IMIDAZO[1,2-b]PYRIDAZINE DERIVATIVES AND THEIR USE AS PDE10 INHIBITORS

Abstract

The present invention relates to novel imidazo[1,2-b]pyridazine derivatives which are inhibitors of the phosphodiesterase 10 enzyme (PDE10) and which are useful for the treatment or prevention of neurological, psychiatric and metabolic disorders in which the PDE10 enzyme is involved. The invention is also directed to pharmaceutical compositions comprising such compounds, to processes to prepare such compounds and compositions, to the use of such compounds or pharmaceutical compositions for the prevention or treatment of neurological, psychiatric and metabolic disorders and diseases.

1 . A compound of formula (I) 
       
         
           
           
               
               
           
         
         or a stereoisomeric form thereof, wherein 
         R 1  is pyridinyl; pyridinyl optionally substituted with halogen, C 1-4 alkyl, trifluoromethyl or C 1-4 alkyloxy; tetrahydropyranyl; or NR 6 R 7 ; 
         R 2  is hydrogen, C 1-4 alkyl, trifluoromethyl, C 3-8 cycloalkyl, or C 1-4 alkyloxy; 
         R 3  is hydrogen, chloro, C 1-4 alkyl, trifluoromethyl, or C 3-8 cycloalkyl; 
         Het is a 5- or 6-membered heterocyclic ring selected from the group consisting of pyridinyl, pyrimidinyl, pyridazinyl, pyrrolyl, oxazolyl, thiazolyl, imidazolyl, pyrazolyl, isothiazolyl, isoxazolyl, oxadiazolyl and triazolyl; 
         R 4  is hydrogen, C 1-4 alkyl, trifluoromethylC 0-4 alkyl, hydroxyC 1-4 alkyl, difluorocyclopropylmethyl, cyclopropyldifluoroethyl, C 3-8 cycloalkyl, C 1-4 alkyloxyC 1-5 alkyl, C 1-4 alkyloxy, trifluoromethylC 0-4 alkyloxy, C 3-8 cycloalkylC 1-4 alkyloxy, C 3-8 cycloalkylC 1-4 alkyl, C 1-6 alkyloxyC 1-4 alkyloxy, tetrahydropyranyl, pyridinylmethyl, NR 6a R 7a C 1-4 alkyl or NR 6a R 7a ; 
         R 5  is hydrogen or C 1-4 alkyl; 
         R 6 , R 6a , R 7  and R 7a  are each independently hydrogen or C 1-4 alkyl, or taken together with N can be a radical of Formula (a), (b) or (c) 
       
       
         
           
           
               
               
           
         
         wherein 
         each R 8 , if present, independently of one another is C 1-4 alkyl; 
         R 9  is hydrogen or C 1-4 alkyloxy; 
         R 10  is hydrogen or C 1-4 alkyl; 
         m is 0, 1, 2, 3, 4 or 5; 
         n is 2, 3, 4, 5 or 6; 
         o is 1 or 2; 
         or a pharmaceutically acceptable salt or a solvate thereof. 
       
     
     
         2 . The compound according to  claim 1 , wherein R 1  is selected from pyridinyl; pyridinyl optionally substituted with halogen, C 1-4 alkyl, trifluoromethyl or C 1-4 alkyloxy; tetrahydropyranyl; and NR 6 R 7 ; wherein R 6  and R 7  taken together with the nitrogen can be a radical of Formula (a), (b) or (c) as defined in  claim 1 ;
 R 2  is selected from hydrogen, methyl, ethyl, cyclopropyl, isopropyl, methoxy and trifluoromethyl;   R 3  is selected from hydrogen, chloro, methyl, trifluoromethyl and cyclopropyl; and   Het is selected from the group consisting of pyridinyl, pyrimidinyl, pyridazinyl, oxazolyl, thiazolyl, pyrazolyl, isothiazolyl, isoxazolyl, oxadiazolyl and triazolyl;   or a pharmaceutically acceptable salt or a solvate thereof.   
     
