IP Library Granted Patent US 8,372,981
Granted Patent B2
US 8,372,981 · App. 12/986,638 · Granted Feb 12, 2013

Nitrogen-containing aromatic derivatives

Inventors: Yasuhiro Funahashi (Nagoya, JP); Masayuki Matsukura (Tsukuba, JP); Tatsuo Watanabe (Inzai, JP); Hiroshi Obaishi (Tsukuba, JP); Junji Matsui (Toride, JP)
Assignee: Eisai R&D Management Co., Ltd.
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Quick Facts
Patent No.
US 8,372,981
App. No.
12/986,638
Granted
Feb 12, 2013
Kind
B2
Abstract

Compounds represented by the following general formula: wherein A g is an optionally substituted 5- to 14-membered heterocyclic group, etc.; X g is —O—, —S—, etc.; Y g is an optionally substituted C 6-14 aryl group, an optionally substituted 5- to 14-membered heterocyclic group, etc.; and T g1 is a group represented by the following general formula: (wherein E g is a single bond or —N(R g2 )—), R g1 and R g2 each independently represent a hydrogen atom, an optionally substituted C 1-6 alkyl group, etc. and Z g represents a C 1-8 alkyl group, a C 3-8 alicyclic hydrocarbon group, a C 6-14 aryl group, etc.), salts thereof or hydrates of the foregoing.

Claims (10)

1. The compound represented by the following general formula or a salt thereof:

wherein W 41 and W are each independently an optionally substituted carbon atom;

X y1 is an optionally substituted group selected from the group consisting of the following formulas:

wherein Z 12 is a hydrogen atom, an optionally substituted C 1-6 alkyl group, an optionally substituted C 2-6 alkenyl group, an optionally substituted C 2-6 alkynyl group, an optionally substituted C 3-8 alicyclic hydrocarbon group, an optionally substituted C 6-14 aryl group, an optionally substituted 5- to 14-membered heterocyclic group, an optionally substituted 5- to 14-membered aromatic heterocyclic group or a group represented by the formula:

 wherein Z 31 , Z 33 and Z 34 are each independently a methylene group, —CO—, —NH— or —O—, and Z 32 is a single bond, a methylene group, —CO—, —NH— or —O—; and

A b11 is (1) an optionally substituted 5- to 14-membered heterocyclic group or (2) a group represented by the formula:

wherein V b11 and V b12 are each independently a single bond, —SO 2 —, —NHCO— or a group represented by the formula —(CH 2 ) b —CO— wherein b is an integer of 0 to 6;

R b13 is a single bond, an optionally substituted C 1-6 alkylene group, an optionally substituted C 3-8 alicyclic hydrocarbon group or an optionally substituted 5- to 14-membered heterocyclic group; and

R b11 and R b12 are each independently a hydrogen atom, a hydroxyl group, a halogen atom, an optionally substituted C 1-6 alkyl group, an optionally substituted C 2-6 alkenyl group, an optionally substituted C 2-6 alkynyl group, an optionally substituted C 3-8 alicyclic hydrocarbon group, an optionally substituted C 6-14 aryl group, an optionally substituted 5- to 14-membered aromatic heterocyclic group or an optionally substituted 5- to 14-membered heterocyclic group.

2. The compound or a salt thereof according to claim 1 , wherein the compound is selected from the group consisting of N-[4-(2-butylaminopyridin-4-yl)oxyphenyl]-N′-(4-fluorophenyl)urea, ethyl (E)-3-[2-[(cyclopropylcarbonyl)amino]-4-(4-{[(4-fluoroanilino)carbonyl]amino}phenoxy)-3-pyridyl]-2-propenoate, N1-Cyclopropylcarbonyl-N-1-[3-(1-ethynyl)-4-(4-{[(4-fluoroanilino)carbonyl]amino}phenoxy)-2-pyridyl]-1-cyclopropanecarboxamide, N4-(4-{4-[(anilinocarbonyl)amino]-3-chlorophenoxy}-2-pyridyl)-1-methyl-4-piperidinecarboxamide, N4-[4-(3-chloro-4-[(cyclopropylamino)carbonyl]amino}phenoxy)-2-pyridyl]-1-methyl-4-piperidinecarboxamide, N4-[4-(3-chloro-4-{[(4-fluoroanilino)carbonyl]amino}phenoxy)-2-pyridyl]-4-piperidinecarboxamide, N4-[4-(3-chloro-4-{[(4-fluoroanilino)carbonyl]amino}phenoxy)-2-pyridyl]-1-methyl-4-piperidinecarboxamide, N1-(4-{4-[(anilinocarbonyl)amino]-3-chlorophenoxy}-2-pyridyl)-2-(1-methyl-4-piperidyl)acetamide, N-[4-(2-cyclobutanecarbonylaminopyridin-4-yl)oxyphenyl]-N′-(2-thiazolyl)urea, N1-[4-{[(cyclopropylamino)carbonyl]amino}-3-chlorophenoxy]-2-pyridyl]-1-cyclopropanecarboxamide, N1-[5-bromo-4-(4-{[(cyclopropylamino)carbonyl]amino}-3-chlorophenoxy)-2-pyridyl]-1-cyclopropanecarboxamide, N1-[4-(3,5-dichloro-4-{[(cyclopropylamino)carbonyl]amino}phenoxy)-2-pyridyl]-1-cyclopropanecarboxamide, N-[4-(2-cyclobutanecarbonylaminopyridin-4-yl)oxyphenyl]-N′-(4-fluorophenyl)urea, N-[4-(2-butanoylaminopyridin-4-yl)oxyphenyl]-N′-(4-fluorophenyl)urea, N-{4-[2-(4-ethoxycarbonylbutanoyl)aminopyridin-4-yl]oxyphenyl}-N′-(4-fluorophenyl)urea, N-[4-(2-nicotinoylaminopyridin-4-yl)oxyphenyl]-N′-(4-fluorophenyl)urea, N-{4-[2-(4-carboxybutanoyl)aminopyridin-4-yl]oxyphenyl}-N′-(4-fluorophenyl)urea, N-(4-{2-[(cyclopropylmethyl)aminocarbonyl]pyridin-4-yl}oxyphenyl)-N′-(4-fluorophenyl)urea and N-{4-[2-(butyroylamino)pyridin-4-yl]oxyphenyl}-N′-cyclopropylurea.

Priority Claims (3)
JP P2000-320420 · Oct 20, 2000 · national
JP P2000-386195 · Dec 20, 2000 · national
JP P2001-046685 · Feb 22, 2001 · national
Continuity (5)
Division 12244227 · Oct 2, 2008
Division 11293785 · Dec 2, 2005
Division 10420466 · Apr 18, 2003
Continuation In Part PCTJP0109221 · Oct 19, 2001
Related Publication 20110118470A1 · May 19, 2011