purified with Mega Bond Elut silica gel (Varian, 5 g).
(E)-5-[(2-Acetylamino-ethoxyimino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-( 2-hydroxy-ethoxy)-benzamide (8.10 mg, 92% yield) was obtained as a pale yellow solid from fractions eluted with 6% methanol/methylene chloride.

'H-NMR(DMSO-d6, 400MHz) 6(PPM) 1.82 (3H, s), 3.36 (2H, t, J = 5.6),3.57(2H, br.s), 3.84 (2H, br.s), 4.15 (2H, t, J = 5.6 Hz), 4.73 (111, s), 6.81 (1 H, m), 7.40 (1 H, d, J = 7.6 Hz), 7.61 (111, d, J = 10.8 Hz), 7.71 (1H, br.s), 8.00 (1H, s), 8.28 (1H, s), 8.90 (0.5H, br.s), 11.98 (0.5H, br.s) ESI(LC/MS positive mode) m/z 581 (M+H) Step E
Synthesis of 5- [(2-acetylamino-ethoxyamino)-methyl] -3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hy droxy-ethoxy)-benzamide (Compound C-7) To (E)-5-[(2-acetylamino-ethoxyimino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2 -hydroxy-ethoxy)-benzamide (57.6 mg, 99.3 mol) obtained in Step D was added dichloromethane (2.5 ml). The mixture was stirred at room temperature, and borane-pyridine complex (80 l, 0.79 mmol) and dichloroacetic acid (67 l, 0.80 mmol) were added thereto.
After stirring for 3 hours, water (10 ml) and saturated aqueous sodium bicarbonate (2 ml) were added to the reaction mixture, which was then extracted with methylene chloride (15 ml and 2x 8 ml). The combined organic layers were washed with aqueous sodium bicarbonate (8 ml) and saturated aqueous sodium chloride(8 ml), dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (methylene chloride/methanol (10:1)) to give 5-[(2-acetylamino-ethoxyamino)-methyl] -3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hy droxy-ethoxy)-benzamide (Compound C-7, 44.0 mg, 76%).

'H-NMR(CD3OD, 270MHz) S(PPM) 1.92 (3H, s), 3.36 (2H, t, J = 5.6), 3.67 (2H, t, J = 5.4 Hz), 3.70 (2H, t, J = 4.8 Hz), 3.93 (2H, t, J = 4.3 Hz), 4.07 (2H, s), 6.59 (1H, td, J = 8.7, 4.5 Hz), 7.34 (1 H, br. d, J = 8.4 Hz), 7.44 (1 H, dd, J = 10.7, 2.0 Hz), 1H is overlapped with the dd peak at 7.44 ppm. 2H is overlapped with the peak of H2O around 3.3ppm.
ESI(LC/MS positive mode) mlz 583 (M+H) [Example 30]
3,4-Difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-propionylamino-eth oxyamino)-methyl]-benzamide (Compound C-34) Step A
Synthesis of (E)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-propionylamino-ethoxyimino)-methyl]-benzamide HO,,-,,,-,, I
HN O
F
HH N
N~ - 0 N \ I F I j I

To a solution of propionic acid (84 l, 1.13 mmol) in methylene chloride (2 ml) were added 1-ethyl-3-(3'-dimethylaminopropyl)carbodiimide hydrochloride (212.0 mg, 1.10 mmol) and N-hydroxybenzotriazole (156.5 mg, 1.17 mmol) at room temperature, and the mixture was stirred at room temperature for 30 minutes to give a solution of an active ester of propionic acid in methylene chloride (0.55 M). To a solution of 5-[(2-amino-ethoxyimino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benzamide (101.9 mg, 0.189 mmol) obtained in Step C of Example 29 in DMF (2.5 ml) were added dimethylaminopyridine (54.0 mg, 0.442 mmol) and the solution of the active ester in methylene chloride (0.55 M, 0.35 ml, 0.193 mmol) obtained above, and the mixture was stirred at room temperature. With monitoring the reaction, 0.18 ml (0.10 mmol) and 0.20 ml (0.11 mmol) of the active ester solution were added after 40 minutes and 13 hours, respectively, and the mixture was stirred for another 8 hours. Water (10 ml) was added to the reaction mixture, which was then extracted with ethyl acetate (20 ml + 3x 10 ml). The combined organic layers were washed with aqueous sodium bicarbonate (2x 15 ml), 0.2 N hydrochloric acid (15 ml), and saturated brine (15 ml), dried over sodium sulfate, and concentrated under reduced pressure.
The resultant residue was triturated with n-hexane/ethyl acetate (3:1) to give an oxime, (E)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-propionylamino-ethoxyimino)-methyl]-benzamide (94.6 mg, 84%) as a pale yellow solid.

ESI(LC/MS positive mode) m/z 595 (M+H) Step B
Synthesis of 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-propionylamino-etho xyamino)-methyl]-benzamide (Compound C-34) HOB -HN O
F
N
H HH
N\/~OA F LI
O F
The oxime, (E)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5 -[(2-propionylamino-ethoxyimino)-methyl]-benzamide (33.0 mg, 51.0 mol) obtained in Step A was suspended in methylene chloride (1 ml), and dichloroacetic acid (60 ml) and borane-pyridine complex (70 l) were added thereto at room temperature. The mixture was stirred at room temperature for 2 hours. Water (6 ml) and aqueous sodium bicarbonate (2 ml) were added to the reaction mixture, which was then extracted with methylene chloride (2x 10 ml). The combined organic layers were washed with aqueous sodium bicarbonate (5-fold dilution of saturated solution, 8 ml) and saturated brine (8 ml), dried over sodium sulfate, and concentrated under reduced pressure. The resultant residue was purified by silica gel column chromatography (methylene chloride/methanol (40:3)) to give 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-propionylamino-etho xyamino)-methyl]-benzamide (Compound C-34, 21.6 mg, 71%) as a colorless syrup.

'H-NMR(CD3OD, 270MHz) S(PPM) 1.09 (314, t, J = 7.8 Hz), 2.17 (2H, q, J = 7.8 Hz), 3.33 (2H, t, J = 5.7 Hz), 3.67 (2H, dd (like t), J = 5.1, 5.7 Hz), 3.70( 2H, br. t, J =
5.1 Hz), 3.93 (2H, br. t, J
= 4.1 Hz), 4.07 (2H, s), 6.58 (114, td, J = 8.9, 4.3 Hz), 7.34 (111, ddd, J =
8.4, 1.6, 1.4 Hz), 7.44 (1H, dd, J = 10.5, 1.9 Hz), 1H is overlapped with the dd peak at 7.44 ppm.
ESI(LC/MS positive mode) m/z 597 (M+H) [Example 31 ]
3,4-Difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-isobutyrylamino-eth oxyamino)-methyl]-benzamide (Compound C-35) Step A
Synthesis of (E)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-isobutyrylamino-ethoxyimino)-methyl] -benzamide HOB/~
HN O
HH F
H / N \
N\/~O~N \ I F

To a solution of isobutyric acid (172 l, 1.85 mmol) in a mixed solvent of methylene chloride and DMF (3 ml and 1 ml) were added 1-ethyl-3-(3'-dimethylaminopropyl)carbodiimide hydrochloride (352.1 mg, 1.84 mmol) and N-hydroxybenzotriazole (250.0 mg, 1.87 mmol) at room temperature, and the mixture was stirred at room temperature for 30 minutes to give a solution of an active ester of isobutyric acid in methylene chloride - DMF
(0.46 M). To a suspension of 5 - [(2-amino-ethoxyimino)-methyl] -3 ,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benzamide (106.7 mg, 0.198 mmol) obtained in Step C of Example 29 in DMF (2 ml) were added dimethylaminopyridine (51.2 mg, 0.419 mmol) and the solution of the active ester in methylene chloride (0.46 M, 0.50 ml, 0.23 mmol) obtained above, and the mixture was stirred at room temperature. With monitoring the reaction, 0.20 ml (0.09 mmol) and 0.20 ml (0.09 mmol) of the active ester solution were added after 20 minutes and 13 hours, respectively, and the mixture was stirred for another 8 hours. Water (10 ml) was added to the reaction mixture, which was then extracted with ethyl acetate (20 ml + 3x 10 ml). The combined organic layers were washed with aqueous sodium bicarbonate (2x 10 ml), 0.2 N hydrochloric acid (15 ml), and saturated brine (10 ml), dried over sodium sulfate, and concentrated under reduced pressure.
The resultant residue was triturated with n-hexane/ethyl acetate (3:1) to give an oxime, (E)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5 - [(2-isobutyrylamino-ethoxyimino)-methyl]-benzamide (98.5 mg, 82%) as a pale yellow solid.
ESI(LC/MS positive mode) m/z 609 (M+H) Step B
Synthesis of 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-isobutyrylamino-etho xyamino)-methyl]-benzamide (Compound C-35) HO,,,,-,,O
I
HN O
F
N
HH ~ ~
N~/~O~N
O F
The oxime, (E)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-isobutyrylamino-ethoxyimino)-methyl]-benzamide (28.8 mg, 47.3 mol) obtained in Step A was suspended in methylene chloride (1 ml), and dichloroacetic acid (60 ml) and borane-pyridine complex (70 l) were added thereto at room temperature. The mixture was stirred at room temperature for 2 hours. Water (6 ml) and aqueous sodium bicarbonate (2 ml) were added to the reaction mixture, which was then extracted with methylene chloride (2x 10 ml). The combined organic layers were washed with aqueous sodium bicarbonate (5-fold dilution of saturated solution, 8 ml) and saturated brine (8 ml), dried over sodium sulfate, and concentrated under reduced pressure. The resultant residue was purified by silica gel column chromatography (methylene chloride/methanol (40:3)) to give 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-isobutyrylamino-etho xyamino)-methyl] -benzamide (Compound C-35, 20.5 mg, 71%) as a colorless syrup.
1H-NMR(CD3OD, 270MHz) 8(PPM) 1.07 (6H, d, J = 6.8 Hz), 2.40 (1H, quinted, J =
6.8 Hz), 3.34 (2H, t, J = 5.4 Hz), 3.67 (2H, t, J = 5.4 Hz), 3.70 (2H, br. t, J = 4.9 Hz), 3.93 (2H, br. t, J =
4.3 Hz), 4.07 (2H, s), 6.58 (1 H, td, J = 8.6, 4.1 Hz), 7.34 (1 H, ddd, J =
8.6, 1.9, 1.1 Hz), 7.44 (111, dd, J = 10.8, 1.9 Hz), 1 H is overlapped with the dd peak at 7.44 ppm.
ESI(LC/MS positive mode) m/z 611 (M+H) [Example 32]
2-(4-Ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)5-[(2-hydroxy-2-methyl -propoxyamino)-methyl]-benzamide (Compound C-29) Step A
(E)-2-(4-Ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)-5-[(2-hydroxy-2-m ethyl-propoxyimino)-methyl]-benzamide HOB/~
O
HN O
F
HO ON I F I( 10 F

(E)-3,4-difluoro-2-(2-fluoro-4-iodophenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-hydroxy-2-methyl-propoxyimino)-methyl]-benzamide (200 mg, 0.35 mmol), Pd(CH3CN)2C12 (4.5 mg, 0.0176 mmol), triphenylphosphine-3,3',3"-trisulfonic acid trisodium salt (25.0 mg, 0.037 mmol), N('Pr)2Et (48.0 mg, 0.37 mmol), trimethylsilyl acetylene (172 mg, 1.76 mmol), and CuI (3.4 mg, 0.0176 mmol) were stirred in MeOH at room temperature for 1 hour, and the solvent was evaporated. The resultant residue was added to THF/H20 containing tetrabutylammonium fluoride (0.35 mmol), and the mixture was stirred for 1 hour. EtOAc was added thereto, and the organic layer was washed with 0.4 N aqueous HC1, dried over Na2SO4, and evaporated. The resultant residue was purified by silica gel chromatography (CH2C12/MeOH as a developing solvent) to give a title compound (99 mg).

'H-NMR(CD3OD, 270MHz) S(PPM) 1.26(6H, s), 3.46(1H, s), 3.71(2H, m), 3.95(2H, m), 4.08(2H, s), 6.85(1H, m), 7.16(d, J=8.9Hz), 7.21(1H, dd, J=13.9, 1.6Hz), 7.82(1H, br.d, J=5.3 Hz), 8.31(1H, s) ESI(LC/MS positive mode) m/z 466 (M+H) Step B
2-(4-Ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)5-[(2-hydroxy-2-methyl -propoxyamino)-methyl]-benzamide (Compound C-29) HOB/~O

HN O
F
, HO
%~ ,a I
O F
F
Using (E)-2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)-5-[(2-hydroxy-2-me thyl-propoxyimino)-methyl]-benzamide obtained in Step A as a starting material, synthesis was performed according to the procedure described in Step C of Example 24 to give 2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)5-[(2-hydroxy-2-methyl-propoxyamino)-methyl]-benzamide (Compound C-29).

'H-NMR(DMSO-d6, 400MHz) 8(PPM) 1.00(6H, s), 3.53(2H,br), 3.81(2H, br), 3.96(2H, d, J=5.9Hz), 4.08(1H, s), 4.40(1H, br), 4.71(1H, br), 6.69(1H, m), 6.97(1H, t, J=5.9Hz), 7.13(1H, d, J=8.8Hz), 7.30(1H, d, J=11.6Hz), 7.49(1H, d, J=6.8Hz), 8.66(1H, br), 11.73(1H, br). The peak of a methylene group is overlapping with that of H2O peak.
ESI(LC/MS positive mode) m/z 468 (M+H) [Example 33]
2-(4-Ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)-5-[(2-hydroxy-ethoxya mino)-methyl]-benzamide (Compound C-2) Step A
Synthesis of (E)-2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)-5-[(2-hydroxy-etho xyimino)-methyl]-benzamide HO~~O
HN O
F
HO,,-,,-~OA
F
F

Starting from (E)3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5- [(2-hydroxy-ethoxyi mino)-methyl]-benzamide obtained in Step B of Example 6, synthesis was performed according to the procedure described in Step A of Example 32 to give (E)-2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)-5-[(2-hydroxy-etho xyimino)-methyl]-benzamide.

'H-NMR(CD3OD, 270MHz) 8(PPM): 3.45(1H, s), 3.72(2H, dd, J=4.9, 4.3Hz), 3.82(2H, dd, J=5.3, 4.6Hz), 3.96(2H, dd, 4.9, 4.3Hz), 4.27(2H, t, J=4.9Hz), 6.85(1H, td, J=8.6, 4.6Hz), 7.18(2H, m), 7.83(1H, dd, J=7.0, 2.0Hz), 8.39(1H,s) ESI(LC/MS positive mode) m/z 438 (M+H) Step B
Synthesis of 2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)-5 - [(2-hydroxy-ethoxya mino)-methyl]-benzamide (Compound C-2) HOB/~
HN O
F
HOB/~ N

HN I I
F
F
Using (E)-2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)-5-[(2-hydroxy-etho xyimino)-methyl]-benzamide obtained in Step A, synthesis was performed according to the procedure described in Step C of Example 24 to give 2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)-5 - [(2-hydroxy-ethoxya mino)-methyl]-benzamide (Compound C-2).

'H-NMR(DMSO-d6, 400MHz) S(PPM) 3.46(2H, t, J=4.7Hz), 3.55(4H,m), 3.82(2H, t, J=4.7Hz), 3.96(2H, d, J=5.8Hz), 4.08(IH, s), 4.53(IH, br), 4.71(1H, br), 6.70(1H, m), 6.85(1H, t, J=5.8Hz), 7.13(1H, d, J=8.3Hz), 7.30(1H, dd, J=12.OHz, 2.0Hz), 7.49(1H, d, J=6.3Hz), 8.66(1H, br), 11.72(IH, br).

ESI(LC/MS positive mode) m/z 440 (M+H) [Example 34]
3,4-Difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-(2-hydroxy-1,1-dimethyl-ethoxymethyl)-N-(2-hydroxy-ethoxy)-benzamide (Compound B-19) Step A
Synthesis of 2-methyl-propane-1,2-diol HO -""-x OH

2-Methyl-propane-1,2-diol is a known compound (CAS No. 558-43-0), and may be prepared by one of the method described in the following literatures:
Zh. Obshch. Khim. 7, 1319 (1937), Chem. Zentralbl. 109, 561 (1938), Meml. Poudres, 28, 263 (1938), and Chem. Zentralbl. 110, 2398 (1939).
Practically, the title compound was prepared by the following procedure.
To a suspension of lithium aluminum hydride (321.3 mg, 8.47 mmol) in THE (5 ml) was added dropwise a solution of 2-hydroxy-2-methyl-propionic acid methyl ester (commercially available, 1.0 g, 8.47 mmol) in THE (3 ml), and the mixture was stirred at room temperature for 4 hours. Water (0.70 ml) was added to the reaction mixture, which was stirred for additional 10 minutes. The resultant mixture was filtered through a mixed bed of celite powder and sodium sulfate powder. The filtrate was concentrated under reduced pressure, and the residue was diluted with THF, dried over sodium sulfate, and concentrated under reduced pressure to give 2-methyl-propane-1,2-diol (659.7 mg, 86%) as an oily crude product.
'H-NMR(DMSO-d6, 270MHz) S(PPM) 1.03 (6H, s), 3.13 (2H, d, J = 5.6 Hz), 4.10 (1H, s), 4.50 (1H,t,J=5.9Hz).

Step B
Synthesis of 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-(2-hydroxy-1,1-dimethyl-ethoxymethyl)-N-(2-h ydroxy-ethoxy)-benzamide (Compound B- 19) HOB -HN O
F
o ~ I a I
HOF
/X\ F
Using 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-formyl-N-(2-hydroxy-ethoxy)-benzamide obtained in Step F of Example 1 as a starting material, and 2-methyl-propane-1,2-diol obtained in Step A instead of ethylene glycol used as a reagent in Step G of Example 1, synthesis similar to that in Step G of Example 1 was performed. The resultant cyclic acetal was subjected to reduction condition similar to that in Step H of Example 1 to give the title compound.

'H-NMR(DMSO-d6, 270MHz) S(PPM) 1.18 (6H, s), 3.35 (2H, overlapped with H2O
peak in DMSO, singlet after addition of D20), 3.37(2H, s), 3.56(2H, dd, J = 4.9, 4.6 Hz), 3.83 (2H, dd, J
= 4.9, 4.6 Hz), 4.50 (2H, s), 4.69 (1H, t, J = 5.6 Hz, disappeared after addition of D20), 4.70 (1H, br. s, disappeared after addition of D20), 6.60(1H, td, J = 8.7, 4.1 Hz), 7.36 (1H, br. d, J = 8.4 Hz),7.46 (1 H, br. d, J = 6.6 Hz), 7.57 (1 H, dd, J = 10.9, 1.8 Hz), 8.61 (1 H, br. s, disappeared after addition of D20), 11.80 (1H, br. s, disappeared after addition of D20).
ESI(LC/MS positive mode) m/z 569(M+H) [Example 35]
Synthesis of 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(2-methanesulfonyl-etho xymethyl)-benzamide (Compound B-12) HO

F
H
N
F

To a suspension of 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-formyl-N-(2-hydroxy-ethoxy)-benzamide (52 mg, 0.108 mmol) obtained in Step F of Example 1 in methylene chloride (anhydrous, 5 mL) were added copper trifluoromethanesulfonate (20 mg, 0.005 mmol), methanesulfonylethanol (200 L), and triethylsilane (500 L, 3.13 mmol) under a nitrogen atmosphere, and the mixture was stirred thoroughly for a whole day and night. After completion of the reaction, the reaction mixture was extracted with ethyl acetate, and the organic layer was washed sequentially with 2%
aqueous EDTA, water, and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The resultant residue was purified by preparative TLC
(No. 5744, Merck, 5% methanol/methylene chloride as a developing solvent) to give 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5 -(2-methanesulfonyl-etho xymethyl)-benzamide (13.3 mg, 21%) as a white solid.

