IL197002A

Method for producing phenoxypyridine derivative

Abstract

This record has no abstract on file.

Term

No projected expiry on record.

22 claims: 3 independent, 19 dependent

1
197002/2 Claims 1. A process for preparing a compound represented by the formula comprising reacting a compound represented by the formula (II) or salt thereof:with a compound represented by the formula (III): H2N, η-R6 (III) 10 15 20 in the presence of a condensation reagent, wherein R1 represents 1) azetidin-l-yl optionally substituted with a substituent selected from Substituent Group A, 2) pyrrolidin-l-yl optionally substituted with a substituent selected from Substituent Group A, 3) piperidin-l-yl optionally substituted with a substituent selected from Substituent Group A, 4) piperazin-l-yl optionally substituted with a substituent selected from Substituent Group A, 5) diazepan-l-yl optionally substituted with a substituent selected from Substituent Group A, 6) morpholin-4-yl optionally substituted with a substituent selected from Substituent Group A, or 7) -NRllaRllb, wherein Rlla represents hydrogen or lib methyl, and R represents n-propyl, n-butyl, pyrrolidir.-3-yl, piperidin-3-yl, piperidin-4-yl or tetrahydropyran-4-yl, and Rllb may be substituted with a substituent selected from Substituent Group B;78 197002/2 10 R2, R3, R4 and R5 may be the same or different and each represents hydrogen or fluorine;Substituent Group A consists of hydroxyl, dimethylaminoacetoxy, methyl, ethyl, dimethylamino, azetidinyl, pyrrolidinyl, piperidinyl and piperazinyl, where each group included in Substituent Grcup A other than hydroxyl and dimethylaminoacetoxy may be substituted with hydroxyl, methyl, dimethylamino, azetidinyl, pyrrolidinyl or piperidinyl;Substituent Group B consists of methyl, ethyl, .i-propyl, acetyl, dimethylamino, diethylamino, azetidinyl, pyrrolidinyl and piperazinyl, where each group included in Substituent Group B may be substituted with methyl or dimethylamino;and R6 represents hydrogen or fluorine.
13
A compound represented by the formula (IV-1) or salt thereof:10 15 20 25 wherein R1 represents 1) azetidin-l-yl optionally substituted with a substituent selected from Substituent Group A, 2) pyrrolidin-l-yl optionally substituted with a substituent selected from Substituent Group A, 3) piperidin-1 -yl optionally substituted with a substituent selected from Substituent Group A, 4) piperazin-l-yl optionally substituted with a substituent selected from Substituent Group A, 5) diazepan-l-yl optionally substituted with a substituent selected from Substituent Group A, 6) morpholin-4-yl optionally substituted with a substituent selected from Substituent Group A, or 7) -NRllaRllb, wherein Rlla represents hydrogen or methyl, and Rllb represents n-propyl, n-butyl, pyrr0lidin-3-yl, piperidin-3-yl, piperidin-4-yl or tetrahydropyran-4-yl, and Rllb may be substituted with a substituent selected from Substituent Group B;R2, R3, R4 and R5 may be the same or different ar.d each represents hydrogen or fluorine;R represents hydrogen, Ci_6 alkyl or benzyl optionally substituted with one or two substituents selected from (1) halogen, (2) hydroxyl, (3) nitro, (4) cyano, (5) trifluoromethyl, (6) Ci_6 alkyl, (7) Ci-6 alkoxy, (8) amino, (9) mono-Ci-6 alkylamino and (10) di-Ci-e alkylamino on the benzene ring;Substituent Group A consists of hydroxyl, dimethylaminoacetoxy, methyl, ethyl, dimethylamino, azetidinyl, pyrrolidinyl, piperidinyl and piperazinyl, where each group included in Substituent Group A other than hydroxyl and dimethylaminoacetoxy may be substituted with hydroxyl, methyl, dimethylamino, azetidinyl, pyrrolidinyl or piperidinyl;and Substituent Group B consists of methyl, ethyl, n-propyl, acetyl, 85 197002/2 dimethylamino, diethylamino, azetidinyl, pyrrolidinyl and piperazinyl, where each group included in Substituent Group B may be substituted with methyl or dimethylamino.
14
A compound represented by the formula (V) or salt thereof:10 15 wherein R2, R3, R4 and R5 have the same definitions as defined in claim 13;R7 represents Ci_6 alkyl or benzyl optionally substituted with one or two substituents selected from (1) halogen, (2) hydroxyl, (3) nitro, (4) cyano, (5) trifluoromethyl, (6) Ci_6 alkyl, (7) Cj-6 alkoxy, (8) amino, (9) mono-Ci-6 alkylamino and (10) di-Ci-6 alkylamino on the benzene ring;and Ar represents phenyl optionally substituted with one or two substituents selected from halogen, methyl, methoxy, nitro, cyano and trifluoromethyl.
15
A compound represented by the formula (VI) or salt thereof:wherein R2, R3, R4 and R5 have the same definicions as defined in claim 13, and R7 has the same definition as defined in claim 14.
16
A compound represented by the formula (VIII) or salt thereof:86 197002/2 10 15 20 wherein R2, R3, R4 and R5 have the same definitions as defined in claim 13, and R7 has the same definition as defined in claim 14. I '
20
A Crystal of N-(2-fluoro-4-{[2-({[4-(4-methylpiperazin-l- 5 yl)piperidin-l-yl]carbonyl}amino)pyridin-4-yl]oxy}phenyl)-N'-(4- fluorophenyl)cyclopropane-1,1 -dicarboxamide.

Independent claims6

413 paragraphs in 13 sections, as filed

γ>τ>Τ£νυρυ3 πύ>ίπ nw'd T>bnn

METHOD FOR PRODUCING PHENOXYPYRIDINE DERIVATIVE FP06-0349-00

DESCRIPTION

METHOD FOR PRODUCING PHENOXYPYRIDINE DERIVATIVE

Technical Field [0001] The present invention relates to processes for preparing phenoxypyridine 5 derivatives (hereafter referred to as "the present compound") useful as an anti tumor agent and an inhibitor for cancer metastasis having inhibitory activity against hepatocyte growth factor receptor (hereafter referred to as "HGFR"), anti-tumor activity, inhibitory activity against angiogenesis, inhibitory activity against cancer metastasis or the like, and to preparation intermediates in the processes. 10 Background Art [0002] Overexpression of HGFR is reported in various kinds of tumors such as a pancreatic cancer, a gastric cancer, a colorectal cancer, a breast cancer, a prostate cancer, a lung cancer, a renal cancer, a brain tumor or an ovarian cancer (nonpatent document 1). HGFR expressed in these cancer cells is considered to be 15 involved in cancer malignancy (aberrant growth, invasion or enhanced metastasis), because HGFR cause autophosphorylation of intracellular tyrosine kinase constitutively or upon stimulation by hepatocyte growth factor (hereafter referred to as "HGF").

[0003] It is also reported that HGFR is expressed in vascular endothelial cells and 20 is involved in tumor angiogenesis since HGF stimulates HGFR to facilitate proliferation and migration of vascular endothelial cells (non-pater.t document 2). [0004] Furthermore, NK4, an antagonistic peptide for HGF, is reported to block HGF-HGFR signal to inhibit invasion of cancer cells and tumor angiogenesis (nonpatent documents 3 and 4). 25 [0005] Therefore, a compound having inhibitory activity against HGFR is expected to be useful as an anti-tumor agent, an angiogenesis inhibitor or an inhibitor for cancer metastasis.

[0006] By the way, patent document 1 discloses compounds similar to the present compounds in structure and processes for preparing the same, but does not disclose 30 the processes for preparing the present compounds according to the present invention and the preparation intermediates in the processes as well as the present compounds.

[0007] 1 FP06-0349-00 [Patent document 1] WO 2005/082855 [Non-patent document 1] Oncology Reports, 5, 1013-1024 (1998) [Non-patent document 2] Advances in Cancer Research, 67, 257-279 (1995) [Non-patent document 3] British Journal of Cancer, 84, 864-873 (2001) [Non-patent document 4] Cancer Sci., 94, 321-327 (2003)

Disclosure of the Invention

Problems to be Solved by the Invention 10 15 20 [0008] An object of the invention is to find processes for preparing phenoxypyridine derivatives having inhibitory activity against HGFR, anti-tumor activity, inhibitory activity against angiogenesis, inhibitory activity against cancer metastasis or the like, and preparation intermediates in the processes.

Means for Solving the Problems [0009] As a result of diligent studies in view of the above situation, the inventors have found processes for preparing phenoxypyridine derivatives suitable for industrial large scale synthesis, and preparation intermediates in the processes, and completed the invention.

[0010] Specifically, the present invention provides [1] to [21] below: [1] A process for preparing a compound represented by the formula (I):

comprising reacting a compound represented by the formula (II) or salt thereof:

with a compound represented by the formula (III): 2 FP06-0349-00 10 15 20 25

in the presence of a condensation reagent, wherein R1 represents 1) azetidin-l-yl optionally substituted with a substituent selected from Substituent Group A, 2) pyrrolidin-l-yl optionally substituted with a substituent selected from Substituent Group A, 3) piperidin-l-yl optionally substituted with a substituent selected from Substituent Group A, 4) piperazin-l-yl optionally substituted with a substituent selected from Substituent Group A, 5) diazepan-l-yl optionally substituted with a substituent selected from Substituent Group A, 6) morpholin-4-yl optionally substituted with a substituent selected from Substituent Group A, or 7) -NRllaRllb, wherein RIla represents hydrogen or methyl, and Rllb represents n-propyl, n-butyl, pyrrolidin-3-yl, piperidin-3-yl, piperidin-4-yl or tetrahydropyran-4-yl, and Rllb may be substituted with a substituent selected from Substituent Group B; R2, R3, R4 and R5 may be the same or different and each represents hydrogen or fluorine;

Substituent Group A consists of hydroxyl, dimethylamir.oacetoxy, methyl, ethyl, dimethylamino, azetidinyl, pyrrolidinyl, piperidinyl and piperazinyl, where each group included in Substituent Group A other than hydroxyl and dimethylaminoacetoxy may be substituted with hydroxyl, methyl, dimethylamino, azetidinyl, pyrrolidinyl or piperidinyl;

Substituent Group B consists of methyl, ethyl, n-propyl, acetyl, dimethylamino, diethylamino, azetidinyl, pyrrolidinyl and piperazinyl, where each group included in Substituent Group B may be substituted with methyl or dimethylamino; and R6 represents hydrogen or fluorine.

[2] The process according to [1], wherein the compound represented by the formula (II) or salt thereof: 3 FP06-0349-00

wherein R1, R2, R3, R4 and R5 have the same definitions as defined in [1], is prepared by hydrolysis or catalytic hydrogenation of a compound represented by the formula (IV) or salt thereof:

wherein R1, R2, R3, R4 and R5 have the same definitions as defined in [1], and R7 represents Ci_6 alkyl or benzyl optionally substituted with one or two substituents selected from (1) halogen, (2) hydroxyl, (3) nitro, (4) cyano, (5) 10 trifluoromethyl, (6) Ci„6 alkyl, (7) Ci_6 alkoxy, (8) amino, (9) mono-Ci.6 alkylamino and (10) di-Ci-6 alkylamino on the benzene ring.

[3] The process according to [2], wherein the compound represented by the formula

15 wherein R1, R2, R3, R4 and R5 have the same definitions as defined in [1], and R7 has the same definition as defined in [2], is prepared by reacting a compound represented by the formula (V): 4 FP06-0349-00

10 15 wherein R2, R3, R4 and R5 have the same definitions as defined in [1], R7 has the same definition as defined in [2], and Ar represents phenyl optionally substituted with one or two substituents selected from halogen, methyl, methoxy, nitro, cyano and trifluoromethyl, with an amine or salt thereof selected from 1) azetidine optionally substituted with a substituent selected from Substituent Group A in [1], 2) pyrrolidine optionally substituted with a substituent selected from Substituent Group A in [1], 3) piperidine optionally substituted with a substituent selected from Substituent Group A in [1], 4) piperazine optionally substituted with a substituent selected from Substituent Group A in [1], 5) diazepane optionally substituted with a substituent selected from Substituent Group A in [1], 6) morpholine optionally substituted with a substituent selected from Substituent Group A in [1], or 7) HNRllaRllb, wherein Rlla and Rllb have the same definitions as defined in [1].

[4] The process according to [3], wherein the compound represented by the formula

20 wherein R2, R3, R4 and R5 have the same definitions as defined in [1], R7 has the same definition as defined in [2], and Ar has the same definition as defined in [3], is prepared by reacting a compound represented by the formula (VI): 5 FP06-0349-00

wherein R2, R3, R4 and R5 have the same definitions as defined in [1], and R7 has the same definition as defined in [2], with a compound represented by the formula (VII):

O Αιχ Λ (V")

^O CI wherein Ar has the same definition as defined in [3], in the presence of a base.

[5] The process according to [4], wherein the compound represented by the formula 10

wherein R2, R3, R4 and R5 have the same definitions as defined in [1], and R7 has the same definition as defined in [2], is prepared by reacting a compound represented by the formula (VIII): 15

wherein R2, R3, R4 and R5 have the same definitions as defined in [1], and R7 has the same definition as defined in [2], with a Hofmann rearrangement reagent. 6 [6] The process according to [5]·, wherein the compound represented by the formula 197002/2

wherein R2 R3, R4 and R5 have the same definitions as defined in [1], and 5 R7 has the same definition as defined in [2], is prepared by reacting a compound represented by the formula (IX):

wherein R2, R3, R4 andR5 have the same definitions as defined in [1], with a compound represented by the formula (X): πθΥ^γ0^7 W 10 ° ° wherein R7 has the same definition as defined in [2], in the presence of a halogenation reagent or a condensation reagent.

[7] The process according to [1J ( wherein the condensation reagent is 4-(4,6-dimethoxy[1.3.5]triazin-2-yl)-4-methyhnoipholinium chloride hydrate or 2-chloro- 15 4,6-dimethoxy-l,3,5-triazine.

[8] The process according to [3], wherein the amine is 1-(2- dimethylaminoethyl)piperazine, 4-(pyirolidin-l-yl)piperidine, 4- (dimethylaimnomethyl)piperidine, 4-(azetidin-l-yl)piperidine, N,N-dimethyl-N-[l-(piperidin-4-yl)azetidin-3-yl]ainine, l-methyl-4-(piperidin-4-yl)piperazine, 4-(1- 20 methylpiperidin-4-yl)piperazine, l-(l-methylazetidin-3-yl)piperazme, 4- (dimethylamino)piperidine5 4-(azetidin-l-ylmethyI)piperidine, 4-(pyirolidin-l- 7 FP06-0349-00 ylmethyl)piperidine, (3S)-3-(dimethylamino)pyrrolidine, (3R)-3- (dimethylamino)pyrrolidine, azetidine, pyrrolidine, morpholine, 1-methylpiperazine, 3-hydroxyazetidine, 3-(azetidin-l-yl)azetidine, 3-(hydroxymethyl)azetidine, 3-(dimethylamino)azetidine, 3- 5 (dimethylaminomethyl)azetidine, 4-hydroxypiperidine, 4- (hydroxymethyl)piperidine, (3R)-3-hydroxypyrrolidine, (3 S)-3-hydroxypyrrolidine, 3- (azetidin-l-ylmethyl)azetidine, 3-(2-dimethylaminoacetoxy)azetidine, 1-methyl- 4- (methylamino)piperidine, N-(l-ethylpiperidin-4-yl)-N-methylimine, N,N-dimethyl-N'-methylpropane-l ,3-diamine or N,N-diethyl-N'-methylpropane-l ,3- 10 diamine.

[9] The process according to [5], wherein the Hofmann rearrangement reagent is iodobenzene diacetate or iodobenzene bis(trifluoroacetate).

[10] The process according to any one of [1] to [3], wherein R1 is 4-[2- (dimethylamino)ethyl]piperazin-1 -yl, 4-pyrrolidin-1 -ylpiperidin-1 -yl, 4- 15 [(dimethylamino)methyl]piperidin-l-yl, 4-azetidin-l-ylpiperid:n-l-yl, 4-[3- (dimethylamino)azetidin-1 -yl]piperidin-1 -yl, 4-(4-methylpiperazin-1 -yl)piperidin-1 -yl, 4-(1 -methylpiperidin-4-yl)piperazin-1 -yl, 4-(1 -methylazetidin-3 -yl)piperazin-1-yl, 4-(dimethylamino)piperidin-l-yl, 4-(azetidin-l-ylmethyl)piperidin-l-yl, 4-(pyrrolidin-1 -ylmethyl)piperidin-1 -yl, (3 S)-3 -(dimethylamino)pynOlidin-1 -yl, 20 (3R)-3-(dimethylamino)pyrrolidin-l-yl, azetidin-l-yl, pyrrolidin-l-yl, morpholin- 4-yl, 4-methylpiperazin-l-yl, 3-hydroxyazetidin-l-yl, l,3'-biazetidin-T-yl, 3-(hydroxymethyl)azetidin-l-yl, 3-(dimethylamino)azetidin-l-yl. 3- [(dimethylamino)methyl] azetidin-1 -yl, 4-hydroxypiperidin-1 -yl·, 4- (hydroxymethyl)piperidin-1 -yl, (3R)-3 -hydroxypyrrolidin-1 -yl, (3 S)-3 - 25 hydroxypyrrolidin-1-yl, 3-(azetidin-l-ylmethyl)azetidin-l-yl, 3-(2- dimethylaminoacetoxy)azetidin-1 -yl, methyl( 1 -methylpiperidin -4-yl)amino, (1 -ethylpiperidin-4-yl)(methyl)amino, [3-(dimethylamino)propyl](methyl)amino or [3 -(diethylamino)propyl] (methyl) amino.

[11] The process according to any one of [1] to [6], wherein the group represented 30 by the formula: 8 FP06-0349-00

is a group represented by the formula:

[12] The process according to any one of [2] to [6], wherein R7 is benzyl.

[13] A compound represented by the formula (IV-1) or salt thereof:

R5

'R71 (IV-1) 10 15 wherein R1 represents 1) azetidin-l-yl optionally substituted with a substituent selected from Substituent Group A, 2) pyrrolidin-l-yl· optionally substituted with a substituent selected from Substituent Group A, 3) piperidin-l-yl optionally substituted with a substituent selected from Substituent Group A, 4) piperazin-l-yl optionally substituted with a substituent selected from Substituent Group A, 5) diazepan-l-yl optionally substituted with a substituent selected from Substituent Group A, 6) morpholin-4-yl optionally substituted with a substituent selected from Substituent Group A, or 7) -NRllaRllb, wherein Rlla represents hydrogen or methyl, and Rllb represents n-propyl, n-butyl, pyrrolidin-3-yl, piperidin-3-yl, piperidin-4-yl or tetrahydropyran-4-yl, and Rllb may be substituted with a substituent selected from Substituent Group B; R2, R3, R4 and R5 may be the same or different and each represents 20 hydrogen or fluorine; 71 R represents hydrogen, Ci-6 alkyl or benzyl optionally substituted with one or two substituents selected from (1) halogen, (2) hydroxyl, (3) nitro, (4) cyano, 9 FP06-0349-00 10 15 20 (5) trifluoromethyl, (6) Ci-6 alkyl, (7) Ci-6 alkoxy, (8) amino, (9) mono-Ci-6 alkylamino and (10) di-Ci-6 alkylamino on the benzene ring;

Substituent Group A consists of hydroxyl, dimethylaminoacetcxy, methyl, ethyl, dimethylamino, azetidinyl, pyrrolidinyl, piperidinyl and piperazinyl, where each group included in Substituent Group A other than hydroxyl and dimethylaminoacetoxy may be substituted with hydroxyl, methyl, dimethylamino, azetidinyl, pyrrolidinyl or piperidinyl; and

[14] A compound represented by the formula (V) or salt thereof:

wherein R2, R3, R4 and R5 have the same definitions as defined in [13]; R7 represents Ci.6 alkyl or benzyl optionally substituted with one or two substituents selected from (1) halogen, (2) hydroxyl, (3) nitro, (4) cyano, (5) trifluoromethyl, (6) Ci.6 alkyl, (7) Ci_6 alkoxy, (8) amino, (9) mor.o-Ci.6 alkylamino and (10) di-Ci-6 alkylamino on the benzene ring; and

Ar represents phenyl optionally substituted with one or two substituents selected from halogen, methyl, methoxy, nitro, cyano and trifluoromethyl.

[15] A compound represented by the formula (VI) or salt thereof:

wherein R2, R3, R4 and R5 have the same definitions as defined in [13], and 10 FP06-0349-00 R has the same definition as defined in [14].

[16] A compound represented by the formula (VIII) or salt thereof: 10

wherein R2, R3, R4 and R5 have the same definitions as defined in [13], and R has the same definition as defined in [14].