     
         3 . The compound according to  claim 1 , wherein
 R 1  is selected from pyridinyl which may be optionally substituted with halogen, C 1-4 alkyl, trifluoromethyl or C 1-4 alkyloxy; morpholinyl; and NR 6 R 7 ; wherein R 6  and R 7  taken together with the nitrogen can be a radical of Formula (a) or (c) wherein n is 3 and o is 1;   Het is selected from pyridinyl and pyrazolyl;   R 4  is hydrogen, C 1-4 alkyl, trifluoromethylC 0-4 alkyl, hydroxyC 1-4 alkyl, difluorocyclopropylmethyl, cyclopropyldifluoroethyl, C 3-8 cycloalkyl, C 1-4 alkyloxyC 1-5  alkyl, C 1-4 alkyloxy, trifluoromethylC 0-4 alkyloxy, C 3-8 cycloalkylC 1-4 alkyloxy, C 1-6 alkyloxyC 1-4 alkyloxy, tetrahydropyranyl, pyridinylmethyl, NR 6a R 7a C 1-4 alkyl or NR 6a R 7a ;   wherein R 6 , R 6a , R 7  and R 7a  are each independently hydrogen or C 1-4 alkyl, or taken together with the nitrogen can be a radical of formula (a), (b) or (c), wherein n is 3, R 9  is hydrogen or C 1-4 alkyloxy, m is 0, o is 1 and R 10  is hydrogen;   
       or a pharmaceutically acceptable salt or a solvate thereof. 
     
     
         4 . The compound according to  claim 1 , wherein
 R 1  is selected from morpholinyl and pyridinyl;   R 2  is selected from hydrogen, methyl, ethyl, methoxy, and cyclopropyl;   R 3  is selected from hydrogen, methyl, and cyclopropyl;   Het is pyridinyl or pyrazolyl;   R 4  is selected from ethyl; isopropyl; isobutyl; 2,2,2-trifluoroethyl; 2-hydroxy-2-methylpropyl; 2,2-difluoro-2-cyclopropylethyl; cyclopropyl; 2-methoxyethyl; (2S)-2-methoxypropyl; 2-ethoxyethyl; ethoxymethyl; 1-ethoxy-1-methylethyl; 1-methoxy-1-methylethyl; 2-methoxy-1,1-dimethylethyl; 3-methoxy-3-methylbutyl; 3-methoxypropyl; 2-methoxy-2-methyl-propyl; 2-methoxyethoxy; 2-methoxy-2-methyl-propoxy; tetrahydro-2H-pyran-4-yl; morpholin-4-yl; piperazin-1-yl; and (3R)-3-methoxypyrrolidin-1-yl;   and R 5  is hydrogen or methyl;   or a pharmaceutically acceptable salt or a solvate thereof.   
     
     
         5 . The compound according to  claim 1 , wherein
 R 1  is selected from morpholin-4-yl, pyridin-3-yl and pyridin-4-yl; and   Het is selected from pyridin-3-yl, pyridin-4-yl and 1H-pyrazol-4-yl;   or a pharmaceutically acceptable salt or a solvate thereof.   
     
     
         6 . The compound according to  claim 1 , wherein
 R 1  is selected from morpholin-4-yl; and   Het is pyridin-3-yl or pyridin-4-yl;   or a pharmaceutically acceptable salt or a solvate thereof.   
     
     
         7 . The compound according to  claim 1 , wherein
 R 1  is morpholin-4-yl;   R 2  is methyl;   R 3  is hydrogen;   Het is pyridin-3-yl;   R 4  is 2-methoxyethyl; and   R 5  is hydrogen;   or a pharmaceutically acceptable salt or a solvate thereof.   
     