1H-NMR(CD3OD, 270MHz) S(PPM) 3.02(3H, s), 3.41(2H, dd, J=5.4, 5.1Hz), 3.71(2H, dd, J=4.8, 4.5Hz), 3.95(4H, m), 4.60(2H, s), 6.63(1H, td, J=8.9, 4.311z), 7.35(1H, br.d, J=8.4Hz), 7.45(1H, dd, J=10.9, 1.8Hz) , 7.50(1H, m) ESI(LC/MS positive mode) m/z 589(M+H) [Example 36]
3,4-Difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(3-oxo-[
1,2]oxazinan-2-ylmethyl)-benzamide (Compound G-1) HO~~O,N O
a F
~zO, (i 0 F

(E)-3,4-Difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(3-methylc arbamoyl-propoxyimino)-methyl]-benzamide (8.0 g, 13.5 mmol) obtained in Step C
of Example 28 was suspended in methylene chloride (240 ml), and borane-pyridine complex (5.45 ml, 53.8 mmol) and dichloroacetic acid (6.65 ml, 80.8 mmol) were added thereto at room temperature.
The reaction mixture was stirred at room temperature for 15 hours, and dichloromethane was removed under reduced pressure with a rotary evaporator. The residue was diluted with 1,2-dichloroethane (240 ml), and the mixture was stirred at 60 C for 8 hours, and filtered. The residue obtained by concentrating the filtrate was diluted with ethyl acetate (800 ml), and washed sequentially with water (400 ml), saturated aqueous sodium bicarbonate (400 ml), and saturated brine (400 ml). The organic layer was dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (CH2C12/MeOH (25:1)) to give 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(3-oxo-[
1,2]oxazinan-2-ylmethyl)-benzamide (Compound G-1, 6.93 g, 91% yield).
This compound may also be obtained as a by-product (18 mg, 35% yield) in a synthesis of 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(3-methylcarbamoyl-pr opoxyamino)-methyl]-benzamide (Compound C-21) in Example 28.

1H-NMR(CD3OD, 400MHz) 6(PPM) 2.10(2H, quinted, J=6.8Hz), 2.53(2H, t, J=6.8Hz), 3.72(2H, t, J=4.4Hz), 3.92(2H, t, J=4.4Hz), 4.04(2H, t, J=6.8Hz), 4.86(2H, s), 6.61 (1H, ddd, J=8.8, 8.8, 3.9Hz), 7.33-7.36(1H, m), 7.41(1H, dd, J=7.0, 1.7Hz), 7.45(1H, dd, J=10.3, 2.0Hz) ESI(LC/MS positive mode) m/z 566 (M+H) [Example 37]
3,4-D iuoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(3 -oxo-isoxazolidin-2-yl methyl)-benzamide (Compound G-2) HO~~O,N 0 F
N I/ F I

To (E)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-methylcarbamoyl -ethoxyimino)-methyl]-benzamide (9.60 g, 15.54 mmol) were added sequentially dichloromethane (300 ml) and borane-pyridine complex (11.70 ml, 115.80 mmol) to give a suspension. This mixture was stirred at room temperature, and dichloroacetic acid (9.51 ml, 115.80 mmol) was added dropwise thereto over 10 minutes. After the mixture was stirred at room temperature for 13 hours, dichloromethane was removed under reduced pressure with a rotary evaporator, and the resultant residue was diluted with 1,2-dichloroethane (300 ml). This mixture was stirred at 60 C for 6 hours, diluted with ethyl acetate, and washed sequentially with 0.1 M aqueous hydrochloric acid, saturated aqueous sodium bicarbonate, and saturated aqueous sodium chloride. The organic layer was dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography to give the title compound (8.28 g, 90% yield).
This compound may also be obtained as a by-product in a synthesis of 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-methylcarbamoyl-eth oxyamino)-methyl]-benzamide (Compound C-6) in Example 27.
1H-NMR(CD3OD, 400MHz) 8(PPM) 2.84(2H, t, J=8.3Hz), 3.70(2H, t, J=4.7Hz), 3.93(2H, t, J=4.7Hz), 4.36(214, t, J=8.3Hz), 4.76(2H, s), 6.62(1H,ddd, J=8.8, 8.8, 3.9Hz), 7.34-7.36(1H, m), 7.39(1H, br.d, J=5.4Hz), 7.45(1H, dd, J=10.5, 1.7Hz) ESI(LC/MS positive mode) m/z 552 (M+H) [Example 38]
2-(4-Ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)-5-(3 -oxo-isoxazolidin-2 -ylmethyl)-benzamide (Compound G-5) HO~~p HN O
F
O
N
F
O F

3,4-Difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(3 -oxo-isoxazol idin-2-ylmethyl)-benzamide (36.9 mg, 66.9 mol) obtained in Example 37, bis(acetonitrile)dichloropalladium (II) (3.5 mg, 13.5 mol), 3,3',3"-phosphinidine-tris(benzenesulfonic acid) trisodium salt (19.0 mg, 33.4 mol), and copper iodide (I) (2.6 mg, 13.6 gmol) were suspended in methanol (2.5 ml) under a nitrogen atmosphere. To this suspension, N,N-diisopropylethylamine (14.0 l, 80.4 mol) and trimethylsilylacetylene (47.3 l, 334.7 gmol) were added at room temperature, and the mixture was stirred for 1 hour. The reaction mixture was diluted with methylene chloride (30 ml), and washed with saturated brine (2x 15 ml). The organic layer was dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The resultant residue was dissolved in THE (2 ml). To this solution, tetrabutylammonium fluoride (1.0 M
solution in THF, 0.10 ml, 0.10 mmol) was added, and the mixture was stirred for 1 hour, and then concentrated under reduced pressure. The resultant residue was purified by preparative TLC
(EtOAc/MeOH
(8:1))to give 2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)-5-(3-oxo-isoxazolidin-2 -ylmethyl)-benzamide (Compound G-5, 11.1 mg, 37%) as a brown oil.

1H-NMR(CD3OD, 270MHz) 8(PPM) 2.85 (2H, t, J = 8.1 Hz), 3,43 (111, s), 3.70 (2H, t, J = 4.6 Hz), 3.93 (2H, t, J = 4.6 Hz), 4.36 (2H, t, J = 8.1 Hz), 4.78 (214, s), 6.75 (1H, dt, J = 4.6, 8.6 Hz), 7.11-7.17 (1 H, m), 7.20 (1 H, dd, J = 1.8, 11.9 Hz), 7.41 (1 H, dd, J =1.8, 7.3 Hz).
ESI(LC/MS positive mode) m/z 450 (M+H) [Example 39]
2-(4-Ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)-5-(3-oxo-[1,2]oxadinan -2-ylmethyl)-benzamide (Compound G-4) HOB/,,O
I
HN O
F
F
O F
Using 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(3-oxo-[1,2]oxazinan-2-ylmethyl)-benzamide obtained in Example 36, synthesis was performed according to the procedure described in Example 38 to give 2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)-5-(3 -oxo-[ 1, 2] oxadinan -2-ylmethyl)-benzamide (Compound G-4).
1H-NMR(CD3OD, 270MHz) 8(PPM) 2.11 (2H, quint., J = 6.9 Hz), 2.54 (2H, t, J =
6.9 Hz), 3,43 (1H, s), 3.70 (2H, t, J = 4.5 Hz), 3.93 (2H, t, J = 4.5 Hz), 4.05 (211, t, J =
6.9 Hz), 4.87 (214, s), 6.75 (1 H, dt, J = 4.6, 8.6 Hz), 7.10-7.17 (1 H, m), 7.19 (1 H, dd, J = 1.9, 11.9 Hz), 7.43 (1 H, dd, J
= 1.9, 7.0 Hz).
ESI(LC/MS positive mode) m/z 464 (M+H) [Example 40]
5-(4,4-Dimethyl-3-oxo-isoxazolidin-2-ylmethyl)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benzamide (Compound G-3) Step A

Synthesis of 3-(1,3-dioxo-1,3-dihydro-isoindol-2-yloxy)-2,2-dimethyl-propionic acid methyl ester To methyl hydroxypivalate (1.31 g, 9.89 mmol) were added tetrahydrofuran (40 ml), hydroxyphthalimide (3.23 g, 19.78 mmol) and triphenylphosphine (6.48 g, 24.73 mmol). After this solution was cooled to 0 C, diisopropyl azodicarboxylate (4.87 ml, 24.73 mmol) was added dropwise to the solution. While being allowed to warm gradually, the reaction mixture was stirred for 12 hours, and concentrated under reduced pressure. The residue was roughly purified by silica gel column chromatography to give the title compound (922 mg).
'H-NMR(CDC13, 400MHz) 8(PPM) 1.35(6H, s), 3.74(3H, s), 4.26(2H, s), 7.27-7.76(2H, m), 7.81-7.85(2H, m) Step B
Synthesis of 3-aminooxy-2,2,N-trimethyl-propionamide '~-'0 O -NN2 To 3-(1,3-dioxo-1,3-dihydro-isoindol-2-yloxy)-2,2-dimethyl-propionic acid methyl ester (800 mg) obtained in Step A was added a 40% solution of methylamine in methanol (6 ml), and the mixture was stirred at 60 C for 13 hours. After the reaction mixture was concentrated under reduced pressure, dichloromethane was added to the residue, and insoluble matter was filtered.
The filtrate was concentrated, and the residue was purified by silica gel column chromatography to give the title compound (202 mg).
'H-NMR(CD3OD, 400MHz) 8(PPM) 1.14(6H, s), 2.71(3H, s), 3.64(2H, s) Step C
Synthesis of 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-[(2-methyl-2-methylcarba moyl-propoxyimino)-methyl]-benzamide N 0"~ F I I
H F

The title compound was synthesized as a mixture of E/Z geometric isomers, using the procedure described in Step C of Example 19, from 3-aminooxy-2,2,N-trimethyl-propionamide obtained in Step B and 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-formyl-N-(2-hydroxy-ethoxy-benzamide obtained in Step F of Example 1.
ESI(LC/MS positive mode) m/z 609 (M+H) Step D
5-(4,4-Dimethyl-3-oxo-isoxazolidin-2-ylmethyl)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benzamide (Compound G-3) HO~~O.N O F
0 ~ N
F b N I

The title compound was synthesized by a similar procedure to that in Example 36 from 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-[(2-methyl-2-methylcarba moyl-propoxyimino)-methyl]-benzamide obtained in Step C.

'H-NMR(CD3OD, 400MHz) 8(PPM) 1.20(6H, s), 3.70(2H, t, J=3.7Hz), 3.92(2H, t, J=3.7Hz), 4.07-4.12(5H, m), 4.77(2H, s), 6.61-6.65(1H, m), 7.35(1H, d, J=8.3Hz), 7.39(1H, d, J=7.3Hz), 7.44(1H, br.d, J=10.7Hz) ESI(LC/MS positive mode) m/z 580 (M+H) [Example 41 ]

5- { [Acetyl-(2-hydroxy-ethoxy)-amino ] -methyl } -3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benzamide (Compound F- 15) HO~~

F
H
H0,,_,,,-~ 0 N
I
N
I
F I

CH3CO2H (300 mg), EDC - HC1(958 mg), and HODhbt (816 mg) were mixed in CH2C12 (5 mL) for 2 hours to give an active ester solution. A portion of this solution (0.2 mL) was added to a solution of 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-hydroxy-ethoxyamin o)-methyl]-benzamide (80 mg) obtained in Example 6 and NEt3 (29 L) in THF, and the mixture was stirred for 12 hours. The reaction mixture was washed with 0.3 N aqueous HCI and aqueous NaHCO3, and subjected to silica gel chromatography (CH2C12/MeOH as a developing solvent) to give the title compound (12.0 mg).

1H-NMR(CD3OD, 400MHz) 8(PPM) 2.21(3H, s), 3.69(2H, t, J=4.5Hz), 3.73(2H, t, J=4.5Hz), 3.92(2H, t, J=4.5Hz), 4.03(2H, t, J=4.5Hz), 4.91(2H, s), 6.60(IH, m), 7.34(1H, d, J=8.3Hz), 7.43(2H, m) ESI(LC/MS positive mode) m/z 584 (M+H) In Examples 42 to 53 below, an alkoxyamine as a starting material was acetylated by a similar procedure to that in Example 41 to give the target compound.

[Example 42]
5- { [Acetyl-(2-hydroxy-ethoxy)-amino] -methyl } -2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluor o-N-(2-hydroxy-ethoxy)-benzamide (Compound F-25) H0~~0 F
H
HO~~0 N
I

'H-NMR(CD3OD, 400MHz) S(PPM) 2.23(3H, s), 3.42(1H, s), 3.69(2H, t, J=4.4Hz), 3.74(2H, t, J=4.4Hz), 3.93(2H, t, J=4.4Hz), 4.03(2H, t, J=4.4Hz), 4.93(2H, s), 6.74(1 H, m), 7.13(1 H, d, J=8.3Hz), 7.18(1H, dd, J=8.3Hz, 2.0Hz), 7.35(1H, d, J=7.4) ESI(LC/MS positive mode) m/z 482 (M+H) [Example 43]
5- { [Acetyl-(3-hydroxy-propoxy)-amino]-methyl } -3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino) -N-(2-hydroxy-ethoxy)-benzamide (Compound F- 16) F
HO~~O ( N
H /
I
N F I

1H-NMR(CD3OD, 400MHz) S(PPM) 1.83(2H, m), 2.21(3H, s), 3.61(2H, t, J=6.3Hz), 3.70(2H, t, J=4.4), 3.92(2H, br), 4.05(2H, t, J=6.3Hz), 4.90(2H, s), 6.61(1H, m), 7.35(1H, d, J=8.8Hz), 7.40(1H, d, J=5.4Hz), 7.44(1H, dd, J=10.7Hz, 1.9Hz) ESI(LC/MS positive mode) m/z 598 (M+H) [Example 44]
5-f [Acetyl-(2-hydroxy-2-methyl-propoxy)-amino] -methyl } -3,4-difluoro-2-(2-fluoro-4-iodo-phe nylamino)-N-(2-hydroxy-ethoxy)-benzamide (Compound F-17) HO~~

F
H
HO/~0 I N
I
~N / F / I

'H-NMR(CD3OD, 400MHz) S(PPM) 1.22(6H, s), 2.20(3H, s), 3.70(2H, t, J=4.4Hz), 3.78(2H, s), 3.92(2H, br), 4.91(2H, s), 6.61(1 H, m), 7.34(1 H, d, J=7.4Hz), 7.43(2H, m) ESI(LC/MS positive mode) m/z 612 (M+H) [Example 45]
5- { [Acetyl-(2-hydroxy-2-methyl-propoxy)-amino]-methyl } -2-(4-ethynyl-2-fluoro-phenylamino) -3,4-difluoro-N-(2-hydroxy-ethoxy)-benzamide (Compound F-26) HO~~

F
H
HOi~O N I

'H-NMR(CD3OD, 400MHz) S(PPM) 1.22(6H, s), 2.21(3H, s), 3.42(1H, s), 3.69(2H, t, J=4.6Hz), 3.79(2H, s), 3.92(2H, t, J=4.6Hz), 4.92(2H, s), 6.74(1 H, m), 7.13(1H, d, J=8.8Hz), 7.19(1 H, dd, J=11.7Hz, 2.0Hz), 7.44(2H, d, J=6.8Hz) ESI(LC/MS positive mode) m/z 510 (M+H) [Example 46]
5- [Acetyl-methoxy-amino-methyl] -3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benzamide (Compound F-2) F
H
O I N

,Y N F11: I

'H-NMR(DMSO-d6, 400MHz) 8(PPM) 2.10(3H, s), 3.55(2H, t, J=4.4Hz), 3.81(2H,br), 4.81(2H, s), 6.63(1H, m), 7.32(1H, br), 7.34(1H, m), 7.56(114, dd, J=10.7Hz, 2.0Hz), 8.53(1H, br), 11.85(1H, br), The peak of CH3(methoxy) was overlapping with that of H2O in solvent.
ESI(LC/MS positive mode) m/z554 (M+H) [Example 47]
5-[(Acetyl-hydroxy-amino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydrox y-ethoxy)-benzamide (Compound F-13) H0~\

H
OH 1 \ I \
N

N / F / I

'H-NMR(DMSO-d6, 400MHz) 6(PPM) 2.01(3H, s), 3.77(2H, br), 3.98(2H,br), 4.71(2H, s), 6.58(1H, m), 7.31(2H, m), 7.53(1H, d, J=10.8Hz), 8.50(1H, br), 9.96(1H, br), 11.81(1H, br), ESI(LC/MS positive mode) m/z540 (M+H) [Example 48]
5-[(Acetoxy-acetyl-amino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy -ethoxy)-benzamide (Compound F-14) I

H
AO N
\ /N FI
X101( The title compound was obtained as a by-product in the preparation of 5-[(Acetyl-hydroxy-amino)-methyl] -3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydrox y-ethoxy)-benzamide in Example 47.
'H-NMR(DMSO-d6, 400MHz) 6(PPM) 1.22(3H, s), 2.17(3H, s), 3.54(2H, br), 3.80(2H,br), 4.85(2H, s), 6.62(1H, m), 7.37(2H, m), 7.56(1H, d, J=6.8Hz), 8.64(1H, br), 11.85(1H, br), ESI(LC/MS positive mode) m/z582 (M+H) [Example 49]
5- { [Acetyl-(2-methyl sulfanyl-ethoxy)-amino] -methyl } -3,4-difluoro-2-(2-fluoro-4-iodo-phenyla mino)-N-(2-hydroxy-ethoxy)-benzamide (Compound F-21) HO,,-,~0 I

F
H
N
N

'H-NMR(DMSO-d6, 400MHz) 8(PPM) 2.04(3H, s), 2.12(3H, s), 2.66(2H, t, J=6.3Hz), 3.80(1H, br), 4.02(2H, m), 4.82(2H, s), 6.62(1H, m), 7.34(2H, d,br, J=8.3Hz), 7.55(1H, dd, J=10.7Hz, 1.7Hz), 8.52(1H, s), 11.8(1H, s). The peaks of two methylene groups are overlapping with that of H2O peak.
ESI(LC/MS positive mode) m/z 614 (M+H) [Example 50]
5-{ [Acetyl-(3-methylsulfanyl-propoxy)-amino]-methyl}-3,4-difluoro-2-(2-fluoro-4-iodo-phenyla mino)-N-(2-hydroxy-ethoxy)-benzamide HO~~

F
H
\SN \
N /
F I

1H-NMR(DMSO-d6, 400MHz) 8(PPM) 1.75(2H, m), 2.04(3H, s), 2.12(3H, s), 2.66(2H, t, J=6.3Hz), 3.80(2H, br), 4.02(2H, m), 4.82(2H, s), 6.62(1H, m), 7.34(2H, d,br, J=8.3Hz), 7.55(1H, dd, J=10.7Hz, 1.7Hz), 8.52(1H, s), 11.8(1H, s). A peak of methylene group is overlapping with that of H2O peak.
ESI(LC/MS positive mode) m/z 628 (M+H) [Example 51]
5- { [Acetyl-(2-acetylamino-ethoxy)-amino] -methyl } -3,4-difluoro-2-(2-fluoro-4-iodo-phenylamin o)-N-(2-hydroxy-ethoxy)-benzamide (Compound F- 18) HO,,_,,-~0 I