[17] The compound or salt thereof according to [13], wherein R1 is 4-[2-(dimethylamino)ethyl]piperazin-1 -yl, 4-pyrrolidin-1 -ylpiperidin-1 -yl, 4- [(dimethylamino)methyl]piperidin-1 -yl, 4-azetidin-1 -ylpiperidin-1 -yl, 4- [3 - (dimethylamino)azetidin-1 -yl]piperidin-1 -yl, 4-(4-methylpiperazin-1 -yl)piperidin-1 -yl, 4-(1 -methylpiperidin-4-yl)piperazin-l -yl, 4-(1 -methylazetidin-3-yl)piperazin-1-yl, 4-(dimethylamino)piperidin-l-yl, 4-(azetidin-l-ylmethyl)piperidin-l-yl, 4-(pyrrolidin-1 -ylmethyl)piperidin-1 -yl, (3 S)-3 -(dimethylamino Ipyrrolidin-1 -yl, (3R)-3-(dimethylamino)pyrrolidin-l-yl, azetidin-l-yl, pyrrolidin-l-yl, morpholin-4-yl, 4-methylpiperazin-l-yl, 3-hydroxyazetidin-l-yl, l,3'-biazetidin-T-yl, 3- 15 (hydroxymethyl)azetidin-l-yl, 3-(dimethylamino)azetidin-l-yl, 3- [(dimethylamino)methyl]azetidin-l-yl, 4-hydroxypiperidin-l-yl, 4- (hydroxymethyl)piperidin-1 -yl, (3 R)-3 -hydroxypyrrolidin-1 -yl, (3 S)-3 - hydroxypyrrolidin-l-yl, 3-(azetidin-l-ylmethyl)azetidin-l-yl, 3-(2- 20 dimethylaminoacetoxy)azetidin-1 -yl, methyl(l -methylpiperidin-4-yl)amino, (1 -ethylpiperidin-4-yl)(methyl)amino, [3-(dimethylamino)propyl](methyl)amino or [3 -(diethylamino)propyl] (methyl)amino.

[18] The compound or salt thereof according to any one of [13] to [16], wherein the group represented by the formula:

25 is a group represented by the formula: 11 FP06-0349-00

10 15 20 [19] The compound or salt thereof according to any one of [14] to [16], wherein R7 is benzyl.

[20] A Crystal of N-(2-fluoro-4-{[2-({[4-(4-methylpiperazir.-l-yl)piperidin-l-yl] carbonyl} amino)pyridin-4-yl] oxy} phenyl)-N'-(4-fluorophenyl) cyclopropane- 1,1 -dicarboxamide.

[21] The crystal according to [20], having diffraction peaks at diffraction angles (20 ± 0.2°) of 6.3°, 12.3° and 17.3° in a powder X-ray diffraction.

Effect of the Invention [0011] The present invention provides processes for preparing phenoxypyridine derivatives having inhibitory activity against HGFR, anti-tumor activity, inhibitory activity against angiogenesis, inhibitory activity against cancer metastasis or the like, which are suitable for industrial large scale synthesis. The present invention also provides preparation intermediates useful in the processes.

Brief Description of the Drawings [0012] Fig.l represents a powder X-ray diffraction pattern for the crystals obtained in Example 9 (Method 3).

Best Mode for Carrying Out the Invention [0013] The symbols and terms as used herein will be defined below and the present invention will be described in details.

[0014] Several of the structural formulas for the compounds throughout the present specification represent only one isomeric form for convenience, but the invention encompasses any and all of the geometric isomers as well as optical isomers based on asymmetric carbons, stereoisomers and tautomers, and mixtures of those isomers, which are implied by the structures of the compounds, without being limited to any of the formulas shown for convenience. The compounds of the invention therefore include all those having asymmetric carbons therein and existing in optically active or racemic form, with no particular restrictions on the invention. There are also no restrictions when polymorphic crystalline forms 25 12 FP06-0349-00 thereof exist, and the compounds may be in one crystalline form or a mixture of different crystalline forms, while anhydrates and hydrates of the compounds of the invention are also included.

[0015] The "salt" is not particularly limited so long as it can fcrm a salt with the 5 compound according to the present invention and includes, for example, a salt with an inorganic acid, a salt with an organic acid, a salt with an inorganic base, a salt with an organic base, a salt with an acidic or basic amino acid or the like.

[0016] The preferable salt with an inorganic acid includes, for example, a salt with hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid or 10 the like. The preferable salt with an organic acid includes, for example, a salt with acetic acid, succinic acid, fumaric acid, maleic acid, tartaric acid, citric acid, lactic acid, stearic acid, benzoic acid, methanesulfonic acid, ethanesulfonic acid, p-toluenesulfonic acid or the like.

[0017] The preferable salt with an inorganic base includes, for example, an alkali 15 metal salt such as sodium salt and potassium salt, an alkali earth metal salt such as calcium salt and magnesium salt, aluminum salt, ammonium salt or the like. The preferable salt with an organic base includes, for example, a salt with diethylamine, diethanolamine, meglumine, Ν,Ν-dibenzylethylenediamine or the like.

[0018] The preferable salt with an acidic amino acid includes, for example, a salt 20 with aspartic acid, glutamic acid or the like. The preferable salt with a basic amino acid includes, for example, a salt with arginine, lysine, ornithine or the like.

[0019] The "halogen" represents fluorine, chlorine, bromine or iodine.

[0020] The "Ci_6 alkyl" represents an alkyl of straight or branched chain having a carbon number of 1 to 6, and includes, for specific example, methyl, ethyl, 1- 25 propyl (n-propyl), 2-propyl (i-propyl), 2-methyl-1 -propyl (i-butyl), 2-methyl-2- propyl (t-butyl), 1-butyl (n-butyl) and 2-butyl (s-butyl).

[0021] The "Ci-6 alkoxy" represents a group obtained by adding oxygen to the terminal of the above defined "Ci_6 alkyl", and includes, for specific example, methoxy, ethoxy, 1-propoxy (n-propoxy), 2-propoxy (i-propoxy), 2-methyl-l- 30 propoxy (i-butoxy), 2-methyl-2-propoxy (t-butoxy), 1-butoxy (n-butoxy), 2-butoxy (s-butoxy) or the like.

[0022] The "mono-Ci„6 alkylamino" represents a group obtained by substituting one hydrogen of amino with the above defined "Ci-6 alkyl", and includes, for 13 specific example, methylamino, ethylamino, 1-propylamino (n-propvlamino), 2- propylamino (i-propylamino), 2-methyl-1-propylamino (i-butylanino), 2-methyl-2- propylamino (t-butylamino), 1-butylamino (n-butylamino), 2-butvlamino (s- butylamino) or the like. 5 [0023] The "di-Ci-6 alkylamino" represents a group obtained by substituting two hydrogen of amino with the same or different groups of the above defined "C,.6 alkyl", and includes, for specific example, Ν,Ν-dimethylamino, N,N-diethylamino, N,N-di-n-propylamino, N,N-di-i-propylamino, N,N-di-n-butylamino, N,N-di-i-butylamino, N,N-di-s-butylamino, N,N-di-t-butylamino, N-ethyl-N-methylamino, 10 N-n-propyl-N-methylamino, N-i-propyl-N-methylamino, N-n-butyl-N- methylamino, N-i-butyl-N-methylamino, N-s-butyl-N-methylamino, N-t-butyl-N-methylamino or the like.

[0024] The "condensation reagent" in the above [1] and [6] represents 4-(4,6-dimethoxy[l .3.5]triazin-2-yl)-4-methylmorpholinium chloride hydrate, 2-chloro- 15 4,6-dimethoxy-1,3,5 -triazine, 2,4,6-trichloro-l,3,5-triazine, dicyclohexyl carbodiimide (DCC), 1-ethyl-3,(3'-dimethylaminopropyl)carbcdiimide HC1 salt (EDC or WSC HC1), O-(lH-benzotiazol-l-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate (HBTU), O-(lH-benzotiazol-l-yl)-N,N,N',N'- tetramethyluronium tetrafluoroborate (TBTU) or the like, and 4-(4,6- 20 dimethoxy[1.3.5]triazin-2-yl)-4-methylmorpholinium chloride hydrate or 2,4,6- trichloro-l,3,5-triazine is preferable.

[0025] The "base" in the above [3] represents potassium carbonate, sodium carbonate, pyridine, triethylamine, diisopropylethylamine or the like, and potassium carbonate is preferable. 25 [0026] The "salt" of the "amine or salt thereof' in the above [3] is not particularly limited so long as it can form salt with amine, and includes, for example, a salt with hydrochloric acid, acetic acid, trifluoroacetic acid or the like.

[0027] The "base" in the above [4] represents pyridine, triethylamine, diisopropylethylamine, potassium carbonate, sodium carbonate or the like, and 30 pyridine is preferable.

[0028] The "Hofmann rearrangement reagent" in the above [5] represents iodobenzene diacetate, iodobenzene bis(trifluoroacetate), sodium hypochlorite, potassium hypobromite, bromine, iodine or the like, and iodobenzene diacetate or 14 FP06-0349-00 iodobenzene bis(trifluoroacetate) is preferable.

[0029] The "halogenation reagent" in the above [6] represents thionyl chloride, oxalyl chloride, phosphorus trichloride, phosphorus oxychloride, phosphorus pentachloride or the like, and thionyl chloride is preferable. 5 [0030] The crystal of N-(2-fluoro-4-{[2-({[4-(4-rnethylpiperazin-l-yl)piperidin-l- yl]carbonyl}amino)pyridin-4-yl]oxy}phenyl)-N'-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide has diffraction peaks at diffraction angles (20 ± 0.2°) of 6.3°, 12.3° and 17.3° in a powder X-ray diffraction, and preferably has diffraction peaks of 6.3°, 12.3°, 17.3°, 18.3°, 18.4°, 19.2°, 19.8°, 20.0°, 20.1°, 20.2°, 22.1° and 23.7°. 10 [0031] As for a diffraction angle (20) in the powder X-ray diffraction analysis, errors in the diffraction angle, generally, may occur within the range of ±0.2°. It is, therefore, to be understood that the values of the diffraction angles may include numerals on the order of ± 0.2°. Accordingly, this invention encompasses not only crystal having completely matching diffraction angles of the peaks in powder X-ray 15 diffraction, but also crystal having matching diffraction angles of the peaks within the errors of about ± 0.2°.

[0032] The respective substituents of the compound represented by the above formula (I) according to the present invention will be described.

[0033] [The definition of R1] 20 R1 represents 1) azetidin-l-yl optionally substituted with a substituent selected from Substituent Group A below, 2) pyrrolidin-l-yl optionally substituted with a substituent selected from Substituent Group A below, 3) piperidin-l-yl optionally substituted with a substituent selected from Substituent Group A below, 4) piperazin-l-yl optionally substituted with a substituent selected from Substituent 25 Group A below, 5) diazepan-l-yl optionally substituted with a substituent selected from Substituent Group A below, 6) morpholin-4-yl optionally substituted with a substituent selected from Substituent Group A below, or 7) -NRllaRIlb, wherein Rlla represents hydrogen or methyl, and Rllb represents n-propyl, n-butyl, pyrrolidin-3-yl, piperidin-3-yl, piperidin-4-yl or tetrahydropyran-4-yl, and Rllb 30 may be substituted with a substituent selected from Substituent Group B below.

Preferable examples of R1 include 4-[2-(dimethylamino)ethyl]piperazin-l- yl, 4-pyrrolidin-l-ylpiperidin-1-yl, 4-[(dimethylamino)methyl]piperidin-l-yl, 4- azetidin-1 -ylpiperidin-1 -yl, 4- [3 -(dimethylamino)azetidin-1 -yl]piperidin-1 -yl, 4-(4- 15 FP06-0349-00 10 15 20 25 30 methylpiperazin-1 -yl)piperidin-1 -yl, 4-(1 -methylpiperidin-4-yl)piperazin-1 -yl, 4-(l-methylazetidin-3-yl)piperazin-l-yl, 4-(dimethylamino)piperidin-l-yl, 4-(azetidin-1 -ylmethyl)piperidin-1 -yl, 4-(pyrrolidin-1 -ylmethyl)pipe:;idin-1 -yl, (3 S)-3 -(dimethylamino)pyrrolidin-1 -yl, (3R)-3 -(dimethylaminc)pyrrolidin-1 -yl, azetidin-l-yl, pyrrolidin-l-yl, morpholin-4-yl, 4-methylpiperazin-l-yl, 3-hydroxyazetidin-l-yl, l,3'-biazetidin-l'-yl, 3-(hydroxymethyl)azetidin-l-yl, 3-(dimethylamino)azetidin-1 -yl, 3 - [(dimethylamino)methyl]azetidin-1 -yl, 4- hydroxypiperidin-l-yl, 4-(hydroxymethyl)piperidin-l-yl, (3R)-3- hydroxypyrrolidin-l-yl, (3S)-3-hydroxypyrrolidin-l-yl, 3-(azetidin-l- ylmethyl)azetidin-1 -yl, 3 -(2-dimethylaminoacetoxy)azetidin-1 -yl, methyl( 1 -methylpiperidin-4-yl)amino, (1 -ethylpiperidin-4-yl)(methyl)amino, [3-(dimethylamino)propyl](methyl)amino, [3-(diethylamino)propyl](methyl)amino or the like.

More preferable examples of R1 include 4-(4-methylpiperazin-l-yl)piperidin-l-yl, 3-hydroxyazetidin-l-yl, (3R)-3-hydroxypyrrolidin-l-yl, (3S)-3-hydroxypyrrolidin-l-yl, methyl(l-methylpiperidin-4-yl)amino or the like.

[0034] [The definition of Substituent Group A]

Substituent Group A represents a group consists of hydroxyl, dimethylaminoacetoxy, methyl, ethyl, dimethylamino, azetidinyl, pyrrolidinyl, piperidinyl and piperazinyl.

Each group included in Substituent Group A other than hydroxyl and dimethylaminoacetoxy may be substituted with hydroxyl, methyl, dimethylamino, azetidinyl, pyrrolidinyl or piperidinyl.

[0035] [The definition of Substituent Group B]

Substituent Group B consists of methyl, ethyl, n-propyl, acetyl, dimethylamino, diethylamino, azetidinyl, pyrrolidinyl and piperazinyl.

Each group included in Substituent Group B may be substituted with methyl or dimethylamino.

[0036] [The definition of R2, R3, R4 and R5] R2, R3, R4 and R5 may be the same or different and each represents hydrogen or fluorine. R2, R3, R4 and R5 may be (1) the case where all represent hydrogen, (2) the case where all represent fluorine, or (3) the case where some represent hydrogen 16 FP06-0349-00 and other represent fluorine, and preferably two or three of R2, R3, R4 and R5 are hydrogen.

Preferable examples of the group represented by the formula:

5 include a group represented by the formula:

[0037] [The definition of R6] R6 represents hydrogen or fluorine.

Preferable examples of R6 include fluorine. 10 [0038] [The definition of R7] R7 represents Ci_6 alkyl or benzyl optionally substituted with one or two substituents selected from (1) halogen, (2) hydroxyl, (3) nitro, (4) cyano, (5) trifluoromethyl, (6) Ci-6 alkyl, (7) Ci_6 alkoxy, (8) amino, (9) mono-C]_6 alkylamino and (10) di-Ci-6 alkylamino on the benzene ring. 15 Preferable examples of R7 include benzyl.

[0039] [The definition of R71] R71 represents hydrogen, Ci_6 alkyl or benzyl optionally substituted with one or two substituents selected from (1) halogen, (2) hydroxyl, (3) nitro, (4) cyano, (5) trifluoromethyl, (6) Ci-6 alkyl, (7) Ci.6 alkoxy, (8) amino, (9) mono-Ci.6 20 alkylamino and (10) di-Ci_e alkylamino on the benzene ring.

Preferable examples of R71 include hydrogen or benzyl.

[0040] [The definition of Ar]

Ar represents phenyl optionally substituted with one or two substituents selected from halogen, methyl, methoxy, nitro, cyano and trifluoromethyl. 25 Preferable examples of Ar include phenyl.

[0041] The preparing process according to the invention will be describe below in 17 FP06-0349-00 detail.

[0042]

H 10

Each symbol has the same definition as mentioned above.

[0043] [Step 1]

This is a step of preparing compound (VIII) by reacting compound (IX) with compound (X) in the presence of a halogenation reagent or a condensation reagent.

As compound (IX) may be used the compounds described in Examples below, publicly known compounds, commercially available compounds or compounds easily prepared by methods those skilled in the art usually carry out.

As compound (X) may be used the compounds described in Examples below, publicly known compounds, commercially available compounds or 18 compounds easily prepared by methods those skilled in the art usually carry out.

The solvent used for this step is not particularly limited so long as it dissolves starting materials to some extent and does not inhibit the reaction, and includes, for example, ether solvents such as tetrahydro furan, 1,2-dimethoxyethane, 5 tert-butyl methyl ether, cyclopentyl methyl ether, diethyl ether, diiscpropyl ether, dibutyl ether and dicyclopentyl ether; aromatic hydrocarbon solvents such as benzene and toluene; aliphatic hydrocarbon solvents such as heptane and hexane; N,N-dimethylformamide; N-methyl-2-pyrrolidone; or a mixed solvent thereof, or the like and tetrahydrofuran is preferable. 10 The halogenation reagent represents thionyl chloride, oxalyl chloride, phosphorus trichloride, phosphorus oxychloride, phosphorus pentachloride or the like, and thionyl chloride is preferable.

The condensation reagent represents 4-(4,6-dimethoxy[l 3.5]triazin-2-yl)-4-methylmorpholinium chloride hydrate, 2-chloro-4,6-dimethoxy-1,3,5-triazine, 15 2,4,6-trichloro-l,3,5-triazine, dicyclohexyl carbodiimide (DCC), 1 -ethyl-3,(31- dimethylaminopropyl)carbodiimide HC1 salt (EDC or WSC HC1), O-(1H-benzotiazol-l-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate (ITBTU), O-(lH-benzotiazol-l-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate (TBTU) or the like, and 4-(4,6-dimethoxy[1.3.5]triazin-2-yl)-4-methylmorpholinium chloride 20 hydrate or 2,4,6-trichloro-1,3,5-triazine is preferable.

The reaction temperature will generally differ depending on the starting materials, the solvent and the other reagents used in the reaction, and it is preferably 0°C to 50°C (internal temperature of the reaction vessel) and more preferably 0°C to 30°C (internal temperature of the reaction vessel). 25 The reaction time will generally differ depending on the starting materials, the solvent, the other reagents used in the reaction and the reaction temperature, and stirring at the above reaction temperature for 1 to 48 hours after the addition of the reagents is preferable and stirring for 4 to 24 hours is more preferable.

Compound (X) can be used in an amount of 1.0- to 3.0-fold molar amount 30 with respect to compound (IX), and preferably it is used in an amount of 1.0- to 1.3-fold molar.

The halogenation reagent can be used in an amount of 1.0- to 2.0-fold molar amount with respect to compound (IX), and preferably it is used in an amount of 19 FP06-0349-00 1.1-fold molar.

The condensation reagent can be used in an amount of 1.0- to 3.0-fold molar amount with respect to compound (IX), and preferably it is used in an amount of 1.1-to 1.3-fold molar. 5 [0044] [Step 2]

This is a step of preparing compound (VI) by reacting compound (VIII) with a Hofmann rearrangement reagent.

The solvent used for this step is not particularly limited so long as it dissolves starting materials to some extent and does not inhibit the reaction, and 10 include, for example, Ν,Ν-dimethylformamide, Ν,Ν-dimethylacetamide, dimethyl sulfoxide, N-methyl-2-pyrrolidone or the like, and Ν,Ν-dimethylformamide or N-methyl-2-pyrrolidone is preferable.

The Hofmann rearrangement reagent represents iodobenzer.e diacetate, iodobenzene bis(trifluoroacetate), sodium hypochlorite, potassium hypobromite, 15 bromine, iodine or the like, and iodobenzene diacetate or iodobenzene bis(trifluoroacetate) is preferable.

The reaction time will generally differ depending on the starting materials, the solvent, the other reagents used in the reaction and the reaction temperature, and stirring at the above reaction temperature for 1 to 24 hours after the addition of the reagents is preferable and stirring for 3 to 5 hours is more preferable. 25 The Hofmann rearrangement reagent can be used in an amount of 1.0- to 3.0-fold molar amount with respect to compound (VIII), and preferably it is used in an amount of 1.0- to 1.2-fold molar.

[0045] [Step 3]

This is a step of preparing compound (V) by reaction compound (VI) with 30 compound (VII) in the presence of a base,

As compound (VII) may be used publicly known compounds, commercially available compounds or compounds easily prepared by methods those skilled in the art usually carry out. 20 FP06-0349-00

The solvent used for this step is not particularly limited so long as it dissolves starting materials to some extent and does not inhibit the reaction, and includes, for example, ether solvents such as tetrahydrofuran, 1,2-dimethoxyethane, tert-butyl methyl ether, cyclopentyl methyl ether, diethyl ether, diisopropyl ether, 5 dibutyl ether and dicyclopentyl ether; aromatic hydrocarbon solvents such as benzene and toluene; aliphatic hydrocarbon solvents such as heptane and hexane; acetonitrile; or a mixed solvent thereof or the like, and a mixed solvent of tetrahydrofuran and acetonitrile is preferable.

The base represents pyridine, triethylamine, diisopropylethylamine, 10 potassium carbonate, sodium carbonate or the like, and pyridine is preferable.

The reaction temperature will generally differ depending on the starting materials, the solvent and the other reagents used in the reaction, and it is preferably -10°C to 50°C (internal temperature of the reaction vessel) and more preferably 0°C to 30°C (internal temperature of the reaction vessel). 15 The reaction time will generally differ depending on the starting materials, the solvent, the other reagents used in the reaction and the reaction temperature, and stirring at the above reaction temperature for 1 to 24 hours after the addition of the reagents is preferable and stirring for 2 to 5 hours is more preferable.

Compound (VII) can be used in an amount of 1.0- to 3.0-fold molar amount 20 with respect to compound (VI), and preferably it is used in an amount of 1.1- to 2.0-fold molar.

