IP Library › Granted Patent US 9,012,458
Granted Patent B2
US 9,012,458 · App. 13/805,826 · Granted Apr 21, 2015

Antitumor agent using compounds having kinase inhibitory effect in combination

Inventors: Takayuki Nakagawa (Tsukuba, JP); Tomohiro Matsushima (Tsukuba, JP); Yasuhiro Funahashi (Andover, MA)
Assignee: Eisai R&D Management Co., Ltd.
A61K31/496A61K31/4427A61K31/4545A61K31/47
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Quick Facts
Patent No.
US 9,012,458
App. No.
13/805,826
Granted
Apr 21, 2015
Kind
B2
Abstract

An antitumor agent for combined use of a compound or pharmaceutically acceptable salt thereof represented by Formula (I) and a compound or pharmaceutically acceptable salt thereof represented by Formula (II) exhibits an excellent antitumor effect compared to cases where these are individually used, and exhibits antitumor effects against various cancer types: wherein R 1 is azetidinyl and the like, R 2 to R 5 is a hydrogen atom or a halogen atom, R 6 is C 3-8 cycloalkyl and the like, R 7 is a hydrogen atom and the like, and R 8 is a halogen atom and the like.

Claims (52)

1. A method of treating a tumor, comprising administering to a patient in need thereof a combination of:

a compound represented by Formula (I) or a pharmaceutically acceptable salt thereof:

wherein R 1 is azetidinyl, piperidinyl, or a formula —NR 11a R 11b , each of which optionally have a substituent selected from Substituent group A, wherein R 11a and R 11b are the same or different and each is a hydrogen atom, C 1-6 alkyl, or piperidinyl optionally having C 1-6 alkyl, Substituent group A consists of hydroxyl, piperazinyl optionally having methyl, and azetidinyl optionally having dimethylamino, and

R 2 to R 5 are the same or different and each is a hydrogen atom or a fluorine atom; and

a compound represented by Formula (II) or a pharmaceutically acceptable salt thereof:

wherein R 6 is C 1-6 alkyl or C 3-8 cycloalkyl,

R 7 is a hydrogen atom, C 1-6 alkyl, or C 1-6 alkoxy, and

R 8 is a hydrogen atom or a halogen atom.

2. The method of claim 1 , wherein the compound represented by Formula (I) is selected from the group consisting of:

N-(2-fluoro-4-{[2-({[4-(4-methylpiperazin-1-yl)piperidin-1-yl]carbonyl}amino)pyridin-4-yl]oxy}phenyl)-N′-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide:

N-[4-({2-[({4-[3-(dimethylamino)azetidin-1-yl]piperidin-1-yl}carbonyl)amino]pyridin-4-yl}oxy)-2-fluorophenyl]-N′-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide:

N-{2,5-difluoro-4-[(2-{[(3-hydroxyazetidin-1-yl)carbonyl]amino}pyridin-4-yl)oxy]phenyl}-N′-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide:

N-{2,5-difluoro-4-[(2-{[4-(4-methylpiperazin-1-yl)piperidin-1-yl]carbonyl}amino)pyridin-4-yl]oxy}phenyl)-N′-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide:

and

N-(2,5-difluoro-4-{[2-({[methyl(1-methylpiperidin-4-yl)amino]carbonyl}amino)pyridin-4-yl]oxy}phenyl)-N′-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide:

and the compound represented by Formula (II) is selected from the group consisting of:

4-[3-chloro-4-(cyclopropylaminocarbonyl)aminophenoxy]-7-methoxy-6-quinolinecarboxamide:

4-[3-chloro-4-(methylaminocarbonyl)aminophenoxy]-7-methoxy-6-quinolinecarboxamide:

4-[3-chloro-4-(ethylaminocarbonyl)aminophenoxy]-7-methoxy-6-quinolinecarboxamide:

N6-methoxy-4-(3-chloro-4-{[(cyclopropylamino)carbonyl)amino]phenoxy}-7-methoxy-6-quinolinecarboxamide:

and

N6-methoxy-4-(3-chloro-4-{[(ethylamino)carbonyl]amino}phenoxy)-7-methoxy-6-quinolinecarboxamide:

3. The method of claim 1 , wherein the compound represented by Formula (I) is N-(2-fluoro-4-{[2-({[4-(4-methylpiperazin-1-yl)piperidin-1-yl]carbonyl}amino)pyridin-4-yl]oxy}phenyl)-N′-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide:

and the compound represented by Formula (II) is 4-[3-chloro-4-(cyclopropylaminocarbonyl)aminophenoxy]-7-methoxy-6-quinolinecarboxamide:

4. The method of claim 1 , comprising simultaneous administration of the compound represented by Formula (I), or a pharmaceutically acceptable salt thereof, and the compound represented by Formula (II), or a pharmaceutically acceptable salt thereof.