F
H H
~N\/~ 1 0 I \ N ( \
0 \ /N / F / I
~0 F

'H-NMR(DMSO-d6, 400MHz) S(PPM) 1.76(3H, s), 2.07(3H, s), 3.23(2H, m), 3.80(2H, br), 3.89(2H, t, J=5.OHz), 4.79(2H, s), 6.64(1H, m), 7.33(2H, m), 7.56(1H, dd, J=10.7Hz, 2.0Hz), 8.00(IH, t, J=5.6Hz), 8.53(1H, br), 11.8(1H, br). A peak of methylene group is overlapping with that of H2O peak.
ESI(LC/MS positive mode) m/z 625 (M+H) [Example 52]
5-{[Acetyl-(2-propionylamino-ethoxy)-amino]-methyl}-3,4-difluoro-2-(2-fluoro-4-iodo-phenyla mino)-N-(2-hydroxy-ethoxy)-benzamide (Compound F-19) F
H H

'iff 'H-NMR(DMSO-d6, 400MHz) 6(PPM) 0.94(3H, t, J=7.7Hz), 2.04(2H, d, J=7.7Hz), 2.07(3H, s), 3.24(2H, m), 3.80(2H, br), 3.89(2H, t, J=5.OHz), 4.79(2H, s), 6.64(1H, m), 7.33(2H, m), 7.55(1H, dd, J=10.7Hz, 2.0Hz), 7.94(1H, t, J=5.lHz), 8.53(1H, br), 11.85(1H, br). A
peak of methylene group is overlapping with that of H2O peak.
ESI(LC/MS positive mode) m/z 639 (M+H) [Example 53]
5- { [Acetyl-(2-isobutyrylamino-ethoxy)-amino]-methyl } -3,4-difluoro-2-(2-fluoro-4-iodo-phenyla mino)-N-(2-hydroxy-ethoxy)-benzamide (Compound F-20) HO,,_,,-~0 I

F
H H

1H-NMR(DMSO-d6, 400MHz) 8(PPM) 0.92(6H, d, J=6.8Hz), 2.07(3H, s), 2.30(1H, hepta, J=6.8Hz), 3.24(2H, m), 3.80(2H, br), 3.90(2H, t, J=5.OHz), 4.79(2H, s), 6.63(1H, m), 7.33(2H, m), 7.55(IH, dd, J=10.7Hz, 1.5Hz), 7.91(1H, t, J=5.6Hz), 8.53(1H, br), 11.84(1H, br). The peak of a methylene group is overlapping with that of H2O peak.
ESI(LC/MS positive mode) m/z 639 (M+H) [Example 54]
3,4-Difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(3-oxo-[
1,4,2]dioxazina n-2-ylmethyl)-benzamide (Compound H-1) HO-,-~0 I

F
H

rl~ I0 I \ N
QYN

3,4-Difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-hydroxy-eth oxyamino)-methyl]-benzamide (100 mg, 0.185 mmol) obtained in Example 6, N,N'-disuccinimidyl carbonate (59 mg, 0.231 mmol) and NEt3 (113 mg, 1.12 mmol) were stirred in a mixed solvent of CH2C12/THF (1 mL/1 mL) at room temperature for 10 hours.
The reaction mixture was purified by silica gel column chromatography (CH2C12/MeOH
as a developing solvent) to give the title compound (12.5 mg).
'H-NMR(DMSO-d6, 400MHz) 8(PPM) 3.54(2H, br), 3.82(2H, br), 4.16(2H, t, J=4.4), 4.42(2H, t, J=4.4Hz), 4.76(2H+1H, s+br), 6.65(1H, m), 7.35(IH, d, J=8.3Hz), 7.40(1H, d, J=6.3Hz), 7.56(1H, d, J=10.8Hz), 8.68(1H, br), 11.88(1H, br) ESI(LC/MS positive mode) m/z 568 (M+H) [Example 55]

2-(4-Ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)-5-(3-oxo-[ 1,4,2]dioxazi nan-2-ylmethyl)-benzamide (Compound H-2) H0~\

F
H
r~ 1p + N , \ /N F
~[

The title compound was synthesized by a similar procedure to that in Example 38 from 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(3 -oxo-[
1,4,2]dioxazinan -2-ylmethyl)-benzamide obtained in Example 54.

'H-NMR(DMSO-d6, 400MHz) S(PPM) 3.54(2H, br), 3.83(2H, br), 4.09(1H, br), 4.17(2H, br), 4.42(2H, br), 4.72(1H, br), 4.78(2H, br), 6.77(1H, br), 7.14(IH, d, J=6.8Hz), 7.31(1H, d, J=11.8Hz), 7.42(1H, d, J=6.4Hz), 8.78(1H, br), 11.87(1H, br) ESI(LC/MS positive mode) m/z 466 (M+H) [Example 56]
3,4-Difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5- {{methoxy-(2-methoxy-acetyl)-amino]-methyl}-benzamide (Compound F-6) HO\,.\O
HN O
F
p \O

N \ I F
O F

To a solution of methoxyacetic acid (9.0 l, 0.12 mmol) in methylene chloride (1 ml) were added 3-hydroxy-4-oxo-3,4-dihydro-1,2,3-benzotriazine (18.9 mg, 0.12 mmol) and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (22.5 mg, 0.12 mmol), and the mixture was stirred for 3 hours. This solution was added dropwise to a solution of 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(methoxyamino-methyl)-benzamide (50.0 mg, 0.10 mmol) obtained in Example 15 in THE (3 ml), and triethylamine (40.9 l, 0.29 mmol) was added thereto. The mixture was stirred for 15 hours. The reaction mixture was diluted with ethyl acetate (45 ml), and washed with saturated aqueous ammonium chloride (20 ml), and then with saturated brine (2x 20 ml). The organic layer was dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The resultant residue was purified by preparative TLC (CH2C12/MeOH (10:1)) to give 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-{[methoxy-(2-methoxy-a cetyl)-amino]-methyl}-benzamide (Compound F-6, 19.1 mg, 34%) as a colorless oil.
iH-NMR(CD3OD, 270MHz) 8(PPM) 3.44 (3H, s), 3.67-3.73 (2H, m), 3.76 (3H, s), 3.89-3.95 (2H, m), 4.30 (2H, s), 4.90 (2H, s), 6.61 (111, dt, J = 4.3, 8.6 Hz), 7.34 (1H, ddd, J = 1.1, 1.9, 8.6 Hz), 7.37-7.43 (111, m),7.44 (111, dd, J = 1.9, 10.8 Hz).
ESI(LC/MS positive mode) m/z 584 (M+H) [Example 57]
3,4-Difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-{ [(2-hydroxy-acetyl)-methoxy-amino]-methyl}
-N-(2-hydroxy-ethoxy)-benzamide (Compound F-5) HO O
I
HN O
F
Hip F
O F

To a solution of acetoxyacetic acid (13.9 mg, 0.12 mmol) in methylene chloride (1 ml) were added 3-hydroxy-4-oxo-3,4-dihydro-1,2,3-benzotriazine (18.9 mg, 0.12 mmol) and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (22.5 mg, 0.12 mmol), and the mixture was stirred for 3 hours. This solution was added dropwise to a solution of 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(methoxyamino-methyl)-benzamide (50.0 mg, 0.10 mmol) obtained in Example 15 in THE (2 ml), and triethylamine (40.9 l, 0.29 mmol) was added thereto. The mixture was stirred for 24 hours. The reaction mixture was diluted with ethyl acetate (45 ml), and washed with saturated aqueous ammonium chloride (20 ml), and then with saturated brine (2x 20 ml). The organic layer was dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The resultant residue was roughly purified by preparative TLC (CH2C12/MeOH (10:1)) to give { [2,3-difluoro-4-(2-fluoro-4-iodo-phenylamino)-5-(2-hydroxy-ethoxycarbamoyl)-benzyl]-metho xy-carbamoyl}acetic acid methyl ester (14.0 mg, containing impurities) as a colorless oil. To a solution of the resultant { [2,3-difluoro-4-(2-fluoro-4-iodo-phenylamino)-5 -(2-hydroxy-ethoxycarbamoyl)-benzyl]-metho xy-carbamoyl} acetic acid methyl ester (14.0 mg, containing impurities) in methanol (1 ml) was added sodium methoxide (3.0 mg, 0.06 mmol), and the mixture was stirred for 2 hours. The reaction mixture was diluted with saturated ammonium chloride, and extracted with methylene chloride (30 ml and 15 ml). The organic layer was dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The resultant residue was purified by preparative TLC (CH2C12/MeOH (10:1)) to give 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5- { [(2-hydroxy-acetyl)-methoxy-amino]-methyl } -N-(2-hydroxy-ethoxy)-benzamide (F-5, 5.8 mg, 12% for 2 steps) as a colorless oil.
IH-NMR(CD3OD, 270MHz) 6(PPM) 3.70 (211, t, J = 4.6 Hz), 3.75 (311, s), 3.92 (211, t, J = 4.6 Hz), 4.36 (211, s), 4.90 (2H, s), 6.61 (111, dt, J = 4.3, 8.9 Hz), 7.31-7.37 (1H, m),7.37-7.43 (1H, m),7.44 (111, dd, J = 1.9, 10.8 Hz).
ESI(LC/MS positive mode) m/z 570 (M+H) [Example 58]
3,4-Diuoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(isobutyryl-methoxy-a mino)-methyl]-benzamide (Compound F-4) HO

HN O
F
H
O N
N
F / I
O

The title compound was prepared by a procedure similar to that in Example 41.
Namely, 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(methoxyamino-methyl)-benzamide obtained in Example 15 was reacted with 4-oxo-4H-benzo[d][1,2,3]triazin-3-yl isobutyrate prepared from isobutyric acid to give 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(isobutyryl-methoxy-am ino)-methyl]-benzamide (88.9 mg, 77%).
'H-NMR(DMSO-d6, 270MHz) 6(PPM) 1.04(6H, d, J=6.8Hz), 2.95(111, m), 3.00(311, s), 3.54(211, m), 3.80(2H, m), 4.75(1H, br.s), 4.85(2H, s), 6.63(1H, td, J=8.6, 3.8Hz), 7.30(IH, br.d, J=6.8Hz), 7.36(1H, d, J=8.4Hz), 7.58(1H, dd, J=10.9, 1.8Hz), 8.53(1H, br.s) ESI(LC/MS positive mode) m/z 582(M+H) [Example 59]
3,4-Difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(methoxy-propionyl-a mino)-methyl]-benzamide (Compound F-3) HO

HN O
F
H
O N
F ltl'l O F

The title compound was prepared by a procedure similar to that in Example 41.
Namely, 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(methoxyamino-methyl)-benzamide obtained in Example 15 was reacted with 4-oxo-4H-benzo[d][1,2,3]triazin-3-yl propionate prepared from propionic acid to give 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(methoxy-propionyl-am ino)-methyl]-benzamide (35.0 mg, 31%).

'H-NMR(DMSO-d6, 270MHz) 6(PPM) 1.02(3H, t, J=7.5Hz), 2.45(2H, q, J=7.5Hz), 3.31(3H, s), 3.54(2H, t, J=4.8Hz), 3.81(2H, t, J=4.8Hz), 4.83(2H, s), 6.64(1H, td, J=8.7,4.3Hz), 7.32(1H, br.s), 7.36(1H, br.d, J=8.4Hz), 7.57(1H, dd, J=10.9, 1.8Hz), 8.62(IH, br.s) ESI(LC/MS positive mode) m/z 568(M+H) [Example 60]
5-[(Acetyl-ethoxy-amino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benzamide (Compound F-10) HO~~
HN O
F
H
O N
' I
N F I

The title compound was prepared by a procedure similar to that in Example 41.
Namely, 5-(ethoxyamino-methyl)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-b enzamide obtained in Example 17 was reacted with 4-oxo-4H-benzo[d][1,2,3]triazin-3-yl acetate prepared from acetic acid to give 5- [(acetyl-ethoxy-amino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-e thoxy)-benzamide (19.3 mg, 71 %).

'H-NMR(DMSO-d6, 270MHz) S(PPM) 1.15(3H, t, J=6.9Hz), 2.10(3H, s), 3.31(3H, s), 3.55(2H, m), 3.82(2H, m), 3.94(2H, q, J=6.9Hz), 4.71(IH, br.s), 4.81(2H, s), 6.64(1H, m), 7.34(1H, m), 7.36(1H, m), 7.58(1H, d, J=9.7Hz), 8.53(1H, br.s), 11.84(1H, br.s) ESI(LC/MS positive mode) m/z 568(M+H) [Example 61 ]
5-[(Ethoxy-propionyl-amino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydro xy-ethoxy)-benzamide (Compound F-11) HO,~~ O

HN O
F
H
N jt:~
O N I I

O

The title compound was prepared by a procedure similar to that in Example 41.
Namely, 5-(ethoxyamino-methyl)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-b enzamide obtained in Example 17 was reacted with 4-oxo-4H-benzo[d][1,2,3]triazin-3-yl propionate prepared from propionic acid to give 5-[(ethoxy-propionyl-amino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydro xy-ethoxy)-benzamide (17.0 mg, 61%).

'H-NMR(CD3OD, 270MHz) S(PPM) 1.12(3H, t, J=7.4Hz), 1.24(3H, t, J=7.lHz), 2.53(2H, q, J=7.4Hz), 3.67(2H, m), 3.92(2H, m), 3.99(2H, q, J=7.lHz), 4.89(2H, s), 6.61(1H, td, J=8.7, 4.3Hz), 7.34(1H, m), 7.38(1H, m), 7.44(1H, dd, J=10.7, 2.0 Hz) ESI(LC/MS positive mode) m/z 582(M+H) [Example 62]
2-(4-Ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)-5-[(isobutyryl-methoxy -amino)-methyl]-benzamide (Compound F-9) HO,,f~

I

F
H
"ej 1 N
N F
O F

Dichlorobis(triphenylphosphine)-palladium (Aldrich, 4 mg, 0.006 mmol), copper iodide (2.2 mg, 0.012 mmol), and N,N-diisopropylethylamine (30 L, 0.175 mmol) were added to a solution of 5-[(acetyl-methoxy-amino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy -ethoxy)-benzamide (67.78 mg, 0.117 mmol) obtained in Example 58 in tetrahydrofuran (anhydrous, 2.0 mL) under a nitrogen atmosphere. The mixture was stirred thoroughly. After a homogenous solution was obtained, trimethylsilylacetylene (65 L, 0.466 mmol) was added to the solution, which was stirred at room temperature for a whole day and night.
After completion of the reaction, the solvent was evaporated under reduced pressure, and the yellowish brown oily residue was extracted with ethyl acetate. The organic layer was washed sequentially with 2% aqueous EDTA, water, and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The resultant residue was purified by silica gel flash chromatography (Mega Bond Elut, Varian, 5% methanol/methylene chloride as an eluent). The resultant 5-[(acetyl-methoxy-amino)-methyl]-3,4-difluoro-2-(2-fluoro-4-trimethylsilanylethynyl-phenyla mino)-N-(2-hydroxy-ethoxy)-benzamide was dissolved in tetrahydrofuran (anhydrous, 2.0 mL), and tetra-n-butylammonium fluoride (1 mol/L solution in tetrahydrofuran, 150 L, 0.150 mmol) was added thereto. The mixture was stirred for 1 day. After completion of the reaction, the solvent was evaporated under reduced pressure, and the yellowish brown oily residue was extracted with ethyl acetate. The organic layer was washed sequentially with diluted (1%) hydrochloric acid, water, and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The resultant residue was purified by silica gel flash chromatography (Mega Bond Elut, Varian, ethyl acetate as an eluent) to give a yellow solid, which was triturated with 10% ethyl acetate/hexane to give a pale yellow solid (23.6 mg, 42% in 2 steps).

1H-NMR(CD3OD, 270MHz) S(PPM) 1.12(6H, d, J=6.8Hz), 3.06(1H, quin., J=6.8Hz), 3.42(1H, s), 3.68(2H, m), 3.78(3H, s), 3.91(2H, m), 4.91(2H, s), 6.73(1H, td, J=8.7, 4.5Hz), 7.14(1H, br.d, J=9.2Hz), 7.19(1H, dd, J=11.9, 1.811z), 7.39(IH, m) ESI(LC/MS positive mode) m/z 480(M+H) [Example 63]
2-(4-Ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)-5-[(methoxy-propionyl-amino)-methyl]-benzamide (Compound F-8) HO

HN O
F
H
N
0 !! \ \

The title compound was synthesized in 2 steps by a procedure similar to that in Example 62 from 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(methoxy-propionyl-am ino)-methyl]-benzamide obtained in Example 59. 6.9 mg (35% in 2 steps).

1H-NMR(CD3OD, 270MHz) S(PPM) 1.12(3H, t, J=7.4Hz), 2.54(1H, q, J=7.4Hz), 3.42(1H, s), 3.70(2H, m), 3.76(3H, s), 3.91(2H, m), 4.90(2H, s), 6.73(1H, td, J=8.6, 4.6Hz), 7.14(1H, br.d, J=9.lHz), 7.19(1H, dd, J=11.9, 1.8Hz), 7.39(1H, br.d, J=5.4Hz) ESI(LC/MS positive mode) m/z 466(M+H) [Example 64]
5-[(Acetyl-methoxy-amino)-methyl]-2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydr oxy-ethoxy)-benzamide (Compound F-7) HOB , HN O
F
H

I ( N F
O

The title compound was synthesized in 2 steps by a procedure similar to that in Example 62 from 5-[(acetyl-methoxy-amino)-methyl] -3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy -ethoxy)-benzamide obtained in Example 46. 191.67 mg (79% in 2 steps).
'H-NMR(CD3OD, 270MHz) 6(PPM) 2.18(3H, s), 3.42(1H, s), 3.68(2H, m), 3.77(3H, s), 3.92(2H, m), 4.90(2H, s), 6.74(1H, td, J=8.6, 4.3Hz), 7.13(1H, br.d, J=9.1Hz), 7.19(1H, dd, J=11.9, 1.8Hz), 7.40(1H, br.d, J=6.4Hz) ESI(LC/MS positive mode) m/z 452(M+H) [Example 65]
5-[(Ethoxy-propionyl-amino)-methyl]-2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hy droxy-ethoxy)-benzamide (Compound F-24) HO

HN O
F
H
O N
I" F
O F
The title compound was synthesized in 2 steps by a procedure similar to that in Example 62 from 5-[(ethoxy-propionyl-amino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydro xy-ethoxy)-benzamide obtained in Example 61. 3.5 mg (45% in 2 steps).
'H-NMR(CD3OD, 270MHz) 8(PPM) 1.11(3H, t, J=7.4Hz), 1.22(3H, t, J=7.1Hz), 2.53(2H, q, J=7.4Hz), 3.39(1H, s), 3.69(2H, m), 3.94(2H, m), 3.97(2H, q, J=7.4Hz), 4.90(2H, s), 6.69(1H, td, J=8.6, 5.4Hz), 7.12(1H, br.d, J=8.7Hz), 7.17(1H, dd, J=12.0, 1.8Hz) , 7.50(1H, br.d, J=5.8 Hz) ESI(LC/MS positive mode) m/z 480(M+H) [Example 66]
5-[(Acetyl-ethoxy-amino)-methyl]-2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydro xy-ethoxy)-benzamide (Compound F-23) HO

F
H
O N
I I
N F
O F

The title compound was synthesized in 2 steps by a procedure similar to that in Example 62 from 5-[(acetyl-ethoxy-amino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-e thoxy)-benzamide obtained in Example 60. 1.8 mg (22%).