The base can be used in an amount of 1.0- to 3.0-fold molar amount with respect to compound (VI), and preferably it is used in an amount of 1.1- to 2.0-fold molar. 25 [0046] [Step 4]

This is a step of preparing compound (IV) or salt thereof by reacting compound (V) with an appropriate amine (or salt thereof) in the presence or absence of a base.

As amine may be used the compounds described in Examples below, 30 publicly known compounds, commercially available compounds or compounds easily prepared by methods those skilled in the art usually carry out.

The solvent used for this step is not particularly limited so long as it dissolves starting materials to some extent and does not inhibit the reaction, and 21 FP06-0349-00 includes, for example, N,N-dimethylformamide, N-methyl-2-pyrrolidone, N,N- dimethylacetamide, dimethyl sulfoxide or the like, and N-methyl-2-pyrrolidone is preferable.

The base represents potassium carbonate, sodium carbonate, pyridine, 5 triethylamine, diisopropylethylamine or the like, and potassium carbonate is preferable.

The reaction temperature will generally differ depending on the starting materials, the solvent and the other reagents used in the reaction, and it is preferably 10°C to 100°C (internal temperature of the reaction vessel) and more 10 preferably 20°C to 50°C (internal temperature of the reaction vessel).

The reaction time will generally differ depending on the starting materials, the solvent, the other reagents used in the reaction and the reaction temperature, and stirring at the above reaction temperature for 1 to 24 hours after the addition of the reagents is preferable and stirring for 1 to 4 hours is more preferable. 15 The amine (or salt thereof) can be used in an amount of 1.0- to 3.0-fold molar amount with respect to compound (V), and preferably it is used in an amount of 1.1 - to 1.3-fold molar.

The base can be used in an amount of 1.0- to 3.0-fold molar amount with respect to compound (V), and preferably it is used in an amount of 1.1- to 1.3-fold 20 molar.

After the above step, the reaction generally used such as oxidation, reduction, esterification, amidation, introduction of protecting groups, deprotection, hydrolysis or the like can be carried out if necessary in order to convert the substituents on R1. 25 [0047] [Step 5]

This is a step of preparing compound (II) or salt thereof by hydrolysis or catalytic hydrogenation of compound (IV) or salt thereof. (1) In the case of hydrolysis

Compound (II) or salt thereof can be prepared by hydrolysis of compound 30 (IV) or salt thereof in the presence of an acid or a base.

The solvent used for this step is not particularly limited so long as it dissolves starting materials to some extent and does not inhibit the reaction, and includes, for example, alcohol solvents such as methanol, ethanol, propanol and 22 FP06-0349-00 butanol; ether solvents such as tetrahydrofuran, 1,2-dimethoxyethane, tert-butyl methyl ether, cyclopentyl methyl ether, diethyl ether, diisopropyl ether, dibutyl ether and dicyclopentyl ether; water; or a mixed solvent thereof oi the like, and a mixed solvent of water and methanol, ethanol or tetrahydrofuran is preferable. 5 The acid represents hydrochloric acid or the like.

The base represents sodium hydroxide, potassium hydroxide, potassium carbonate, sodium carbonate or the like.

The reaction temperature will generally differ depending on the starting materials, the solvent and the other reagents used in the reaction, and it is 10 preferably 0°C to 80°C (internal temperature of the reaction vessel) and more preferably 30°C to 50°C (internal temperature of the reaction vessel).

The acid can be used in an amount of 1.0- to 5.0-fold molar amount with respect to compound (IV), and preferably it is used in an amount of 1.0- to 2.0-fold molar.

The base can be used in an amount of 1.0- to 5.0-fold mclar amount with 20 respect to compound (IV), and preferably it is used in an amount of 1.0- to 2.0-fold molar. (2) In the case of catalytic hydrogenation

This is a step of preparing compound (II) or salt thereof by catalytic hydrogenation of compound (IV) or salt thereof in the presence of a reduction 25 catalyst under a hydrogen atmosphere.

The solvent used for this step is not particularly limited so long as it dissolves starting materials to some extent and does not inhibit the reaction, and includes, for example, alcohol solvents such as methanol, ethanol, propanol and butanol; ether solvents such as tetrahydrofuran, 1,2-dimethoxyethane, tert-butyl 30 methyl ether, cyclopentyl methyl ether, diethyl ether, diisopropyl ether, dibutyl ether and dicyclopentyl ether; N,N-dimethylformamide; N-methyl-2-pyrrolidone; formic acid; water; or a mixed solvent thereof, and a mixed solvent of water, methanol and tetrahydrofuran, a mixed solvent of water, ethanol and 23 FP06-0349-00 tetrahydrofuran, or a mixed solvent of water and ethanol is preferable.

The reduction catalyst represents palladium on carbon, palladium hydroxide, platinum oxide, Raney nickel or the like, and palladium on carbon is preferable.

This step can be carried out under a hydrogen atmosphere at 0.1 MPa 5 (ordinary pressure) to 1.0 MPa, and more preferably under a hydrogen atmosphere at 0.1 MPa to 0.3 MPa.

When formic acid or a mixed solvent containing formic acid is used as a solvent for this step, this step can be carried out without using hydrogen gas.

The reaction temperature will generally differ depending on the starting 10 materials, the solvent and the other reagents used in the reaction, and it is preferably 0°C to 50°C (internal temperature of the reaction vessel) and more preferably 20°C to 30°C (internal temperature of the reaction vessel).

The reaction time will generally differ depending on the starting materials, the solvent, the other reagents used in the reaction and the reaction temperature, 15 and stirring at the above reaction temperature for 1 to 48 hours after the addition of the reagents is preferable and stirring for 3 to 18 hours is more preferable.

The reduction catalyst can be used in an amount of 0.1- to 5.0-fold molar amount with respect to compound (IV), and preferably it is used in an amount of 0.5- to 1.5-fold molar. 20 [0048] [Step 6]

This is a step of preparing compound (I) by reacting compound (II) or salt thereof with compound (III) in the presence of a condensation reagent and in the presence or absence of a base.

As compound (III) may be used publicly known compounds, commercially 25 available compounds or compounds easily prepared by methods those skilled in the art usually carry out.

The solvent used for this step is not particularly limited so long as it dissolves starting materials to some extent and does not inhibit the reaction, and includes, for example, ether solvents such as tetrahydrofuran, 1,2-c.imethoxyethane, 30 tert-butyl methyl ether, cyclopentyl methyl ether, diethyl ether, ciisopropyl ether, dibutyl ether and dicyclopentyl ether; alcohol solvents such as ethanol, 1-propanol, 2-propanol; N,N-dimethylformamide; N-methyl-2-pyrrolidone; N,N-dimethylformamide; or a mixed solvent thereof, and a mixed solvent of 24 tetrahydrofuran and Ν,Ν-dimethylformamide or a mixed solvent of tetrahvdrofuran and 2-propanol is preferable.

The condensation reagent represents 4-(4,6-dimethoxy[l.3.5’ triazin-2-yl)-4- methylmorpholinium chloride hydrate, 2-chloro-4,6-dimethoxy-1,3,5-triazine, 5 2,4,6-trichloro-l,3,5-triazine, dicyclohexyl carbodiimide (DCC), 1-ethyl-3,(3'- dimethylaminopropyl)carbodiimide HC1 salt (EDC or WSC HC1). O-(1H-benzotiazol-l-yl)-N,N,N',N'-tetramethyluronium hexafluorophosphate (HBTU), 0-(1 H-benzotiazol-1 -yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate (7BTU) or the like, and 4-(4,6-dimethoxy[1.3.5]triazin-2-yl)-4-methyhnorpholinium chloride 10 hydrate or 2,4,6-trichloro-l ,3,5-triazine is preferable.

The base represents N-methylmorpholine, pyridine, triethylamine, diisopropylethylamine, 1 -methylimidazole, potassium carbonate, sodium carbonate or the like, and N-methylmorpholine is preferable.

The reaction temperature will generally differ depending on the starting 15 materials, the solvent and the other reagents used in the reaction, and it is preferably -10°C to 50°C (internal temperature of the reaction vessel) and more preferably 20°C to 30°C (internal temperature of the reaction vessel·).

The reaction time will generally differ depending on the stalling materials, the solvent, the other reagents used in the reaction and the reaction temperature, 20 and stirring at the above reaction temperature for 1 to 48 hours after the addition of the reagents is preferable and stirring for 3 to 18 hours is more preferable.

Compound (III) can be used in an amount of 1.0- to 3.0-fold molar amount with respect to compound (II), and preferably it is used in an amount of 1.0- to 2.0-fold molar. 25 The condensation reagent can be used in an amount of 1.0- to 3.0-fold molar amount with respect to compound (II), and preferably it is used in an amount of 1.0- to 2.0-fold molar.

The base can be used in an amount of 1.0- to 10-fold molar amount with respect to compound (II), and preferably it is used in an amount of 2.0- to 4.0-fold 30 molar.

Examples [0049] Examples are illustrated below for the purpose of the easy understanding of the present invention, but the present invention is not limited to these Examples. 25 FP06-0349-00 10 15 20 [0050] [Production Example 1) tert-Butyl [l-f2-dimethvlaminoacetvDpiperidin-4-yl] carbamate

H 0 1 o Ν,Ν-Dimethylglycine (2.97 g), 1-hydroxybenzotriazole (3.89 g) and l-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (5.27 g) were added to a solution of 4-(tert-butoxycarbonylamino)piperidine (5.0 g) in N,N-dimethylformamide (70 ml), followed by stirring at room temperature under a nitrogen atmosphere for 46 hours. Ethyl acetate (400 ml), brine (200 ml) and a IN aqueous solution of sodium hydroxide (50 ml) were added to the reaction mixture, followed by stirring at room temperature for 30 minutes, and the mixture was partitioned. The aqueous layer was extracted with ethyl acetate. The organic layer was collected, washed with a IN aqueous solution of sodium hydroxide and brine in this order, and dried over anhydrous sodium sulfate. The dried organic layer was concentrated under reduced pressure to give the title compound (8.03 g, quant.) as white crystals. ESI-MS (m/z): 286[M+H]+.

[0051] (Production Example 2) N-[l-f2-Dimethylaminoethyllpiperidin-4-yl]-N- methylamine

I A solution of tert-butyl [l-(2-dimethylaminoacetyl)piperidin-4-yf carbamate (7.07 g) in tetrahydro furan (100 ml) was stirred with cooling on ice under a nitrogen atmosphere. Lithium aluminium hydride (280 mg) was added thereto, followed by stirring on an ice bath for 15 minutes, then at room temperature for 15 minutes. The reaction mixture was heated and refluxed under a nitrogen atmosphere at 100°C for 11 hours. The reaction mixture was cooled on ice. Water (2.8 ml), a 5N aqueous solution of sodium hydroxide (2.8 ml) and water (14.0 ml) was added thereto in this order, followed by stirring for 2 hours. Insoluble matter was removed by filtration. The filtrate was concentrated to give the title compound (4.65 g, quant.) as a yellow oil. 25 26 FP06-0349-00

10 15 20 !H-NMR Spectrum (CDC13) δ (ppm): 1.34-1.43 (2H, m), 1.87-1.90 (2H, m), 2.02-2.08 (2H, m), 2.25 (6H, s), 2.31-2.50 (7H, m), 2.90 (2H, m), 3.14-3.27 (1H, m). ESI-MS (m/z): 186[M+H]+.

[0052] (Production Example 3) (4-Benzovlpiperazin-l-vl)acetic acid ethyl ester o-/ '— o o l-(Ethoxycarbonylmethyl)piperazine (5.1 g) was dissolved in tetrahydrofuran (300 ml) under a nitrogen atmosphere, and triethylamine (8.25 ml) and benzoyl chloride (3.44 ml) was added thereto with cooling in an ice water bath. The reaction mixture was brought to room temperature, followed by stirring for 4 hours. The reaction mixture was partitioned between ethyl acetate (200 ml) and a saturated aqueous solution of sodium hydrogencarbonate (100 ml). The separated organic layer was washed with a saturated aqueous solution of sodium hydrogencarbonate (100 ml), water (100 ml) and brine (100 ml), and dried over sodium sulfate. The solvent was distilled off under reduced pressure to give the title compound (8.19 g, quant.) as a colorless oil. ’H-NMR Spectrum (CDC13) δ (ppm): 1.28 (3H, t, J=7.2 Hz), 2.20-2.85 (4H, m), 3.26 (2H, m), 3.48 (2H, m), 3.85 (2H, m), 4.19 (2H, m), 7.41 (5H, in).

[0053] (Production Example 4) l-(Azetidin-l-yl)-2-(4-benzoylpiperazin-l- vDethanone

iP o o

Methanol (300 ml) and water (50 ml) were added to (4-benzoylpiperazin-l-yl)acetic acid ethyl ester (8.19 g), and lithium hydroxide (1.34 g) v/as added thereto with cooling in an ice water bath, followed by stirring for 10 minutes. The reaction mixture was brought to room temperature, followed by stirring for 24 hours. After adding IN hydrochloric acid (55.9 ml), the reaction mixture was concentrated under reduced pressure, and ethanol (200 ml) was added to the resultant residue. The precipitated insoluble matter was removed by filtration through celite. The

25 27 FP06-0349-00 5 10 15 20 filtrate was concentrated under reduced pressure to give a crude product of (4-benzoylpiperazin-l-yl) acetic acid (8.6 g) as a white solid. N,N-Dimethylformamide (80 ml) was added to (4-benzoylpiperazin-l-yl)acetic acid (2 g) at room temperature under a nitrogen atmosphere, and azetidine hydrochloride (1.51 g), triethylamine (4.49 ml), l-ethyl-3-(3-dimethylaminopropvl)carbodiimide hydrochloride (3.09 g) and 1-hydroxybenzotriazole (2.18 g) were added in this order, followed by stirring at room temperature for 66 hours. Ethyl acetate (100 ml) and a saturated aqueous solution of sodium hydrogencarbonate (50 ml) were added to the reaction mixture, which was partitioned. The organic layer was washed with a saturated aqueous solution of sodium hydrogencarbonate (50 ml), water (50 ml) and brine (50 ml) in this order, and dried over anhydrous sodium sulfate. The residue obtained by distilling off the solvent under reduced pressure was purified by silica gel column chromatography (Fuji Silysia NH, eluent; ethyl acetate). The residue obtained by concentrating the fractions containing the target compound under reduced pressure was suspended by the addition of diethyl ether (10 ml). The solid was collected by filtration, and dried under aeration to give the title compound (731.5 mg) as white powder. ’H-NMR Spectrum (CDC13) δ (ppm): 2.40-2.80 (6H, m), 3.03 (2H, s), 3.47 (2H, m), 3.83 (2H, m), 4.06 (2H, m), 4.22 (2H, m), 7.30-7.50 (5H, m).

[0054] (Production Example 5) l-r2-(Azetidin-l-yl)ethyn-4-benzy'piperazine

Lithium aluminium hydride (405 mg) was suspended in tetrahydrofuran (10 ml) under a nitrogen atmosphere with stirring in an ice water bath, l-(azetidin-l-yl)-2-(4-benzoylpiperazin-l-yl)ethanone (730 mg) and tetrahydrofuran (5 ml x 3) was added thereto. The reaction mixture was stirred at 60°C for 3 hours. The reaction mixture was allowed to cool down to room temperature, and water (0.4 ml), a 5N aqueous solution of sodium hydroxide (0.4 ml) and water (1.2 ml) were added thereto, followed by stirring for 13 hours. The insoluble matter in the reaction mixture was removed by filtration through celite, and washed with ethyl acetate (100 ml). The solvent was distilled off under reduced pressure to give a crude 30 28 FP06-0349-00 product of the title compound (687 mg) as a pale yellow oil. ESI-MS (m/z): 260[M+H]+.

[0055] (Production Example 6) l-[2-fAzetidin-l-yl)ethyllpiperazine trihydrochloride hl

hL· 3HCI 10 15 l-[2-(Azetidin-l-yl)ethyl]-4-benzylpiperazine (687 mg) was dissolved in methanol (30 ml), and 20% palladium hydroxide on carbon (372 mg) was added thereto, followed by stirring under a pressurized hydrogen atmosphere (0.4 MPa) for 10 hours. The catalyst was removed by filtration and washed with methanol. 4N hydrochloric acid in ethyl acetate (1.33 ml) was added to the filtrate, followed by stirring. Excess hydrochloric acid was removed by pressure reduction in the system with stirring. The solvent was distilled off to give the title compound (736 mg, quant.) as a pale brown oil. ESI-MS (m/z): 170[M+H]+.

[0056] (Production Example 7) l-Benzhydrylazetidin-3-one

20 25 A solution of pyridine sulfur trioxide complex (19.7 g) in dimethyl sulfoxide (80 ml) was added dropwise to a mixture of l-benzhydrylazetidin-3-ol hydrochloride (5.52 g) and triethylamine (27.9 ml) at room temperature. The reaction mixture was stirred at 50°C for 30 minutes. The reaction mixture was allowed to cool down to room temperature, and poured into ice water. This wa.s extracted with ethyl acetate, and the organic layer was washed with brine. Activated carbon (5 g) was added to the organic layer, followed by stirring at room temperature for 3 days. The activated carbon was removed by filtration, and the filtrate v/as concentrated. The residue was dissolved in methanol (200 ml), and activated carbon (10 g) was added thereto, followed by stirring at room temperature for 3 days. The activated carbon was removed by filtration, and the filtrate was concentrated. The residue 29 FP06-0349-00 5 10 was purified by silica gel column chromatography (eluent; heptane.ethyl acetate = 4:1, then 2:1). The fractions containing the target compound were concentrated to give the target compound (3.21 g) as a pale yellow oil. Hexane was added thereto to precipitate crystals, and the crystals were collected by filtration. Drying under aeration gave the title compound (1.11 g, 23.4%) as white crystals. Hexane was added to the residue obtained by concentration of the filtrate, which was allowed to stand at room temperature. After crystals precipitated, the supernatant was removed using a pipette. These were dried under reduced pressure to give the title compound (940 mg, 19.8%) as pale yellow crystals. ’H-NMR Spectrum (CDC13) δ (ppm): 4.01 (4H, s), 4.60 (1H, s), 7.22 (2H, m), 7.30 (4H, m), 7.48 (4H, m).

[0057] [Production Example 8~) 3-[Azetidin-l-yll-l-benzhvdrylazetidine

15 20 25

Azetidine hydrochloride (326 mg) was added to a solution of 1-benzhydrylazetidin- 3-one (750 mg) in dichloromethane (12 ml), followed by stirring at room temperature. Sodium triacetoxyborohydride (1.01 g) was added thereto, followed by stirring at room temperature for 25 hours. Sodium carbonate: (until bubbling stopped), water (50 ml) and ethyl acetate (100 ml) was added to the reaction mixture. The organic layer was separated, washed with brine and dried over anhydrous sodium sulfate. The dried organic layer was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (Fuji Silysia NH, eluent; heptane:ethyl acetate =1:1, 1:2, then ethyl acetate ) to give the title compound (643 mg,73.1%) as a pale yellow solid. 1 H-NMR Spectrum (CDC13) δ (ppm): 2.06 (2H, m), 2.91 (2H, m), 3.16-3.24 (7H, m), 4.35 (1H, s), 7.15 (2H, m), 7.25 (4H, m), 7.40 (4H, d, J=7.6 Hz). ESI-MS (m/z): 279[M+H]+.

[0058] [Production Example 91 3-[Azeti din-1-yljazeti dine dihydrochloride 30 FP06-0349-00

10 4N hydrochloric acid in ethyl acetate (1.16 ml) was added to a solution of 3-(azetidin-l-yl)-l-benzhydrylazetidine (643 mg) in ethyl acetate, and the mixture was concentrated. The resultant residue was dissolved in methanol (65 ml), and 20% palladium hydroxide (811 mg) was added thereto. This mixiure was stirred under a pressurized hydrogen atmosphere (0.3 to 0.4 MPa) at room temperature for 4 hours. The catalyst was removed by filtration, and the filtrate was concentrated. The solid was suspended by the addition of heptane to the residue. The supernatant was removed using a pipette and the residue was concentrated under reduced pressure to give a crude product of the title compound (471.2 mg) as a pale yellow oil. ESI-MS (m/z): 113[M+H]+.

[0059] (Production Example 101 l-Benzhydryl-S-fmethanesulfonyloxylazetidine

15 20 25 A suspension of l-benzhydrylazetidin-3-ol (15.0 g) in pyridine (100 ml) was cooled down to -20°C under a nitrogen atmosphere, and methanesulfonyl chloride (6.33 ml) was added dropwise. The reaction mixture was stirred under a nitrogen atmosphere at -20°C for 1 hour, then in a water bath for 2.5 days. The reaction mixture was partitioned after addition of water and ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium hydrogencarbonate, water and brine, and dried over anhydrous sodium sulfate. The solvent was concentrated under reduced pressure. Ethanol (10 ml) and hexane (50 ml) was added to the residue, and the precipitated crystals were suspended. The crystals were collected by filtration and washed with hexane. This was dried under aeration at room temperature to give the title compound (5.943 g, 44.8%) as pale yellow crystals. The filtrate was concentrated, and the residue was purified by silica gel column chromatography (eluent; heptane: ethyl acetate = 2:1, 1:1, heptane: ethyl 31 FP06-0349-00 5 acetate:methanol = 50:50:1, 40:60:1, then ethyl acetate methanol = 100:1). The fractions containing the target compound were concentrated to give the title compound (1.58 g, 11.9%) as pale yellow crystals. ’H-NMR Spectrum (CDC13) δ (ppm): 2.99 (3H, s), 3.18-3.21 (2H, m), 3.62-3.66 (2H, m), 4.40 (1H, s), 5.11 (1H, m), 7.18-7.22 (2H, m), 7.26-7.31 (4H, m), 7.39 (4H, d, J=7.2 Hz).

