3-heteroaryl-3,5-dihydro-4-oxo-4h-pyridazino[4,5-b]indole-1-carboxamide derivatives, their preparation and therapeutic use

Abstract

A subject-matter of the invention is the compounds of general formula (I) in which X represents a hydrogen or halogen atom; R 1 represents a hydrogen atom or a (C 1 -C 4 )alkyl group; R 2 and R 3 each represent, independently of one another, a hydrogen atom or a (C 1 -C 4 )alkyl group or else R 2 and R 3 form, with the nitrogen atom which carries them, a pyrrolidinyl, piperidinyl, morpholinyl or 4-alkylpiperazinyl group; and Het represents a heteroaromatic group of pyridinyl, 1-oxidopyridinyl, quinolinyl, isoquinolinyl, pyrimidinyl, pyrazinyl or pyridazinyl type, it being possible for the heteroaromatic group to carry one or more halogen atoms and/or one or more (C 1 -C 4 )alkyl or (C 1 -C 4 )alkoxy groups; in the form of bases, of addition salts with acids, of solvates or of hydrates, the pharmaceutical compositions comprising them, processes for their preparation and synthetic intermediates.

1 . A method for the treatment of a pathology in which the peripheral benzodiazepine receptors are involved which comprises administering to a patient in need of said treatment a therapeutically effective amount of a compound of formula (I): 
     
       
         
         
             
             
         
       
     
     wherein:
 X represents a hydrogen or halogen atom, 
 R 1  represents a hydrogen atom or a (C 1 -C 4 )alkyl group; 
 R 2  and R 3  each represent, independently of one another, a hydrogen atom or a (C 1 -C 4 )alkyl group or else R 2  and R 3  form, with the nitrogen atom which carries them, a pyrrolidinyl, piperidinyl, morpholinyl or 4-alkylpiperazinyl group; and 
 Het represents a heteroaryl group selected from pyridinyl, 1-oxidopyridinyl, quinolinyl, isoquinolinyl, pyrimidinyl, pyrazinyl and pyridazinyl, optionally substituted with one or more halogen atoms,(C 1 -C 4 )alkyl or (C 1 -C 4 )alkoxy groups; or 
 a hydrate or a pharmaceutically acceptable salt thereof; and 
 wherein said pathology is selected from the group consisting of motor neuron condition, neurodegenerative disease of the central nervous system, sleep disorder, pathologies associated with the heart valves, inflammatory heart disease, side effects due to cardiotoxic medicaments or as a result of heart surgery, atherosclerosis and its thromboembolic complications, restenosis, conditions related to incorrect proliferation or incorrect migration of smooth muscle cells, cancer, cutaneous stress, and chronic inflammatory disease. 
 
   
   
       2 . The method according to  claim 1  wherein, for said compound of formula (I),
 X represents a halogen atom;   R 1  represents a (C 1 -C 4 )alkyl;   R 2  and R 3  each represent, independently of one another, a hydrogen atom or   (C 1 -C 4 )alkyl group, or else R 2  and R 3  form, with the nitrogen atom which carries them, a pyrrolidinyl, piperidinyl, morpholinyl or 4-alkylpiperazinyl group; and   Het represents a heteroaryl group selected from pyridinyl, quinolinyl, isoquinolinyl, pyrimidinyl, pyrazinyl and pyridazinyl, optionally substituted with one or more halogen atoms, (C 1 -C 4 )alkyl groups or (C 1 -C 4 )alkoxy groups.   
   