'H-NMR(CD3OD, 270MHz) S(PPM) 1.25(3H, t, J=7.1Hz), 2.18(3H, s), 3.43(1H, s), 3.63(2H, m), 3.68(2H, m), 4.01(2H, q, J=7.1Hz), 4.90(2H, s), 6.74(IH, td, J=8.6, 4.5Hz), 7.14(l H, br.d, J=8.2Hz), 7.20(lH, dd, J=11.9, 1.8Hz) , 7.40(1H, m) ESI(LC/MS positive mode) m/z 466(M+H) [Example 67]
3,4-Difluoro-2-(2-fluoro-4-iodo-phenylamino)-5- [(formyl-methoxy-amino)-methyl]-N-(2-hydro xy-ethoxy)-benzamide (Compound F-1) F
H
O N
~N F
I

O F

Ethyl formate (0.2 mL) was added to 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(methoxyamino-methyl)-benzamide (Compound C-24, 50 mg, 0.0978 mmol) obtained in Example 15, and the mixture was heated to reflux at 80 C for 1 hour.
After completion of the reaction, the reaction mixture was concentrated under reduced pressure. The resultant white solid was fractionated by TLC (No. 5715, Merck, 5%
methanol/methylene chloride as a developing solvent), and the resultant white solid was further triturated with 10% methylene chloride/hexane to give 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-[(formyl-methoxy-amino)-methyl]-N-(2-hydrox y-ethoxy)-benzamide (Compound F-1, 18.2 mg, 35%) as a white solid.

1H-NMR(DMSO-d6, 400MHz, at 80 C) 8(PPM) 3.55(2H, dd, J=5.4, 4.911z), 3.69(3H, s), 3.84(2H, dd, J=5.4, 4.9Hz), 4.77(2H, s), 6.65(l H, td, J=8.9, 3.9Hz), 7.35(1H, d, J=8.3Hz), 7.45(1H, d, J=7.3Hz), 7.51(1H, dd, J=11.0, 2.0Hz), 8.35(IH, br.s) ESI(LC/MS positive mode) m/z 540(M+H) [Example 68]
3,4-Difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(2-oxo-pyrrolidin-l-ylm ethyl)-benzamide (Compound H-3) HO

HN O
F
H
N
gN ilt F )"I
O F

Methyl 4-amino-butyrate hydrochloride (commercially available, 48 mg, 0.312 mmol) and sodium cyanoborohydride (20 mg, 0.312 mmol) were added to a solution of 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-formyl-N-(2-hydroxy-ethoxy)-benzamide (50 mg, 0.104 mmol) obtained in Step F of Example 1 in methanol (2.0 mL). The mixture was stirred at room temperature for 18 hours. Then, the reaction vessel was equipped with a reflex condenser, and the mixture was heated at 80 C for 2 hours. After completion of the reaction, the reaction mixture was extracted with ethyl acetate, and the organic layer was washed sequentially with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The resultant residue was purified by silica gel flash chromatography (Mega Bond Elut, Varian, 5% methanol/methylene chloride as an eluent) to give 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(2-oxo-pyrrolidin- l -ylm ethyl)-benzamide (Compound H-3, 26.8 mg, 47%) as a white solid.

'H-NMR(CD3OD, 270MHz) 8(PPM) 2.06(2H, m), 2.43(2H, dd, J=8.4, 7.7Hz), 3.44(2H, dd, J=7.1, 6.9Hz), 3.70(2H, dd, J=4.8, 4.514z), 3.93(2H, dd, J=4.9, 4.0Hz), 4.53(2H, s), 6.62(1H, td, J=8.7, 4.3Hz), 7.32(114, m), 7.35(IH, m), 7.45(1H, dd, J=10.7, 2.011z) ESI(LC/MS positive mode) m/z 550(M+H) [Example 69]
3,4-D iuoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(2-oxo-piperidin- l -ylme thyl)-benzamide (Compound H-4) HO~~
HN O
F
H
N
N F
O

Methyl 5-amino-pentanoate hydrochloride {see J. Org. Chem. (1968) 15811 (128 mg, 0.178 mmol) and sodium cyanoborohydride (45 mg, 0.718 mmol) were added to a solution of 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-formyl-N-(2-hydroxy-ethoxy)-benzamide (115 mg, 0.239 mmol) obtained in Step F of Example 1 in tetrahydrofuran (anhydrous, 4.0 mL). The mixture was stirred at room temperature for 1.5 hours. Then, the reaction vessel was equipped with a reflux condenser, and the mixture was heated at 60 C for 2 days. After completion of the reaction, the reaction mixture was extracted with ethyl acetate, and the organic layer was washed sequentially with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The resultant residue was purified by silica gel flash chromatography (Mega Bond Elut, Varian, 4% methanol/methylene chloride as an eluent) to give 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(2-oxo-piperidin-1-ylmet hyl)-benzamide (Compound H-4, 42.7 mg, 37%) as a white solid.

'H-NMR(CD3OD, 270MHz) 8(PPM) 1.85(4H, m), 2.42(2H, m), 3.40(2H, m) 3.70(2H, dd, J=4.9, 4.3Hz), 3.92(2H, dd, J=4.9, 4.3Hz), 4.65(2H, s), 6.56(IH, td, J=8.9, 4.3Hz), 7.34(1H, m), 7.35(1H, m), 7.45(1H, dd, J=10.7, 2.0Hz) ESI(LC/MS positive mode) m/z 564(M+H) [Example 70]
3,4-Difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-[(2-hydroxy-acetylamino)-methyl]-N-(2-hydro xy-ethoxy)-benzamide (Compound E-5) Step A
Synthesis of 5-aminomethyl-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-benzoic acid trifluoroacetate F

F

tert-Butyl carbamate (commercially available, 187 mg, 1.602 mmol), trifluoroacetic acid (123 L, 1.602 mmol), and triethylsilane (255 L, 1.602 mmol) were added sequentially to a suspension of 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-formyl-benzoic acid (225 mg, 0.534 mmol) obtained in Step A of Example 5 in acetonitrile (anhydrous, 20 mL). The mixture was stirred at room temperature for 5 days. After completion of the reaction, the reaction mixture was evaporated under reduced pressure, and the resultant residue was extracted with ethyl acetate. The organic layer was washed sequentially with water and saturated brine, dried over anhydrous sodium sulfate, and evaporated under reduced pressure. The resultant crude product was purified by silica gel flash chromatography (Mega Bond Elut, Varian, 5%
methanol/methylene chloride as an eluent) to give 5-(tert-butoxycarbonylamino-methyl)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-benzoic acid. [LC/MS m/z 523(M+1)]. Then, trifluoroacetic acid (0.5 mL) was added to a solution of the resultant product in methylene chloride (20 mL), and the mixture was stirred at room temperature for 14 hours. After completion of the reaction, the reaction mixture was evaporated under reduced pressure, and the resultant residue was recrystallized from a mixed solvent of diethyl ether:hexane (1:1) to give 5-aminomethyl-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-benzoic acid trifluoroacetate (285 mg, 99% in 2 steps) as white crystals.

'H-NMR(CD3OD, 270MHz) S(PPM) 4.19(2H, s), 6.84(IH, td, J=8.6, 4.8Hz), 7.44(1H, br.d, J=10.lHz), 7.51(1H, dd, J=10.4, 2.0Hz), 8.06(1H, dd, J=7.8, 1.8Hz) ESI(LC/MS positive mode) m/z 423(M+H) Step B
Synthesis of 5-(acryloylamino-methyl)-N-[2-(tert-butyl-dimethyl-silanyloxy)-ethoxy]-3,4-difluoro-2-(2-fluor o-4-iodo-phenylamino)-benzamide ao iii 0 F
F
F

Acryloyl chloride (100 L, 0.986 mmol) and triethylamine (689 L, 4.93 mmol) were added to a solution of hydroxy-pyrrolidine-2,5-dione (commercially available, 227 mg, 1.973 mmol) in methylene chloride (anhydrous, 2 niL), and the mixture was stirred at room temperature for 30 minutes.
5-aminomethyl-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-benzoic acid (150 mg, 0.355 mmol) obtained in Step A was added to this solution, and the mixture was stirred for 1 hour.
After completion of the reaction, the reaction mixture was evaporated under reduced pressure, and the resultant residue was extracted with ethyl acetate. The organic layer was washed sequentially with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to give 5-(acryloylamino-methyl)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-benzoic acid as a white solid. This product was confirmed for the structure by LC/MS. LC/MS (positive mode) m/z 477(M+1). This compound was dissolved in methylene chloride (anhydrous, 10 mL) under argon flow. N,N-diisopropylethylamine (250 L, 1.42 mmol), O-[2-(tert-butyl-dimethyl-silanyloxy)-ethyl]-hydroxylamine (135 mg, 0.71 mmol), 1-hydroxy-lH-benzotriazole (71mg, 0.533 mmol), and (3-dimethylamino-propyl)-ethyl-carbodiimide hydrochloride (102 mg, 0.533 mmol) were added sequentially to the solution. The mixture was stirred at room temperature for 20 hours.
After completion of the reaction, the reaction mixture was evaporated under reduced pressure, and the resultant residue was extracted with ethyl acetate. The organic layer was washed sequentially with water and saturated brine, dried over anhydrous sodium sulfate, and evaporated under reduced pressure. The resultant crude product was purified by silica gel flash chromatography (Mega Bond Elut, Varian, 40% ethyl acetate/hexane as an eluent) and preparative TLC (No. 5744, Merck, 40% ethyl acetate/hexane as a developing solvent) to give 5-(acryloylamino-methyl)-N- [2-(tert-butyl-dimethyl-silanyloxy)-ethoxy]-3,4-difluoro-2-(2-fluor o-4-iodo-phenylamino)-benzamide (7.4 mg, 3%) as a waxy solid.

'H-NMR(CDC13, 270MHz) 5(PPM) 0.07(6H, s), 0.09(9H, s), 3.89(2H, m), 4.07(2H, m), 4.51(2H, d, J=6.lHz), 5.71(2H, dd, J=10.1, 1.5Hz), 6.12(1H, dd, J=17.OHz, 10.2Hz), 6.20(1H, br.s), 6.33(1H, dd, J=17.0, 1.511z), 6.56(1H, td, J=8.7,5.3Hz), 7.30(1H, dt, J=8.6, 3.0Hz), 7.38(1H, dd, J=10.2, 2.0Hz), 7.40(IH, m), 8.57(1H, br.s) ESI(LC/MS positive mode) m/z 650(M+H) Step C
Synthesis of N-[2-(tert-butyl-dimethyl-silanyloxy)-ethoxy]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-[( 2-hydroxy-acetylamino)-methyl] -benzamide b o i 0,- ~0~ F
---p N I N **&
HHO-'Y / F I

Aqueous osmium tetroxide (4%, 0.1 mL) and sodium metaperiodate (12 mg, 0.056 mmol) were added to a solution of 5-(acryloylamino-methyl)-N-[2-(tert-butyl-dimethyl-silanyloxy)-ethoxy]-3,4-difluoro-2-(2-fluor o-4-iodo-phenylamino)-benzamide (7.3 mg, 0.011 mmol) obtained in Step B in tetrahydrofuran (4 mL) and water (1 mL). The mixture was stirred for 3 hours. After the disappearance of the starting material was confirmed by LC/MS, the reaction mixture was extracted with ethyl acetate.
The organic layer was washed sequentially with water and saturated brine, dried over anhydrous sodium sulfate, and concentrated under reduced pressure to give N-[2-(tert-butyl-dimethyl-silanyloxy)-ethoxy]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-[( 2-oxo-acetylamino)-methyl]-benzamide. Subsequently, this was dissolved in methanol (2.0 mL). Sodium borohydride (3 mg, 0.079 mmol) was added to this solution at room temperature, and the mixture was stirred for 1 hour. After completion of the reaction, the reaction mixture was extracted with ethyl acetate, and the organic layer was washed sequentially with water and saturated brine, dried over anhydrous sodium sulfate, and evaporated under reduced pressure.
The resultant crude product was purified by silica gel flash chromatography (Mega Bond Elut, Varian, 60% ethyl acetate/hexane as an eluent) to give N- [2-(tert-butyl-dimethyl-silanyloxy)-ethoxy] -3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5 - [( 2-hydroxy-acetylamino)-methyl]-benzamide (4.34 mg, 60% in 2 steps) as a pale yellow solid.
ESI(LC/MS positive mode) m/z 654(M+H) Step D
Synthesis of 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-[(2-hydroxy-acetylamino)-methyl]-N-(2-hydrox y-ethoxy)-benzamide (Compound E-5) HO~,,,,,O

~

OH

F

Tetra-n-butylammonium fluoride (1 mol/L solution in tetrahydrofuran, 0.5 mL, 0.500 mmol) was added to a solution of N-[2-(tert-butyl-dimethyl-silanyloxy)-ethoxy]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-[( 2-hydroxy-acetylamino)-methyl]-benzamide (4.34 mg, 0.00665 mmol) obtained in Step C in tetrahydrofuran (anhydrous, 1 mL) at room temperature. The mixture was stirred for 1.5 hours.
After completion of the reaction, the reaction mixture was extracted with ethyl acetate, and the organic layer was washed sequentially with water and saturated brine, dried over anhydrous sodium sulfate, and evaporated under reduced pressure. The resultant crude product was purified sequentially with silica gel flash chromatography (Mega Bond Elut, Varian, 5%
methanol/methylene chloride as an eluent) and preparative TLC (No. 5715, Merck, 7%
methanol/methylene chloride as a developing solvent) to give 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-[(2-hydroxy-acetylamino)-methyl]-N-(2-hydrox y-ethoxy)-benzamide (Compound E-5, 1.4 mg, 39%) as a white solid.

1H-NMR(CD3OD, 270MHz) S(PPM) 3.71(2H, dd, J=7.4, 4.714z), 3.94(2H, dd, J=7.4, 4.7Hz), 4.03(2H, s), 4.50(2H, s), 6.55(1H, td, J=8.6, 5.3Hz), 7.32(1H, m), 7.42(1H, dd, J=10.7, 1.8Hz), 7.45(1H, dd, J=5.8, 2.1Hz) ESI(LC/MS positive mode) m/z 540(M+H) [Example 71 ]
3,4-Difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(2-oxo-tetrahydro-pyrim idin- 1 -ylmethyl)-benzamide (Compound H-6) Step A
Synthesis of 5-[(3-amino-propylamino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy -ethoxy)-benzamide HOB/,,O
I
HN O
F
H
N
H2N~/N I F 1 / I
F

3,4-Difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-formyl-N-(2-hydroxy-ethoxy)-benzam ide obtained in Step F of Example 1 was reacted with propane- 1,3-diamine in THE The thus-obtained imine was reduced with sodium borohydride in methanol to give the title compound.

ESI(LC/MS positive mode) m/z 539 (M+H) Step B
Synthesis of 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(2-oxo-tetrahydro-pyrimi din- l-ylmethyl)-benzamide (Compound H-6) HO -O

HN O
F
HN'N F / 1 O F
The amine synthesized in Step A (66.4 mg, 0.1233 mmol) was dissolved in THF:CH3CN
(1:1 v/v, 3.0 ml). N,N-disuccinimidyl carbonate (47.4 mg, 1.5 eq., 0.1849 mmol) and triethylamine (103.1 l, 6.0 eq., 0.7398 mmol) were added sequentially to this solution, and the mixture was stirred at room temperature for 20 hours. The solvent was removed under reduced pressure, and the residue was purified by LC/MS to give white crystals (42.6 mg).
'H-NMR(DMSO-d6, 400MHz) 6(PPM) 1.83(2H, t, J=5.2Hz), 3.14(2H, t, J=5.6Hz), 3.23(2H, t, J=5.6Hz), 3.51-3.58(2H, m), 3.82(2H, brt), 4.49(2H, s), 6.41(1H, brs), 6.61(1H, dt, J=3.9, 8.3Hz), 7.28(1H, d, J=6.4Hz), 7.34(IH, d, J=7.9Hz), 7.56(1H, d, J=10.8Hz) , 8.48(1H, s), 12.0(IH, s) ESI(LC/MS positive mode) m/z 565 (M+H) [Example 72]
3,4-Difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(2-oxo-oxazolidin-3 -yl methyl)-benzamide (Compound H-5) HO\ .- ,a O F

O N F I i O F

Step A
Synthesis of 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5- { [(E)-2-hydroxy-ethylim ino ] -methyl } -b enzamide HO~\ is 0 H F
N

HO "~ N I
F
The title compound was synthesized by reacting 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-formyl-N-(2-hydroxy-ethoxy)-benzamide obtained in Step F of Example 1 with ethanolamine in THF.

1H-NMR(CD3OD, 400MHz) S(PPM) 3.72-3.74(4H, m), 3.81-3.84(2H, m), 3.96-3.99(2H, m), 6.64-6.68(1H, m), 7.36(1H, d, J=8.79Hz), 7.43(1H, d, J=9.99Hz), 8.13(1H, d, J=5.6Hz), 8.50(1H, s) ESI(LC/MS positive mode) m/z 524 (M+H) Step B
Synthesis of 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-hydroxy-ethylamino) -methyl]-benzamide O HH F

\ N \
HO~~N ( F I I

Sodium borohydride was added to a solution of the imine, 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5 -I [(E)-2-hydroxy-ethylim ino]-methyl}-benzamide obtained in Step Ain MeOH at 0 C. While being allowed to warm gradually, the mixture was stirred overnight. The solvent was removed under reduced pressure, and the residue was purified with a silica gel column (CH2C12:MeOH (4:1 to 2:1)) to give the title compound as a white solid.

'H-NMR(CD3OD, 400MHz) 8(PPM) 2.80(2H, t, J=5.38Hz), 3.69-3.72(4H, m), 3.92-3.95(4H, m), 6.59(1H, dt, J=3.9, 8.3Hz), 7.34(1H, d, J=10.3Hz), 7.44(1H, dd, J=1.95, 10.311z), 7.49(1H, d, J=7.3Hz) ESI(LC/MS positive mode) m/z 526 (M+H) Step B' (an alternative to Step B) 3,4-Difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-hydroxy-eth ylamino)-methyl]-benzamide obtained in Step B can be prepared in 1 step by reductive amination of 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-formyl-N-(2-hydroxy-ethoxy)-benzamide obtained in Step F of Example 1. Namely, 2-aminoethanol (0.070 ml), acetic acid (0.080 ml), and sodium cyanoborohydride (44 mg) were added to a solution of an aldehyde, 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-formyl-N-(2-hydroxy-ethoxy)-benzamide (65.7 mg, 0.136 mmol) in methanol (2 ml) at room temperature. The mixture was stirred overnight.
Water (6 ml), saturated brine (3 ml), and aqueous sodium bicarbonate (2 ml) were added, and the reaction mixture was extracted with ethyl acetate (2x 10 ml). The combined organic layers were washed with saturated brine (10 ml), dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The residue was triturated with ethyl acetate/n-hexane (2:1) to give 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-hydroxy-ethylamino) -methyl]-benzamide (60.4 mg, 84%) as a colorless solid.