[0060] (Production Example 11) l-Benzhydryl-3-cyanoazetidine

10 15 20

Water (7.2 ml) and sodium cyanate (3.48 g) were added to a solution of 1-benzhydryl-3-(methanesulfonyloxy)azetidine (7.52 g) in N,N-dimethylformamide (60 ml), followed by stirring at 65°C for 9 hours. Water, sodium carbonate and ethyl acetate were added to the reaction mixture, which was partitioned. The aqueous layer was extracted with ethyl acetate. The organic layer was collected, washed with brine, and dried over anhydrous sodium sulfate. This was concentrated under reduced pressure, and the resultant crystals were suspended by addition of diethyl ether (10 ml). The crystals were collected by filtration, and washed with diethyl ether. This was dried under aeration to give the title compound (5.43 g, 92.3%) as pale yellow crystals. Ή-NMR Spectrum (CDC13) δ (ppm): 3.20-3.31 (3H, m), 3.47 (2H, m), 4.36 (1H, s), 7.19-7.23 (2H, m), 7.26-7.30 (4H, m), 7.39 (4H, m).

[0061] (Production Example 12) l-Benzhydrylazetidine-3-carboxylic acid

O

Potassium hydroxide (6.48 g) and water (3.25 ml) were added to a solution of 1-benzhydryl-3-cyanoazetidine (5.43 g) in methoxyethanol (54 ml), followed by stirring at 100°C for 4 hours. The reaction mixture was allowed to cool down to room temperature, and poured into ice. After pH of the mixture was adjusted to 5 with IN hydrochloric acid, sodium chloride was added thereto. This was extracted 32 FP06-0349-00 5 10 with a mixed solvent of ethyl acetate and tetrahydrofuran. The organic layer was washed with brine, and dried over anhydrous sodium sulfate. The dried organic layer was concentrated under reduced pressure to give a crude product of the title compound as pale yellow crystals. The crystals were suspended by the addition of diethyl ether (15 ml). The crystals were collected by filtration and washed with diethyl ether. This was dried under aeration to give the title compound (4.20 g, 71.7%) as pale yellow crystals. ’H-NMR Spectrum (CDC13) δ (ppm): 3.00-3.90 (5H, m), 4.95 (1H, s), 7.25-7.28 (2H, m), 7.33 (4H, m), 7.53 (4H, m).

[0062] (Production Example 13) Methyl l-benzhydrylazetidine-3-carboxylate 0

15 20

Potassium carbonate (6.53 g) and iodomethane (0.976 ml) were added to a solution of l-benzhydrylazetidine-3-carboxylic acid (4.20 g) in N,N-dimethylformamide (45 ml), followed by stirring at room temperature for 20.5 hours. The reaction mixture was poured into ice water, and extracted with ethyl acetate. The organic layer was washed with brine, and dried over anhydrous sodium sulfate. The solvent was distilled off, and the residue was purified by silica gel column chromatography (eluent; heptane:ethyl acetate = 5:1, then 3:1). The fractions containing the target compound were concentrated to give the title compound (3.57 g, 80.8%) as yellow crystals. ’H-NMR Spectrum (CDC13) δ (ppm): 3.26 (2H, m), 3.31 (1H, m), 3.44 (2H, m), 3.69 (3H, s), 4.38 (1H, s), 7.16-7.20 (2H, m), 7.25-7.28 (4H, m), 7.39-7.41 (4H, m). ESI-MS (m/z): 282[M+H]+.

[0063] (Production Example 141 Methyl azetidine-3-carboxylate hydrochloride

O

HN 25

OMe HCI 4N hydrochloric acid in ethyl acetate (12.7 ml) and 20% palladium hydroxide (3.57 g) were added to a solution of methyl l-benzhydrylazetidine-3-carboxvlate (3.57 g) in methanol (360 ml), followed by stirring under a pressurized hydrogen 33 FP06-0349-00 atmosphere (0.4 MPa) at room temperature for 11 hours. The catalyst was removed by filtration, and washed with methanol and water. The filtrate was concentrated to give a crude product of the target compound as a pale yellow oil, which was used in the next reaction supposing that the reaction proceeded quantitatively and 1.93 g of the product was obtained. ESI-MS (m/z): 116[M+H]+.

[0064] (Production Example 15) Methyl l-tert-butoxyca.':bony.'iazetidine-3- carboxylate 10 15 20 25 30

O OMe

A crude product of methyl azetidine-3-carboxylate hydrochloride (calculated as 1.93 g of pure product) was dissolved in water (26 ml), sodium hydro gencarbonate (3.2 g), then a solution of di-t-butyl dicarbonate (2.91 g) in tetrahydrofuran (13 ml) were added with stirring and cooling in an ice bath, followed by stirring at the same temperature for 0.5 hours. The reaction mixture was stirred at room temperature for 19.5 hours. Tetrahydrofuran in the reaction mixture was distilled off, extraction was performed with ethyl acetate. The organic layer was washed with brine (70 ml) and dried over anhydrous sodium sulfate. The concentrated organic layer and the aqueous layer were combined, and tetrahydrofuran (50 ml) was added thereto. This was stirred with cooling in an ice bath, and sodium hydrogencarbonate (3.2 g), then di-t-butyl dicarbonate (2.91 g) were again added thereto. The reaction mixture was stirred at the same temperature for 0.5 hours, then at room temperature for 2.5 days. The reaction mixture was partitioned, and the aqueous layer was extracted with ethyl acetate. The organic layers were combined, and dried over anhydrous sodium sulfate. The solvent was distilled off, and the residue was purified by silica gel column chromatography (eluent; heptane:ethyl acetate = 2:1, 1:1, ethyl acetate, then ethyl acetate:methanol = 10:1). The fractions containing the target compound were concentrated to give the title compound (370 mg, 13.5%) as a colorless oil. Ή-NMR Spectrum (CDC13) δ (ppm): 1.44 (9H, s), 3.35 (1H, m), 3.75 (3H, s), 4.10 (4H, d, J=7.6 Hz).

[0065] (Production Example 16) tert-Butyl 3-(hydroxymethyl)azetidine-l- 34 FP06-0349-00 carboxylate >r°YN 1 o 10 15

Lithium aluminium hydride (128 mg) was placed in a round bottomed flask, and suspended in tetrahydrofuran (30 ml). The suspension was cooled in an ice bath, and a solution of methyl l-tert-butoxycarbonylazetidine-3-carboxylate (970 mg) in tetrahydrofuran (10 ml) was added gradually, followed by stirring at the same temperature under a nitrogen atmosphere for 1 hour. Water (0.13 ml), a 5N aqueous solution of sodium hydroxide (0.13 ml) and water (0.39 ml) was added to the reaction mixture with cooling in an ice bath, followed by stirring at the same temperature for 1 hour. Insoluble matter in the reaction mixture was removed by filtration. The filtrate was concentrated to give the title compound (805 mg, 95.3%) as a colorless oil. ’H-NMR Spectrum (CDC13) δ (ppm): 1.44 (9H, s), 2.71 (1H, m), 3.69 (2H, dd, J=5.2, 8.4 Hz), 3.79 (2H, d, J=6.8 Hz), 4.00 (2H, m).

[0066] (Production Example 17) 3-(Hydroxymethyl) azetidine trifluoro acetate

OH

CF3CO2H 20 25

Trifluoroacetic acid (0.413 ml) was added to tert-butyl 3-(hydroxymethyl)azetidine-l-carboxylate (125 mg) with cooling in an ice bath, followed by stirring at the same temperature for 30 minutes. Then the reaction mixture was stirred at room temperature for 1.5 hours. The reaction mixture was concentrated to give a crude product of the title compound (209.8 mg) as a yellow oil. ESI-MS (m/z): 88[M+H]+.

[0067] (Production_Example_18)_tert-Butyl_3^ [fmethanesulfonyloxylmethyl] azetidine-1 -carboxylate ^^Q.SOaMe

>°YN 1 O 35 FP06-0349-00

Triethylamine (1.80 ml) was added to a solution of tert-butyl 3-(hydroxymethyl)azetidine-l-carboxy late (806 mg) in tetrahydrofuran (25 ml). This was cooled on ice under a nitrogen atmosphere, and methanesulfonvl chloride (0.499 ml) was added dropwise, followed by stirring at the same temperature for 30 5 minutes. The reaction mixture was partitioned after the addition of ethyl acetate (100 ml) and water (70 ml). The aqueous layer was extracted with ethyl acetate. The combined organic layer was washed with brine, and dried over anhydrous sodium sulfate. The solvent was distilled off, and the residue was purified by silica gel column chromatography (eluent; ethyl acetate). The fractions containing the 10 target compound were concentrated to give the title compound (1.05 g, 92.0%) as a colorless oil. Ή-NMR Spectrum (CDC13) δ (ppm): 1.44 (9H, s), 2.93 (1H, m), 3.05 (3H, s), 3.72 (2H, dd, >5.0, 9.0 Hz), 4.06 (2H, m), 4.35 (2H, d, >6.8 Hz). ESI-MS (m/z): 288[M+Na]+. 15 [0068] (Production Example 19) tert-Butyl 3-(dimethylaminom5thyl)azetidine-l- carboxylate 1 0 A 2M solution of dimethylamine in tetrahydrofuran (20 ml) was added to a solution of tert-butyl 3-[(methanesulfonyloxy)methyl]azetidine-l-carboxylate (1.05 g) in 20 methanol (20 ml), and the reaction mixture was heated in a sealed tube at 70°C for 40 hours. The reaction mixture was allowed to cool down to room temperature. The reaction mixture was concentrated, and partitioned between ethyl acetate and a saturated aqueous solution of sodium hydrogencarbonate. The organic layer was washed with brine, and dried over anhydrous sodium sulfate. The solvent was 25 distilled off to give the title compound (678 mg, 79.9%) as a yellow oil. Ή-NMR Spectrum (CDC13) δ (ppm): 1.43 (9H, s), 2.22 (6H, s), 2.50 (2H, d, >7.6

Hz), 2.69 (1H, m), 3.59 (2H, dd, >5.2, 8.4 Hz), 4.16 (2H, m). ESI-MS (m/z): 215[M+H]+, 269[M+Na+MeOH]+.

[0069] (Production Example 20) S-fDimethylaminomethyllazetidine 30 bistrifluoroacetate 36 FP06-0349-00 hnJ ι

2 CF3CO2H

Trifluoroacetic acid (1.95 ml) was added to tert-butyl 3-(dimethylaminomethyl)azetidine-l-carboxylate (678 mg) with cooling on ice, followed by stirring at the same temperature for 30 minutes. Then, the reaction 5 mixture was stirred at room temperature for 1.5 hours. The reaction mixture was concentrated and azeotropically distilled with toluene to give a crude product of the title compound (1.79 g) as a yellow oil. ESI-MS (m/z): 115[M+Na]+.

[0070] (Production Example 21) tert-Butyl 3-methoxyazetidine-l-carboxylate □ Γ— >°YN 10 1 0 A suspension of sodium hydride (2.89 g) in tetrahydrofuran (50 ml) was stirred with cooling in an ice bath. A solution of tert-butyl 3-hydroxyazetidine-l-carboxylate (5.00 g) in tetrahydrofuran (50 ml) was gradually added, followed by stirring at the same temperature for 30 minutes. Then, the reaction mixture was 15 stirred at room temperature for 30 minutes. The reaction mixture was stirred with cooling in an ice bath again for 15 minutes. Iodomethane (3.09 ml) was added dropwise to the reaction mixture, followed by stirring for 2 hours. Water was gradually added to the reaction mixture. When bubbling stopped, the organic layer was separated. The aqueous layer was extracted with ethyl acetate. The organic 20 layers were combined, washed with brine, and dried over anhydrous sodium sulfate.

The solvent was distilled off, and the residue was purified by silica gel column chromatography (eluent; heptane:ethyl acetate = 3:1, 2:1, 1:1, then ethyl acetate). The fractions containing the target compound were concentrated to give the title compound (1.80 g, 33.3%) as a colorless oil. The fractions containing the starting 25 material were concentrated and collected (2.10 g, 42.0%). Ή-NMR Spectrum (CDC13) δ (ppm): 1.44 (9H, s), 3.28 (3H, s), 3.82 (2H, m), 4.06 (2H, m), 4.14 (lH,m).

[0071] fProduction Example 22) 3-Methoxyazetidine trifluoroacetate 37 FP06-0349-00 /^Ox ΗΝ-/

CF3CO2H tert-Butyl 3-methoxyazetidine-l-carboxylate (125 mg) was dissolved in dichloromethane (0.618 ml), and trifluoroacetic acid (0.618 ml) was added thereto, followed by stirring at room temperature for 3.5 hours. The reaction mixture was 5 concentrated to give a crude product of the target compound (232 mg) as a yellow oil. ESI-MS (m/z): 88[M+H]+.

[0072] (Production Example 23) 3-(Azetidin-l-ylcarbonyl)-l-benzhvdrylazetidine 10 l-Benzhydrylazetidine-3-carboxylic acid (1.52 g) was dissolved in N,N- dimethylformamide (30 ml) at room temperature under a nitrogen atmosphere. Triethylamine (3.17 ml), BOP reagent (benzotriazole-1-yl-oxy-tris-(dimethylamino)-phosphonium hexafluorophosphate; 5.03 g) and azetidine hydrochloride (1.06 g) were added in this order, followed by stirring for 24 hours. 15 A IN aqueous solution of sodium hydroxide (50 ml) was added to the reaction mixture, followed by stirring. Then the reaction mixture was extracted after addition of ethyl acetate (100 ml). The separated organic layer was washed with a IN aqueous solution of sodium hydroxide, water and brine, and dried over anhydrous sodium sulfate. To the residue (1.83 g) obtained by distilling off the 20 solvent were added ethyl acetate (2 ml) and tert-butyl methyl ether (10 ml) to precipitate crystals. The crystals were collected by filtration, and dried under aeration to give the title compound (1.14 g, 65%) as pale yellow crystals. Ή-NMR Spectrum (CDClj) δ (ppm): 2.15-2.30 (2H, m), 3.20-3.50 (5H, m), 3.90- 4.10 (4H, m), 4.45 (1H, s), 7.15-7.45 (10H, m). 25 ESI-MS (m/z): 307[M+H]+.

[0073] (Production Example 24) 3-(Azetidin-l-ylmethyl)-l-benzhydrylazetidine 38 FP06-0349-00

Lithium aluminium hydride (300 mg) was suspended in tetrahydrofuran (10 ml) at room temperature under a nitrogen atmosphere, and a solution of 3-(azetidin-l-ylcarbonyl)-l-benzhydrylazetidine (1.14 g) in tetrahydrofuran (30 ml) was added dropwise. After the addition, the reaction mixture was stirred at 60°C for 2 hours. After the reaction mixture was cooled in an ice water bath, water (0.3 ml), a 5N aqueous solution of sodium hydroxide (0.3 ml) and water (0.9 ml) were added, followed by stirring overnight. Insoluble matter was removed by filtration, and washed with ethyl acetate (100 ml). The filtrate was concentrated under reduced pressure to give the title compound (1.115 g, quant.) as a pale brown oil. ]H-NMR Spectrum (CDC13) δ (ppm): 2.07 (2H, m), 2.40-2.60 (3H, n), 2.74 (2H, m), 3.11-3.15 (4H,m), 3.32 (2H, m), 4.29 (1H, s), 7.14-7.40 (10H, m). ESI-MS (m/z): 293[M+H]+.

[0074] [Production Example 25) 3-[Azetidin-l-ylmethyl)azetidme dihydrochloride 15

20 25 3-(Azetidin-l-ylmethyl)-l-benzhydrylazetidine (1.115 g) was dissolved in methanol (25 ml). 10% palladium on carbon (1.1 g) was added under a nitrogen atmosphere, followed by stirring under a pressurized hydrogen atmosphere (0.4 MPa) for 12 hours. After replacing the air of the vessel by nitrogen, the catalyst was removed by filtration, and washed with methanol. 4N hydrochloric acid in ethyl acetate (4 ml) was added to the reaction mixture, which was concentrated under reduced pressure. Heptane (25 ml) was added to the residue, and the supernatant was removed. This procedure was repeated once more. The resultant residue was dried under reduced pressure for 2 days to give the title compound (680 mg, 90%) as a pale brown oil. ESI-MS (m/z): 127[M+H]+.

[0075] [Production Example 26) l-Benzhydrvl-3-[hydroxymethyl]azetidine 39 FP06-0349-00

10 15 20 l-Benzhydryl-3-azetidinecarboxylic acid (3.12 g) was suspended in tetrahydrofuran (60 ml), and cooled in an ice-methanol bath under a nitrogen atmosphere. Triethylamine (1.96 ml) was added dropwise, and a solution of ethyl chlorocarbonate (1.34 ml) in tetrahydrofuran (5 ml) was added dropwise over 20 minutes. After the addition, the reaction mixture was stirred at the same temperature for 30 minutes. The reaction mixture was filtered, and the residue was washed with tetrahydrofuran (30 ml). The filtrate was added dropwise to a solution of an aqueous (15 ml) solution of sodium borohydride (1.33 g) cooled in an ice water bath over 15 minutes. After the addition, the reaction mixture was stirred at room temperature. IN hydrochloric acid (35 ml) was gradually added to the reaction mixture to degrade excess sodium borohydride, and a IN aqueous solution of sodium hydroxide (35 ml) was added. This was extracted with ethyl acetate (100 ml). The organic layer was washed with brine, and dried over anhydrous sodium sulfate. The solvent was concentrated, and the residue was dried under reduced pressure to give the title compound (1.59 g, 54%) as a pale brown solid. ^d-NMR Spectrum (CDC13) δ (ppm): 2.57 (1H, m), 3.03 (2H, m), 3.24 (2H, m), 3.80 (2H, d, J=5.2 Hz), 4.33 (1H, s), 7.15-7.45 (10H, m). ESI-MS (m/z): 254[M+H]+.

[0076] (Production Example 27) 3-fHydroxymethyl)azetidine hydrochloride hnj HC1 l-Benzhydryl-3-(hydroxymethyl)azetidine (1.59 g) was dissolved in methanol (30 ml) and palladium hydroxide on carbon (1.0 g) was added under a nitrogen atmosphere, followed by stirring under a pressurized hydrogen atmosphere (0.4 25 MPa). After replacing the air of the vessel by nitrogen, the catalyst was removed by filtration and washed with methanol. 4N hydrochloric acid in ethyl acetate (2 ml) was added to the reaction mixture, which was concentrated under reduced pressure. Heptane (15 ml) was added to the residue, and the supernatant was 40 FP06-0349-00 removed. This procedure was repeated once more. The residue was dried under reduced pressure overnight to give a crude product of the title compound (832 mg) as a pale yellow oil. ESI-MS (m/z): 88[M+H]+.

[0077] (Production Example 281 l-(Benzyloxy)-2.5-difluoro-4-nitrobenzene

10 15

Potassium carbonate (11.1 g) was added to a solution of 2,4,5-trifluoronitrobenzene (9.48 g) and benzyl alcohol (5.54 ml) in Ν,Ν-dimethylformamide (40 ml), followed by stirring at room temperature for 60 hours. Water (120 ml) was added to the reaction mixture at 0°C, followed by stirring at 4°C for 24 hours. The precipitated crystals were collected by filtration, and washed with water. The crystals were dried under reduced pressure to give the title compound (11.5 g, 81%) as pale yellow crystals. 'H-NMR Spectrum (DMSO-d6) δ (ppm): 5.35 (2H, s), 7.40-7.50 (5H, n), 7.64 (1H, dd, J=7.2, 13.2 Hz), 8.20 (1H, dd, J=7.2, 10.8 Hz).

[0078] (Production Example 291 4-Amino-2.5-difluorophenol

NH, 20 25 10% palladium on carbon (921 mg) was added to a solution of l-(berzyloxy)-2,5-difluoro-4-nitrobenzen (9.21 g) in methanol (300 ml), followed by stirring at room temperature under hydrogen atmosphere for 24 hours and 20 minutes. The air of the flask was replaced with nitrogen to stop the reaction, and the catalyst was removed by filtration using celite. The filtrate was distilled off under reduced pressure to give the title compound (4.96 g, 99%) as a pale brown solid. ]H-NMR Spectrum (DMSO-d6) δ (ppm): 4.67 (1H, s), 6.53-6.64 (1H, m), 9.03 (1H, s).

