New Compounds

Abstract

The present invention provides new compounds of formula Ia and Ib: as well as a process for their preparation and new intermediates used therein, pharmaceutical formulations containing said therapeutically active compounds and to the use of said active compounds in therapy.

1 - 41 . (canceled) 
   
   
       42 . A method of prevention and/or treatment of conditions associated with glycogen synthase kinase-3, comprising administering to a mammal, including man in need of such prevention and/or treatment, a therapeutically effective amount of a compound of formula Ia 
     
       
         
         
             
             
         
       
     
     wherein the compound is in the form of a base or a pharmaceutically acceptable salt thereof, and wherein:
 P is a 6-membered ring containing one nitrogen; 
 R 1  is hydrogen; 
 R 2  is C 0-6 alkylcyano; 
 R 3  is C 0-6 alkylNR 4 R 5 ; 
 m is 1; 
 n is 1; 
 R 4  is selected from the group consisting of hydrogen, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 0-6 alkylC 3-6 cycloalkyl, C 0-6 alkylaryl, C 0-6 alkylheteroaryl, C 1-6 alkylNR 14 R 15 , and a 5- or 6-membered heterocyclic group containing one or two heteroatoms independently selected from N, O, and S, wherein the heterocyclic group is optionally substituted by a group Y; 
 R 5  is selected from the group consisting of hydrogen, C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 0-6 alkylC 3-6 cycloalkyl, C 0-6 alkylaryl, C 0-6 alkylheteroaryl, and C 1-6 alkylNR 14 R 15 ; 
 or R 4  and R 5  together with the N to which they are attached may form a 6-membered heterocyclic group containing one nitrogen and one oxygen; and 
 
     wherein any C 1-6 alkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 0-6 alkylC 3-6 cycloalkyl, C 0-6 alkylaryl, and C 0-6 alkylheteroaryl group defined under R 2  to R 5  is optionally substituted by one or more groups Z;
 R 14  and R 15  are independently selected from hydrogen, C 1-6 alkyl, and C 0-6 alkylC 3-6 cycloalkyl, wherein R 14  and R 15  optionally together form a 5- or 6-membered heterocyclic group containing one or more heteroatoms independently selected from N, O, and S, wherein the heterocyclic group is optionally substituted by a group Y; 
 Z is independently selected from the group consisting of oxo, halogen, nitro, CN, OR 16 , C 1-6 alkyl, C 0-6 alkylaryl, C 0-6 alkylC 3-6 cycloalkyl, fluoromethyl, difluoromethyl, trifluoromethyl, fluoromethoxy, difluoromethoxy, trifluoromethoxy, OC 1-6 alkylNR 16 R 17 , NR 16 R 17 , CONR 16 R 17 NR 16 (CO)R 17 , O(CO)C 1-6 alkyl, (CO)OC 1-6 alkyl, COR 16 , (SO 2 )NR 16 R 17 , SO 2 R 16 , SOR 16 , (CO)C 1-6 alkylNR 16 R 17 , (SO 2 )C 1-6 alkylNR 16 R 17 , phenyl, heteroaryl, and a 5- or 6-membered heterocyclic group containing one or two heteroatoms independently selected from N, O, and S, wherein the phenyl, heteroaryl, and heterocyclic groups are optionally substituted by a group Y; 
 Y is selected from the group consisting of oxo, halogen, nitro, CN, OR 16 , C 1-6 alkyl, C 0-6 alkylaryl, C 0-6 alkylC 3-6 cycloalkyl, fluoromethyl, difluoromethyl, trifluoromethyl, fluoromethoxy, difluoromethoxy, trifluoromethoxy, OC 1-6 alkylNR 16 R 17 , NR 16 R 17 , CONR 16 R 17 , NR 16 (CO)R 17 , O(CO)C 1-6 alkyl, (CO)OC 1-6 alkyl, COR 16 , (SO 2 )NR 16 R 17 , SO 2 R 16 , SOR 16 , (CO)C 1-6 alkylNR 16 R 17  (SO 2 )C 1-6 alkylNR 16 R 17 , phenyl, C 0-6 alkylaryl, and heteroaryl, wherein the phenyl, C 0-6 alkylaryl, and heteroaryl groups are optionally substituted with one or more substituents selected from the group consisting of halogen, nitro, CN, OR 16 , C 1-6 alkyl, fluoromethyl, difluoromethyl, trifluoromethyl, fluoromethoxy, difluoromethoxy, and trifluoromethoxy; 
 R 16  and R 17  are independently selected from hydrogen and C 1-6 alkyl, and wherein R 16  and R 17  optionally together form a 5- or 6-membered heterocyclic group containing one or more heteroatoms independently selected from N, O, and S. 
 