Step C

3,4-Diuoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(2-oxo-oxazolidin-3-yl methyl)-benzamide (Compound H-5) HO,,,,-5 ,O
I
HN O
F
H
N
O N
F
O F

Using 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-hydroxy-ethylamino) -methyl]-benzamide obtained in Step B (or Step B') as a starting material, synthesis was performed according to the procedure described in Step B of Example 27 to give 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(2-oxo-oxazolidin-3-ylm ethyl)-benzamide (Compound H-5).

'H-NMR(DMSO-d6, 400MHz) 6(PPM) 3.49-3.59(4H, m), 3.83-3.85(2H, m), 4.28-4.32(2H, m), 4.42(2H, s), 6.87(1H, td, J=8.8, 3.9Hz), 7.36(1H, d,J=7.9Hz), 7.46(1H, d, J=8.4Hz), 7.57(1H, dd, J=1.9, 10.8Hz), 8.76(1H, s), 12.3(1H, s) ESI(LC/MS positive mode) m/z 552 (M+H) [Example 73]
5 -(2,3 -Dioxo-morpholin-4-ylmethyl)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydrox y-ethoxy)-benzamide (Compound H-7) HO~~ N

HN O
F
O

O N F
O F

4-Dimethylaminopyridine (12.1 mg) and dibenzotriazol-1-yl oxalate (9.2 mg, 27.4 mol) were added to a solution of 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-hydroxy-ethylamino) -methyl]-benzamide (15.9 mg, 30.2 mol) obtained in Step B (or Step B') of Example 72 in anhydrous N,N-dimethylformamide (1.5 ml) at room temperature. The mixture was stirred at room temperature for 2 hours. Water (6 ml) and 1 N hydrochloric acid (0.5 ml) were added, and the reaction mixture was extracted with ethyl acetate (2x 10 ml). The combined organic layers were washed with saturated brine (8 ml), dried over anhydrous sodium sulfate, and concentrated under. reduced pressure. The residue was purified with a preparative silica gel plate (No. 5744, Merck, CH2Cl2/MeOH (10:1) as a developing solvent) to give 5-(2,3-dioxo-morpholin-4-ylmethyl)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydrox y-ethoxy)-benzamide (Compound H-7, 1.0 mg, 6% yield).

'H-NMR(DMSO-d6, 270MHz) S(PPM) 3.57 (211,br.s), 3.70 (2H, t, J = 6.1 Hz), 3.86 (2H, t, J =
4.9 Hz), 4.55 (2H, t, J = 5.4 Hz), 4.66 (2H, s), 6.67 (1H, td, J = J = 8.4, 4.3 Hz), 7.32 - 7.40 (2H, m), 7.59 (1 H, dd, J = 10.8, 1.4 Hz).
ESI(LC/MS positive mode) m/z 580(M+H) [Example 74]
5-{ [Acetyl-(2-hydroxy-ethyl)-amino]-methyl}-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benzamide (Compound E-6) HO,,-,~O
HN O
HH F
O / .N \
HO~~N FI I

F
Using 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-hydroxy-ethylamino) -methyl]-benzamide obtained in Step B (or Step B') of Example 72 as a starting material, synthesis was performed according to the procedure described in Example 41 to give 5- { [acetyl-(2-hydroxy-ethyl)-amino] -methyl } -3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-( 2-hydroxy-ethoxy)-benzamide (Compound E-6).

'H-NMR(DMSO-d6, 270MHz) S(PPM) 2.07 (3H x 1/3, s), 2.12 (3H x 2/3, s), 3.47 -3.56 (4H, m), 3.83 (2H, t, J = 4.5 Hz), 4.58 (2H x 2/3, s), 4.69 (2H x 1/3, s), 6.61 (1H, td, J = 8.9, 4.3 Hz), 7.24 (I H, d, J = 7.4 Hz), 7.3 5 (1 H, d, J = 8.6 Hz), 7.5 7 (1 H, d, J = 7.6 Hz), ESI(LC/MS positive mode) m/z 568(M+H) [Test Example I]
[Measurement of MEK inhibitory activity]
MEK inhibitory activities were measured for Compounds B-l, B-2, B-6, B-9, B-12, C-1, C-6, C-7, C-8, C-10, C-13, C-24, C-28, C-31, F-1, F-2, F-3, F-4, F-5, F-6, F-7, F-8, F-9, G-1, G-2, G-3, G-4, and G-5 obtained in the Examples, and the following known compounds, P
(W002/06213, Example 9), Q (W002/06213, Example 39), and R (W099/01426, Example 95).
HO H
H F
--. O -N 0 N
F
F (p) N O Chiral O F
O
O N
F
F
(Q) O N~
G O
N

(R) Compound P was prepared according to the description (Example 9) of W002/06213.
Compound Q was prepared according to the description (Example 39) of WO02/06213.
Compound R was prepared according to the description (Example 95) of WO99/01426.
For the measurement of MEK inhibitory activities, an assay system was constructed so that phosphorylation of MBP (Myelin Basic Protein) could occur in proportion to the MEK
kinase activity, with adjusting the amount of the enzyme and the like, according to the method of Raf-1 Kinase Cascade Assay Kit (cat. 17-172, Upstate Biotechnology Inc., New York, USA).
[y3 PI ATP (Amersham Biosciences) was used as a radioisotope.
The amount of the 33P-labelled MBP was measured using Microbeta 1450 (PerkinElmer Inc., Massachusetts, USA), and 50% inhibitory concentration (IC50) was calculated.
Results are shown in Table 2.
[Test Example 2]
[Measurement of growth inhibitory activity against cancer cells]
Growth inhibitory activities against cancer cells based on MEK inhibitory activities were measured for Compounds B-1, B-2, B-6, B-9, B-12, C-1, C-6, C-7, C-8, C-10, C-13, C-24, C-28, C-31, F-1, F-2, F-3, F-4, F-5, F-6, F-7, F-8, F-9, G-1, G-2, G-3, G-4, and G-5 obtained in the Examples, and the known compounds, P, Q, and R shown above.
The growth inhibitory activities against cancer cells were measured using Cell Counting Kit-8 (Dojindo Laboratories).
Human colon cancer cell line HT-29 obtained from American Type Culture Collection (Virginia, USA) and human non-small cell lung carcinoma cell line QG56 obtained from Immuno-Biological Laboratories Co., Ltd. were plated onto 96-well culture plate at a density of 2000 cells/well, a designated concentration of MEK inhibitor was added, and the cells were incubated for 4 days.
On the 4th day of culture, a solution of Cell Counting Kit-8 was added, and absorbance (measurement wavelength: 450 nm; reference wavelength: 615 nm) was measured according to the protocol attached to the kit, and 50% inhibitory concentration (IC50) was calculated.
Results are shown in Table 2.
[Test Example 3]
[Measurement of stability against mouse liver microsome]
A variety of metabolic enzymes exist in the liver, and play a key role in the foreign substance detoxication. Many enzymes involved in drug metabolism (e.g., cytochrome P450) are localized in the endoplasmic reticulum in the cells, and are collected in the microsome fraction during preparation from the cells. The stability in liver microsome is used universally as a simple measure for evaluation of drug metabolism.
There is a correlation between in vitro intrinsic clearance calculated from the stability in human liver microsome and human in vivo clearance (Ito K. et al. Annu. Rev.
Pharmacol.
Toxicol. 1998, 38: 461-99, Naritomi Y. et al. Drug Metab. Dispos. 2001, 29:1316-24, Yuichi Sugiyama et al., Pharmacokinetics - Understanding by exercises, Nanzando).
Clearance is an important parameter that determines a blood concentration. The better the drug stability in liver microsome is, the smaller the clearance is and the higher the blood concentration is. A drug having a good stability in liver microsome can achieve a certain blood concentration with a lower dose, compared to a drug having a poor stability.
Compounds B-1, B-2, B-6, B-9, B-12, C-1, C-2, C-6, C-7, C-10, C-24, C-28, C-29, C-31, C-34, C-35, F-1, F-2, F-5, F-7, G-1, G-2, G-3, G-4, and G-5 obtained in the Examples, and the known compounds, P, Q, and R shown above were incubated with mouse liver microsome (1 mg protein/mL) in 50 mM phosphate buffer (pH 7.4) containing 5 mM MgCl2 and 2 mM
NADPH (the reduced form of nicotinamide adenine dinucleotide phosphate) at 37 C for 1 hour.
After the enzyme reaction was terminated with the addition of a three-fold volume of acetonitrile, the reaction mixture was centrifuged at 1500 rpm for 10 minutes, and the resultant supernatant was used as a test sample to measure the stability in human liver microsome by quantitating the compound in the sample using HPLC/MS.
Table 3 shows the stability of the test compounds in mouse liver microsome.
When a test compound has a longer half-life, the compound is metabolically very stable, and can produce a high blood concentration.
[Test Example 4]
[Measurement of water solubility]
Biopharmaceutical Classification System (BCS) is widely used to scientifically classify oral formulations in regard to membrane permeability and solubility. Drugs having good membrane permeability and good solubility are classified into Class 1, and guaranteed that they are absorbed almost perfectly after oral administration, and that the variability among individuals is small (Lenneras H. et al. J. Pharm. Pharmacol. 2005, 57: 273-85, Kasim NA
et al. Mol.
Pharmaceutics 2004, 1: 85-96).
Excessive amount of each of Compounds B-1, B-2, B-6, B-9, B-12, C-1, C-2, C-6, C-7, C-10, C-24, C-28, C-29, C-31, C-34, C-35, F-i, F-2, F-5, F-7, G-1, G-2, G-3, G-4, and G-5 obtained in the Examples, and the known compounds, P, Q, and R shown above was added to a glass vessel, to which 50 mM phosphate buffer (pH 6.5) was added. The vessel was sealed, sonicated at room temperature (20 C) for 10 minutes, and agitated on an agitator for 2 hours.
After dissolution equilibrium was achieved, the reaction mixture was filtered through a membrane filter, and the solute concentration in the filtrate was determined by HPLC.
Results are shown in Table 3.
[Test Example 5]
[Measurement of tumor growth suppressive activity]
A mouse model carrying human cancer was used to measure tumor growth suppressive activity of Compounds B-1, C-i, C-10, C-13, F-1, F-2, F-5, G-1, G-2, G-3, G-4, and H-3 obtained in the Examples, and the known compound, Q shown above.
Human colon cancer cell line HT 29 (obtained from American Type Culture Collection) was inoculated subcutaneously to BALB/c nu/nu mice. The test compound was dissolved in the vehicle (10% Cremophor, 10% ethanol, and 80% distilled water for injection), and orally given to the mice once a day for 14 consecutive days after the average tumor volume (0.5x long diameter x short diameter) reached to about 200 mm3. One day after the last administration, the tumor volume was measured, and the tumor growth suppression rate, (1-tumor volume increase in the group received the test compound/tumor volume increase in the group received the vehicle) x 100, of each of the test compounds was determined compared to the group received the vehicle. The higher value (%) indicates the stronger tumor suppressive activity.
Results of the tumor growth suppression rate at maximum tolerance dose (MTD) are shown in Table 4.
Table 4 shows very high tumor growth suppression rates of the compounds of this invention, indicating that they have very strong effect of tumor regression, compared to control compound Q, which has the tumor growth suppression rate of 66 - 82%.
[Test Example 6]
Anti-Type II collagen antibody-induced arthritis in mice]
Suppressive effects of compounds B-1 and G-2 obtained in Examples on arthritis development were determined using anti-Type II collagen antibody (anti-CII)-induced arthritis (J
Immunol. 2002 Aug 1; 169(3):1459-66).
Anti-CII (10 mg/mL of antibody cocktail for arthritis, code No. 62200, Chondrex) was administered intravenously at 1 mg/body/100 L to BALB/c mice (female mice of 5 weeks old were purchased from Charles River Japan, Inc., and used at 5 animals per group after 1 week acclimation), and after 3 days, LPS (lipopolysaccharide) solution (0111:B4 250 pg/mL, code No.
62200, Chondrex) was administered intraperitoneally at 25 g/0.1 mL/body. The test compounds were dissolved in the vehicle (10% Cremophor, 10% ethanol, and 80%
distilled water for injection), and orally administered 1 hour before, 1, 2, 4-8, and 11 days after LPS
administration (once a day, 1 mg/kg).
Arthritis score was evaluated with the full score 4 points per limb, and 16 points per animal. Score indicates as follows:
0.5: erythema is observed at 1 joint;
1: erythema is observed at 2 joints. Or reddening of the upper surface of the paws is observed, but swelling is not observed;
2: Slight swelling is observed;
3: Moderate swelling is observed on the upper surface of the paws;
4: Severe swelling is observed on the upper surface of the paws and digits.
In the group received the vehicle, arthritis developed the day after LPS
administration.
On the other hand, arthritis development was strongly suppressed in both groups received B-1 and G-2. Results of suppressive effect on arthritis development (arthritis score; mean +/-standard deviation) are shown in Figure 1. Figure 1 shows that the present compounds are effective anti-arthritis drugs.

[Table 2]

Growth inhibitory activity against cancer cats MEK inhibitory activity HT29 OG56 Compound No. Structure 1C50 ( M) IC50 (pM) 1C50 (pM) O,,,-0.N O F
N
B-1 O I I 0.021 0.016 0.02 F I
F
O~ O.N O F

O I \ 0.032 0.0405 0.0388 0"' F

0-.-0 O F
N
B-6 0.._0 I F I 1 0.023 0.01 0.034 F

N
O~ :;56, F
B-9 O.,~O 0.015 0.029 0.138 F
F
N F
B-12 . N . 0.031 0.0062 0.028 a-C-1 0 JJ 0.019 0.029 0.094 C!O'F v`1 F
O,_,,-,O N O F
N
C-6 ^ (~ ! 0.049 0.031 0.154 N O.N F ' 1 F
o~Q
O F
C-7 0.14 0.028 0.084 ~TM~10 F
O F
o-'- NO F
C-8 p N4 0.032 0.0086 0.023 lg_,_ON F F I

u -1'O
N O F
C-10 N- (I
0.019 0.04 0.092 O~~0.N F 1 F

N O F
C-13 ~N0 N I 0.028 0.0059 0.012 O N ( F 1 F
O,-~-Q
N O F
C-24 N I 0.068 0.014 0.041 F
Of0 N O F
C-28 N i 0.068 0.059 0.221 O~O"N i F 1 O..~O
N O F
C-31 0 N 0.012 0.0083 0.022 0 N Z F ' 1 F
O--Q
N O F
F-1 N 0.035 0.0026 0.02 (N I5F
O F
OZI-O
N O F
F-2 1 1 0.0086 0.0033 0.017 O F
O~Q
N O F
F-3 N 0.029 0.0073 0.01 ~N ' / F'' I
O F
O~Q
N O F
F-4 N, 0.035 0.01032 0.02155 /y N F I
O
O--Q
N O F
F-5 QZN~. 0.043 0.0048 0.0051 O-fN F I
O F
O..--Q
N O F
F-6 QZN 0.028 0.0046 0.0046 -OWN F I
O F
0-,,-o N O F
F-7 10 0.048 0.0074 0.0092 -i(N ' F

Oro NO F
F-8 0 N,( 0.065 0.012 0.017 i1rN I~F
O F
OHO
N O F
F-9 OZ N 0.07 0.011 0.02 F
O
O-~.Q
N O F
G-1 (P I N 0.0088 0.0015 0.021 N ' F ' I
O F
ON O F

G-2 CN ~ 0.0072 0.0034 0.0086 F I
O F
-~o N O F
G-3 N i N 0.037 0.0051 0.038 F I
O F
0-,--0 NO F
G-4 ~N 0.0 56 0.0057 0.021 N

O.1-O
F
G-5 To I ~N.yL 0.04 0.016 0.058 (NF O F

N O
P i I 0.002 0.0059 0.017 , - - - o N 0 F Chiral Q O (~ 0.0052 0.005 0.01 F
F
O N
O

R 0.13 0.1 0.13 F

[Table 3]
Stability against mouse liver microsome Water solubili Conpound No Structure ( M) T7/2 (nun) OHO-N O F

B-1 Oti0 ( 1-1 F I 728 >360 F

Of :;/ N 0 F
B-2 N 811 >360 OHO F
F
O-/~O'N O F
N
B-6 O O 519 >360 F

p~-0. ;5F F
O N
B-9 O~~O 958 >360 I
F
0.^p F
B-12 159 >360 ~SniO F

cO

F
F
0-.4 C-2 0,-- 2913 >360 F
O-.O,N 0 N
C-6 291 >360 N O_N i F i F
.~Q

o F
o`-0 O F
C-10 "~ Y"_F 557 114 O^~O F
F
O-^4 ~Fl C-24 `9- 45 Ofp O F
C-28 7 0 " " , 206 >360 0 f4 C-29 0x0 ( 237 >360 F

orb N O F
C-31 0 N 613 >360 S,,O"N r F
F

O F
C-34 r+. 427 238 O F

F
C-35 219 >360 O
o,--o N O F

`N FbI
O F
0,-~ 4 ~ I ~ F ~ I
O F
O./-0 N O F

OWN F
O F
'~- 0 F

O F \

F
G-1 YN- 88 >360 F
O.N O F

G-2 O ~N I 216 >360 F
O F
O-O
N O F
G-3, 39 >360 N F I
O
Of0 N O F
G-4 ~o N 344 >360 N F
O

N O F
G-5 N 95 >360 N
O F

~Fl P <
F

~~O,N O F Chiral O

F I
F
O N~
p R I \ / ( <<2 11 F

[Table 4]

Tumor growth suppression rate at maximum tolerance dose (MTD) Compound No. Structure 1 day after Iast administration O- O.I N 0 F
N
B-1 96%
O~'O F
F
o1 C-1 N O N F 93%
OfONF
F

N O F
C-10 NIA 107%
O^/.O. N i F i t F
O".
O F
C-13 ,N~`0 N i 97%
O i F I
F
o.-Q
N O F
F-1 Q Z N 101%
(N F I
O F
o`n`o N O F
F-2 113%
F
O F

O F
F-5 Q~N~ 99%
O~YN ' F 1 O F
0"1.0 O F
124%
G-1 - ~N,riIL,1 O F
Oro N 0 F

G-2 O I (~ 105%
~N F I
O F
~'O
N O F
G-3 N 104%
](N I i F I I

N O F
G-4 ~QJ(N15 112%
N F
O F ~

107%
cII1tiIL / I

O F
O-N O F Chiral O
O NI 66%^-82%
F I
F
Test Examples 1 - 3 described above were performed according to "Development of pharmaceuticals, Vol. 15, "Physicochemical property of formulation", edited by Koichiro Miyajima, Professor of Kyoto University, pages 45 to 48", and Test Example 4 described above was performed according to "2.2 Method for measuring solubility, 2.2.1 Equilibrium method, a.
Stirring method, Hirokawa Publishing Co."

Industrial Applicability The compounds according to the present invention and the pharmaceutically acceptable salts thereof have a MEK inhibitory effect, a cell growth inhibitory effect, are excellent in stability in vivo and solubility in water, and are useful as preventing agents or therapeutic agents for proliferative diseases, e.g., cancers and joint diseases with inflammation.