[0079] (Example 11 l-fBenzyloxycarbonyllcyclopropanecarboxylic acid 41 FP06-0349-00 10 15 20 25

Ο Ο (Method 1) 1,1-Cyclopropanedicarboxylic acid (5.02 g) was dissolved in tetrahydrofuran (50 ml) under a nitrogen atmosphere, and triethylamine (5.38 ml) was added dropwise with stirring and cooling in an ice water bath. After stirring at the same temperature for 30 minutes, thionyl chloride (2.82 ml) was added dropwise with cooling in ice water bath. After stirring at the same temperature for 30 minutes, a solution of benzyl alcohol (4.39 ml) in tetrahydrofuran (25 ml) was added with cooling in an ice water bath, and the reaction mixture was gradually brought to room temperature and stirred overnight. A 2N aqueous solution of sodium hydroxide (100 ml) was added to the reaction mixture, and tetrahydrofuran was distilled off under reduced pressure. tert-Butyl methyl ether (25 ml) was added to the resultant aqueous solution, followed by stirring. The organic layer and the aqueous layer were separated. The aqueous layer was cooled in an ice water bath, and 2N hydrochloric acid (50 ml) was added to adjust pH 4. Ethyl acetate (150 ml) was added, and the reaction mixture was stirred for a while. The organic layer was separated, washed with brine, and dried over anhydrous sodium sulfate. The residue obtained by distilling off the solvent was dried under reduced pressure to give the title compound (6.29 g, 74%) as a pale yellow oil. 'H-NMR Spectrum (DMSO-d6) δ (ppm): 1.30-1.40 (4H, m), 5.15 (2H, s), 7.30-7.38 (5H, m). ESI-MS (m/z): 243[M+Na]+. (Method 2) 1,1-Cyclopropanedicarboxylic acid (50 g) was dissolved in acetonitrile (500 ml) under a nitrogen atmosphere, and N-methylimidazole (31 ml) was added dropwise with stirring and cooling in an ice water bath. After stirring at the same temperature for 30 minutes, thionyl chloride (29 ml) was added dropwise. After stirring at the same temperature for 30 minutes, a mixed solution of benzyl alcohol (45.7 g) and N-methylimidazole (31 ml) was added with cooling in an ice water bath, and the reaction mixture was stirred at the same temperaPrre for 6 hours. A 2N aqueous solution of sodium hydroxide (900 ml) was added to adjust pH 8. tert- 30 42 FP06-0349-00 5 10 20 25

Butyl methyl ether (500 ml) was added to the resultant solution, and the mixture was stirred. The organic layer and the aqueous layer were separated, and the organic layer was extracted with a 5% aqueous solution of sodium hydrogencarbonate (200 ml). The aqueous layers were combined, cooled in an ice water bath, and 5N hydrochloric acid (300 ml) was added to adjust pH 4. Ethyl acetate (1000 ml) was added, and the mixture was stirred for a while. The organic layer was separated, washed with brine, and dried over anhydrous sodium sulfate. The residue obtained by distilling off the solvent was dissolved in methanol (120 ml), and water (120 ml) was added dropwise with stirring at room temperature. After stirring at room temperature for 30 minutes, and with cooling in an ice water bath for 2 hours, the precipitated solid was suction filtered, and washed with water (60 ml, twice). The resultant solid was dried under reduced pressure at 40°C to give the title compound (59 g, 69%).

[0080] (Example 2) 4-f 4-Amino-3-fluorophenoxy)pyridine-2-carboxamide 15

(Method 1) 4-Amino-3-fluorophenol (5.7 g) was dissolved in dimethyl sulfoxide (57 ml) under a nitrogen stream, potassium tert-butoxide (5.6 g) was added at room temperature, and the reaction mixture was stirred for 15 minutes. 4-Chloropvridine-2-carboxamide (5.0 g) was added to the reaction mixture, followed by stirring in an oil bath at 80°C (external temperature) under a nitrogen stream for 50 minutes. The reaction mixture was allowed to cool down to room temperature. A IN aqueous solution of sodium hydroxide (85.5 ml) was added to the reaction mixture, followed by stirring. The precipitated solid was collected by filtration and washed with water. The residue was dried under aeration and then dried by hot air at 100°C to give the title compound (5.88 g, 74.3%) as pale brown powder. 'H-NMR Spectrum (DMSO-d6) δ (ppm): 5.18-5.30 (2H, m), 6.80 (1H, dd, >2.4, 8.4 Hz), 6.81-6.90 (1H, m), 7.02 (1H, dd, >2.4, 11.6 Hz), 6.99-7.14 (1H, m), 7.32- 43 FP06-0349-00 7.39 (1H, m), 7.69 (1H, brs), 8.10 (1H, brs), 8.48 (1H, m). (Method 2)

Potassium tert-butoxide (214 g) was dissolved in dimethyl sulfoxide (750 ml) and tetrahydrofuran (250 ml) under a nitrogen stream, and a solution of 4-amino-3- 5 fluorophenol 1/2 naphthalene-2,6-disulfonate (242 g) and 4-chlorcpyridine-2- carboxamide (100 g) in dimethyl sulfoxide (1000 ml) was added dropwise to the solution with stirring and cooling on ice. The reaction mixture was stirred at room temperature for 30 minutes, then in an oil bath at 90°C (external temperature) for 2 hours. The reaction mixture was allowed to cool down to room temperature, and 10 water (3000 ml) was added, and the reaction mixture was stirred for 2 hours. The precipitated crystals were collected by filtration, and washed with water (500 ml, twice). The residue was suspended in water (2000 ml), stirred for 30 minutes, collected by filtration again, and washed with water (500 ml, twice). Drying by hot air at 60°C gave the title compound (119 g, 75.3%). 15 [0081] (Example_3)_1 -[4-(2-Carbamoylpyridin-4-yloxv)-2- fluorophenylcarbamovllcyclopropanecarboxylic acid benzyl ester

A mixture of l-(benzyloxycarbonyl)cyclopropanecarboxylic acid (11.5 g), 20 tetrahydrofuran (148 ml) and N-methylmorpholine (10.9 g) was stirred with cooling on ice. Thionyl chloride (6.19 g) was added dropwise at the internal temperature between 4.4°C and 25.2°C, and the reaction mixture was stirred for 47 minutes. 4-(4-Amino-3-fluorophenoxy)pyridine-2-carboxamide (9.89 g) was added over 2 minutes at the internal temperature between 1.9°C and 13.4°C, and 25 the reaction mixture was stirred for 4 hours and 40 minutes with keeping the internal temperature between 3°C and 6°C. The reaction mixture was partitioned after the addition of ethyl acetate (346 ml), a 2N aqueous solution of sodium hydroxide (100 ml), tetrahydrofuran (49 ml) and water (20 ml). The organic layer 44 FP06-0349-00 10 15 20 was washed twice with a 5% aqueous solution of sodium chloride (49 ml). The organic layer was concentrated under reduced pressure, and the precipitated crystals were triturated with a mixed solvent of ethyl acetate (15 ml) and heptane (15 ml). This was filtered and washed with a mixed solvent of etayl acetate (5 ml) and heptane (5 ml) to give the title compound (13.44 g). ^-NMR Spectrum (DMSO-de) δ (ppm): 1.58 (4H, s), 5.20 (2H, s), 7.06-7.11 (1H, m), 7.19-7.23 (1H, m), 7.31-7.44 (7H, m), 7.72 (1H, s), 8.13 (1H, s), 8.51-8.56 (1H, m), 8.75 (1H, t, J=8.4 Hz), 10.71 (1H, s). (Method 2) N-Methylmorpholine (12.8 g) was added to a solution of 2-chloro-4,6-dimethoxy-1,3,5-triazine (24.5 g) in tetrahydrofuran (625 ml) with stirring at room temperature, at the internal temperature between 25.0°C and 27.5°C. After stirring at room temperature for 50 minutes, l-(benzyloxycarbonyl)cyclopropanecarboxylic acid (24.5 g) was added at the same temperature. After 10 minutes, 4-(4-amino-3-fluorophenoxy)pyridine-2-carboxamide (25.5 g) was added with stirring at room temperature. The reaction mixture was stirred at room temperature for 12 hours and 50 minutes. A 5% aqueous solution of sodium hydrogencarbonate (1250 ml) was added to the reaction mixture, followed by stirring at room temperature for 3 hours. The mixture was filtered, and the collected crystals were washed with water (100 ml). The crystals were dried at 60°C for 13 hours to give the target title compound (45.4 g).

[0082] (Example_4)_1 -r4-f2-Aminopyridin-4-yloxy)-2- iluorophenylcarbamoyllcyclopropanecarboxylic acid benzyl ester

25 (Method 1) l-[4-(2-Carbamoylpyridin-4-yloxy)-2-fluorophenylcarbamoyl]- cyclopropanecarboxylic acid benzyl ester (2 g) was dissolved in N,N-dimethylformamide (20 ml) at room temperature, and water (0.481 ml) was added. 45 FP06-0349-00

Iodobenzene diacetate (2.87 g) was added at room temperature with stirring, and the reaction mixture was stirred for 2.5 hours. Water (40 ml) was added to the reaction mixture, and the reaction was quenched by the addition of a 2N aqueous solution of sodium hydroxide until pH became 11, and ethyl acetate was added and 5 the layers were separated. The organic layer was washed with water and a 5% aqueous solution of sodium chloride, dried over magnesium sulfate, filtered, and concentrated. The resultant crude brown oil was purified by silica gel column chromatography (eluent; heptane:ethyl acetate = 1:1, then 1:2) to give the title compound (819 mg) as cream crystals. 10 ^-NMR Spectrum (DMSO-d6) δ (ppm): 1.50-1.60 (4H, brs), 3.30 (2H, s), 5.19 (2H, s), 5.85 (1H, d, J=2.4 Hz), 5.96 (1H, m), 6.15 (1H, dd, J=2.4 Hz, 6.4 Hz), 6.96 (1H, m), 7.20 (1H, dd, J=2.4 Hz, 11.2 Hz), 7.30-7.42 (4H, m), 7.81 (1H, d, J=5.6 Hz), 7.96 (1H, m), 10.62 (1H, s). (Method 2) 15 1 - [4-(2-Carbamoylpyridin-4-yloxy)-2- fluorophenylcarbamoyl]cyclopropanecarboxylic acid benzyl ester (10 g) was dissolved in N,N-dimethylformamide (100 ml) at room temperature, and water (2.41 ml) was added. Iodobenzene diacetate (7.91 g) was added with stirring at room temperature, the reaction mixture was stirred for 3 hours, iodobenzene 20 diacetate (360 mg) was further added, and the reaction mixture was stirred for 2 hours. Ethyl acetate (100 ml) and a 5% aqueous solution of sodium hydrogencarbonate (100 g) were added to the reaction mixture, and layers were separated. The organic layer was washed with water, dried over magnesium sulfate, filtered, and concentrated. Ethyl acetate (30 ml) was added to the resultant 25 crude crystals, and the mixture was heated and stirred at 60°C. After confirming the crystals were dissolved, the mixture was allowed to cool down to room temperature. Seed crystals obtained in Method 1 (50 mg) were added, and the mixture was stirred for 30 minutes. After confirming the precipitation of the crystals, heptane (100 ml) was added, and the mixture was further stirred for 30 30minutes. The crystals were collected by filtration and dried to give the title compound (6.84 g). (Method 3) l-[4-(2-Carbamoylpyridin-4-yloxy)-2- 46 FP06-0349-00 fluorophenylcarbamoyl]cyclopropanecarboxylic acid benzyl ester (17.9 g) was dissolved in N-methyl-2-pyrrolidone (125 ml) at room temperature, and water (7.2 ml) was added. Iodobenzene diacetate (14.1 g) was added with stirring at room temperature, followed by stirring for 4 hours and 7 minutes. Ethyl acetate (268 ml) 5 and a IN aqueous solution of sodium hydroxide (179 ml) were added to the reaction mixture, and the layers were separated. The organic layer was washed with a 5% aqueous solution of sodium chloride (179 ml) three times and water (179 ml) once, dried over magnesium sulfate, filtered, and concentrated. Toluene (72 ml) was added to the resultant crystals, and the mixture was heated and stirred at 10 90°C. After confirming the crystals were dissolved, the mixture was allowed to cool down to room temperature. The precipitated crystals were collected by filtration, washed with toluene (18 ml), and dried under reduced pressure at 50°C for 4 hours to give the title compound (11.9 g) as pale orange crystals.

[0083] (Example_5)_1 -[2-Fluoro-4-(2-phenoxycarbonylaminopyridin-4- 15 yloxylphenylcarbamoyl] cyclopropanecarboxylic acid benzyl ester

Tetrahydro furan (41 ml), acetonitrile (41 ml) and pyridine (2.07 g) was added to 1-[4-(2-aminopyridin-4-yloxy)-2-fluorophenylcarbamoyl]cyclopropimecarboxylic acid benzyl ester (6.0 g, content 5.51 g), which was dissolved by stirring. Phenyl 20 chloroformate (4.1 g) was added dropwise to this solution with cooling on ice at the internal temperature between 8.8°C and 14.9°C. The reaction mixture was stirred at the same temperature for 2 hours and 9 minutes, then at room temperature for 3 hours and 5 minutes. The precipitate was collected by filtration, washed with a mixed solvent of tetrahydro furan and acetonitrile (2:1, 16 ml), and dried under 25 aeration to give the target title compound (6.39 g).

[0084] [Example 6) 1 -[2-Fluoro-4-(2-[ [4-(4-methylpiperazin-1 -yl)piperidine-1 - carbonyl] amino} piperidin-4-yloxvlphenylcarbamoyl] cyclopropanecarboxylic acid benzyl ester 47 FP06-0349-00 oxj ο ο

10 15 20 25 (Method 1)

Potassium carbonate (772 mg) was added to a mixture of l-[2-fluoro-4-(2-phenoxycarbonylaminopyridin-4-yloxy)phenylcarbamoyl]cyclopropanecarboxylic acid benzyl ester (2.75 g) and Ν,Ν-dimethylformamide (13.8 ml) was added, followed by stirring. l-Methyl-4-(piperidin-4-yl)piperazine (1.02 g) was added, followed by stirring for 6 hours. The reaction mixture was partitioned after the addition of ethyl acetate (41 ml) and water (27.5 ml). The resultant organic layer was washed with water (13.8 ml, three times), dried over sodium sulfate, and filtered, and the filtrate was concentrated. The resultant residue was purified by silica gel column chromatography (Fuji Silysia ΝΉ, eluent; ethyl acetate methanol = 30:1). The eluate was concentrated under reduced pressure, and the precipitate appeared by the addition of tert-butyl methyl ether (3 ml) and the application of a stimulus. tert-Butyl methyl ether (40 ml) was further added, followed by stirring overnight. The resultant precipitate was collected by filtration, washed with tertbutyl methyl ether (3 ml), and dried under aeration to give the target title compound (1.61 g). Ή-NMR Spectrum (DMSO-d6) δ (ppm): 1.20-1.34 (2H, m), 1.57 (4H, s), 1.72 (2H, d, J=10.8 Hz), 2.12 (3H, s), 2.18-2.40 (4H, m), 2.45 (3H, brs), 2.74 (2H, t, J=11.6 Hz), 3.30 (2H, s), 4.10 (2H, d, J=13.6 Hz), 5.20 (2H, s), 6.43-6.55 (1H, m), 6.97-7.10 (1H, m), 7.22-7.29 (1H, m), 7.30-7.44 (6H, m), 7.98-8.08 (1H, m), 8.13 (1H, d, J=6.0 Hz), 9.21 (1H, s), 1O.67(1H, s). (Method 2) l-Methyl-4-(piperidin-4-yl)piperazine (1.46 g) was added to a mixture of l-[2-fluoro-4-(2-phenoxycarbonylaminopyridin-4- yloxy)phenylcarbamoyl]cyclopropanecarboxylic acid benzyl ester (3.60 g) and N-methyl-2-pyrrolidone (25 ml), followed by stirring with heating at 40°C for 1 hour and 51 minutes. The reaction mixture was partitioned after the addition of ethyl 48 FP06-0349-00 5 10 acetate (180 mL) and water (90 mL). The resultant organic layer was washed with water (36 ml, twice) and a 10% aqueous solution of sodium chloride (36 ml), dried over anhydrous magnesium sulfate (10 g), and filtered, and the filtrate was concentrated. The resultant residue was purified by silica gel column chromatography (Fuji SilysiaNH, eluent; heptane:ethyl acetate = 1:1, ethyl acetate, ethyl acetate:isopropyl alcohol = 9:1). The eluate was concentrated under reduced pressure, and the precipitate appeared after the addition of tert-butyl methyl ether (60 ml) and seed crystals obtained in (Method 1). The resultant precipitate was collected by filtration, washed with tert-butyl methyl ether (10 ml)., and dried under reduced pressure at 40°C for 2 hours to give the target title compound (2.57 g). [0085] (Example 71 l-[2-Fhioro-4-(2-{[4-(4-methylpiperazin-l-yr)piperidine-l- carbonyllaminolpiperidin-4-yloxyiphenylcarbamovncyclopropanecarboxylic acid benzyl ester trihydrochloride

15 20 25 (Method 1) 1 -[2-Fluoro-4-(2- {[4-(4-methylpiperazin-1 -yl)piperidine-1 - carbonyl]amino}piperidin-4-yloxy)phenylcarbamoyl]cyclopropanecarbcxylic acid benzyl ester (189 mg) was dissolved in ethyl acetate (6 ml), and 4N hydrochloric acid in ethyl acetate (0.3 ml) was added. The resultant mixture was concentrated under reduced pressure, and methanol (0.5 ml) and ethyl acetate (4 ml) was added. The precipitate obtained by filtration was hygroscopic, thus it was collected using methanol (10 ml). The collected solution was again concentrated under reduced pressure, and methanol (0.5 ml) and tert-butyl methyl ether (4 ml) was added. The precipitate was filtered to give the title compound (102 mg). hd-NMR Spectrum (DMSO-d<;) δ (ppm): 1.58 (4H, s), 1.60-1.74 (2H, m), 2.17 (2H, d, J=10.4 Hz), 2.83 (3H, s), 2.91 (2H, t, J=12.4 Hz), 3.50-3.57 (9H, m), 4.39 (2H, d, J=12.8 Hz), 5.20 (2H, s), 7.03-7.09 (1H, m), 7.13-7.19 (1H, m), 7.30-7.42 (6H, m), 49 FP06-0349-00 7.46 (1H, dd, J=2.4, 8.8 Hz), 8.14 (1H, t, J=8.8 Hz), 8.30 (1H, d, 1=7.2 Hz), 10.78 (1H, s), 10.93 (1H, brs). (Method 2) l-Methyl-4-(piperidin-4-yl)piperazine (812 mg) was added to a mixture of l-[2- 5 fluoro-4-(2-phenoxycarbonylaminopyridin-4- yloxy)phenylcarbamoyl]cyclopropanecarboxylic acid benzyl ester (2.0 g) and N-methyl-2-pyrrolidone (14 ml), followed by stirring at 40°C for 2 hours and 31 minutes. The reaction mixture was partitioned after the addition of ethyl acetate (60 ml) and water (40 ml). The organic layer was washed with a 5% aqueous

10 solution of sodium chloride (10 ml, three times) and water (10 ml). 4N

Hydrochloric acid in ethyl acetate (0.5 ml) was added to a portion (10 ml) of the resultant organic layer, and seed crystals obtained in (Method 1) were added. Isopropyl alcohol (1 ml) was added, and the precipitate appeared after sonication. The resultant precipitate was filtered, and washed with ethyl acetate (2 ml) to give 15 the title compound (322 mg). (Method 3) 1 -Methyl-4-(piperidin-4-yl)piperazine (2.68 g) was added to a mixture of l-[2-fluoro-4-(2-phenoxycarbonylaminopyridin-4- yloxy)phenylcarbamoyl]cyclopropanecarboxylic acid benzyl ester (6.63 g) and N- 20 methyl-2-pyrrolidone (33 ml), followed by stirring at 40°C for 2 hours and 10 minutes. The reaction mixture was partitioned after the addition of ethyl acetate (132 ml) and water (99 ml). The organic layer was washed with a 5% aqueous solution of sodium chloride (33 ml, twice) and water (33 ml). 4N hydrochloric acid in ethyl acetate (10 ml) was added to isopropyl alcohol (13 ml), then the above 25 washed organic layer (8 ml) was added dropwise thereto, the seed crystals obtained in (Method 2) was added, and the organic layer was father added dropwise. During the addition, isopropyl alcohol (13 ml) was added, and the mixture was treated with sonication, and the drop continued. After the completion of the addition, the mixture was stirred for 5 hours and 38 minutes. The precipitate was filtered, 30 washed with a mixed solvent of ethyl acetate and isopropyl alcohol (5:1, 20 ml), and the solvent was replaced by ethyl acetate (20 ml). Drying under aeration under a nitrogen stream and drying under reduced pressure at 40°C for 2 hours gave the target title compound (6.12 g). 50 FP06-0349-00 5 10 15 20 25 (Method 4) A solution of l-methyl-4-(piperidin-4-yl)piperazine in N-methyl-2-pyrrolidone (24.8%, 26.3 g) was added to a mixture of l-[2-fluoro-4-(2- phenoxycarbonylaminopyridin-4-yloxy)phenylcarbamoyl]cycloprcpanecarboxylic acid benzyl ester (16.1 g) and N-methyl-2-pyrrolidone (46 ml), washing with N-methyl-2-pyrrolidone (15 ml) was performed. The mixture was stirred at 37°C for 1 hour and 52 minutes. The reaction mixture was partitioned after the addition of ethyl acetate (242 ml) and water (242 ml). The organic layer was washed with IN hydrochloric acid (81 ml). The aqueous layer was separated, ethyl acetate (161 ml) was added, and a 2N aqueous solution of sodium hydroxide (81 mL) was added, and the partition was performed. The organic layer was separated and washed with a 1% aqueous solution of sodium chloride (81 g), and the organic layer (151.3 g) was collected. A portion (104.2 g) of the above organic layer was added to ethanol (48 ml), and concentrated hydrochloric acid (7.41 ml) was added to the mixture with stirring on ice. A portion (ca.15 ml) of the rest of the organic layer was added and seed crystals (48.3 mg) were added, and the mixture was stirred at room temperature for 1 hour and 14 minutes. The whole amount of the rest of the organic layer was added dropwise over 29 minutes, followed by stirring for 16 hours and 19 minutes. The precipitate was removed by filtration, washed with a mixed solvent of ethyl acetate and ethanol (3:1, 32.4 ml), and the solvent was replaced by ethyl acetate (32.2 ml). Drying under aeration under a nitrogen stream and drying under reduced pressure at 40°C for 2 hours and 20 minutes gave the title compound (15.0 g).