5. The method of claim 1 , comprising separate administration of the compound represented by Formula (I), or a pharmaceutically acceptable salt thereof, and the compound represented by Formula (II), or a pharmaceutically acceptable salt thereof.

6. The method of claim 1 , wherein the tumor is melanoma, pancreatic cancer, gastric cancer, ovarian cancer, or glioblastoma.

7. A pharmaceutical composition comprising:

a compound represented by Formula (I) or a pharmaceutically acceptable salt thereof:

wherein R 1 is azetidinyl, piperidinyl, or a formula —NR 11a R 11b , each of which optionally have a substituent selected from Substituent group A, wherein R 11a and R 11b are the same or different and each is a hydrogen atom, C 1-6 alkyl, or piperidinyl optionally having C 1-6 alkyl,

Substituent group A consists of hydroxyl, piperazinyl optionally having methyl, and azetidinyl optionally having dimethylamino, and

R 2 to R 5 are the same or different and each is a hydrogen atom or a fluorine atom; and

a compound represented by Formula (II) or a pharmaceutically acceptable salt thereof:

wherein R 6 is C 1-6 alkyl or C 3-8 cycloalkyl,

R 7 is a hydrogen atom, C 1-6 alkyl, or C 1-6 alkoxy, and

R 8 is a hydrogen atom or a halogen atom.

8. The pharmaceutical composition of claim 7 , wherein the compound represented by Formula (I) is selected from the group consisting of:

N-(2-fluoro-4-{[2-({[4-(4-methylpiperazin-1-yl)piperidin-1-yl]carbonyl}amino)pyridin-4-yl]oxy}phenyl)-N′-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide:

N-[4-({2-[({4-[3-(dimethylamino)azetidin-1-yl]piperidin-1-yl}carbonyl)amino]pyridin-4-yl}oxy)-2-fluorophenyl]-N′-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide:

N-{2,5-difluoro-4-[(2-{[(3-hydroxyazetidin-1-yl)carbonyl]amino}pyridin-4-yl)oxy]phenyl}-N′-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide:

N-{2,5-difluoro-4-[(2-{[4-(4-methylpiperazin-1-yl)piperidin-1-yl]carbonyl}amino)pyridin-4-yl]oxy}phenyl)-N′-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide:

and

N-(2,5-difluoro-4-{[2-({[methyl(1-methylpiperidin-4-yl)amino]carbonyl}amino)pyridin-4-yl]oxy}phenyl)-N′-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide:

and the compound represented by Formula (II) is selected from the group consisting of:

4-[3-chloro-4-(cyclopropylaminocarbonyl)aminophenoxy]-7-methoxy-6-quinolinecarboxamide:

4-[3-chloro-4-(methylaminocarbonyl)aminophenoxy]-7-methoxy-6-quinolinecarboxamide:

4-[3-chloro-4-(ethylaminocarbonyl)aminophenoxy]-7-methoxy-6-quinolinecarboxamide:

N6-methoxy-4-(3-chloro-4-{[(cyclopropylamino)carbonyl)amino]phenoxy}-7-methoxy-6-quinolinecarboxamide:

and

N6-methoxy-4-(3-chloro-4-{[(ethylamino)carbonyl]amino}phenoxy)-7-methoxy-6-quinolinecarboxamide:

9. The pharmaceutical composition of claim 7 , wherein the compound represented by Formula (I) is N-(2-fluoro-4-{[2-({[4-(4-methylpiperazin-1-yl)piperidin-1-yl]carbonyl}amino)pyridin-4-yl]oxy}phenyl)-N′-(4-fluorophenyl)cyclopropane-1,1-dicarboxamide:

and the compound represented by Formula (II) is 4-[3-chloro-4-(cyclopropylaminocarbonyl)aminophenoxy]-7-methoxy-6-quinolinecarboxamide:

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 28, 2013
From: NAKAGAWA, TAKAYUKI; MATSUSHIMA, TOMOHIRO; FUNAHASHI, YASUHIRO
To: EISAI R&D MANAGEMENT CO., LTD.
Reel/Frame 029704/0431 →
Priority Claims (2)
JP P2010-145030 · Jun 25, 2010 · national
JP P2010-273921 · Dec 8, 2010 · national
Continuity (1)
Related Publication 20130123274A1 · May 16, 2013