     
         8 . The compound of formula (I) according to  claim 1 , selected from the group consisting of
 3-[6-(2-methoxyethyl)-3-pyridinyl]-2-methyl-8-(4-morpholinyl)-imidazo[1,2-b]pyridazine,   3-[6-(2-methoxyethyl)-3-pyridinyl]-2-methyl-8-(4-morpholinyl)-imidazo[1,2-b]pyridazine hydrochloride,   3-[6-(2-methoxyethyl)-3-pyridinyl]-2-methyl-8-(4-morpholinyl)-imidazo[1,2-b]pyridazine maleate,   3-[6-(2-methoxyethyl)-3-pyridinyl]-2-methyl-8-(4-morpholinyl)-imidazo[1,2-b]pyridazine monohydrate,   3-[6-(3-methoxypropyl)-3-pyridinyl]-2-methyl-8-(4-morpholinyl)-imidazo[1,2-b]pyridazine,   3-[6-(2-methoxy-2-methylpropyl)-3-pyridinyl]-2-methyl-8-(4-morpholinyl)-imidazo[1,2-b]pyridazine,   3-[6-(2-methoxy-1,1-dimethylethyl)-3-pyridinyl]-2-methyl-8-(4-morpholinyl)-imidazo[1,2-b]pyridazine,   3-[6-(1-ethoxy-1-methylethyl)-3-pyridinyl]-2-methyl-8-(4-morpholinyl)-imidazo[1,2-b]pyridazine,   3-[6-(1-methoxy-1-methylethyl)-3-pyridinyl]-2-methyl-8-(4-morpholinyl)-imidazo[1,2-b]pyridazine,   3-[6-(2-methoxy-2-methylpropyl)-3-pyridinyl]-2-methyl-8-(4-pyridinyl)-imidazo[1,2-b]pyridazine,   3-[6-(2-methoxyethoxy)-5-methyl-3-pyridinyl]-2-methyl-8-(4-pyridinyl)-imidazo[1,2-b]pyridazine,   3-[6-(2-methoxyethoxy)-3-pyridinyl]-2-methyl-8-(3-pyridinyl)-imidazo[1,2-b]pyridazine,   2-cyclopropyl-3-[6-(2-methoxyethyl)-3-pyridinyl]-8-(4-pyridinyl)-imidazo[1,2-b]pyridazine,   3-[6-(2-methoxyethyl)-3-pyridinyl]-8-(4-morpholinyl)-imidazo[1,2-b]pyridazine,   2-methoxy-3-[6-(2-methoxyethyl)-3-pyridinyl]-8-(4-morpholinyl)-imidazo[1,2-b]pyridazine,   6-cyclopropyl-3-[6-(2-methoxyethyl)-3-pyridinyl]-2-methyl-8-(4-morpholinyl)-imidazo[1,2-b]pyridazine,   6-cyclopropyl-3-[6-(2-methoxyethyl)-3-pyridinyl]-2-methyl-8-(4-pyridinyl)-imidazo[1,2-b]pyridazine,   2-cyclopropyl-3-[6-(2-methoxyethyl)-3-pyridinyl]-6-methyl-8-(4-morpholinyl)-imidazo[1,2-b]pyridazine,   3-[6-(2-methoxyethoxy)-3-pyridinyl]-2-methyl-8-(4-morpholinyl)-imidazo[1,2-b]pyridazine,   3-[6-(ethoxymethyl)-3-pyridinyl]-2-methyl-8-(4-morpholinyl)-imidazo[1,2-b]pyridazine,   3-[6-(2-methoxy-2-methylpropoxy)-3-pyridinyl]-2-methyl-8-(4-morpholinyl)-imidazo[1,2-b]pyridazine,   2-methyl-8-(4-morpholinyl)-3-[6-(4-morpholinyl)-3-pyridinyl]-imidazo[1,2-b]pyridazine,   3-[6-(2-methoxyethyl)-3-pyridinyl]-2-methyl-8-(4-pyridinyl)-imidazo[1,2-b]pyridazine,   3-[6-(2-methoxyethoxy)-3-pyridinyl]-2-methyl-8-(4-pyridinyl)-imidazo[1,2-b]pyridazine,   3-[6-(2-methoxyethoxy)-3-pyridinyl]-2-methyl-8-(4-pyridinyl)-imidazo[1,2-b]pyridazine hydrochloride,   