[0086] (Example 8) l-[2-Fluoro-4-(2-{r4-f4-methylpiperazin-l -yl)piperidine-l- carbony 11 amino} pvridin-4-vloxvlphenvlcarbamoyllcvclopropanec.arboxvlic acid

(Method 1) 1 - [2-Fluoro-4-(2- {[4-(4-methylpiperazin-1 -yl)piperidine-1 - 51 FP06-0349-00 carbonyl]amino}pyridin-4-yloxy)phenylcarbamoyl]cyclopropanecarboxylic acid benzyl ester (800 mg) was dissolved in a mixed solvent of tetrahydrofiiran (4 ml) and ethanol (4 ml), palladium on carbon (400 mg) was added, and the mixture was stirred at room temperature under a hydrogen atmosphere (0.15 MPa) for 4 hours. 5 Water (4 ml) was added to the reaction mixture, which was filtered, and the residue was washed with a 50% aqueous ethanol (8 ml) and water (4 ml), and the filtrate was concentrated. Tetrahydro furan (8 ml) and ethanol (8 ml) was added to the residue, which was concentrated. Tetrahydrofiiran (8 ml), ethyl acetate (8 ml) and ethanol (2 ml) were added to the residue, which was concentrated. 10 Tetrahydrofiiran (8 ml) and ethanol (16 ml) were added to the residue, which was concentrated to precipitate crystals. The crystals were suspended in tetrahydrofiiran (16 ml), stirred at room temperature for 40 minutes, filtered, and dried to give the title compound (550 mg) as white crystals. rH-NMR Spectrum (DMSO-d6) δ (ppm): 1.15-1.23 (2H, m), 1.24-1.38 (4H, m), 15 1.70-1.80 (2H, m), 2.41-2.50 (2H, brs), 2.50 (3H, s), 2.60-2.90 (9H, m), 4.10-4.18 (2H, m), 6.60 (1H, dd, J=2.4 Hz, 5.6 Hz), 6.93 (1H, d, >8.8 Hz), 7.17 (1H, dd, >2.4 Hz, 11.6 Hz), 7.33 (1H, d, >2.4 Hz), 8.10 (1H, d, >5.6 Hz), 8.35 (1H, t, >8.8 Hz), 9.21 (1H, s). (Method 2) 20 1 - [2-Fluoro-4-(2- {[4-(4-methylpiperazin-1 -yl)piperidine-1 - carbonyl]amino}pyridin-4-yloxy)phenylcarbamoyl]cyclopropanecarboxylic acid benzyl ester (500 mg) was dissolved in a mixed solvent of tetrahydrofiiran (2.5 ml), ethanol (2.5 ml) and water (1.5 ml), palladium on carbon (100 mg) was added, and the mixture was stirred at room temperature under a hydrogen atmosphere (0.15 25 MPa) for 3 hours. The reaction mixture was filtered, and the residue was washed with a 90% aqueous ethanol (1 ml), and the filtrate was concentrated. Addition of ethanol to the residue and subsequent concentration were repeated three times. Ethanol (2.5 ml), tetrahydrofiiran (2.5 ml) and the seed crystals obtained in (Method 1) were added to the residue, and the mixture was stirred at room 30 temperature for 1 hour. Ethyl acetate (5 ml) was added, and the mixture was further stirred for 1 hour. The crystals were filtered and dried, to give the title compound (420 mg) as white crystals. (Method 3) 52 FP06-03 49-00 5 10 15 1 - [2-Fluoro-4-(2- {[4-(4-methylpiperazin-1 -yl)piperidine-1 - carbonyl] amino} pyridin-4-yloxy)phenylcarbamoyl] cyclopropanecarboxylic acid benzyl ester hydrochloride (2 g) was dissolved in water (20 ml) and ethyl acetate (20 ml), and a 2N aqueous solution of sodium hydroxide (4 ml) was added, and the layers were separated. The organic layer was washed with water and concentrated. Addition of tetrahydrofuran and subsequent concentration was repeated three times. The residue was dissolved in a mixed solvent of tetrahydrofuran (8 ml) and water (1.6 ml), and palladium on carbon (200 mg) was added, and the mixture was stirred at room temperature under a hydrogen atmosphere (0.2 MPa) for 5 hours. Tetrahydrofuran (4 ml) and methanol (6 ml) were added to the reaction mixture, which was filtered. The residue was washed with 90% aqueous methanol (3 ml). Tetrahydrofuran (12 ml) and the seed crystals obtained in (Method 1) were added to the filtrate, and the mixture was stirred at room temperature for 1 hour. Ethyl acetate (32 ml) was added, and the mixture was stirred for 14 hours. The crystals were filtered and dried to give the title compound (1.2 g) as white crystals.

[0087] (Example 8-2] l-r2-Fluoro-4-(2-{[4-(4-methylpiperazin-l-yl]piperidine-l- carbonvl] amino ] pyridin-4-vloxylphenvlcarbamoyl] cyclopropanecarboxylic acid trihydro chloride

20 (Method 1) 1 - [2-Fluoro-4-(2- {[4-(4-methylpiperazin-1 -yl)piperidine-1 - carbonyl]amino}pyridin-4-yloxy)phenylcarbamoyl]cyclopropanecarboxylic acid benzyl ester trihydrochloride (2 g) was dissolved in a mixed solvent of water (4 ml) and ethanol (8 ml), palladium on carbon (100 mg) was added, and the mixture was 25 stirred at room temperature under a hydrogen atmosphere (ca. 1 atmospheric pressure) for 5 hours and 10 minutes. The reaction mixture was filtered, and the residue was washed with a mixed solvent of water (1 ml) and ethanol (2 ml). 53 FP06-0349-00

Ethanol (20 ml) was added to the filtrate, which was concentrated. Addition of ethanol (10 ml) to the residue and subsequent concentrate were repeated four times.

The mixture was filtered with heating and ethyl acetate (40 ml) was added dropwise with stirring at the same time. After stirring at room temperature for 25 5 hours and 30 minutes, the crystals were filtered with washing with a mixed solvent of ethanol (2 ml) and ethyl acetate (2 ml) and dried to give the title compound (1.56 g) as a white solid. *H-NMR Spectrum (DMSO-d6) δ (ppm): 1.50-1.78 (8H, m), 2.04-2.22 (2H, m), 2.46 (3H, s), 2.80-3.90 (9H, m), 4.22-4.40 (2H, m), 7.01 (1H, brs), 7.13 (1H, d, 10 3=9.6 Hz), 7.22 (1H, s), 7.43 (1H, d, >12.4 Hz), 8.22-8.32 (2H, m), 11.30 (1H, s). (Method 2) 1 - [2-Fluoro-4-(2- {[4-(4-methylpiperazin-1 -yl)piperidine-1 - carbonyl]amino}pyridin-4-yloxy)phenylcarbamoyl]cyclopropanecarboxylic acid benzyl ester trihydrochloride (5 g) was dissolved in a mixed solvent of water (10 15 ml) and ethanol (20 ml), and palladium on carbon (250 mg) was added, and the mixture was stirred at room temperature under a hydrogen atmosphere (0.2 MPa) for 7 hours and 50 minutes. The reaction mixture was filtered, and the residue was washed with a mixed solvent of water (6 ml) and ethanol (10 ml). Ethanol (50 ml) was added to the filtrate, which was azeotropically distilled off and concentrated, 20 and water (0.6 g) and ethanol (8.3 ml) were added. 2-Propanol (10 ml) was added to the solution, followed by stirring at room temperature for 5 minutes. l-[2-Fluoro-4-(2- {[4-(4-methylpiperazin-1 -yl)piperidine-1 -carbonyl] amino} pyridin-4-yloxy)phenylcarbamoyl]cyclopropanecarboxylic acid trihydrocbloride (150 mg) was added, followed by stirring for 13 hours and 45 minutes. 2-Propanol (50 ml) 25 was further added, and the mixture was stirred at room temperature for 24 hours and 35 minutes. The crystals were filtered and dried to give the title compound (4.26 g) as a white solid.

[0088] (Example 9) N-(2-Fluoro-4-([2-(fr4-(4-methylpiperazm-l-yl)piperidin-l- yl] carbonyl) 3ΐηϊηο)ρνΓΪάπι-4-γ1]οχν}ρ1ΐ6ην1)-Ν'-(4-ί1ηοΓορίΐ6ηνΓ)ονο1ορΓθρηη6- 30 1.1 -dicarboxamide 54 FP06-0349-00 10 15 20 25

(Method 1) 4-(4,6-Dimethoxy[l,3,5]triazin-2-yl)-4-methylmorpholinium chloride hydrate (164 mg) was added to a suspension of l-[2-fluoro-4-(2-{[4-(4-methylpiperazin-l-yl)piperidine-1 -carbonyl] amino} pyridin-4- yloxy)phenylcarbamoyl]cyclopropanecarboxylic acid (100 mg) in mixture of tetrahydrofuran (1 ml), Ν,Ν-dimethylformamide (0.2 ml) and 4-fluoroaniline (0.0526 ml), followed by stirring at room temperature for 2.5 hours. A 5% aqueous solution of sodium hydrogencarbonate was added to the reaction mixture to quench the reaction, and ethyl acetate was added and the layers were separated. The organic layer was washed with water and concentrated. The residue was purified by silica gel column chromatography (Fuji Silysia NH, eluent; ethyl acetate, ethyl acetate:methanol = 95:5). The eluate was concentrated. Ethyl acetate (2 ml) was added to the resultant residue, followed by stirring at room temperature for 30 minutes. Heptane (2 ml) was added, and the mixture was stirrec. for 30 minutes. The crystals were collected by filtration and dried to give the title compound (74 mg) as white crystals. ’H-NMR Spectrum (DMSO-d6) δ (ppm): 1.22-1.33 (2H, m), 1.54-1.63 (4H, m), 1.68-1.78 (2H, m), 2.12 (3H, s), 2.12-2.40 (5H, m), 2.40-2.60 (4H, m), 2.68-2.78 (2H, m), 4.06-4.14 (2H, m), 6.60 (1H, dd, J=2.4 Hz, 5.6 Hz), 7.00 (1H, m), 7.19 (2H, t, >8 Hz), 7.22 (1H, dd, J=2.4 Hz, 11.2 Hz), 7.40 (1H, s), 7.61 (2H, dd, J=5.2 Hz, 8 Hz), 7.93 (1H, t, J=8.8 Hz), 8.13 (1H, d, J=5.6 Hz), 9.21 (1H, s), 9.90 (1H, brs), 10.55 (1H, brs). (Method 2) 4-(4,6-Dimethoxy[l,3,5]triazin-2-yl)-4-methylmorpholinium chloride hydrate was added to a suspension of l-[2-fluoro-4-(2-{[4-(4-methylpiperazin-l-yl)-piperidine-1 -carbonyl] -amino} -pyridin-4-yloxy)phenylcarbamoyl] -cyclopropanecarboxylic acid (500 mg, 0.925 mmol) in a mixture of tetrahydrofuran (4.5 ml), N,N- 55 FP06-0349-00 dimethylformamide (1 ml) and 4-fluoroaniline (0.131 ml), followed by stirring at room temperature for 16 hours. Ethyl acetate (7.5 ml) was added to the reaction mixture, and a 5% aqueous solution of sodium hydrogencarbonate (7.5 ml) was added to quench the reaction, and the layers were separated. IN hydrochloric acid 5 (5 ml) was added to the organic layer, and the layers were separated.

Tetrahydro furan (7.5 ml) was added to the aqueous layer, and a 2N aqueous solution of sodium hydroxide (3 ml) was added to effect neutralization, and ethyl acetate (7.5 ml) was added and the layers were separated. The organic layer was washed with water and concentrated. Addition of ethyl acetate to the residue and 10 subsequent concentration were repeated three times.

To the residue was added ethyl acetate until the whole weight reached to 2.34 g, and the seed crystals obtained in (Method 1) was added, and the mixture was stirred at room temperature for 30 minutes. Ethyl acetate (2.5 ml) was added, and the mixture was stirred for 1 hour, heptane (5 ml) was added and the mixture was 15 stirred for 2 hours. The crystals were collected by filtration and dried to give the title compound (427 mg) as white crystals. (Method 3) N-Methylmorpholine (419 g) was added to a solution of 2-chloro-4,5-dimethoxy-1,3,5-triazine (238 g) in a mixture of tetrahydrofuran (4400 g) and 2-propanol 20 (2159 g) with stirring, and tetrahydrofuran (122 g) was used for washing, and the mixture was stirred at 25°C for 33 minutes. l-[2-Fluoro-4-(2-{[4-(4-methylpiperazin-1 -yl)piperidine-1 - carbonyl] amino} piperidin-4- yloxy)phenylcarbamoyl]-cyclopropanecarboxylic acid benzyl ester trihydrochloride (550 g) was added to the reaction mixture, tetrahydrofuran (245 g) 25 was used for washing, 4-fluoroaniline (132 g) was added, tetrahydrofuran (122 g) was used for washing, and the mixture was stirred at 25°C for 4 hours and 20 minutes. Isopropyl acetate (7194 g) and a IN aqueous solut:.on of hydrochloric acid (5593 g) were added to the reaction mixture, and the layers were separated. Tetrahydrofuran (1147 g) and isopropyl acetate (7194 g) were added to the aqueous 30 layer, a 2N aqueous solution of sodium hydroxide (5401 g) was added to effect neutralization, and the layers were separated. The organic layer was washed with a 5% aqueous solution of sodium chloride (1650 g) twice, and water (1650 g) once, and concentrated until the liquid volume became ca. 3 L. Isopropyl acetate (1440 56 FP06-0349-00 5 g) was added to the concentrated solution, and the mixture was stirred at 25°C for 1 hour and 20 minutes. Isopropyl acetate (959 g) was added, ar.d the mixture was stirred at the same temperature for 3 hours and 7 minutes. Isopropyl acetate (2398 g) was added, and the mixture was stirred at the same temperature for 16 hours and 28 minutes. The precipitated crystals were collected by filtration and dried to give the title compound (408 g) as white crystals.

[0089] (Example 10) 4-(4-Amino-2.5-difluorophenyllpyridine-2-carboxamide

NK2

F 10 15 20 25 4-Amino-2,5-difluorophenol (4.95 g) was dissolved in dimethyl· sulfoxide (50 ml) under a nitrogen stream, and potassium tert-butoxide (4.05 g) was added at room temperature, and the mixture was stirred for 25 minutes. 4-Chloropyridine-2-carboxamide (2.70 g) was added to the mixture, which was stirred at 80°C for 2.5 hours. The reaction mixture was allowed to cool down to room temperature, and a IN aqueous solution of sodium hydroxide (74.25 ml) was added, and the mixture was stirred for 10 hours. The precipitated solid was collected by filtration, and the resultant solid was washed with water. The solid was dried by hot air at 100°C for 24 hours to give the title compound (3.38 g, 74%) as purple powder. ^d-NMR Spectrum (DMSO-d6) δ (ppm): 5.57 (2H, d, J=6.0 Hz), 6.75-6.80 (1H, m), 7.17-7.20 (1H, m), 7.26 (1H, dd, J=7.2, 10.8 Hz), 7.38 (1H, m), 7.73 (1H, s), 8.14 (1H, s), 8.52(1 H, d, J=5.6 Hz). ESI-MS (m/z): 288[M+Na]+.

[0090] fExample 11) Benzyl l-{[(4-(r2-faminocarbonyI)pyridin-4-yl]oxy}-2,5- difluorophenyllamino] carbonyl) cyclopropanecarboxylate

l-[(Benzyloxy)carbonyl]cyclopropanecarboxylic acid (1.04 g) was dissolved in 57 FP06-0349-00 5 10 15 20 tetrahydrofuran (15 ml) under a nitrogen atmosphere. N-Methylmorpholine (0.520 ml) was added at 0°C, and the mixture was stirred for 15 minutes. Thionyl chloride (0.345 ml) was added to the mixture at 0°C, and the mixture was stirred at the same temperature for 30 minutes. 4-(4-Amino-2,5-difluorophenoxy)pyridine-2-carboxamide (500 mg) and N-methylmorpholine (0.520 ml) was added, and the mixture was stirred at room temperature for 2 hours and 50 minutes. The reaction mixture was partitioned after the addition of a IN aqueous solution of sodium hydroxide (15 ml) and ethyl acetate (20 ml). The organic layer was washed with a IN aqueous solution of sodium hydroxide (15 ml), water (15 ml) and brine (15 ml), and dried over anhydrous magnesium sulfate. The desiccant, was removed by filtration, and the filtrate was concentrated under reduced pressure. The resultant residue was purified by silica gel column chromatography (Fuji SilysiaNH, eluent; heptane:ethyl acetate = 1:1, then 1:2). The fractions containing the target compound was concentrated under reduced pressure to give the title compound (822.7 mg, 93%) as white powder. ^-NMR Spectrum (DMSO-d6) δ (ppm): 1.58-1.63 (4H, m), 5.20 (2H, s), 7.24-7.27 (1H, m), 7.30-7.42 (5H, m), 7.43 (1H, d, J=2.8 Hz), 7.63-7.71 (1H, m), 7.72-7.78 (1H, m), 8.13-8.22 (2H, m), 8.56 (1H, d, J=5.6 Hz), 10.93 (1H, brs). ESI-MS (m/z): 490[M+Na]+.

[0091] (Example 12) Benzyl l-r({4-[(2-aniinopvridm-4-yl)oxy1-2,5- difluorophenyl)amino)carbonyl1cyclopropanecarboxylate

Benzyl l-{ [(4-{[2-(aminocarbonyl)pyridin-4-yl]oxy )-2,5- difluorophenyl)amino]carbonyl}cyclopropanecarboxylate (1.55 g) was dissolved in N,N-dimethylformamide (33 ml). Water (0.299 ml) and iodobenzene diacetate (1.18 g) were added at room temperature, and the mixture was stirred for 15 hours and 20 minutes. Iodobenzene diacetate (215 mg) was added again and the mixture was stirred for 2 hours and 20 minutes. Water (150 ml) was added to the mixture, and the mixture was stirred for 1 hour, and partitioned after the addition of a 25 58 FP06-0349-00 5 10 15 saturated aqueous solution of sodium hydrogencarbonate (200 ml) and ethyl acetate (300 ml). The organic layer was washed with water (200 ml, twice) and brine (150 ml), and dried over anhydrous magnesium sulfate. The desiccant was removed by filtration, and the filtrate was concentrated under reduced pressure. The resultant residue was purified by silica gel column chromatography (Fuji Silysia NH, eluent; heptane:ethyl acetate = 1:2). The fractions containing the target compound were concentrated under reduced pressure to give the title compound (1.217 g, 83%) as a pale yellow solid. Ή-NMR Spectrum (DMSO-d6) δ (ppm): 1.54-1.65 (4H, m), 5.19 (2H, s), 5.83 (1H, d, J=2.0 Hz), 5.99 (2H, brs), 6.18 (1H, dd, J=2.4, 5.6 Hz), 7.30-7.45 (5H, m), 7.52 (1H, dd, J=7.2, 10.8 Hz), 7.82 (1H, d, J=5.6 Hz), 8.05-8.20 (1H, m), 10.86 (1H, brs). ESI-MS (m/z): 440[M+H]+.

[0092] (Example 13) Benzyl l-ff[4-f{2-[fphenoxycarbonyr)amino]pyridin-4- yl} oxy)-2,5 -difluorophenyl] amino} carbonyl) cyclopropanecarboxvlate

Benzyl l-[({4-[(2-aminopyridin-4-yl)oxy]-2,5- difluorophenyl}amino)carbonyl]cyclopropanecarboxylate (1.15 g) was dissolved in tetrahydrofuran (12 ml) under a nitrogen atmosphere. Pyridir.e (0.424 ml) and phenyl chloroformate (0.657 ml) were added at room temperature, and the mixture was stirred for 20 minutes. A saturated aqueous solution of sodium hydrogencarbonate (36 ml) and hexane (36 ml) were added to the mixture, and the mixture was stirred for 55 minutes. The precipitated solid was collected by filtration. The resultant solid was washed with hexane and dried under aeration and dried by hot air (60°C) for 5 hours. Water (150 ml) was added to the solid, and the mixture was stirred for 2 hours, and the solid was collected by filtration, and the resultant solid was washed with water. The solid was dried by hot air (60°C) for 3 days to give the title compound (1.117 g, 76%) as a white solid. lH-NMR Spectrum (CDC13) δ (ppm): 1.69-1.90 (4H, m), 5.19 (2H, s), 6.62 (1H, dd, 25 59 FP06-0349-00 J=2.4, 6.0 Hz), 6.95-7.04 (1H, m), 7.12-7.21 (1H, m), 7.28-7.45 (9H, m), 7.56 (1H, d, J=2.4 Hz), 8.19 (1H, d, J=6.0 Hz), 8.34 (1H, dd, J=7.2, 12.0 Hz), 8.49 (1H, brs), 11.27 (1H, brs).

