Nitrogen-containing compounds having kinase inhibitory activity and drugs containing the same
View Patent ↗An objective of the present invention is to provide compounds having Rho kinase inhibitory activity. The compounds according to the present invention are those represented by formula (I) or pharmaceutically acceptable salts or solvates thereof: Het—X—Z (I) wherein Het represents a monocyclic or bicyclic heterocyclic group containing at least one nitrogen atom, for example, pyridyl or phthalimide; X represents group (i) —NH—C(═O)—NH—Q1-, group (ii) —NH—C(═O)—Q2-, wherein Q1 and Q2 represent a bond, alkylene, or alkenylene, or the like; and Z represents hydrogen, halogen, a monocyclic, bicyclic, or tricyclic carbocyclic group, a heterocyclic group or the like, for example, optionally substituted phenyl.
1. A compound represented by formula (I) or a pharmaceutically acceptable salt or solvate thereof:
Het—X—Z (I)
wherein
Het represents
wherein R 12 represents a hydrogen atom or a halogen atom;
X is —N(—R 1 )—Q6-Q7-
wherein
R 1 represents a hydrogen atom,
Q6 represents a five- to seven-membered saturated heterocyclic group and the heterocyclic groups are optionally substituted by an oxygen atom, hydroxyl, or C 1-4 alkyl,
Q7 represents
—(CH 2 )n1-CR 2a R 2b —(CH 2 )n2-
wherein
n1 and n2 are each an integer of 0 to 3,
when n2 is 2 or 3, —CH 2 —CH 2 — in —(CH 2 )n2- may represent —CH═CH— or —C≡C—,
R 2a and R 2b , which may be the same or different, represent
a hydrogen atom,
a halogen atom,
C 1-6 alkyl optionally substituted by hydroxyl,
carboxyl,
C 1-4 alkoxycarbonyl,
cyano,
Z represents
a hydrogen atom,
a halogen atom,
a three- to seven-membered saturated or unsaturated monocyclic carbocyclic or heterocyclic group,
a nine- to twelve-membered bicyclic saturated or unsaturated carbocyclic or heterocyclic group, or
a thirteen- to fifteen-membered tricyclic saturated or unsaturated carbocyclic or heterocyclic group, wherein the carbocyclic and heterocyclic groups are optionally substituted by a halogen atom; hydroxyl; nitro; amino; C 1-4 alkyl optionally substituted by a halogen atom; C 1-4 alkoxy of which the alkyl portion is optionally substituted by a halogen atom; C 1-4 alkoxycarbonyl of which the alkyl portion is optionally substituted by a halogen atom; C 1-4 alkylcarbonyl of which the alkyl portion is optionally substituted by a halogen atom; C 1-4 alkylcarbonyloxy of which the alkyl portion is optionally substituted by a halogen atom; or benzyloxy of which the phenyl portion is optionally substituted by a halogen atom.
2. The compound according to claim 1 , wherein Q6 represents a five- to seven-membered saturated Q6 represents a five- to seven-membered saturated heterocyclic group containing one nitrogen atom and the heterocyclic groups are optionally substituted by an oxygen atom; and Q7 represents —(CH 2 )n1-CR 2a R 2b —(CH 2 )n2-, wherein n1 is an integer of 0 or 1, n2 is 0, R 2a represents a hydrogen atom, and R 2b represents a hydrogen atom, C 1-4 alkyl, or optionally substituted phenyl.
3. The compound according to claim 1 wherein Q6 represents a five- to seven-membered saturated heterocyclic group containing one nitrogen atom and the heterocyclic groups are optionally substituted by an oxygen atom; and Q7 represents —(CH 2 )n1-CR R 2b R 2b (CH 2 )n2-, wherein n1 and n2 are each an integer of 0 to 3, R 2a represents a hydrogen atom, and R 2b represents a hydrogen atom, optionally substituted C 1-6 alkyl, carboxyl, C 1-4 alkoxycarbonyl, cyano.
4. The compound according to claim 2 , wherein Q6 represents a five- to seven-membered saturated heterocyclic group which is optionally substituted by an oxygen atom and contains one nitrogen atom.
5. The compound according to claim 3 , wherein Q6 represents a five- to seven-membered saturated heterocyclic group containing one nitrogen atom and the heterocyclic groups are optionally substituted by an oxygen atom; and Q7 represents —(CH 2 )n1-CR 2a R 2b —(CH 2 )n2- wherein n1 and n2, which may be the same or different, are each an integer of 0 to 3, R 2a represents a hydrogen atom, and R 2b represents a hydrogen atom or optionally substituted C 1-4 alkyl.
6. The compound according to claim 3 , wherein Q6 represents a five- to seven-membered saturated heterocyclic group containing one nitrogen atom and the heterocyclic groups are optionally substituted by an oxygen atom; and Q7 represents —(CH 2 )n1-CR 2a R 2b —(CH 2 )n2-wherein n1 and n2 are each 0, R 2a represents a hydrogen atom, and R 2b represents optionally substituted C 1-6 alkyl, carboxyl, C 1-4 alkoxycarbonyl, cyano.