   
   
       43 . A method according to  claim 42  wherein in said compound of formula Ia,
 R 5  is C 1-6 ylNR 14 R 15 , and   R 4  is selected from hydrogen, C 1-6 alkyl; or   R 4  and R 5  together with the N to which they are attached form a 6-membered heterocyclic group containing one or more heteroatoms selected independently from N and O, wherein said heterocyclic group may optionally be substituted by a group Y;   
     and wherein R 14  and R 15  may together form a 5-membered heterocyclic group containing one or more heteroatoms, selected independently from N, and O
 Y is selected from C 1-6 alkyl, C 0-6 alkylaryl, NR 16 R 17 , phenyl, wherein the phenyl may be optionally substituted with nitro and trifluoromethyl; 
 
     wherein R 16  and R 17  may together form a 5-membered heterocyclic group containing one N heteroatom, 
     in the form of a base or a pharmaceutically acceptable salt thereof. 
   
   
       44 . A method according to  claim 42  wherein in said compound of formula Ia,
 P is pyridyl; R 2  is CN; R 3  is C 0-6 alkylNR 4 R 5 ; wherein R 4  and R 5  may together form a 5- or 6-membered heterocyclic group containing one or more heteroatoms selected independently from N and O,   in the form of a base or a pharmaceutically acceptable salt thereof.   
   
   
       45 . A method according to  claim 42  wherein in said compound of formula Ia, R 4  and R 5  together form a 6-membered heterocyclic group containing one or more heteroatoms selected independently from N and O,
 in the form of a base or a pharmaceutically acceptable salt thereof.   
   
   
       46 . A method according to  claim 42  wherein in said compound of formula Ia is a compound selected from: 
     2-Hydroxy-3-{5-[(4-methylpiperazin-1-yl)carbonyl]pyridin-2-yl}-1H-indole-5-carbonitrile; 
     2-Hydroxy-3-[6-(2-morpholin-4-ylethoxy)pyrimidin-4-yl]-1H-indole-5-carbonitrile; 
     3-(5-{[3-(Dimethylamino)pyrrolidin-1-yl]methyl}pyridin-2-yl)-2-hydroxy-1H-indole-5-carbonitrile; 
     2-Hydroxy-3-{5-[(4-methylpiperidin-1-yl)methyl]pyridin-2-yl}-1H-indole-5-carbonitrile; 
     3-[5-(Azetidin-1-ylmethyl)pyridin-2-yl]-2-hydroxy-1H-indole-5-carbonitrile; 
     2-Hydroxy-3-[5-(piperidin-1-ylmethyl)pyridin-2-yl]-1H-indole-5-carbonitrile; 
     3-[5-(Morpholin-4-ylcarbonyl)pyridin-2-yl]-5-nitro-1H-indol-2-ol, or 
     2-Hydroxy-3-[5-(morpholin-4-ylsulfonyl)pyridin-2-yl]-1H-indole-5-carbonitrile; 
     or a pharmaceutically acceptable salt thereof. 
   