Claims (53)

1. A compound represented by the following formula (1), or a pharmaceutically acceptable salt thereof, wherein R1 represents a halogen atom, an alkenyl group, or an alkynyl group;
R2 represents a halogen atom or an alkyl group; the alkyl group may be substituted by a hydroxyl group;
R3 represents a hydrogen atom or a halogen atom;
R4 represents a hydrogen atom, an alkyl group, an alkenyl group, or an alkynyl group; the alkyl group, the alkenyl group, and the alkynyl group may have one to three substituents selected from the group consisting of -ORa, -NRaRb, -NRaCORb, a heterocyclic group, and a heteroaryl group; the heterocyclic group and the heteroaryl group may have one to three substituents selected from the group consisting of a C1-5 alkyl group, -ORa, and -NRaRb;
X represents a group represented by the following formula (i);
.cndot.-Y-Z-W (i) wherein Y represents -O-, -NR8O-, -ONR8-, -NR8CO-, or -NR8SO2-;
Z represents an C1-8 alkylene chain which may be substituted by one to three groups represented by W';
where R8 represents a hydrogen atom, an alkyl group, -ORa, or -COR9; and the alkyl group may be substituted by a halogen atom, -ORa, or -NRaRb;
R9 represents a hydrogen atom, an alkyl group, or -ORa; and the alkyl group may be substituted by a halogen atom, -ORa, or -NRaRb;
R8 and R9 may be linked to the alkylene chain of Z or form a heterocyclic group through a linkage to the substituent represented by Ra or Rb of W
or alternatively, X represents a group represented by the following formula (ii):
wherein Y1 and Y2, which may be the same or different, each represent a single bond, -CO-, -COO-, -O-, -OCO-, -NRa-, or -SO2-;
Z' represents a CI-5 chain which may be substituted by one to three groups represented by W';
in the above formulae (i) and (ii), W and W', which may be the same or different, each represent a C1-5 alkyl group, a halogen atom, an oxo group, -ORa, -COORa, -COOCORa, -CO-halogen atom, -OCORa, -CONRaRb, -SRa, -SORa, -SO2Ra, -NRaRb, -NRaCORb, -NRaSO2Rb, -SO2NRaRb, a heterocyclic group, or a heteroaryl group; the heterocyclic group and the heteroaryl group may have a substituent selected from the group consisting of a C1-5 alkyl group, -ORa, and -NRaRb; the alkyl group may be substituted by a hydroxyl group, a C1-alkoxy group, or an amino group;
the above substituents except the oxo group and the halogen may be linked to each other to form a cycloalkyl group or a heterocyclic group; the cycloalkyl group or the heterocyclic group may have a substituent selected from the group consisting of, -ORa, -NRaRb, and a C1-5 alkyl group that may be substituted with -ORa;
Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1-5 alkyl group; the alkyl group may be substituted by one to three groups selected from the group consisting of a hydroxyl group, a C1-5 alkoxy group, and an amino group;
provided that, when X is the group represented by the above formula (i) and Y
is not -O-, W is a hydrogen atom.
2. The compound according to claim 1, or a pharmaceutically acceptable salt thereof, wherein X represents the group -Y-Z-W of the formula (i) and Z represents a C1-5 alkylene chain, wherein the alkylene chain may have one to three substituents selected from the group consisting of a C1-5 alkyl group, a halogen atom, -ORa, -NRaRb, and an oxo group; the above substituents except the oxo group and the halogen atom may be linked to each other to form a cycloalkyl group or a heterocyclic group;
the cycloalkyl group or the heterocyclic group may have a substituent selected from the group consisting of -ORa, -NRaRb, and a C1-5 alkyl group that may be substituted with -ORa;
Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1-5 alkyl group; and the alkyl group may be substituted by a hydroxyl group, a C1-5 alkoxy group, or an amino group.
3. The compound according to claim 1 or 2, or a pharmaceutically acceptable salt thereof, wherein X represents the group -Y-Z-W of the formula (i), wherein the alkylene chain of Z is any one of the groups represented by the following formulae:
-CH2-, -(CH2)2-, -(CH2)3-, -(CH2)4-, -CH2CH(Me)-, -CH2C(Me)2-, -C(Me)2CH2-, -(CH2)2CH(Me)-, -(CH2)2C(Me)2-, -CH(Me)(CH2) 2-, -C(Me)2(CH2)2-, -CH2CH(Me)CH2-, -CH2C(Me)2CH2-, -CH2C(CH2CH2)CH2-, -CO-, -CH2CO-, -COCH2-, -(CH2)2CO-, -CO(CH2)2-, -CHOH-, -CH2CH(OH)-, -CH(OH)CH2-, -CH2CH(OH)CH2-, -CH(OH)CH2CH2-, and -CH2CH2CH(OH)-.
4. The compound according to any one of claims 1 to 3, or a pharmaceutically acceptable salt thereof, wherein X represents -Y-Z-W of the formula (i), wherein R8 represents a hydrogen atom, a hydroxyl group, a C1-5 alkyl group, or -COR9;
R9 represents a hydrogen atom, a hydroxyl group, a C1-5 alkyl group, or a C1-5 alkoxy group;
the alkyl group and the alkoxy group represented by R8 and R9 may be substituted by one to three hydroxyl groups at arbitrary positions of the hydrocarbon moiety.
5. The compound according to any one of claims 1 to 4, or a pharmaceutically acceptable salt thereof, wherein X represents -Y-Z-W of the formula (i), wherein R8 represents a hydrogen atom, a hydroxyl group, a methyl group, an ethyl group, an n-propyl group, an i-propyl group, an n-butyl group, an i-butyl group, a t-butyl group, a sec-butyl group, a 1,1-dimethylpropyl group, a 2,2-dimethylpropyl group, a 1,2-dimethylpropyl group, a pentyl group, a formyl group, an acetyl group, a 2-methoxyacetyl group, a 2-ethoxyacetyl group, a 2-hydroxyacetyl group, a propionyl group, a 2-methylpropionyl group, a 2-methoxypropionyl group, a 2-ethoxypropionyl group, a 2-hydroxypropionyl group, a 3-methoxypropionyl group, a 3-ethoxypropionyl group, a 3-hydroxypropionyl group, a methoxy group, an ethoxy group, an n-propyloxy group, an i-propyloxy group, a hydroxymethyl group, or a 2-hydroxyethyl group.
6. The compound according to any one of claims 1 to 5, or a pharmaceutically acceptable salt thereof, wherein X represents -Y-Z-W of the formula (i), wherein Y represents -O-, -NHO-, -N(COCH3)O-, -N(COCH2OH)O-, -N(COCH2CH3)O-, -N(COCH(OH)CH3)O-, -N(COCH2CH2OH)O-, -N(COCH(OH)CH2OH)O-, -N(COCH2CH2CH3)O-, -N(COCH2CH2CH2OH)O-, -N(COCH(OH)CH2CH3)O-, -N(COCH2CH(OH)CH3)O-, -NHCO-, or -NHSO2-.
7. The compound according to claim 1, or a pharmaceutically acceptable salt thereof, wherein X represents a group represented by the formula (ii) and X is any one of the groups represented by the following formulae:

wherein Z' represents a C1-5 alkylene chain which may be substituted by one to three groups represented by W';
W' represents a C1-5 alkyl group, a halogen atom, an oxo group, -ORa, -CONRaRb, -SRa, -SORa, -SO2Ra, -NRaRb, -NRaCORb, -NRaSO2Rb, -SO2NRaRb, a heterocyclic group, or a heteroaryl group;
the heterocyclic group and the heteroaryl group may have substituents selected from the group consisting of a C1-5 alkyl group, -ORa, and -NRaRb; the alkyl group may be substituted by a hydroxyl group, a C1-5 alkoxy group, or an amino group;
the above substituents except the oxo group and the halogen may be linked to each other to form a cycloalkyl group or a heterocyclic group; the cycloalkyl group or the heterocyclic group may have a substituent selected from the group consisting of -ORa, -NRaRb, and a C1-5 alkyl group that may be substituted with -ORa;
Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1-5 alkyl group; and the alkyl group may be substituted by a hydroxyl group, a C1-5 alkoxy group, or an amino group.
8. The compound according to any one of claims 1 or 7, or a pharmaceutically acceptable salt thereof, wherein X represents the group represented by the formula (ii), wherein W' represents any one of the groups represented by the formulae:
-Me, -Et, -n-Pr, -i-Pr, -CH2OH, -CH2CH2OH, -CH(OH)CH3, -OH, -OMe, -OEt, -OCH2OH, -O(CH2)2OH, -O(i-Pr), -O(n-Pr), -CONH2, -CONHMe, -CONHEt, -CONH(n-Pr), -CONH(i-Pr), -CONMe2, -CON(Et)Me, -SO2Me, -SOMe, -SMe, -NH2, -NHMe, -NHCH2OH, -NH(CH2)2OH, -N(Me)CH2CH2OH, -NHEt, -NMe2, -N(Et)Me, -NHCOMe, -NMeCOMe, -NHCOEt, -NHCO(n-Pr), and -NHCO(i-Pr).
9. The compound according to any one of claims 1, 7, and 8, or a pharmaceutically acceptable salt thereof, wherein X represents the group represented by the formula (ii), wherein the alkylene chain of Z' is any one of the groups represented by the following formulae:
-CH2-, -(CH2) 2-, -(CH2)3-, -(CH2)4-, -CH2CH(Me)-, -CH2C(Me)2-, -C(Me)2CH2-, -(CH2)2CH(Me)-, -(CH2)2C(Me)2-, -CH(Me)(CH2)2-, -C(Me)2(CH2)2-, -CH2CH(Me)CH2-, -CH2C(Me)2CH2-, -CHOH-, -CH2CH(OH)-, -CH(OH)CH2-, -CH2CH(OH)CH2-, -CH(OH)CH2CH2-, -CH2CH2CH(OH)-, -CO-, -CH2CO-, -COCH2-, -(CH2)2CO-, -CO(CH2)2-, and -CH2CH(OH)CH2-.
10. The compound according to any one of claims 1, 7, 8, and 9, or a pharmaceutically acceptable salt thereof, wherein X represents the group represented by the formula (ii) and X is any one of the groups represented by the following formulae:

wherein the alkylene chain may be substituted at arbitrary positions by one to three substituents selected from the group consisting of a CI-5 alkyl group, a halogen atom, -ORa, -NRaRb, and an oxo group; Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1-5 alkyl group; the alkyl group may be substituted by a hydroxyl group, a C1-5 alkoxy group, or an amino group; Ra represents a hydrogen atom or a C1-5 alkyl group; and the alkyl group may be substituted by a hydroxyl group, a C1-5 alkoxy group, or an amino group.
11. The compound according to claim 1, or a pharmaceutically acceptable salt thereof, wherein X represents the group represented by the following formula (iii) or (iv):

wherein n represents an integer ranging from 1 to 5 and n' represents an integer ranging from 0 to 5; the repeated units represented by -(CH2)n- or -(CH2)n'- in the formulae may be substituted at arbitrary positions in the hydrocarbon moiety by one to three substituents selected from the group consisting of a C1-5 alkyl group, a halogen atom, -ORa, -NRaRb, and an oxo group; Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1-5 alkyl group; and the alkyl group may be substituted by a hydroxyl group, a C1-5 alkoxy group, or an amino group.
12. The compound according to claim 1, or a pharmaceutically acceptable salt thereof, wherein X represents a group selected from the group consisting of a 2-hydroxyethoxy group, a 3-hydroxy-2-dimethylpropoxy group, a 3-hydroxypropoxy group, a 2-carbamoylethoxy group, a 2-methylcarbamoylethoxy group, a 2-methanesulfonyl-ethoxy group, a 2-acetylamino-ethoxy group, a 2-hydroxyethoxyamino group, a 3-hydroxypropionyl amino group, a 2-hydroxyethanesulfonamide group, a 1-hydroxymethyl-cyclopropylmethoxy group, a 2,3-dihydroxy-propoxy group, a 1H-imidazol-2-ylmethoxy group, a 2-methylcarbamoyl-ethoxyamino group, a 2-acetylamino-ethoxyamino group, a 2-methanesulfonyl-ethoxyamino group, a 1H-imidazol-2-ylmethoxyamino group, a 3-hydroxypropoxyamino group, a 2-(2-hydroxyethoxy)-ethoxy group, a 2-methylaminoethoxy group, a 2-(2-hydroxyethylamino)-ethoxy group, a 2-morpholin-4-yl-ethoxy group, a 2-(4-hydroxy-piperidin-1-yl)-ethoxy group, a 2-methylamino-ethoxyamino group, a 2,3-dihydroxy-propoxyamino group, a formyl-methoxyamino group, an acetyl-methoxyamino group, a methoxy-propionylamino group, an isobutyryl-methoxy-amino group, a (2-hydroxy-acetyl)-methoxyamino group, a methoxy-(2-methoxy-acetyl)-amino group, an acetyl-ethoxy-amino group, an ethoxy-propionyl-amino group, an acetyl-isopropoxy-amino group, an acetylhydroxyamino group, an acetoxy-acetyl-amino group, an acetyl-(2-hydroxy-ethoxy)-amino group, an acetyl-(3-hydroxy-propoxy)-amino group, an acetyl-(2-hydroxy-2-methyl-propoxy)-amino group, an acetyl-(2-acetylamino-ethoxy)-amino group, an acetyl-(2-propionylamino-ethoxy)-amino group, an acetyl-(2-isobutyrylamino-ethoxy)-amino group, an acetyl-(2-methylsulfanyl-ethoxy)-amino group, an acetyl-(3-methylsulfanyl-propoxy)-amino group, a 2-hydroxy-1,1-dimethyl-ethoxy group, a methylcarbamoylmethoxyamino group, an ethylcarbamoylmethoxyamino group, a propylcarbamoylmethoxyamino group, an isopropylcarbamoyl-methoxyamino group, a dimethylcarbamoylmethoxyamino group, a 2-ethylcarbamoyl-ethoxyamino group, a 2-propylcarbamoyl-ethoxyamino group, a 2-isopropylcarbamoyl-ethoxyamino group, a 3-methylcarbamoyl-propoxyamino group, a 2-methoxycarbonyl-ethoxyamino group, a methoxyamino group, a methoxy-methyl-amino group, an ethoxyamino group, an isopropoxyamino group, a 2-hydroxy-2-methyl-propoxyamino group, a 2-methylsulfanyl-ethoxyamino group, a 2-methanesulfinyl-ethoxyamino group, a 3-methylsulfanyl-propoxyamino group, a 3-methanesulfinyl-propoxyamino group, a 2-propionylamino-ethoxyamino group, a 2-isobutyrylamino-ethoxyamino group, a 2-hydroxy-acetylamino group, and an acetyl-(2-hydroxy-ethyl)-amino group.
13. The compound according to claim 1, or a pharmaceutically acceptable salt thereof, wherein X represents a group selected from the group consisting of a 3-oxo-[1,2]oxazinan-2-yl group, a 3-oxo-isoxazolidin-2-yl group, a 4,4-dimethyl-3-oxo-isoxazolidin-2-yl group, a 4-hydroxy-3-oxo-[1,2]oxazinan-2-yl group, a 3-oxo-[1,4,2]dioxazinan-2-yl group, a 2-oxo-pyrrolidin-1-yl group, a 2-oxo-piperidin-1-yl group, a 2-oxo-oxazolidin-3-yl group, a 2-oxo-tetrahydro-pyrimidin-1-yl group, and a 2,3-dioxo-morpholin-4-yl group.
14. The compound according to any one of claims 1 to 13, or a pharmaceutically acceptable salt thereof, wherein R1 represents an iodine atom, a bromine atom, a vinyl group, or an ethynyl group.
15. The compound according to any one of claims 1 to 14, or a pharmaceutically acceptable salt thereof, wherein R1 represents an iodine atom or an ethynyl group.
16. The compound according to any one of claims 1 to 15, or a pharmaceutically acceptable salt thereof, wherein R2 represents a chlorine atom, a fluorine atom, a methyl group, or a hydroxymethyl group.
17. The compound according to any one of claims 1 to 16, or a pharmaceutically acceptable salt thereof, wherein R2 represents a fluorine atom.
18. The compound according to any one of claims 1 to 17, or a pharmaceutically acceptable salt thereof, wherein R3 represents a fluorine atom.
19. The compound according to any one of claims 1 to 18, or a pharmaceutically acceptable salt thereof, wherein R4 represents a C1-5 alkyl group substituted by one to three hydroxyl groups.
20. The compound according to any one of claims 1 to 19, or a pharmaceutically acceptable salt thereof, wherein R4 represents a group selected from the group consisting of the groups represented by the following formulae:

21. The compound according to claim 1, or a pharmaceutically acceptable salt thereof, wherein Ra and Rb, which may be the same or different, each represent a group selected from the group consisting of a hydrogen atom, a methyl group, an ethyl group, an n-propyl group, an i-propyl group, an n-butyl group, an i-butyl group, a t-butyl group, a sec-butyl group, a 1,1-dimethylpropyl group, a 2,2-dimethylpropyl group, a 1,2-dimethylpropyl group, a pentyl group, a hydroxymethyl group, a 1- hydroxyethyl group, a 1-hydroxy-1-methylethyl group, a 2-hydroxy-1-methylethyl group, a 2-hydroxy-1,1-dimethylethyl group, a 2-hydroxyethyl group, a 1-hydroxypropyl group, a 2-hydroxypropyl group, and a 3-hydroxypropyl group.
22. The compound according to any one of claims 1 to 6, or a pharmaceutically acceptable salt thereof, wherein X represents -Y-Z-W of the formula (i), wherein W and W', which may be the same or different, each represent a group selected from the group consisting of -OH, -OMe, -OEt, -OCH2OH, -O(CH2)2OH, -O(i-Pr), -O(n-Pr), -COOH, -COOMe, -COOEt, -COOCOMe, -COCl, -CONH2, -CONHMe, -CONHEt, -CONH(n-Pr), -CONH(i-Pr), -CONMe2, -CON(Et)Me, -SO2Me, -SOMe, -SMe, -NH2, -NHMe, -NHCH2OH, -NH(CH2)2OH, -N(Me)CH2CH2OH, -NHHEt, -NMe2, -N(Et)Me, -NHCOMe, -NMeCOMe, -NHCOEt, -NHCO(n-Pr), and -NHCO(i-Pr); and W is a hydrogen atom when Y is not -O-.
23. The compound according to claim 1, or a pharmaceutically acceptable salt thereof, wherein the compound represented by the above formula (1) is any one selected from the group consisting of:
(1) B-1 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(2-hydroxy-ethoxymethy l)-benzamide, (2) B-2 2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)-5-(2-hydroxy-ethoxyme thyl)-benzamide, (3) B-3 N-(2,3-dihydroxy-propoxy)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-(2-hydroxy-ethoxy methyl)-benzamide, (4) B-4 2-(2-chloro-4-iodo-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)-5-(2-hydroxy-ethoxymeth yl)-benzamide, (5) B-5 3,4-difluoro-2-(2-fluoro-4-vinyl-phenylamino)-N-(2-hydroxy-ethoxy)-5-(2-hydroxy-ethoxymeth yl)-benzamide, (6) B-6 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(3-hydroxypropoxymeth yl)-benzamide, (7) B-7 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-(3-hydroxy-2,2-dimethyl-propoxymethyl)-N-(2-hydroxy-ethoxy)-benzamide, (8) B-8 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(1-hydroxymethyl-cyclo propylmethoxymethyl)-benzamide, (9) B-9 5-(2,3-dihydroxy-propoxymethyl)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benzamide, (10) B-10 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(2-methylcarbamoyl-eth oxymethyl)-benzamide, (11) B-11 5-(2-acetylamino-ethoxymethyl)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-et hoxy)-benzamide, (12) B-12 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(2-methanesulfonyl-etho xymethyl)-benzamide, (13) B-13 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(1H-imidazol-2-yl methoxymethyl)-benzamide, (14) B-14 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[2-(2-hydroxy-ethoxy)-et hoxymethyl]-benzamide, (15) B-15 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(2-methylamino-ethoxy methyl)-benzamide, (16) B-16 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[2-(2-hydroxy-ethylamin o)-ethoxymethyl]-benzamide, (17) B-17 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(2-morpholin-4-yl-ethox ymethyl)-benzamide, (18) B-18 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[2-(4-hydroxy-piperidin-1-yl)-ethoxymethyl]-benzamide, and (19) B-19 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-(2-hydroxy-1,1-dimethyl-ethoxymethyl)-N-(2-h ydroxy-ethoxy)-benzamide.
24. The compound according to claim 1, or a pharmaceutically acceptable salt thereof, wherein the compound represented by the above formula (1) is any one selected from the group consisting of:
(1) C-1 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-hydroxy-ethoxyamin o)-methyl]-benzamide, (2) C-2 2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)-5-[(2-hydroxy-ethoxya mino)-methyl]-benzamide, (3) C-3 N-(2,3 -dihydroxy-propoxy)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-[(2-hydroxy-ethoxy amino)-methyl]-benzamide, (4) C-4 2-(2-chloro-4-iodo-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)-5-[(2-hydroxy-ethoxyamin o)-methyl] -benzamide, (5) C-5 3,4-difluoro-2-(2-fluoro-4-vinyl-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-hydroxy-ethoxyami no)-methyl]-benzamide, (6) C-6 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5 - [(2-methylcarbamoyl-eth oxyamino)-methyl]-benzamide, (7) C-7 5-[(2-acetylamino-ethoxyamino)-methyl] -3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hy droxy-ethoxy)-benzamide, (8) C-8 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-methanesulfonyl-eth oxyamino)-methyl]-benzamide, (9) C-9 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(1H-imidazol-2-ylmeth oxyamino)-methyl] -benzamide, (10) C-10 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5- [(3 -hydroxy-propoxyami no)-methyl] -benzamide, (11) C-11 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-methylamino-ethoxy amino)-methyl]-benzamide, (12) C-12 5-[(2,3 -dihydroxy-propoxyamino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-h ydroxy-ethoxy)-benzamide, (13) C-13 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(methylcarbamoylmetho xyamino-methyl)-benzamide, (14) C-14 5-(ethylcarbamoylmethoxyamino-methyl)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-h ydroxy-ethoxy)-benzamide, (15) C-15 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(propylcarbamoylmetho xyamino-methyl)-benzamide, (16) C-16 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(isopropylcarbamoyl-m ethoxyamino)-methyl] -benzamide, (17) C-17 5-(dimethylcarbamoylmethoxyamino-methyl)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-( 2-hydroxy-ethoxy)-benzamide, (18) C-18 5-[(2-ethylcarbamoyl-ethoxyamino)-methyl] -3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2 -hydroxy-ethoxy)-benzamide, (19) C-19 5-[(2-propylcarbamoyl-ethoxyamino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-( 2-hydroxy-ethoxy)-benzamide, (20) C-20 5-[(2-isopropylcarbamoyl-ethoxyamino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benzamide, (21) C-21 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5- [(3 -methylcarbamoyl-pr opoxyamino)-methyl] -benzamide, (22) C-22 3 -[N- [2,3 -difluoro-4-(2-fluoro-4-iodo-phenylamino)-5-(2-hydroxyethoxycarbamoyl)benzyl] amin ooxy]propionic acid methyl ester, (24) C-24 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(methoxyamino-methyl)-benzamide, (25) C-25 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(methoxy-methyl-amino )-methyl] -benzamide, (26) C-26 5-(ethoxyamino-methyl)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-b enzamide, (27) C-27 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(isopropoxyamino-meth yl)-benzamide, (28) C-28 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)5-[(2-hydroxy-2-methyl-pro poxyamino)-methyl]-benzamide, (29) C-29 2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)5-[(2-hydroxy-2-methyl-propoxyamino)-methyl]-benzamide, (30) C-30 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-methylsulfanyl-ethox yamino)-methyl]-benzamide, (31) C-31 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-methanesulfinyl-etho xyamino)-methyl]-benzamide, (32) C-32 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(3-methylsulfanyl-propo xyamino)-methyl]-benzamide, (33) C-33 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(3-methanesulfinyl-prop oxyamino)-methyl]-benzamide, (34) C-34 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-propionylamino-eth oxyamino)-methyl]-benzamide, and (35) C-35 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(2-isobutyrylamino-etho xyamino)-methyl] -benzamide.
25. The compound according to claim 1, or a pharmaceutically acceptable salt thereof, wherein the compound represented by the above formula (1) is any one selected from the group consisting of:
(1) E-1 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(3-hydroxy-propionyla mino)-methyl]-benzamide (2) E-2 2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)-5-[(3-hydroxy-propiony lamino)-methyl]-benzamide (3) E-3 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5- [(2-hydroxy-ethanesulfonylamino)-methyl]-N-( 2-hydroxy-ethoxy)-benzamide, (4) E-4 2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-5-[(2-hydroxy-ethanesulfonylamino)-methyl]-N-(2-hydroxy-ethoxy)-benzamide, (5) E-5 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-[(2-hydroxy-acetylamino)-methyl]-N-(2-hydrox y-ethoxy)-benzamide, and (6) E-6 5-{[acetyl-(2-hydroxy-ethyl)-amino]-methyl}-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-( 2-hydroxy-ethoxy)-benzamide.
26. The compound according to claim 1, or a pharmaceutically acceptable salt thereof, wherein the compound represented by the above formula (1) is any one selected from the group consisting of:
(1) F-1 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-[(formyl-methoxy-amino)-methyl]-N-(2-hydrox y-ethoxy)-benzamide, (2) F-2 5-[acetyl-methoxy-amino-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benzamide, (3) F-3 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(methoxy-propionyl-am ino)-methyl]-benzamide, (4) F-4 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-[(isobutyryl-methoxy-am ino)-methyl] -benzamide, (5) F-5 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-{[(2-hydroxy-acetyl)-methoxy-amino]-methyl}-N-(2-hydroxy-ethoxy)-benzamide, (6) F-6 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-{[methoxy-(2-methoxy-a cetyl)-amino]-methyl}-benzamide, (7) F-7 5-[(acetyl-methoxy-amino)-methyl]-2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydr oxy-ethoxy)-benzamide, (8) F-8 2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)-5-[(methoxy-propionyl-amino)-methyl]-benzamide, (9) F-9 2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)-5-[(isobutyryl-methoxy-amino)-methyl]-benzamide, (10) F-10 5-[(acetyl-ethoxy-amino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-e thoxy)-benzamide, (11) F-11 5- [(ethoxy-propionyl-amino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydro xy-ethoxy)-benzamide, (12) F-12 5-[(acetyl-isopropoxy-amino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydro xy-ethoxy)-benzamide, (13) F-13 5-[(acetyl-hydroxy-amino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy -ethoxy)-benzamide, (14) F-14 5-[(acetoxy-acetyl-amino)-methyl]-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benzamide, (15) F-15 5- {[acetyl-(2-hydroxy-ethoxy)-amino]-methyl}-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N
-(2-hydroxy-ethoxy)-benzamide, (16) F-16 5- {[acetyl-(3-hydroxy-propoxy)-amino]-methyl}-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benzamide, (17) F-17 5- {[acetyl-(2-hydroxy-2-methyl-propoxy)-amino]-methyl}-3,4-difluoro-2-(2-fluoro-4-iodo-phen ylamino)-N-(2-hydroxy-ethoxy)-benzamide, (18) F-18 5- {[acetyl-(2-acetylamino-ethoxy)-amino]-methyl}-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino )-N-(2-hydroxy-ethoxy)-benzamide, (19) F-19 5-{[acetyl-(2-propionylamino-ethoxy)-amino]-methyl}-3,4-difluoro-2-(2-fluoro-4-iodo-phenyla mino)-N-(2-hydroxy-ethoxy)-benzamide, (20) F-20 5-{[acetyl-(2-isobutyrylamino-ethoxy)-amino]-methyl}-3,4-difluoro-2-(2-fluoro-4-iodo-phenyla mino)-N-(2-hydroxy-ethoxy)-benzamide, (21) F-21 -{[acetyl-(2-methylsulfanyl-ethoxy)-amino]-methyl}-3,4-difluoro-2-(2-fluoro-4-iodo-phenylam ino)-N-(2-hydroxy-ethoxy)-benzamide, (22) F-22 5 -{[acetyl-(3-methylsulfanyl-propoxy)-amino]-methyl}-3,4-difluoro-2-(2-fluoro-4-iodo-phenyla mino)-N-(2-hydroxy-ethoxy)-benzamide, (23) F-23 5-[(acetyl-ethoxy-amino)-methyl]-2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydrox y-ethoxy)-benzamide, (24) F-24 5-[(ethoxy-propionyl-amino)-methyl]-2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hy droxy-ethoxy)-benzamide, (25) F-25 5- {[acetyl-(2-hydroxy-ethoxy)-amino]-methyl}-2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluor o-N-(2-hydroxy-ethoxy)-benzamide, and (26) F-26 5-{[acetyl-(2-hydroxy-2-methyl-propoxy)-amino]-methyl}-2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)-benzamide.
27. The compound according to claim 1, or a pharmaceutically acceptable salt thereof, wherein the compound represented by the above formula (1) is any one selected from the group consisting of (1) G-1 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(3-oxo-[1,2]oxazinan-2-ylmethyl)-benzamide, (2) G-2 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(3-oxo-isoxazolidin-2-yl methyl)-benzamide, (3) G-3 5-(4,4-dimethyl-3-oxo-isoxazolidin-2-ylmethyl)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-benzamide, (4) G-4 2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)-5-(3-oxo-[ 1,2]oxazinan-2-ylmethyl)-benzamide, (5) G-5 2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)-5-(3-oxo-isoxazolidin-2 -ylmethyl)-benzamide, (6) G-6 N-(2,3-dihydroxy-propoxy)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-(3-oxo-[ 1,2]oxazin an-2-ylmethyl)-benzamide, (7) G-7 N-(2,3-dihydroxy-propoxy)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-5-(3-oxo-isoxazolidin -2-ylmethyl)-benzamide, and (8) G-8 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(4-hydroxy-3-oxo-[ 1,2]0 xazinan-2-ylmethyl)-benzamide.
28. The compound according to claim 1, or a pharmaceutically acceptable salt thereof, wherein the compound represented by the above formula (1) is any one selected from the group consisting of:
(1) H-1 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(3-oxo-[1,4,2]dioxazinan -2-ylmethyl)-benzamide, (2) H-2 2-(4-ethynyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-ethoxy)-5-(3-oxo-[1,4,2]dioxazi nan-2-ylmethyl)-benzamide, (3) H-3 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(2-oxo-pyrrolidin-1-ylm ethyl)-benzamide, (4) H-4 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(2-oxo-piperidin-1-ylmet hyl)-benzamide, (5) H-5 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(2-oxo-oxazolidin-3-ylm ethyl)-benzamide, (6) H-6 3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydroxy-ethoxy)-5-(2-oxo-tetrahydro-pyrimi din-1-ylmethyl)-benzamide, and (7) H-7 -(2,3-dioxo-morpholin-4-ylmethyl)-3,4-difluoro-2-(2-fluoro-4-iodo-phenylamino)-N-(2-hydrox y-ethoxy)-benzamide.
29. A synthetic intermediate (E) of the compound represented by the formula (1) according to claim 1, wherein the intermediate is represented by the following formula (6):
wherein R1 represents a halogen atom, an alkenyl group, or an alkynyl group;
R2 represents a halogen atom or an alkyl group; the alkyl group may be substituted by a hydroxyl group;
R3 represents a hydrogen atom or a halogen atom;
in the above formula (6), the group represented by the following formula (a):
represents a 3- to 1 0-membered heterocyclic group that may have one to three substituents selected from the group consisting of a C1-5 alkyl group, a halogen atom, -OR
a, -NR a R b, and an oxo group;
the above substituents except the oxo group and the halogen atom may be linked to each other to form a cycloalkyl group or a heterocyclic group; the cycloalkyl group or the heterocyclic group may have a substituent selected from the group consisting of -OR a, NR a R b, and a C1-5 alkyl group that may be substituted with -OR a;
R a and R b, which may be the same or different, each represent a hydrogen atom or a C1-5 alkyl group; the alkyl group may be substituted by a hydroxyl group, a C1-5 alkoxy group, or an amino group;
U represents -O-, -CONRd-, -S-, -SO-, -SO2-, -NRd-, -NRdCO-, -NRdSO2-, -SO2NRd-, a divalent heterocyclic group, or a divalent heteroaryl group; Rd represents a hydrogen atom or a C1-5 alkyl group; the alkyl group may be substituted by a hydroxyl group, a C1-5 alkoxy group, or an amino group;
R1, R2, R3, and U may have protecting group(s) required for the synthesis.
30. The synthetic intermediate (E) according to claim 29, wherein R1 represents an iodine atom, a bromine atom, an ethynyl group, or a vinyl group;
R2 represents a chlorine atom or a fluorine atom;
R3 represents a fluorine atom; and U represents -O-.
31. The synthetic intermediate (E) according to claim 29, wherein the heterocyclic group represented by the formula (a) is a [1,3]dioxoran-2-yl group or a[l,3]dioxan-2-yl group, which may be substituted by a hydroxyl group or a C1-5 alkyl group.
32. A synthetic intermediate (F) of the compound represented by the formula (1) according to claim 1, wherein the intermediate is represented by the following formula (7):
wherein R1 represents a halogen atom, an alkenyl group, or an alkynyl group;
R2 represents a halogen atom or an alkyl group; the alkyl group may be substituted by a hydroxyl group;
R3 represents a hydrogen atom or a halogen atom;
R4 represents a hydrogen atom, an alkyl group, an alkenyl group, or an alkynyl group; the alkyl group, the alkenyl group, and the alkynyl group may have one to three substituents selected from the group consisting of -OR a, -NR a R b, -NR a COR b, a heterocyclic group, and a heteroaryl group; the heterocyclic group and the heteroaryl group may have one to three substituents selected from the group consisting of a C1-5 alkyl group, -OR a, and -NR a R
b; R a and R b, which may be the same or different, each represent a hydrogen atom or a C1-5 alkyl group; the alkyl group may be substituted by a hydroxyl group, a C1-5 alkoxy group, or an amino group;
in the above formula (7), the group represented by the following formula (a):
represents a 3- to 10-membered heterocyclic group that may have one to three substituents selected from the group consisting of a C1-5 alkyl group, a halogen atom, -OR
a, -NR a R b, and an oxo group;
the above substituents except the oxo group and the halogen atom may be linked to each other to form a cycloalkyl group or a heterocyclic group; the cycloalkyl group or the heterocyclic group may have a substituent selected from the group consisting of -OR a, NR a R b, and a C1-5 alkyl group that may be substituted with -OR a;
R a and R b, which may be the same or different, each represent a hydrogen atom or a C1-5 alkyl group; and the alkyl group may be substituted by a hydroxyl group, a C1-5 alkoxy group, or an amino group;
U represents -O-, -CONRd-, -S-, -SO-, -SO2-, -NRd-, -NRdCO-, -NRdSO2-, -SO2NRd-, a divalent heterocyclic group, or a divalent heteroaryl group; Rd represents a hydrogen atom or a C1-5 alkyl group; the alkyl group may be substituted by a hydroxyl group, a C1-5 alkoxy group, or an amino group;
R1, R2, R3, and U may have protecting group(s) required for the synthesis.
33. The synthetic intermediate (F) according to claim 32, wherein R1 represents an iodine atom, a bromine atom, an ethynyl group, or a vinyl group;
R2 represents a chlorine atom or a fluorine atom;
R3 represents a fluorine atom;
R4 represents a hydroxy alkyl group, in whichthe hydroxy moiety may be protected; and U represents -O-.
34. The synthetic intermediate (F) according to claim 32, wherein the heterocyclic group represented by the formula (a) is a [1,3]dioxolan-2-yl group or a[1,3]dioxan-2-yl group, which may be substituted by a hydroxyl group or a C1-5 alkyl group.
35. A synthetic intermediate (I) of the compound represented by the formula (1) according to claim 1, wherein the intermediate is represented by the following formula (10):

wherein R1 represents a halogen atom, an alkenyl group, or an alkynyl group;
R2 represents a halogen atom or an alkyl group; the alkyl group may be substituted by a hydroxyl group;
R3 represents a hydrogen atom or a halogen atom;
Z represents a C1-8 alkylene chain which may be substituted by one to three groups represented by W';
W or W', which may be the same or different, each represent a hydrogen atom, a C1-5 alkyl group, a halogen atom, an oxo group, -ORa, -COORa, -COOCORa, -CO-[halogen atom], -OCORa, -CONRaRb, -SRa, -SORa, -SO2Ra, -NRaRb, -NRaCORb, -NRaSO2Rb, -SO2NRaRb, a heterocyclic group, or a heteroaryl group;
the heterocyclic group and the heteroaryl group may have a substituent selected from the group consisting of a C1-5 alkyl group, -ORa, and -NRaRb; the alkyl group may be substituited by a hydroxyl group, a C1-5 alkoxy group, or an amino group;
the above substituents except the oxo group and the halogen atom may be linked to each other to form a cycloalkyl group or a heterocyclic group; the cycloalkyl group or the heterocyclic group may have a substituent selected from the group consisting of -ORa, -NRaRb, and a C1-5 alkyl group that may be substituted with -ORa;
Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1-5 alkyl group; and the alkyl group may be substituted a hydroxyl group, a C1-5 alkoxy group, or an amino group; and R1, R2, R3, Z, W and W' may have protecting group(s) required for the synthesis.
36. The synthetic intermediate according to claim 35, which is a synthetic intermediate (K) represented by the following formula (12):

wherein R1 represents a halogen atom, an alkenyl group, or an alkynyl group;
R2 represents a halogen atom or an alkyl group; the alkyl group may be substituted by a hydroxyl group;
R3 represents a hydrogen atom or a halogen atom;
Z' represents a C1-5 alkylene chain that may be substituted by one to three groups represented by W';
W' represents any one of the groups represented by the formulae:
-OH, -OMe, -OEt, -OCH2OH, -O(CH2)2OH, -O(i-Pr), -O(n-Pr), -CONH2, -CONHMe, -CONHEt, -CONH(n-Pr), -CONH(i-Pr), -CONMe2, -CON(Et)Me, -SO2Me, -SOMe, -SMe, -NH2, -NHMe, -NHCH2OH, -NH(CH2)2OH, -N(Me)CH2CH2OH, -NHEt, -NMe2, -N(Et)Me, -NHCOMe, -NMeCOMe, -NHCOEt, -NHCO(n-Pr), and -NHCO(i-Pr);
Q represents -ORc, -OCORc, -NRcRd, or a halogen atom; Rc and Rd, which may be the same or different, each represent a hydrogen atom or a C1-5 alkyl group;
R1, R2, and R3 are defined herein above; and R1, R2, R3, Z', Q and W' may have protecting group(s) required for the synthesis.
37. The synthetic intermediate according to claim 35 or 36, wherein R1 represents an iodine atom, a bromine atom, an ethynyl group, or a vinyl group;
R2 represents a chlorine atom or a fluorine atom; and R3 represents a fluorine atom.
38. A synthetic intermediate (L) of the compound represented by the formula (1) the according to claim 1, wherein the intermediate is represented the following formula (13):