[0093] [Example 14) Benzyl l-[((2,5-difluoro-4-[(2-([(3-hydroxyazetidin-l-5 yDcarbonyl] amino) pyridin-4- yDoxy1phenyl}amino)carbonyl]cyclopropanecarboxylate

Triethylamine (0.100 ml) was added to a mixture of benzyl l-({[4-({2-[(phenoxycarbonyl)amino]pyridin-4-yl}oxy)-2,5- 10 difluorophenyl] amino }carbonyl)cyclopropanecarboxylate (200 mg), 3- hydroxyazetidine hydrochloride (39.1 mg) and Ν,Ν-dimethylformamide (4.0 ml) at room temperature under a nitrogen atmosphere, and the mixture was stirred for 6 hours and 10 minutes. 3-Hydroxyazetidine hydrochloride (10.0 mg) and triethylamine (0.025 ml) were added at room temperature, and the mixture was 15 stirred for 1 hour and 20 minutes. A saturated aqueous solution of sodium hydrogencarbonate (16 ml) and hexane (5 ml) were added to the mixture, and the precipitated solid was collected by filtration. The solid was washed with water (2 ml, three times), and dried under aeration. The resultant solid was purified by silica gel column chromatography (Fuji Silysia NH, eluent; ethyl acetate, then ethyl 20 acetate:methanol = 10:1). The fractions containing the target compound was concentrated under reduced pressure to give the title compound (86.7 mg, 45%) as a white solid. JH-NMR Spectrum (CDC13) δ (ppm): 1.72-1.86 (4H, m), 3.93 (2H, dd, J=4.4, 10.0 Hz), 4.26-4.32 (2H, m), 4.66-4.73 (1H, m), 5.20 (2H, s), 6.54 (1H, dd, J=2.0, 6.0 25 Hz), 6.89 (1H, brs), 7.00 (1H, dd, J=7.2, 10.4 Hz), 7.30-7.43 (5H, m), 7.65 (1H, d, J=2.0 Hz), 8.04 (1H, d, J=6.0 Hz), 8.34 (1H, dd, J=7.2,12.0 Hz), 11.27 (1H, brs). ESI-MS (m/z): 537[M-H]'.

[0094] (Example_15)_14((2,5-Difhioro-4-[(2-{rf3-hydroxyazetidin-1- yDcarbonyl] amino (pyridin-4- 60 FP06-0349-00 ylloxylphenyllaminolcarbonyllcyclopropanecarboxylic acid triethylamine salt

B enzyl 1 - [({2,5 -difluoro -4- [(2- {[(3 -hy droxyazeti din-1 -yl)carbonyl] amino} pyridin-4-yl)oxy]phenyl}amino)carbonyl]cyclopropanecarboxylate (84.2 mg) was 5 dissolved in tetrahydrofuran and methanol (1:1) (2 ml) under a nitrogen atmosphere. 10% palladium on carbon (33.2 mg) was added and the air in the reaction vessel was replaced by hydrogen, and the mixture was stirred at room temperature for 20 hours. The air in the reaction vessel was replaced by nitrogen, and triethylamine (0.0435 ml) was added, and the mixture was stirred for 30 minutes. The catalyst 10 was removed by filtration, and washed with methanol. The filtrate was concentrated under reduced pressure to give the title compound (75.3 mg, 88%) as a white solid. ESI-MS (m/z): 447 [M-H]'.

[0095] (Example_161_N-{2.5-Difluoro-4-Γ(2-{[f3-hydroxyazetidin-1 - 15 yllcarbonyl] amino} pyridin-4-yl]oxylphenyl} -N'-f 4-fluorophenyl)cyclopropane- 1,1-dicarboxamide

4-(4,6-Dimethoxy[l,3,5]triazin-2-yl)-4-methylmorpholinium chloride hydrate (80.8 mg) was added to a mixture of l-[({2,5-difluoro-4-[(2-{[(3-hydroxyazetidin-l- 20 yl)carbonyl] amino }pyridin-4- yl)oxy]phenyl}amino)carbonyl]cyclopropanecarboxylic acid triethylamine salt (75.3 mg), 4-fluoroaniline (0.026 ml) and tetrahydrofuran (1.0 ml) at room temperature under a nitrogen atmosphere, and the mixture was stirred for 5 hours. 4-(4,6-Dimethoxy[l,3,5]triazin-2-yl)-4-methylmorpholinium chloride hydrate (80.8

25 mg) was added at room temperature, and the mixture was stirred for 87 hours. A 61 FP06-0349-00 5 10 15 saturated aqueous solution of sodium hydrogencarbonate (5 ml) was added to the reaction mixture and stirred, and the mixture was partitioned after the addition of ethyl acetate (20 ml) and water (20 ml). The organic layer was washed with brine (10 ml), and dried over anhydrous magnesium sulfate. The desiccant was removed by filtration, and the filtrate was concentrated under reduced pressure. The resultant residue was purified by silica gel column chromatography (Fuji Silysia NH, eluent; ethyl acetate, ethyl acetatermethanol - 10:1). The fractions containing the target compound was concentrated under reduced pressure to give the title compound (68.1 mg, 92%) as a white solid. ^-NMR Spectrum (DMSO-d6) δ (ppm): 1.54-1.68 (4H, m), 3.65-3.72 (2H, m), 4.09-4.15 (2H, m), 4.33-4.41 (1H, m), 5.60 (1H, d, >6.4 Hz), 6.62-6.66 (1H, m), 7.14-7.22 (2H, m), 7.50-7.65 (4H, m), 8.05-8.15 (1H, m), 8.13 (1H, d, J=5.6 Hz), 9.19 (1H, brs), 9.79-9.84 (1H, m), 10.95-11.02 (1H, m). ESI-MS (m/z): 540[M-H]’.

[0096] (Example 17) Benzyl l-({r(2.5-difluoro-4-(2-[3-methyl-3-(l- methvlpiperidin-4-yl)ureido1pyridin-4- yl} oxy)phenyl] amino} carbonyDcyclopropanecarboxylate

Benzyl l-({[4-({2-[(phenoxycarbonyl)amino]pyridin-4-yl}oxy)-2,5- difluorophenyl] amino }carbonyl)cyclopropanecarboxylate (200 mg) was suspended in N-methylpyrrolidinone (2.0 ml) under a nitrogen atmosphere. l-Methyl-4-(methylamino)piperidine (0.104 ml) was added at room temperature, and the mixture was stirred overnight. A saturated aqueous solution of sodium hydrogencarbonate (10 ml) was added to the reaction mixture, and the mixture was stirred. Extraction was performed with ethyl acetate (20 ml). The organic layer was washed with water (10 ml), a saturated aqueous solution of ammonium chloride (10 ml) and brine (10 ml), dried over anhydrous sodium sulfate. The desiccant was removed by filtration, and the filtrate was concentrated under reduced pressure. The resultant residue was purified by silica gel column 25 62 FP06-0349-00 10 chromatography (Fuji Silysia NH, eluent; ethyl acetate, then ethyl acetate:methanol = 95:5). The fractions containing the target compound was concentrated under reduced pressure, and the residue was dried under reduced pressure to give the title compound (62.3 mg, 29%) as white powder. Ή-NMR Spectrum (CDC13) δ (ppm): 1.60-1.90 (8H, m), 2.05-2.20 (2H, m), 2.32 (3H, s), 2.89 (3H, s), 2.90-3.00 (2H, m), 4.19 (1H, m), 5.20 (2H, s), 6.53 (1H, dd, J=2.4, 5.6 Hz), 7.00 (1H, brs), 7.20 (1H, m), 7.30-7.45 (5H, m), 7.68 (1H, d, J=2.4 Hz), 8.06 (1H, d, J=5.6 Hz), 8.33 (1H, dd, J=7.2,12.0 Hz), 11.27 (1H, brs). ESI-MS (m/z): 616[M+Na]+.

[0097] (Example 18) l-(([(2,5-Difluoro-4-{2-[3-methyl-3-(l-methylpiperidin-4- yl)ureido]pyridin-4-yl ] oxylpheny 11 amino }carbonyl)cyclopropanecarboxylic acid

I H 15 20

Benzyl l-({[(2,5-difluoro-4-{2-[3-methyl-3-(l-methylpiperidin-4- yl)ureido]pyridin-4-yl} oxy)phenyl]amino}carbonyl)cyclopropaiecarboxylate (61.0 mg) was dissolved in tetrahydrofuran and methanol (1:1) (4.0 ml) under a nitrogen atmosphere, and 10% palladium on carbon (45 mg) was added. The air in the reaction vessel was replaced by hydrogen, and the mixture was stirred at room temperature for 3.5 hours. The air in the reaction vessel was replaced by nitrogen, and the mixture was diluted with the addition of tetrahydrofuran and methanol (1:1) (4.0 ml). The catalyst was removed by filtration, and washed with methanol. The filtrate was distilled off under reduced pressure to give the title compound (49.2 mg, 95%) as a white solid. ESI-MS (m/z): 502[M-H]‘.

[0098] (Example 19) N-(2,5-Difhioro-4-{[2-({[methyl(l-methylpiperidin-4- yl)amino]carbonyl]aminolpyridin-4-yl]oxy]phenyl)-N'-(4- fluorophenyllcyclopropane-1.1 -dicarboxamide 25 63 FP06-0349-00 10 15 20

4-(4,6-Dimethoxy[l,3,5]triazin-2-yl)-4-methylmorpholinium chloride hydrate (57.6 mg) was added to a mixture of l-({[(2,5-difluoro-4-{2-[3-methyl-3-(l-methylpiperidin-4-yl)ureido]pyridin-4- yl}oxy)phenyl]amino}carbonyl)cyclopropanecarboxylic acid (49.2 mg), 4-fluoroaniline (0.0186 ml) and tetrahydrofuran (2 ml) at room temperature under a nitrogen atmosphere, and the mixture was stirred for 15 hours. A saturated aqueous solution of sodium hydrogencarbonate (5 ml) was added to the reaction mixture, and the mixture was stirred. The mixture was partitioned after the addition of ethyl acetate (20 ml) and water (15 ml). The organic layer was washed with brine (10 ml), and dried over anhydrous sodium sulfate. The desiccant was removed by filtration, and the filtrate was concentrated under reduced pressure. The resultant residue was purified by silica gel column chromatography (Fuji Silysia NH, eluent; ethyl acetate, then ethyl acetate:methanol = 95:5). The fractions containing the target compound was concentrated under reduced pressure to give the title compound (41.5 mg, 71%) as a white solid. ’H-NMR Spectrum (CDC13) δ (ppm): 1.61-1.83(8H, m), 2.03-2.10 (2H, m), 2.28 (3H, s), 2.88 (3H, s), 2.90-2.94 (2H, m), 4.10-4.20 (1H, m), 6.55 (1H, dd, >2.4, 5.6 Hz), 6.98-7.08 (3H, m), 7.15 (1H, s), 7.46-7.50 (2H, m), 7.67 (1H, d, >2.4 Hz), 8.08 (1H, d, >5.6 Hz), 8.29 (1H, dd, >7.2,12.0 Hz), 8.57 (1H, s), 9.59 (1H, s). ESI-MS (m/z): 597[M+H]+.

[0099] (Example 20) Benzyl l-[({2,5-difluoro-4-[(2-{[((S)-3-hydroxypyrrolidin-l- yljcarbonyll amino} pyridin-4- ylloxvlphenyl}amino)carbonyl]cyclopropanecarboxylate 25

64 FP06-0349-00 (S)-3-Hydroxypyrrolidine (0.0577 ml) was added to a mixture of benzyl l-({[4- ({2-[(phenoxycarbonyl)amino]pyridin-4-yl}oxy)-2,5- difluorophenyl] amino }carbonyl)cyclopropanecarboxylate (200 mg) and N- methylpyrrolidinone (4.0 ml) at room temperature under a nitrogen atmosphere, 5 and the mixture was stirred for 2 hours. A saturated aqueous solution of sodium hydrogencarbonate (20 ml) was added to the mixture, and the mixture was stirred for 30 minutes. The precipitated solid was collected by filtration, and the solid was washed with water (20 ml, three times), and the solid was dried by hot air (80°C) for 1 day to give the title compound (159.0 mg, 81%) as a white solid. 10 'H-NMR Spectrum (CDC13) δ (ppm): 1.71-1.88 (4H, m), 2.00-2.17 (2H, m), 3.47- 3.69 (4H, m), 4.53-4.59 (1H, m), 5.20 (2H, m), 6.54 (1H, dd, J=2.0, 5.6 Hz), 7.00 (1H, dd, J=7.2, 10.4 Hz), 7.08 (1H, brs), 7.30-7.44 (5H, m), 7.70 (1H, d, J=2.0 Hz), 8.05 (1H, d, J=5.6 Hz), 8.31-8.38 (1H, m), 11.27 (1H, brs). ESI-MS (m/z): 551[M-H]’. 15 [0100] (Example 21] l-[({2,5-Difluoro-4-[(2-{r(fS)-3-hvdroxvpyrrolidin-l- vf)carbonynamino)pyridin-4- yl)oxy1phenyl}amino)carbonyl]cyclopropanecarboxylic acid triethylamine salt

Benzyl 1 - [({2,5-difluoro-4- [(2- {[((S)-3 -hydroxypyrrolidin-1 - 20 yl)carbonyl]amino}pyridin-4- yl)oxy]phenyl}amino)carbonyl]cyclopropanecarboxylate (156.8 mg) was dissolved in tetrahydro furan and methanol (1:1) (4 ml) under a nitrogen atmosphere. 10% palladium on carbon (60.4 mg) was added, and the air in the reaction vessel was replaced by hydrogen, and the mixture was stirred at room temperature for 19 25 hours. The air in the reaction vessel was replaced by nitrogen, and triethylamine (0.0991 ml) was added, and the mixture was stirred for 30 minutes. The catalyst was removed by filtration, and washed with methanol. The filtrate was concentrated under reduced pressure to give the title compound (174.9 mg, quant.) as a white solid. 65 FP06-0349-00 ESI-MS (m/z): 461 [M-H]'.

[0101] (Example 22) N-i2,5-Difluoro-4-[(2-([((S)-3-hydroxypyrrolidin-l- yl)carbonvl]amino]pyridin-4-yl)oxy]phenyn-N'-(4-fluorophenyl)cyclopropane- 1,1-dicarboxamide

10 15 20 4-(4,6-Dimethoxy[l,3,5]triazin-2-yl)-4-methylmorpholinium chloride hydrate (365 mg) was added to a mixture of l-[({2,5-difluoro-4-[(2-{[((S)-3-hydroxypyrrolidin-1 -yl)carbonyl] amino} pyridin-4- yl)oxy]phenyl}amino)carbonyl]cyclopropanecarboxylic acid triethylamine salt (175 mg), 4-fluoroaniline (0.0587 ml) and tetrahydrofuran (4.0 ml) at room temperature under a nitrogen atmosphere, and the mixture was stirred for 68 hours and 30 minutes. A saturated aqueous solution of sodium hydrogencarbonate (10 ml) was added to the mixture and stirred, and the mixture was partitioned after the addition of ethyl acetate and tetrahydrofuran (1:1) (40 ml) and water (30 ml). The organic layer was washed with brine (20 ml), and dried over anhydrous magnesium sulfate. The desiccant was removed by filtration, and the filtrate was concentrated under reduced pressure. The resultant residue was purified by silica gel column chromatography (Fuji SilysiaNH, eluent; ethyl acetate, then eth.yl acetate:methanol = 10:1). The fractions containing the target compound were concentrated under reduced pressure to give the title compound (128.5 mg, 75%) as a white solid. lH-NMR Spectrum (CDC13) δ (ppm): 1.67-1.77 (4H, m), 2.00-2.16 (2H, m), 3.46-3.67 (4H, m), 4.52-4.58 (1H, m), 6.55-6.59 (1H, m), 6.97-7.10 (4H, m), 7.45-7.52 (2H, m), 7.67 (1H, d, J=2.0 Hz), 8.07 (1H, d, J=5.6 Hz), 8.28 (1H, dd, J=7.6, 12.0 Hz), 8.64-8.70 (1H, m), 9.49-9.55 (1H, m). ESI-MS (m/z): 554[M-H]'.

[0102] (Example 23) Benzyl l-[([2,5-difluoro-4-r(2-[[((R)-3-hydroxvpyrrolidin-l- yl)carbonyllamino)pvridin-4- yl)oxy]phenyl }amino)carbonyl]cyclopropanecarboxylate 25 66 FP06-0349-00

10 15 20

Ν,Ν-Diisopropylethylamine (0.249 ml) was added to a mixture of benzyl l-({[4-({2-[(phenoxycarbonyl)amino]pyridin-4-yl}oxy)-2,5- difluorophenyl]amino}carbonyl)cyclopropanecarboxylate (200 mg), (R)-3-hydroxypyrrolidine hydrochloride (88.2 mg) and N-methylpyrrolidinone (4.0 ml) at room temperature under a nitrogen atmosphere, and the mixture was stirred for 5 hours. (R)-3-Hydroxypyrrolidine hydrochloride (44.1 mg) and N,N- diisopropylethylamine (0.125 ml) were added at room temperature, and the mixture was stirred for 15 hours and 40 minutes. A saturated aqueous solution of sodium hydrogencarbonate (20 ml) was added to the mixture to quench the reaction, and the mixture was partitioned after the addition of ethyl acetate and tetrahydrofuran (1:1) (50 ml) and (30 ml). The organic layer was washed with brine (30 ml), and dried over anhydrous magnesium sulfate. The desiccant was removed by filtration, and the filtrate was concentrated under reduced pressure. The resultant residue was purified by silica gel column chromatography (Fuji Silysia NH, eluent; ethyl acetate, then ethyl acetate:methanol = 10:1). The fractions containing the target compound were concentrated under reduced pressure to give the title compound (178.2 mg, 90%) as a white solid. ’H-NMR Spectrum (CDC13) δ (ppm): 1.71-1.88 (4H, m), 2.00-2.17 (2H, m), 3.47-3.69 (4H, m), 4.53-4.59 (1H, m), 5.20 (2H, m), 6.54 (1H, dd, >2.0, 5.6 Hz), 7.00 (1H, dd, >7.2, 10.4 Hz), 7.08 (1H, brs), 7.30-7.44 (5H, m), 7.70 (1H, d, >2.0 Hz), 8.05 (1H, d, >5.6 Hz), 8.31-8.38 (1H, m), 11.27 (1H, brs). ESI-MS (m/z): 551[M-H]'.

[0103] (Example 24) l-[f[2,5-Difluoro-4-r(2-{r((R)-3-hydroxypyrrolidin-l- yl)carbonvl1amino}pyridin-4- yl)oxy]phenyl}amino)carbonyllcyclopropanecarboxylic acid triethylamine salt 25 67 FP06-0349-00

Benzyl 1 - [({2,5-difluoro-4- [(2- {[((R)-3 -hy droxypyrrolidin-1 - yl)carbonyl] amino }pyridin-4- yl)oxy]phenyl}amino)carbonyl]cyclopropanecarboxylate (156.8 mg) was dissolved 5 in tetrahydro furan and methanol (2:1) (6 ml) under a nitrogen atmosphere. 10% palladium on carbon (68.6 mg) was added, and the air in the reaction vessel was replaced by hydrogen, and the mixture was stirred at room temperature for 16 hours and 30 minutes. The air in the reaction vessel was replaced by nitrogen, and triethylamine (0.112 ml) was added, and the mixture was stirred for 30 minutes. 10 The catalyst was removed by filtration, and washed with methanol. The filtrate was concentrated under reduced pressure to give the title compound (185.3 mg, quant.) as a white solid. ESI-MS (m/z): 461 [M-H]', [0104] (Example 25) N-{2,5-Difluoro-4-[(2-{r((R')-3-hvdroxypyrrolidin-l- 15 yl')carbonyl1amino}pyridin-4-yl]oxy1phenyl}-N'-(4-fluorophenyl')cyclopropane- 1,1-dicarboxamide

4-(4,6-Dimethoxy[l,3,5]triazin-2-yl)-4-methylmorpholinium chloride hydrate (388 mg) was added to a mixture of l-[({2,5-difluoro-4-[(2-{[((R)-3-hydroxypyrrolidin- 20 1 -yl)carbonyl] amino} pyridin-4- yl)oxy]phenyl}amino)carbonyl]cyclopropanecarboxylic acid triethylamine salt (185.3 mg), 4-fluoroaniline (0.0623 ml) and tetrahydro furan (4.0 ml) at room temperature under a nitrogen atmosphere, and the mixture was stirred for 68 hours. A saturated aqueous solution of sodium hydrogencarbonate (10 ml) was added to 25 the reaction mixture and stirred, and the mixture was partitioned after the addition 68 FP06-0349-00 of ethyl acetate and tetrahydrofuran (1:1) (40 ml) and water (30 ml). The organic layer was washed with brine (20 ml), and dried over anhydrous magnesium sulfate.

The desiccant was removed by filtration, and the filtrate was concentrated under reduced pressure. The resultant residue was purified by silica gel column 5 chromatography (Fuji Silysia NH, eluent; ethyl acetate, then ethyl acetate methanol = 10:1). The fractions containing the target compound were concentrated under reduced pressure to give the title compound (132.8 mg, 73%) as a. white solid. ’H-NMR Spectrum (CDC13) δ (ppm): 1.67-1.77 (4H, m), 2.00-2.16 (2H, m), 3.46-3.67 (4H, m), 4.52-4.58 (1H, m), 6.55-6.59 (1H, m), 6.97-7.10 (4H, m), 7.45-7.52 10 (2H, m), 7.67 (1H, d, J=2.0 Hz), 8.07 (1H, d, J=5.6 Hz), 8.28 (1H, dd, J=7.6, 12.0

Hz), 8.64-8.70 (1H, m), 9.49-9.55 (1H, m). ESI-MS (m/z): 554[M-H]'.