7. The compound according to claim 3 , wherein Q6 represents a five- to seven-membered saturated heterocyclic group containing one nitrogen atom and the heterocyclic groups are optionally substituted by an oxygen atom; and Q7 represents —(CH 2 )n1-CR 2a R 2b —(CH 2 )n2- wherein n1 is an integer of 0 to 3, n2 is 0, and R 2a and R 2b represent a halogen atom.
8. The compound according to claim 1 , wherein Q6 represents any one of the following groups:
wherein the bond with * represents a bond to Q7 and the bond without * represents a bond to group —N(—R 1 )—.
9. The compound according to claim 1 , wherein Z represents
a hydrogen atom,
a halogen atom,
a three- to seven-membered saturated or unsaturated carbocyclic group,
a five- to seven-membered saturated or unsaturated heterocyclic group containing one nitrogen atom and/or one oxygen atom,
a nine- or ten-membered unsaturated bicyclic carbocyclic group,
a nine- or ten-membered unsaturated bicyclic heterocyclic group containing one nitrogen atom and/or one or two oxygen atoms, or
a thirteen- to fifteen-membered unsaturated tricyclic carbocyclic group or heterocyclic group.
10. The compound according to claim 9 , wherein Z represents a hydrogen atom, a halogen atom, phenyl, cyclopropyl, cyclohexyl, furanyl, pyridyl, piperidyl, naphthyl, naphthalenyl, indenyl, indolyl, imidazolyl, thienyl, 1,3-benzodioxole, fluorenyl, or carbazolyl and these groups are optionally substituted by a halogen atom; hydroxyl; nitro; amino; C 1-4 alkyl which is optionally substituted by a halogen atom; C 1-4 alkoxy of which the alkyl portion is optionally substituted by a halogen atom; C 1-4 alkoxycarbonyl of which the alkyl portion is optionally substituted by a halogen atom; C 1-4 alkylcarbonyl of which the alkyl portion is optionally substituted by a halogen atom; C 1-4 alkylcarbonyloxy of which the alkyl portion is optionally substituted by a halogen atom; or benzyloxy of which the phenyl portion is optionally substituted by a halogen atom.
11. The compound according to claim 1 , wherein
Z represents a hydrogen atom, a halogen atom, phenyl, cyclopropyl, cyclohexyl, furanyl, pyridyl, piperidyl, naphthyl, naphthalenyl, indenyl, indolyl, imidazolyl, thienyl, 1,3-benzodioxole, fluorenyl, or carbazolyl and these groups are optionally substituted by a halogen atom; hydroxyl; nitro; amino; C 1-4 alkyl which is optionally substituted by a halogen atom; C 1-4 alkoxy of which the alkyl portion is optionally substituted by a halogen atom; C 1-4 alkoxycarbonyl of which the alkyl portion is optionally substituted by a halogen atom; C 1-4 alkylcarbonyl of which the alkyl portion is optionally substituted by a halogen atom; C 1-4 alkylcarbonyloxy of which the alkyl portion is optionally substituted by a halogen atom; or benzyloxy of which the phenyl portion is optionally substituted by a halogen atom.
12. A compound selected from the group consisting of the following compounds:
(269) N-(5-isoquinolyl)-N-[1-(4-methylpentyl)-3-piperidyl]amine;
(273) N-(5-isoquinolyl)-N-[1-(4,4,4-trifluoro-butyl)-3-piperidyl]amine;
(276) N-(5-isoquinolyl)-N-[1-(2,4,6-trifluorobenzyl)-3-piperidyl]amine;
(278) N-(5-isoquinolyl)-N-[1-(2-methylbutyl)-3-piperidyl]amine;
(297) N-[1-(4-fluorobenzyl)-3-piperidyl]-N-(5-isoquinolyl)amine;
(299) N-(5-isoquinolyl)-N-{1-[4-(trifluoromethyl)benzyl]-3-piperidyl}amine;
(301) N-[1-(3,4-difluorobenzyl)-3-piperidyl]-N-(5-isoquinolyl)amine;
(318) N-(5-isoquinolyl)-N-(1-propyl-4-piperidyl)-amine;
(319) N-(1-isobutyl-4-piperidyl)-N-(5-isoquinolyl)amine;
(320) N-[1-(2-ethylbutyl)-4-piperidyl]-N-(5-isoquinolyl)amine;
(321) N-[1-(cyclopropylmethyl)-4-piperidyl]-N-(5-isoquinolyl)amine; and
(322) N-[1-(3-fluoropropyl)-4-piperidyl]-N-(5-isoquinolyl)amine.
13. A compound selected from the group consisting of the following compounds,
N-(1-Isopentyl-3-piperidyl)-N-(5-isoquinolyl)amine and
N-(5-Isoquinolyl)-N-[1-(2,4,6-trifluorobenzyl)-3-piperidyl]amine.
14. A pharmaceutical composition comprising a pharmaceutically effective amount of the compound according to claim 1 , a pharmaceutically acceptable salt or solvate thereof.
15. A pharmaceutical composition comprising a pharmaceutically effective amount of the compound according to claim 12 .
16. A method for treating hypertension comprising the step of administering a pharmaceutically effective amount of the compound of claim 1 or a pharmaceutically acceptable salt or solvate thereof together with a pharmaceutically acceptable carrier, to a mammal in need thereof.
17. The method of claim 16 , wherein the mammal is a human.