2-cyclopropyl-3-[6-(2-methoxyethyl)-3-pyridinyl]-8-(4-morpholinyl)-imidazo[1,2-b]pyridazine,   3-[6-(2-methoxyethyl)-3-pyridinyl]-2,6-dimethyl-8-(4-morpholinyl)-imidazo[1,2-b]pyridazine,   3-[6-(2-methoxyethyl)-3-pyridinyl]-2,6-dimethyl-8-(4-pyridinyl)-imidazo[1,2-b]pyridazine,   3-[6-(2-ethoxyethyl)-3-pyridinyl]-2-methyl-8-(4-morpholinyl)-imidazo[1,2-b]pyridazine,   3-[2-(2-methoxyethyl)-4-pyridinyl]-2-methyl-8-(4-morpholinyl)-imidazo[1,2-b]pyridazine,   2-methyl-8-(4-morpholinyl)-3-[6-(tetrahydro-2H-pyran-4-yl)-3-pyridinyl]-imidazo[1,2-b]pyridazine,   3-(6-ethyl-3-pyridinyl)-2-methyl-8-(4-morpholinyl)-imidazo[1,2-b]pyridazine,   3-[6-(3-methoxy-3-methylbutyl)-3-pyridinyl]-2-methyl-8-(4-morpholinyl)-imidazo[1,2-b]pyridazine,   2-methyl-8-(4-morpholinyl)-3-[6-(1-piperazinyl)-3-pyridinyl]-imidazo[1,2-b]pyridazine,   2-methyl-3-[6-(4-morpholinyl)-3-pyridinyl]-8-(4-pyridinyl)-imidazo[1,2-b]pyridazine,   2-methyl-3-[6-(1-methylethyl)-3-pyridinyl]-8-(4-morpholinyl)-imidazo[1,2-b]pyridazine,   3-(6-cyclopropyl-3-pyridinyl)-2-methyl-8-(4-morpholinyl)-imidazo[1,2-b]pyridazine,   3-[6-[(3R)-3-methoxy-1-pyrrolidinyl]-3-pyridinyl]-2-methyl-8-(4-morpholinyl)-imidazo[1,2-b]pyridazine,   2-methyl-3-[1-(2-methylpropyl)-1H-pyrazol-4-yl]-8-(4-morpholinyl)-imidazo[1,2-b]pyridazine,   3-[1-(2-methoxyethyl)-1H-pyrazol-4-yl]-2-methyl-8-(4-morpholinyl)-imidazo[1,2-b]pyridazine,   3-[1-(2-methoxy-2-methylpropyl)-1H-pyrazol-4-yl]-2-methyl-8-(4-morpholinyl)-imidazo[1,2-b]pyridazine,   2-cyclopropyl-3-[1-(2-methoxy-2-methylpropyl)-1H-pyrazol-4-yl]-8-(4-morpholinyl)-imidazo[1,2-b]pyridazine,   2-cyclopropyl-3-[6-(2-methoxy-2-methylpropyl)-3-pyridinyl]-8-(4-morpholinyl)-imidazo[1,2-b]pyridazine hydrochloride,   2-cyclopropyl-3-[6-(2-methoxy-2-methylpropyl)-3-pyridinyl]-8-(4-morpholinyl)-imidazo[1,2-b]pyridazine,   3-[6-(2-methoxy-2-methylpropyl)-3-pyridinyl]-2,6-dimethyl-8-(4-pyridinyl)-imidazo[1,2-b]pyridazine,   2-cyclopropyl-3-[6-(2-methoxy-2-methylpropyl)-3-pyridinyl]-8-(4-pyridinyl)-imidazo[1,2-b]pyridazine,   5-[2-cyclopropyl-8-(4-morpholinyl)imidazo[1,2-b]pyridazin-3-yl]-α,α-dimethyl-2-pyridineethanol,   3-[6-(4-morpholinyl)-3-pyridinyl]-8-(4-pyridinyl)-imidazo[1,2-b]pyridazine,   2,6-dimethyl-8-(4-morpholinyl)-3-[6-(4-morpholinyl)-3-pyridinyl]-imidazo[1,2-b]pyridazine,   2-cyclopropyl-6-methyl-3-[6-(4-morpholinyl)-3-pyridinyl]-8-(4-pyridinyl)-imidazo[1,2-b]pyridazine,   2-cyclopropyl-3-[6-(2-methoxyethoxy)-3-pyridinyl]-6-methyl-8-(4-pyridinyl)-imidazo[1,2-b]pyridazine,   2-methyl-8-(4-morpholinyl)-3-[2-(4-morpholinyl)-4-pyridinyl]-imidazo[1,2-b]pyridazine,   