[0105] The preparing process according to the present invention can be carried out by performing a reaction similar to the above Examples using as a starting material 15 the amine described in the above Production Example or a publicly known amine.

[0106] Pharmacological Test Examples

The biological activity and pharmaceutical effect (inhibitory activity for hepatocyte growth factor receptor, anti-tumor activity, inhibitory activity for angiogenesis, and inhibitory activity for cancer metastasis) of the compound 20 according to the present invention were evaluated by methods described below.

Abbreviations and terms used in the following Pharmacological Test Examples are listed as follows: (Abbreviation List) HGFR (Hepatocyte growth factor receptor) 25 DNA (Deoxyribonucleic acid)

Human placenta (Human placenta) PCR (Polymerase chain reaction) VEGFR2 (Vascular endothelial growth factor receptor 2) FGFR1 (Fibroblast growth factor receptor 1) 30 PDGFRP (Platelet derived growth factor receptor β) EGFR (Epidermal growth factor receptor) FBS (Fetal bovine serum) PBS (Phosphate buffered saline) 69 FP06-0349-00

Tris (Tris(hydroxymethyl)aminomethane, Tris(buffer)) PMSF (Phenylmethylsulfonyl fluoride) NP-40 (Nonidet P-40) EGTA (O,O-Bis(2-aminoethyleneglycol)-N,N,N',N'-tetraacetic acid) 5 SDS (Sodium dodecyl sulfate) BSA (Bovine serum albumin)

Hepes (N-[2-hydroxyethyl]piperazine-N'-[2-ethanesulfonic acid], Hepes(buffer)) ATP (Adenosine 5’-triphosphate) EDTA (Ethylenediamine tetraacetic acid) 10 HTRF (Homogenous Time-Resolved Fluorescence) HRP (Horseradish peroxidase) ELISA (Enzyme-linked immunosorbent assay) [0107] Pharmacological Test Example 1: Inhibitory activity against receptor tyrosine kinase activity 15 1. Cloning of receptor tyrosine kinases, and preparation of the recombinant baculovirus solutions

The cytoplasmic domain of HGFR (GenBank Accession No. J02958) is a 1.3kb DNA fragment beginning with Lys974 and including a stop codon, and described by Park et al. (Proc. Natl. Acad. Sci. U.S.A. 84(18), 6379-6383, 1987). 20 The DNA fragment was isolated from the human placental cDNA library (purchased from Clontech) by PCR (TaKaRa Ex Taq™ Kit, purchased from TaKaRa) using two kinds of primers (SEQ ID NO: 1, 5’- CCGGCCGGATCCAAAAAGAGAAAGCAAATTAAA-3’ and SEQ ID NO: 2, 5’-TTAATTCTGCAGCTATGATGTCTCCCAGAAGGA-3’, purchased from 25 Invitrogen). The DNA fragment was cloned into a baculovirus transplace vector (pFastBac™-HT (purchased from GIBCO BRL)) to produce a recombinant construct. The construct was transfected into insect cells (Spodoptera frugiperda 9(Sf9)) to produce a solution of HGFR transfected baculovirus (preparation of a recombinant baculovirus can be found in the standard text (Bac-to-Bac Baculovirus 30 Expression System (GIBCO BRL)). The cloning of the other receptor tyrosine kinases and preparation of the recombinant baculovirus solutions were prepared using a cytoplasmic fragment starting from Lys791 (VEGFR2, GenBank Accession

No.L04947), a cytoplasmic fragment starting from Lys398 (FGFR1, GenBank 70 FP06-0349-00

Accession No.X52833) and a cytoplasmic fragment starting from Lys558 (PDGFRP, GenBank Accession No.M21616) in stead of HGFR in the above method. EGFR was purchased from Sigma (Production No. E-2645).

[0108] 2. Expression and purification of receptor tyrosine kinases 5 To the suspension of Sf9 cells (3xl08 cells) in SF-900II medium (purchased from Invitrogen) containing 2% FBS was added a solution of HGFR transfected baculovirus above (4ml), followed by a shaking culture at 27 °C for 48 hrs. The cells infected with the HGFR transfected baculovirus were centrifuged at 1,000 rpm, 4 °C for 5 min to remove the supernatant. The precipitated infected cells were 10 suspended in 80 ml of ice-cold PBS, and centrifuged at 1,000 rpm, 4 °C for 5 min to remove the supernatant. The precipitated infected cells were suspended in 40 ml of ice-cold Lysis Buffer (50 mM Tris-HCl (pH 8.5), 5 mM 2-meicaptoethanol, 100 mM KC1, 1 mM PMSF and 1 % (v/v) NP-40). The suspension was centrifuged at 12,000 rpm, 4 °C for 30 min to provide a supernatant. 15 The supernatant was loaded onto an Ni-NTA agarose column (3 ml, purchased from Qiagen) equilibrated with 30 ml of Buffer A (20 mM Tris-HCl (pH 8.5), 5 mM 2-mercaptoethanol, 500 mM KC1, 20 mM imidazole and. 10 % (v/v) glycerol). The column was washed with 30 ml of Buffer A, 6 ml of Buffer B (20 mM Tris-HCl (pH 8.5), 5 mM 2-mercaptoethanol, 1 M KC1, and 10 % (v/v) 20 glycerol) and 6 ml of Buffer A in this order. Then, the column was eluted with 6 ml of Buffer C (20 mM Tris-HCl (pH 8.5), 5 mM 2-mercaptoethanol, 100 mM KC1, 100 mM imidazole, and 10 % (v/v) glycerol) to provide a fraction. The fraction was entrapped in a dialysis membrane (purchased from Spectrum Laboratories), dialyzed at 4 °C overnight with 1 L of dialysis buffer (20 mM Tris-HCl (pH 7.5), 25 10 % (v/v) glycerol, 1 mM dithiothreitol, 0.1 mM NasVCL and 0.1 mM EGTA), and stored at -80 °C until used. An aliquot of the dialyzed fraction was subjected to SDS electrophoresis, and then a recombinant protein (His6-HGFR, the HGFR cytoplasmic domain fused with six histidine at the N terminus) detected at a molecular weight of about 60 kDa when stained with Coomassie Brilliant Blue, 30 was determined with regard to protein content using BSA (purchased from Sigma) as a standard. The VEGFR2 cytoplasmic domain, the FGFR1 cytoplasmic domain,

and the PDGFRP cytoplasmic domain were fused with six histidine at the N terminus by the similar method to produce respective recombinant proteins (His6- 71 FP06-0349-00 VEGFR2, His6-FGFR1, and His6- PDGFRP).

[0109] 3. Assay for the inhibitory activity against HGFR tyrosine kinase activity

To each well of a 96-well round plate (purchased from NUNC, Production

No. 163320) were added 10 μΐ of a solution for kinase reaction (200 mM Hepes 5 (pH 7.4), 80 mM MgCl2, 16 mM MnCl2 and 2 mM Na3VO4), 250 ng of biotinylated poly(Glu4: Tyrl) (biotin-poly(GT), purchased from Japan Schering) (6 μΐ, 15-fold diluted with distilled water), 30 ng of His6-HGFR (10 μΐ, 60-fold diluted with 0.4 % BSA) and a test substance dissolved in dimethyl sulfoxide (4 μΐ, 100-fold diluted with 0.1 % BSA) to mess up to 30 μΐ. To the well was added 10 10 μΐ of 4 μΜ ATP (purchased from Sigma) diluted with distilled water to incubate at 30 °C for 10 min, followed by adding 10 μΐ of 500 mM EDTA (pH 8.0) (purchased from Wako Pure Chemicals) to provide a kinase reaction solution.

The tyrosine-phosphorylated biotin-poly(GT) was detected using the Homogenous Time-Resolved Fluorescence (HTRF) method (Analytical 15 Biochemistry, 269, 94-104, 1999). That is, to each well of a 96-well half-area black plate (purchased from COSTAR, Production No. 3694) were added 20 μΐ of the above kinase reaction solution and 30 μΐ of a dilution solution (50 mM Hepes (pH 7.4), 20 mM MgCl2, 4 mM MnCl2, 0.5 mM Na3VO4, 0.1 % BSA and 100 mM EDTA). To the well was added 7.5 ng of an europium cryptate-labelled anti- 20 pho spho tyro sine antibody (Eu(K)-PY20, purchased from Japan Schering) (25 μΐ, 250-fold diluted with 20 mM Hepes (pH 7.0), 0.5 M KF and 0.1 % BSA) and 250 ng of XL665-labelled streptavidin (XL665-SA, purchased from Japan Schering) (25 μΐ, 62.5-fold diluted with 20 mM Hepes (pH 7.0), 0.5 Μ KF and 0.1 % BSA), and using a discovery HTRF microplate analyzer (Packard), the well was instantly 25 irradiated at an excitation wavelength of 337 nm to determine fluorescence intensities at 665 nm and 620 nm. The tyrosine phosphorylation rate of a biotin-poly(GT) was calculated using a delta F% value described in the text of a HTRF standard experiment method by Japan Schering. While defining the delta F% value of a well added with His6-HGFR and no test substance as 100 % and the delta F% 30 value of a well added with no His6-HGFR and no test substance as 0 %, ratio (%) of the delta F% value of each well added with the test substance was calculated.

The ratio (%) was used to calculate the concentration (IC50) cf the test substance necessary to inhibit HGFR kinase activity by 50%, and the results are shown in 72 FP06-0349-00

Table 1.

[0110] [Table 1] Example IC50 (μΜ) 9 0.053 16 0.004 19 0.049 22 0.016 25 0.010 10 15 20 25 [0111] 4. Assay for the inhibitory activity against receptor tyrosine kinase activities

other than HGFR

The inhibitory activity against tyrosine kinase activities of VEGFR2, FGFR1, and EGFR were determined by the similar manner as in the assay for the inhibitory activity against E1GFR tyrosine kinase activity described above, using 15 ng of His6-VEGFR2, 15 ng of His6-FGFR1 or 23ng of EGFR, respectively instead of HGFR.

The inhibitory activity against PDGFRp tyrosine kinase activity was evaluated by obtaining a kinase reaction solution by the above method using 50 ng of His6-PDGFRP, followed by detecting the tyrosine phosphorylated biotin-poly(GT) by a method described below.

To each well of a 96-well streptavidin-coated plate (purchased from PIERCE, Production No. 15129) were added 34 μΐ of the kinase reaction solution and 16 μΐof a dilution solution, followed by incubation at room temperature for 30 min. Then, the well was washed three times with 150 μΐ of a washing solution (20 mM Tris-HCl (pH 7.6), 137 mM NaCl, 0.05 % Tween-20 and C.l % BSA), and to the well was added 70 μΐ of anti-phosphotyrosine (PY20)-HRP conjugate (purchased from Transduction Laboratories, Production No. P-11625) (2,000-fold diluted with 20 mM Tris-HCl (pH 7.6), 137 mM NaCl, 0.05 % Tween-20 and 1% BSA), followed by incubation at room temperature for 1 hr. Then, each well was washed three times with 150 μΐ of the washing solution, and supplied with 100 μΐ of TMB Membrane Peroxidase Substrate (purchased from Funakoshi, Production No. 50-5077-03). After incubating the same at room temperature for 10 min, 100 μΐ of 1 M phosphoric acid was added to each well, and using a Plate Reader MTP-500 (Corona Electric), the absorbance of the well was instantly determined at 450 nm. While defining the absorbance of a well supplied with His6-PDGFRp and no 73 FP06-0349-00 10 15 20 25 test substance as 100 % and the absorbance of a well supplied with no His6-PDGFR-β and no test substance as 0 %, the absorbance ratio (%) of each well supplied with the test substance was calculated. The absorbance ratio (%) was used to calculate the concentration (IC50) of the test substance necessary to inhibit PDGFRP kinase activity by 50 %.

[0112] Pharmacological Test Example 2: Inhibitory activity against the proliferation of human gastric cancer cells (MKN-45]

Human gastric cancer cells (MKN-45) were suspended in a 1 % FBS- containing RPMI1640 medium (purchased from Sigma). The cell suspension (lx 104 cells/ml) was added in a 96-well plate for cell culture (purchased from NUNC, Production No. 167008) at 0.1 ml/well, and then cultured in a 5 % CO2 incubator (37 °C) overnight. After the culture, each well was supplied with 0.1 ml of a test substance diluted with a 1 % FBS-containing RPMI1640 medium, followed by culturing in a 5 % CO2 incubator (37 °C) for 3 days. After the culture, each well was supplied with 10 μΐ of Cell Counting Kit-8 (purchased from DOJINDO, Production No. 343-07623), followed by incubation in a 5 % CO2 incubator (37 °C) for about 1.5 hrs. After the incubation, using the Plate Reader MTP-500 (Corona Electric), the absorbance of each well was determined at a measurement wavelength of 450 nm and a reference wavelength of 660 nm. The ratio (%) of absorbance of each well supplied with a test substance to absorbance of the well supplied with no test substance was calculated, and the ratio was used to calculate the concentration (IC50) of the test substance necessary to inhibit the cell proliferation by 50%, and the results are shown in Table 2.

[0113] [Table 2] Example IC50 (μΜ) 9 0.017 16 0.005 19 0.0049 22 0.0024 25 0.0022

[0114] Pharmacological Test Example 3: Inhibitory activity against the HGFR

autophosphorylation using ELISA 1. Preparation of cell extract

Human gastric cancer cells (MKN-45) were suspended in a 1 % FBS- 74 FP06-0349-00 containing RPMI1640 medium (purchased from Sigma). The cell suspension (lx 105 cells/ml) was put in a 96-well plate for cell culture (purchased from NUNC,

Production No. 167008) at 0.1 ml/well, and then cultured in a 5 % CO2 incubator (37 °C) overnight. After the culture, from each well was removed the supernatant, 5 followed by adding 0.05 ml of a 1 % FBS-containing RPMI1640 medium. Then, the well was supplied with 0.05 ml of the test substance dissolved in dimethyl sulfoxide (diluted with a 1 % FBS-containing RPMI1640 medium), followed by culturing in a 5 % CO2 incubator (37 °C) for 1 hr. From each well was removed the supernatant, and each well was washed with 150 μΐ of PBS, followed by adding 10 100 μΐ of a lysis buffer (50 mM Hepes (pH 7.4), 150 mM NaCl, 10 % (v/v) glycerol, 1 % Triton X-100, 1.5 mM MgCl2, 1 mM EDTA (pH 8.0), 100 mM NaF, 1 mM PMSF, 10 μg/ml Aprotinin, 50 pg/ml Leupeptin, 1 pg/rn. Pepstatin A and 1 mM NaaVCU). The plate was shaken at 4 °C for 1 hr to prepare the cell extract. [0115] 2. Preparation of an anti-phosphotyrosine antibody-immcbilized plate 15 To a 96-well plate for ELISA (purchased from COSTAR, Production No. 3369) was added 50 μΐ of 60 mM bicarbonate buffer (pH 9.6) containing 50 pg/ml of an anti-phosphotyrosine antibody (PY20, purchased from Transduction Laboratory, Production No. P-11120). The plate was incubated at 4 °C overnight. [0116] 3. Assay for inhibitory activity against HGFR autophosphorylation

I 20 Each well of the plate prepared in 2. was washed three times with 200 μΐ of PBS, and supplied with 150 μΐ of 3 % BSA/PBS, followed by incubating at room temperature for 2 hrs. Each well was washed three times with 200 μΐ of PBS, and supplied with 50 μΐ of the above cell extract, followed by incubating at 4 °C overnight. After the incubation, each well was washed three times with 250 μΐ of a 25 washing solution (0.1 % BSA, 20 mM Tris-HCl (pH 7.6), 137 mM NaCl, and 0.05 % Tween-20), and supplied with 70 μΐ of anti-HGFR antibody (h-Met(C-12), purchased from Santa Cruz, Production No. sc-10) 2,000-fold diluted with a reaction solution (1 % BSA, 20 mM Tris-HCl (pH 7.6), 137 mM NaCl and 0.05 % Tween-20), followed by incubating at room temperature for 1 hr. The well was 30 washed three times with 250 μΐ of the washing solution, and supplied with 70 μΐ of peroxidase-labelled anti-rabbit IgG antibody (purchased frcm Cell Signaling,

Production No. 7074) 2,000-fold diluted with the reaction solution, followed by incubating at room temperature for 1 hr. Each well was washed three times with 75 FP06-0349-00 5 10 20 25 250 μΐ of the washing solution, and supplied with 70 μΐ of TM3 Membrane Peroxidase Substrate (purchased from Funakoshi, Production No. 50-5077-03), followed by incubating at room temperature for 10 min. Each well was supplied with 70 μΐ of 1 M phosphoric acid, and using the Plate Reader MTP-500 (Corona Electric), the absorbance of the well was instantly determined at a measurement wavelength of 450 nm. While defining the absorbance of a well supplied with the cell extract having no test substance as 100% HGFR autophosphorylation activity, and the absorbance of a well supplied with 50 μΐ of the lysis buffer as 0% HGFR autophosphorylation activity, the HGFR autophosphorylation activity (%) was calculated for each well. The concentration of the test substance was changed by several levels to calculate HGFR autophosphorylation activities (%) in respective cases, and to calculate the concentration (IC50) of the test substance necessary to inhibit HGFR autophosphorylation activity by 50%, and the results are shown in Table 3. 15 [0117] [Table 3] Example IC50 (μΜ) 9 0.016 16 0.0084 19 0.011 22 0.0045 25 0.0034 [0118] Measurement of powder X-ray diffraction

With regard to the crystals obtained in Example 9 (Method 3), about 5 mg of sample was ground in a mortar and then sampled on an aluminum pan for measurement. Measurement was carried out under the conditions below. Apparatus: X-ray DSC system TTR-III (manufactured by Rigaku Denki KK) X-ray: CuKa

Goniometer: TTR-III horizontal goniometer

Counter: scintillation counter

Tube voltage: 50 kV

Tube current: 300 mA

Scan speed: 5°/min

Scan axis: 2Θ/Θ

Scan range: 20 = 5° to 35° 76 FP06-0349-00

Divergent slit: 0.5 mm

Divergent vertical limited slit: 2 mm

Scattering slit: open

Receiving slit: open

Sampling width: 0.02°

Accumulation: 1 [0119] The powder X-ray diffraction pattern of the crystals obtained in Example 9 (Method 3) is shown in Fig. 1, and the representative peaks and their relative intensities of diffraction angles (20) of the crystals are shown in table 4. 10 [0120] [Table 4] 2Θ Relative Intensity 6.3 100 12.3 52 17.3 58 18.3 31 18.4 19 19.2 19 19.8 29 20.0 15 20.1 18 20.2 21 22.1 19 23.7 18

Industrial Applicability 15 [0121] The processes for preparing phenoxypyridine derivatives according to the present invention can provide phenoxypyridine derivatives useful as anti-tumor agents, angiogenesis inhibitors or inhibitors for cancer metastasis against various kinds of tumors such as a pancreatic cancer, a gastric cancer, a colorectal cancer, a breast cancer, a prostate cancer, a lung cancer, a renal cancer, a brain tumor or an ovarian cancer. 77 cra&amp;’an , crnxan rwzn ατα inia^n pnow pnszn irn πτ “|»oa ,ρνιη ηχΰπ naoana ma™ na^maa np’ioa .zruwan rwaa mpnan pmi1? oxnm οιηπη Pi?

.(moia nannn) cras^an mwa

18 members in 9 offices

This recordMember, by publication datePriority claim

Priority claims16

Priority claims
Document	Office	Kind	Date
82419206	United States of America	P	2006-08-31
82419206	United States of America	P	2006-08-31
2006285327	Japan	A	2006-10-19
2006285327	Japan	A	2006-10-19
85511706	United States of America	P	2006-10-30
85511706	United States of America	P	2006-10-30
2007066635	Japan	W	2007-08-28
2007066635	Japan	W	2007-08-28
2006285327	–	–	–
60824192	–	–	–
60855117	–	–	–
JP20060285327	–	–	–
PCTJP2007066635	–	–	–
US20060824192P	–	–	–
US20060855117P	–	–	–
WO2007JP66635	–	–	–

Members18

Family members, oldest first
Document	Office	Kind
AU2007289787A1	Australia	A1	2008-03-06
CA2661702A1	Canada	A1	2008-03-06
WO2008026577A1	World Intellectual Property Organization (WIPO)	A1	2008-03-06
US2008214815A1	United States of America	A1	2008-09-04
KR20090042760A	Republic of Korea	A	2009-04-30
EP2058302A1	European Patent Office (EPO)	A1	2009-05-13
CN101454286A	China	A	2009-06-10
IL197002A0	Israel	A0	2009-11-18
JPWO2008026577A1	Japan	A1	2010-01-21
US7790885B2	United States of America	B2	2010-09-07
EP2058302A4	European Patent Office (EPO)	A4	2010-10-06
CN101454286B	China	B	2011-07-20
AU2007289787B2	Australia	B2	2012-03-29
JP5145231B2	Japan	B2	2013-02-13
IL197002AThis record	Israel	A	2013-02-28
EP2058302B1	European Patent Office (EPO)	B1	2013-04-17
CA2661702C	Canada	C	2014-05-13
KR101432318B1	Republic of Korea	B1	2014-08-20

3 legal events, as the office reported them to INPADOC

Over the term

Point at a mark for the event

Events

Legal events, newest first
	Event	Code
2018-04-30	Patent not in force due to non-payment of renewal feesMM9K	MM9K
2013-07-31	Patent renewedKB	KB
2013-06-27	Patent grantedGrantedFF	FF