   
       3 . The method according to  claim 1  wherein the compound is selected from the group consisting of: 
     7-fluoro-N,N, 5-trimethyl-4-oxo-3-(pyridin-2-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     7-fluoro-N,N,5-trimethyl-4-oxo-3-(pyridin-3-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     7-fluoro-N,N,5-trimethyl-4-oxo-3-(pyridin-4-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide hydrochloride (1:1); 
     7-fluoro-N,N,5-trimethyl-4-oxo-3-(2-methoxypyridin-5-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     7-fluoro-N,N,5-trimethyl-4-oxo-3-(quinolin-3-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     1-[[7-fluoro-5-methyl-3-(pyrimidin-2-yl)-4-oxo-3,5-dihydro-4H-pyridazino[4,5-b]indol-1-yl]carbonyl]pyrrolidine; 
     4-methyl-1-[[7-fluoro-5-methyl-3-(pyridin-3-yl)-4-oxo-3,5-dihydro-4H-pyridazino[4,5-b]indol-1-yl]carbonyl]piperazine hydrochloride (1:1); 
     1-[[7-fluoro-5-methyl-3-(pyridin-3-yl)-4-oxo-3,5-dihydro-4H-pyridazino[4,5-b]indol-1-yl]carbonyl]pyrrolidine; 
     7-fluoro-N,5-dimethyl-4-oxo-3-(pyridin-3-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     7-fluoro-5-methyl-4-oxo-3-(pyridin-3-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     7-chloro-N,N,5-trimethyl-4-oxo-3-(pyridin-2-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     7-chloro-N,N,5-trimethyl-4-oxo-3-(pyridin-3-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide hydrochloride (1:1); 
     7-chloro-N,N,5-trimethyl-4-oxo-3-(pyridin-4-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     7-chloro-N,N,5-trimethyl-4-oxo-3-(pyridin-4-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide hydrochloride (1:1); 
     7-chloro-N,N,5-trimethyl-4-oxo-3-(5-methylpyridin-2-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     7-chloro-N,N,5-trimethyl-4-oxo-3-(2-methoxypyridin-5-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     7-chloro-N,N,5-trimethyl-4-oxo-3-(2-methylpyridin-5-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     7-chloro-N,N,5-trimethyl-4-oxo-3-(2-bromopyridin-5-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     7-chloro-N,N,5-trimethyl-4-oxo-3-(quinolin-3-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     7-chloro-N,N,5-trimethyl-4-oxo-3-(isoquinolin-4-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     7-chloro-N,N,5-trimethyl-4-oxo-3-(6-methylpyridazin-3-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     7-chloro-N,N,5-trimethyl-4-oxo-3-(pyrimidin-5-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     7-chloro-N,N,5-trimethyl-4-oxo-3-(pyrimidin-2-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     7-chloro-N,N,5-trimethyl-4-oxo-3-(pyrazin-2-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     1-[[7-chloro-5-methyl-3-(pyridin-3-yl)-4-oxo-3,5-dihydro-4H-pyridazino[4,5-b]indol-1-yl]carbonyl]pyrrolidine hydrochloride (1:1); 
     4-methyl-1-[[7-chloro-5-methyl-3-(pyridin-3-yl)-4-oxo-3,5-dihydro-4H-pyridazino[4,5-b]indol-1-yl]carbonyl]piperazine hydrochloride (1:1); 
     1-[[7-chloro-5-methyl-3-(pyridin-4-yl)-4-oxo-3,5-dihydro-4H-pyridazino[4,5-b]indol-1-yl]carbonyl]pyrrolidine; 
     7-chloro-N,5-dimethyl-4-oxo-3-(pyridin-4-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     7-chloro-5-methyl-4-oxo-3-(pyridin-4-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     7-chloro-N,N,5-trimethyl-4-oxo-3-(4-methoxypyridin-2-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     1-[[7-chloro-5-methyl-3-(pyridin-4-yl)-4-oxo-3,5-dihydro-4H-pyridazino[4,5-b]indol-1-yl]carbonyl]morpholine; 
     7-chloro-N,N,-diethyl-5-methyl-4-oxo-3-(pyridin-4-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     7-chloro-N-ethyl-N, 5-dimethyl-4-oxo-3-(pyridin-4-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     1-[[7-chloro-5-methyl-3-(pyridin-4-yl)-4-oxo-3,5-dihydro-4H-pyridazino[4,5-b]indol-1-yl]carbonyl]piperidine; 
     7-chloro-N,N,5-trimethyl-4-oxo-3-(2-methylpyridin-4-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     1-[[7-chloro-5-methyl-3-(2-methylpyridin-4-yl)-4-oxo-3,5-dihydro-4H-pyridazino[4,5-b]indol-1-yl]carbonyl]pyrrolidine; 
     7-chloro-N,N,5-trimethyl-3-(1-oxidopyridin-4-yl)-4-oxo-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     7-chloro-3-(2-methoxypyridin-4-yl)-N,N, 5-trimethyl-4-oxo-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; and 
     3-(2-bromopyridin-4-yl)-7-chloro-N,N,5-trimethyl-4-oxo-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     or a pharmaceutically acceptable salt or a hydrate thereof. 
   