wherein R1 represents a halogen atom, an alkenyl group, or an alkynyl group;
R2 represents a halogen atom or an alkyl group; the alkyl group may be substituted by a hydroxyl group;
R3 represents a hydrogen atom or a halogen atom;
R4 represents a hydrogen atom, an alkyl group, an alkenyl group, or an alkynyl group; the alkyl group, the alkenyl group, and the alkynyl group may have one to three substituents selected from the group consisting of -ORa, -NRaRb, -NRaCORb, a heterocyclic group, and a heteroaryl group; the heterocyclic group and the heteroaryl group may have one to three substituents selected from the group consisting of a C1-5 alkyl group, -ORa, and -NRaRb; Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1-5 alkyl group; the alkyl group may be substituted by a hydroxyl group, a C1-5 alkoxy group, or an amino group;
Z' represents a C1-5 alkylene chain that may have one to three groups represented by W';
W' represents the group represented by any one of the groups represented by the following formulae:
-OH, -OMe, -OEt, -OCH2OH, -O(CH2)2OH, -O(i-Pr), -O(n-Pr), -CONH2, -CONHMe, -CONHEt, -CONH(n-Pr), -CONH(i-Pr), -CONMe2, -CON(Et)Me, -SO2Me, -SOMe, -SMe, -NH2, -NHMe, -NHCH2OH, -NH(CH2)2OH, -N(Me)CH2CH2OH, -NHEt, -NMe2, -N(Et)Me, -NHCOMe, -NMeCOMe, -NHCOEt, -NHCO(n-Pr), and -NHCO(i-Pr);
Q represents -ORc, -OCORc, -NRcRd, or a halogen atom; Rc and Rd, which may be the same or different, each represent a hydrogen atom or a C1-5 alkyl group; and R1, R2, R3, R4, Z', Q, and W' may have protecting group(s) required for the synthesis].
39. The synthetic intermediate (L) according to claim 38, wherein R1 represents an iodine atom, a bromine atom, an ethynyl group, or a vinyl group;
R2 represents a chlorine atom or a fluorine atom;
R3 represents a fluorine atom; and R4 represents a hydroxy alkyl group, in which the hydroxy alkyl moiety may be protected.
40. A method for producing any one of the compounds (M), (N), (M'), and (N'), wherein the method comprises reacting a reducing agent, in a solvent at neutral pH or in the presence of an acid, with a synthetic intermediate (E) represented by the following formula (6) or a synthetic intermediate (F) represented by the following formula (7):

wherein R1 represents a halogen atom, an alkenyl group, or an alkynyl group;
R2 represents a halogen atom or an alkyl group; the alkyl group may be substituted by a hydroxyl group;
R3 represents a hydrogen atom or a halogen atom;
R4 represents a hydrogen atom, an alkyl group, an alkenyl group, or an alkynyl group;
the alkyl group, the alkenyl group, and the alkynyl group may have one to three substituents selected from the group consisting of -ORa, -NRaRb, -NRaCORb, a heterocyclic group, and a heteroaryl group; the heterocyclic group and the heteroaryl group may have one to three substituents selected from the group consisting of a C1-5 alkyl group, -ORa, and -NRaRb;
Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1-5 alkyl group; and the alkyl group may be substituted by a hydroxyl group, a C1-5 alkoxy group, or an amino group;
in the formulae (6) and (7), the group represented by the following formula (a):
represents a 3- to 10-membered heterocyclic group that may have one to three substituents selected from the group consisting of a C1-5 alkyl group, a halogen atom, -ORa, -NRaRb, and an oxo group;
the above substituents except the oxo group and the halogen atom may be linked to each other to form a cycloalkyl group or a heterocyclic group; the cycloalkyl group or the heterocyclic group may have a substituent selected from the group consisting of -ORa, -NRaRb, and a C1-5 alkyl group that may be substituted with -ORa;
Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1-5 alkyl group; and the alkyl group may be substituted by a hydroxyl group, a C1-5 alkoxy group, or an amino group;
U represents -O-, -CONRd-, -S-, -SO-, -SO2-, -NRd-, -NRdCO-, -NRdSO2-, -SO2NRd-, a divalent heterocyclic group, or a divalent heteroaryl group; Rd represents a hydrogen atom or a C1-5 alkyl group; the alkyl group may be substituted by a hydroxyl group, a C1-5 alkoxy group, or an amino group; and R1, R2, R3, and U may have protecting group(s) required for the synthesis to thereby obtain the compounds (M), (N), (M'), and (N') represented by the formulae (14), (15), (14'), and (15'), respectively:

wherein R1, R2, R3, R4, and U are defined herein above in formulae (6) and (7);
Z corresponds to the alkylene chain constituting the ring in the above formula (a); Z represents a C1-8 alkylene chain, which may be substituted by one to three groups represented by W'; W' represents any one of substituents selected from the group consisting of a C1-5 alkyl group, a halogen atom, -ORa, -NRaRb, and an oxo group; the above substituents except the oxo group and the halogen atom may be linked to each other to form a cycloalkyl group or a heterocyclic group;
Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1-5 alkyl group; the alkyl group may be substituted by a hydroxyl group, a C1-5 alkoxy group, or an amino group.
41. A method for producing compound (I) or compound (J), wherein the method comprises reacting a reducing agent, in a solvent at neutral pH or in the presence of an acid, with a synthetic intermediate (G) of the compound represented by the formula (1) according to claim 1, wherein (G) is represented by the following formula (8):

wherein R1 represents a halogen atom, an alkenyl group, or an alkynyl group;
R2 represents a halogen atom or an alkyl group; the alkyl group may be substituted by a hydroxyl group;
R3 represents a hydrogen atom or a halogen atom;
Z represents a C1-8 alkylene chain that may have one to three substituents represented by W' ;
W or W', which may be the same or different, each represent a hydrogen atom, a alkyl group, a halogen atom, an oxo group, -ORa, -COORa, -COOCORa, -CO-[halogen atom], -OCORa, -CONRaRb, -SRa, -SORa, -SO2Ra, -NRaRb, -NRaCORb, -NRaSO2Rb, -SO2NRaRb, a heterocyclic group, or a heteroaryl group;
the heterocyclic group and the heteroaryl group may have a substituent selected from the group consisting of a C1-5 alkyl group, -ORa, and -NRaRb; the alkyl group may be substituted by a hydroxyl group, a C1-5 alkoxy group, or an amino group;
the above substituents except the oxo group and the halogen may be linked to each other to form a cycloalkyl group or a heterocyclic group; the cycloalkyl group or the heterocyclic group may have a substituent selected from the group consisting of -ORa, -NRaRb, and a C1-5 alkyl group that may be substituted with -ORa;
Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1-5 alkyl group; the alkyl group may be substituted by a hydroxyl group, a C1-5 alkoxy group, or an amino group; and R1, R2, R3, Z, W, and W' may have protecting group(s) required for the synthesis, or a synthetic intermediate (H) of the compound represented by the formula (1) according to claim 1, wherein (H) is represented by the following formula (9):

wherein R1 represents a halogen atom, an alkenyl group, or an alkynyl group;
R2 represents a halogen atom or an alkyl group; the alkyl group may be substituted by a hydroxyl group;
R3 represents a hydrogen atom or a halogen atom;
R4 represents a hydrogen atom, an alkyl group, an alkenyl group, or an alkynyl group;
the alkyl group, the alkenyl group, and the alkynyl group may have one to three substituents selected from the group consisting of -ORa, -NRaRb, -NRaCORb, a heterocyclic group, and a heteroaryl group; the heterocyclic group and the heteroaryl group may have one to three substituents selected from the group consisting of a C1-5 alkyl group, -ORa, and -NRaRb;
Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1-5 alkyl group; and the alkyl group may be substituted by a hydroxyl group, a C1-5 alkoxy group, or an amino group;
Z represents a C1-8 alkylene chain that may be substituted by one to three groups represented by W';
W or W', which may be the same or different, each represent a hydrogen atom, a alkyl group, a halogen atom, an oxo group, -ORa, -COORa, -COOCORa, -CO-[halogen atom], -OCORa, -CONRaRb, -SRa, -SORa, -SO2Ra, -NRaRb, -NRaCORb, -NRaSO2Rb, -SO2NRaRb, a heterocyclic group, or a heteroaryl group;
the heterocyclic group and the heteroaryl group may have a substituent selected from the group consisting of a C1-5 alkyl group, -ORa, and -NRaRb; the alkyl group may be substituted by a hydroxyl group, a C1-5 alkoxy group, or an amino group;
the above substituents except the oxo group and the halogen atom may be linked to each other to form a cycloalkyl group or a heterocyclic group; the cycloalkyl group or the heterocyclic group may have a substituent selected from the group consisting of -ORa, -NRaRb, and a C1-5 alkyl group that may be substituted with -ORa;
Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1-5 alkyl group; and the alkyl group may be substituted by a hydroxyl group, a C1-5 alkoxy group, or an amino group;
R1, R2, R3, Z, W, and W' may have protecting group(s) required for the synthesis, to thereby obtain compound (I) represented by the following formula (10):

or compound (J) represented by the following formula (11):
in the formulae (10) and (11), R1, R2, R3, R4, Z, W, and W' are defined herein above in formulae (8) and (9).
42. A method for producing compound (O) or compound (P), wherein the method comprises allowing a synthetic intermediate (K) or (L) to intramolecularly cyclize at neutral pH
or in the presence of an acid or a base in a solvent that optionally contains a peptide condensing agent, wherein the synthetic intermediates (K) and (L) are represented by the following formulae (12) and (13), respectively:

n the above formulae (12) and (13), R1 represents a halogen atom, an alkenyl group, or an alkynyl group;
R2 represents a halogen atom or an alkyl group; the alkyl group may be substituted by a hydroxyl group;
R3 represents a hydrogen atom or a halogen atom;
R4 represents a hydrogen atom, an alkyl group, an alkenyl group, or an alkynyl group;
the alkyl group, the alkenyl group, and the alkynyl group may have one to three substituents selected from the group consisting of -ORa, -NRaRb, -NRaCORb, a heterocyclic group, and a heteroaryl group; the heterocyclic group and the heteroaryl group may have one to three substituents selected from the group consisting of a C1-5 alkyl group, -ORa, and -NRaRb;
Ra and Rb, which may be the same or different, each represent a hydrogen atom or a CI-5 alkyl group; and the alkyl group may be substituted by a hydroxyl group, a C1-5 alkoxy group, or an amino group;
Z' represents a C1-5alkylene chain that may be substituted by one to three groups represented by W';
W' represents any one of the groups of -OH, -OMe, -OEt, -OCH2OH, -O(CH2)2OH, -O(i-Pr), -O(n-Pr), -CONH2, -CONHMe, -CONHEt, -CONH(n-Pr), -CONH(i-Pr), -CONMe2, -CON(Et)Me, -SO2Me, -SOMe, -SMe, -NH2, -NHMe, -NHCH2OH, -NH(CH2)2OH, -N(Me)CH2CH 2OH, -NHEt, -NMe2, -N(Et)Me, -NHCOMe, -NMeCOMe, -NHCOEt, -NHCO(n-Pr), and -NHCO(i-Pr);

Q represents -ORc, -OCORc, -NRcRd, or a halogen atom; Re and Rd, which may be the same or different, each represent a hydrogen atom or a C1-5 alkyl group;
R1, R2, R3, R4, Z', W', and Q may have protecting group(s) required for the synthesis, to thereby obtain compound (O) represented by the following formula (16):

or compound (P) represented by the following formula (17):
in the formula (16) and (17), R1, R2, R3, R4, and Z' are defined herein above in formulae (12) and (13).
43. A method for producing compound (S) or compound (T), wherein the method comprises reacting, in the presence of a base or an acid, or at neutral pH, in a solvent that optionally contains a condensing agent, the synthetic intermediate (I) of the compound represented by the formula (1) according to claim 1, the intermediate being represented by the following formula (10):

or the synthetic intermediate (J)of the compound represented by the formula (1) according to claim 1, the intermediate being represented by the following formula (11):

in the formulae (10) and (11), R1 represents a halogen atom, an alkenyl group, or an alkynyl group;
R2 represents a halogen atom or an alkyl group; the alkyl group may be substituted by a hydroxyl group;
R3 represents a hydrogen atom or a halogen atom;
R4 represents a hydrogen atom, an alkyl group, an alkenyl group, or an alkynyl group;
the alkyl group, the alkenyl group, and the alkynyl group may have one to three substituents selected from the group consisting of -ORa, -NRaRb, -NRaCORb, a heterocyclic group, and a heteroaryl group; the heterocyclic group and the heteroaryl group may have one to three substituents selected from the group consisting of a C1-5 alkyl group, -ORa, and -NRaRb; Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1-5 alkyl group; the alkyl group may be substituted by a hydroxyl group, a C1-5 alkoxy group, or an amino group;
Z represents a C1-8 alkylene chain that may be substituted by one to three groups represented by W';
W or W', which may be the same or different, each represent a hydrogen atom, a alkyl group, a halogen atom, an oxo group, -ORa, -COORa, -COOCORa, -CO-[halogen atom], -OCORa, -CONRaRb, -SRa, -SORa, -SO2Ra, -NRaRb, -NRaCORb, -NRaSO2Rb, -SO2NRaRb, a heterocyclic group, or a heteroaryl group;
the heterocyclic group and the heteroaryl group may have a substituent selected from the group consisting of a C1-5 alkyl group, -ORa, and -NRaRb; the alkyl group may be substituted by a hydroxyl group, a C1-5 alkoxy group, or an amino group;
the above substituents except the oxo group and the halogen may be linked to each other to form a cycloalkyl group or a heterocyclic group; the cycloalkyl group or the heterocyclic group may have a substituent selected from the group consisting of -ORa, -NRaRb, and a C1-5 alkyl group that may be substituted with -ORa;

Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1-5 alkyl group; the alkyl group may be substituted by a hydroxyl group, a C1-5 alkoxy group, or an amino group;
R1, R2, R3, R4, Z, W, and W' may have protecting group(s) required for the synthesis with a carboxylic acid derivative represented by the following formula:

wherein R9 represents a hydrogen atom, an alkyl group, or -ORa; the alkyl group may be substituted by a halogen atom, -ORa, or -NRaRb;
Q represents -ORc, -OCORc, -NRcRd, or a halogen atom; Re and Rd, which may be the same or different, each represent a hydrogen atom or a C1-5 alkyl group;
Ra and Rb, which may be the same or different, each represent a hydrogen atom or a C1-5 alkyl group; and the alkyl group may be substituted by a hydroxyl group, a C1-5 alkoxy group, or an amino group;
R9 and Q may have protecting group(s) required for the synthesis, to thereby obtain compound (S) represented by the following formula (18):
or compound (T) represented by the following formula (19):
in the formulae (18) and (19), R1, R2, R3, R4, Z, and W are defined herein above in formulae (10) and (11); and R9 is the carboxylic acid derivative defined herein above.
44. A pharmaceutical composition comprising a compound according to any one of claims 1 to 28 or a pharmaceutically acceptable salt thereof and a pharmaceutically acceptable excipient.
45. An MEK inhibitor comprising a compound according to any one of claims 1 to 28 or a pharmaceutically acceptable salt thereof.
46. A preventive or therapeutic agent for a proliferative disease, which comprises a compound according to any one of claims 1 to 28 or a pharmaceutically acceptable salt thereof.
47. The preventive or therapeutic agent for a proliferative disease according to claim 46, wherein the proliferative disease is a cancer.
48. The preventive or therapeutic agent for a proliferative disease according to claim 47, wherein the cancer is breast, lung, colorectal, prostate, liver, ovarian, uterine, or pancreatic cancer.
49. Use of a compound according to any one of claims 1 to 28 or a pharmaceutically acceptable salt thereof in the production of a preventive or therapeutic agent for a disease to which MEK inhibition is effective.
50. A preventive or therapeutic agent for a joint disorder with inflammation, wherein the agent comprises a compound according to any one of claims 1 to 28 or a pharmaceutically acceptable salt thereof.
51. The preventive or therapeutic agent for a joint disorder with inflammation according to claim 50, wherein the joint disorder with inflammation is osteoarthritis or rheumatoid arthritis.
52. A compound (O represented by the following formula (16):

wherein R1 represents a halogen atom, an alkenyl group, or an alkynyl group;
R2 represents a halogen atom or an alkyl group; the alkyl group may be substituted by a hydroxyl group;
R3 represents a hydrogen atom or a halogen atom;
Z' represents a C1-5 alkylene chain that may be substituted by one to three groups represented by W';
W' represents any one of the groups of -OH, -OMe, -OEt, -OCH2OH, -O(CH2)2OH, -O(i-Pr), -O(n-Pr), -CONH2, -CONHMe, -CONHEt, -CONH(n-Pr), -CONH(i-Pr), -CONMe2, -CON(Et)Me, -SO2Me, -SOMe, -SMe, -NH2, -NHMe, -NHCH2OH, -NH(CH2)2OH, -N(Me)CH2CH2OH, -NHEt, -NMe2, -N(Et)Me, -NHCOMe, -NMeCOMe, -NHCOEt, -NHCO(n-Pr), and -NHCO(i-Pr);
R1, R2, R3, Z', and W' may have a protecting group(s) required for the synthesis.
53. A method for producing compound (I-g) represented by the following formula, wherein the method comprises reacting a compound (XXV) represented by the following formula with a hydroxylamine derivative (VI) represented by NH2OR4, in a solvent in the presence of a condensing agent for peptide synthesis and in the presence or absence of a base, wherein R1 represents a halogen atom, an alkenyl group, or an alkynyl group;
R2 represents a halogen atom or an alkyl group; the alkyl group may be substituted by a hydroxyl group;
R3 represents a hydrogen atom or a halogen atom;
R4 represents a hydrogen atom, an alkyl group, an alkenyl group, or an alkynyl group; the alkyl group, the alkenyl group, and the alkynyl group may have one to three substituents selected from the group consisting of -ORa, -NRaRb, -NRaCORb, a heterocyclic group, and a heteroaryl group; the heterocyclic group and the heteroaryl group may have one to three substituents selected from the group consisting of a C1-5 alkyl group, -ORa, and -NRaRb; Ra and Rb, which may be the same or different, each represents a hydrogen atom or a C1-5 alkyl group; the alkyl group may be substituted by a hydroxyl group, a CI-5 alkoxy group, or an amino group;
Z' represents a C1-5 alkylene chain that may be substituted by one to three groups represented by W';
W' represents any one of the groups of -OH, -OMe, -OEt, -OCH2OH, -O(CH2)2OH, -O(i-Pr), -O(n-Pr), -CONH2, -CONHMe, -CONHEt, -CONH(n-Pr), -CONH(i-Pr), -CONMe2, -CON(Et)Me, -S2Me, -SOMe, -SMe, -NH2, -NHMe, -NHCH2OH, -NH(CH2)2OH, -N(Me)CH2CH2OH, -NHEt, -NMe2, -N(Et)Me, -NHCOMe, -NMeCOMe, -NHCOEt, -NHCO(n-Pr), and -NHCO(i-Pr);
R1, R2, R3, R4, Z', and W' may have a protecting group(s) required for the synthesis.
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