3-{1-[2,2-difluorocyclopropyl)methyl]-1H-pyrazol-4-yl}-2-methyl-8-morpholin-4-ylimidazo[1,2-b]pyridazine,   2-methyl-3-[1-(2-methylpropyl)-1H-pyrazol-4-yl]-8-(4-pyridinyl)-imidazo[1,2-b]pyridazine,   6-cyclopropyl-3-[1-(2-methoxyethyl)-1H-pyrazol-4-yl]-2-methyl-8-(4-morpholinyl)-imidazo[1,2-b]pyridazine,   2-ethyl-3-[1-(2-methoxyethyl)-1H-pyrazol-4-yl]-8-(4-morpholinyl)-imidazo[1,2-b]pyridazine,   3-[1-[(2S)-2-methoxypropyl]-1H-pyrazol-4-yl]-2-methyl-8-(4-morpholinyl)-imidazo[1,2-b]pyridazine,   3-[1-(2-methoxyethyl)-1H-pyrazol-4-yl]-2,6-dimethyl-8-(4-morpholinyl)-imidazo[1,2-b]pyridazine,   3-[1-(2-methoxyethyl)-1H-pyrazol-4-yl]-2,6-dimethyl-8-(4-pyridinyl)-imidazo[1,2-b]pyridazine,   2-methyl-8-(4-pyridinyl)-3-[1-(2,2,2-trifluoroethyl)-1H-pyrazol-4-yl]-imidazo[1,2-b]pyridazine,   2-cyclopropyl-3-[1-(2-methoxyethyl)-1H-pyrazol-4-yl]-8-(4-pyridinyl)-imidazo[1,2-b]pyridazine,   2-cyclopropyl-3-[1-(2-methoxy-2-methylpropyl)-1H-pyrazol-4-yl]-8-(4-pyridinyl)-imidazo[1,2-b]pyridazine,   6-chloro-3-[1-(2-methoxyethyl)-1H-pyrazol-4-yl]-2-methyl-8-(4-pyridinyl)-imidazo[1,2-b]pyridazine, and   2-cyclopropyl-3-[1-(2-methylpropyl)-1H-pyrazol-4-yl]-8-(4-pyridinyl)-imidazo[1,2-b]pyridazine,   
       and the stereoisomeric forms, the pharmaceutically acceptable salts and the solvates thereof. 
     
     
         9 . A pharmaceutical composition comprising a therapeutically effective amount of a compound according to  claim 1  and a pharmaceutically acceptable carrier or excipient. 
     
     
         10 . (canceled) 
     
     
         11 . A method for the treatment or prevention of a central nervous system disorder selected from the group of psychotic disorders; drug induced psychosis; anxiety disorders; movement disorders; mood disorders; neurodegenerative disorders; disorders or conditions comprising as a symptom a deficiency in attention and/or cognition; drug addiction disorders; pain and metabolic disorders. 
     
     
         12 . The method of  claim 11 , wherein the psychotic disorder is selected from the group consisting of schizophrenia, delusional disorder, schizoaffective disorder, schizophreniform disorder and substance-induced psychotic disorder. 
     
     
         13 . (canceled) 
     
     
         14 . A process for preparing a pharmaceutical composition wherein a pharmaceutically acceptable carrier is intimately mixed with a therapeutically effective amount of a compound as defined in  claim 1 . 
     
     
         15 . (canceled)