   
       4 . The method according to  claim 1  wherein the compound is selected from the group consisting of: 
     7-chloro-N,N,5-trimethyl-4-oxo-3-(2-methoxypyridin-5-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     7-chloro-N,N,5-trimethyl-4-oxo-3-(2-methylpyridin-5-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; and 
     7-chloro-N,N,5-trimethyl-4-oxo-3-(2-bromopyridin-5-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     or a pharmaceutically acceptable salt or a hydrate thereof. 
   
   
       5 . A method for the treatment of a pathology in which the peripheral benzodiazepine receptors are involved which comprises administering to a patient in need of said treatment a therapeutically effective amount of a compound of formula (I): 
     
       
         
         
             
             
         
       
     
     wherein:
 X represents a hydrogen or halogen atom; 
 R 1  represents a hydrogen atom or a (C 1 -C 4 )alkyl group; 
 R 2  and R 3  each represent, independently of one another, a hydrogen atom or a (C 1 -C 4 )alkyl group or else R 2  and R 3  form, with the nitrogen atom which carries them, a pyrrolidinyl, piperidinyl, morpholinyl or 4-alkylpiperazinyl group; and 
 Het represents a heteroaryl group selected from pyridinyl, 1-oxidopyridinyl, quinolinyl, isoquinolinyl, pyrimidinyl, pyrazinyl and pyridazinyl, optionally substituted with one or more halogen atoms,(C 1 -C 4 )alkyl or (C 1 -C 4 )alkoxy groups; or 
 a hydrate or a pharmaceutically acceptable salt thereof; and 
 wherein said pathology is selected from the group consisting of stroke, cranial and medullar trauma, multiple sclerosis, Alzheimer's disease, and Parkinson's disease. 
 
   
   
       6 . The method according to  claim 5 , wherein for said compound of formula (I),
 X represents a halogen atom;   R 1  represents a (C 1 -C 4 )alkyl;   R 2  and R 3  each represent, independently of one another, a hydrogen atom or a   (C 1 -C 4 )alkyl group, or else R 2  and R 3  form, with the nitrogen atom which carries them, a pyrrolidinyl, piperidinyl, morpholinyl or 4-alkylpiperazinyl group; and   Het represents a heteroaryl group selected from pyridinyl, quinolinyl, isoquinolinyl, pyrimidinyl, pyrazinyl and pyridazinyl, optionally substituted with one or more halogen atoms, (C 1 -C 4 )alkyl groups or (C 1 -C 4 )alkoxy groups.   
   
   
       7 . The method according to  claim 5  wherein the compound is selected from the group consisting of: 
     7-fluoro-N,N, 5-trimethyl-4-oxo-3-(pyridin-2-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     7-fluoro-N,N,5-trimethyl-4-oxo-3-(pyridin-3-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     7-fluoro-N,N,5-trimethyl-4-oxo-3-(pyridin-4-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide hydrochloride (1:1); 
     7-fluoro-N,N,5-trimethyl-4-oxo-3-(2-methoxypyridin-5-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     7-fluoro-N,N,5-trimethyl-4-oxo-3-(quinolin-3-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     1-[[7-fluoro-5-methyl-3-(pyrimidin-2-yl)-4-oxo-3,5-dihydro-4H-pyridazino[4,5-b]indol-1-yl]carbonyl]pyrrolidine; 
     4-methyl-1-[[7-fluoro-5-methyl-3-(pyridin-3-yl)-4-oxo-3,5-dihydro-4H-pyridazino[4,5-b]indol-1-yl]carbonyl]piperazine hydrochloride (1:1); 
     1-[[7-fluoro-5-methyl-3-(pyridin-3-yl)-4-oxo-3,5-dihydro-4H-pyridazino[4,5-b]indol-1-yl]carbonyl]pyrrolidine; 
     7-fluoro-N,5-dimethyl-4-oxo-3-(pyridin-3-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     7-fluoro-5-methyl-4-oxo-3-(pyridin-3-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     7-chloro-N,N,5-trimethyl-4-oxo-3-(pyridin-2-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     7-chloro-N,N,5-trimethyl-4-oxo-3-(pyridin-3-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide hydrochloride (1:1); 
     7-chloro-N,N,5-trimethyl-4-oxo-3-(pyridin-4-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     7-chloro-N,N,5-trimethyl-4-oxo-3-(pyridin-4-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide hydrochloride (1:1); 
     7-chloro-N,N,5-trimethyl-4-oxo-3-(5-methylpyridin-2-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     7-chloro-N,N,5-trimethyl-4-oxo-3-(2-methoxypyridin-5-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     7-chloro-N,N,5-trimethyl-4-oxo-3-(2-methylpyridin-5-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     7-chloro-N,N,5-trimethyl-4-oxo-3-(2-bromopyridin-5-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     7-chloro-N,N,5-trimethyl-4-oxo-3-(quinolin-3-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     7-chloro-N,N,5-trimethyl-4-oxo-3-(isoquinolin-4-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     7-chloro-N,N,5-trimethyl-4-oxo-3-(6-methylpyridazin-3-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     7-chloro-N,N,5-trimethyl-4-oxo-3-(pyrimidin-5-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     7-chloro-N,N,5-trimethyl-4-oxo-3-(pyrimidin-2-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     7-chloro-N,N,5-trimethyl-4-oxo-3-(pyrazin-2-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     1-[[7-chloro-5-methyl-3-(pyridin-3-yl)-4-oxo-3,5-dihydro-4H-pyridazino[4,5-b]indol-1-yl]carbonyl]pyrrolidine hydrochloride (1:1); 
     4-methyl-1-[[7-chloro-5-methyl-3-(pyridin-3-yl)-4-oxo-3,5-dihydro-4H-pyridazino[4,5-b]indol-1-yl]carbonyl]piperazine hydrochloride (1:1); 
     1-[[7-chloro-5-methyl-3-(pyridin-4-yl)-4-oxo-3,5-dihydro-4H-pyridazino[4,5-b]indol-1-yl]carbonyl]pyrrolidine; 
     7-chloro-N,5-dimethyl-4-oxo-3-(pyridin-4-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     7-chloro-5-methyl-4-oxo-3-(pyridin-4-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     7-chloro-N,N,5-trimethyl-4-oxo-3-(4-methoxypyridin-2-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     1-[[7-chloro-5-methyl-3-(pyridin-4-yl)-4-oxo-3,5-dihydro-4H-pyridazino[4,5-b]indol-1-yl]carbonyl]morpholine; 
     7-chloro-N,N,-diethyl-5-methyl-4-oxo-3-(pyridin-4-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     7-chloro-N-ethyl-N, 5-dimethyl-4-oxo-3-(pyridin-4-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     1-[[7-chloro-5-methyl-3-(pyridin-4-yl)-4-oxo-3,5-dihydro-4H-pyridazino[4,5-b]indol-1-yl]carbonyl]piperidine; 
     7-chloro-N,N,5-trimethyl-4-oxo-3-(2-methylpyridin-4-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     1-[[7-chloro-5-methyl-3-(2-methylpyridin-4-yl)-4-oxo-3,5-dihydro-4H-pyridazino[4,5-b]indol-1-yl]carbonyl]pyrrolidine; 
     7-chloro-N,N,5-trimethyl-3-(1-oxidopyridin-4-yl)-4-oxo-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     7-chloro-3-(2-methoxypyridin-4-yl)-N,N, 5-trimethyl-4-oxo-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; and 
     3-(2-bromopyridin-4-yl)-7-chloro-N,N,5-trimethyl-4-oxo-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     or a pharmaceutically acceptable salt or a hydrate thereof. 
   
   
       8 . The method according to  claim 5  wherein the compound is selected from the group consisting of: 
     7-chloro-N,N,5-trimethyl-4-oxo-3-(2-methoxypyridin-5-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     7-chloro-N,N,5-trimethyl-4-oxo-3-(2-methylpyridin-5-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; and 
     7-chloro-N,N,5-trimethyl-4-oxo-3-(2-bromopyridin-5-yl)-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-carboxamide; 
     or a pharmaceutically acceptable salt or a hydrate thereof.