   
       47 . A method according to  claim 42  wherein in said compound of formula Ia is a compound selected from: 
     2-Hydroxy-3-{4-[(4-methylpiperazin-1-yl)carbonyl]pyridin-2-yl}-1H-indole-5-carbonitrile; 
     2-Hydroxy-3-{5-[(4-methylpiperazin-1-yl)methyl]pyridin-2-yl}-1H-indole-5-carbonitrile; 
     2-Hydroxy-3-{5-[(4-methylpiperazin-1-yl)sulfonyl]pyridin-2-yl}-1H-indole-5-carbonitrile; 
     2-Hydroxy-3-{5-(pyrrolidin-1-ylmethyl)pyridin-2-yl}-1H-indole-5-carbonitrile; 
     2-Hydroxy-3-{5-[(4-methyl-1,4-diazepan-1-yl)methyl]pyridin-2-yl}-1H-indole-5-carbonitrile; 
     2-Hydroxy-3-{5-[(4-pyrrolidin-1-ylpiperidin-1-yl)methyl]pyridin-2-yl}-1H-indole-5-carbonitrile; 
     3-{5-[(4-Methylpiperazin-1-yl)sulfonyl]pyridin-2-yl}-1H-indol-2-ol; 
     6-Chloro-3-{5-[(4-methylpiperazin-1-yl)sulfonyl]pyridin-2-yl}-1H-indol-2-ol; 
     6-Bromo-3-[5-(morpholin-4-ylmethyl)pyridin-2-yl]-1H-indol-2-ol; 
     5-Bromo-3-[5-(morpholin-4-ylmethyl)pyridin-2-yl]-1H-indol-2-ol; 
     3-Fluoro-3-[5-(morpholin-4-ylmethyl)pyridin-2-yl]-2-oxoindoline-6-carbonitrile; 
     3-{5-[(4-Benzylpiperazin-1-yl)sulfonyl]pyridin-2-yl}-2-hydroxy-1H-indole-5-carbonitrile; 
     2-Hydroxy-3-{5-[(4-isopropylpiperazin-1-yl)sulfonyl]pyridin-2-yl}-1H-indole-5-carbonitrile; 
     3-{5-[(4-Ethylpiperazin-1-yl)sulfonyl]pyridin-2-yl}-2-hydroxy-1H-indole-5-carbonitrile; 
     3-[5-(Morpholin-4-ylmethyl)pyridin-2-yl]-5-thien-2-yl-1H-indol-2-ol; 
     5-(2-Furyl)-3-[5-(morpholin-4-ylmethyl)pyridin-2-yl]-1H-indol-2-ol; 
     3-{3-Bromo-5-[(4-methylpiperazin-1-yl)sulfonyl]pyridin-2-yl}-5-nitro-1H-indol-2-ol; 
     3-[5-(Morpholin-4-ylmethyl)pyridin-2-yl]-5-(trifluoromethyl)-1H-indol-2-ol; 
     6-(2-Hydroxy-5-nitro-1H-indol-3-yl)-N-(2-morpholin-4-ylethyl)nicotinamide; 
     6-(2-Hydroxy-5-nitro-1H-indol-3-yl)-N-methyl-N-(1-methylpiperidin-4-yl)nicotinamide; 
     5-Nitro-3-{5-[(4-pyrrolidin-1-ylpiperidin-1-yl)carbonyl]pyridin-2-yl}-1H-indol-2-ol; 
     3-(5-{[3-(Dimethylamino)pyrrolidin-1-yl]carbonyl}pyridin-2-yl)-5-nitro-1H-indol-2-ol; 
     6-(5-Cyano-2-hydroxy-1H-indol-3-yl)-N-methyl-N-(2-pyrrolidin-1-ylethyl)pyridine-3-sulfonamide; 
     3-{5-[(4-Methylpiperazin-1-yl)sulfonyl]pyridin-2-yl}-5-(2-methyl-1,3-thiazol-4-yl)-1H-indol-2-ol; 
     3-[5-(Morpholin-4-ylmethyl)pyridin-2-yl]-5-nitro-1H-indol-2-ol; 
     6-(5-Cyano-2-hydroxy-1H-indol-3-yl)-N-(2-pyrrolidin-1-ylethyl)pyridine-3-sulfonamide; 
     2-Hydroxy-3-[5-(morpholin-4-ylmethyl)pyridin-2-yl]-1H-indole-5-carbonitrile; 
     2-Hydroxy-3-[5-(morpholin-4-ylmethyl)pyridin-2-yl]-1H-indole-6-carbonitrile; 
     5,6-Dibromo-3-[5-(morpholin-4-ylmethyl)pyridin-2-yl]-1H-indol-2-ol, or 
     2-Hydroxy-3-{5-[(4-methylpiperazin-1-yl)sulfonyl]pyridin-2-yl}-1H-indole-6-carbonitrile; 
     or a pharmaceutically acceptable salt thereof. 
   
   
       48 . A method of prevention and/or treatment according to  claims 42  wherein said condition associated with glycogen synthase kinase-3 is selected from: dementia, Alzheimer's Disease, Parkinson's Disease, Frontotemporal dementia Parkinson's Type, Parkinson dementia complex of Guam, HIV dementia, diseases with associated neurofibrillar tangle pathologies and dementia pugilistica. 
   
   
       49 . A method according to  claim 48 , wherein the condition is Alzheimer's Disease. 
   
   
       50 . A method of prevention and/or treatment according to  claim 42  wherein said condition is selected from: amyotrophic lateral sclerosis, corticobasal degeneration, Down syndrome, Huntington's Disease, postencephalitic parkinsonism, progressive supranuclear palsy, Pick's Disease, Niemann-Pick's Disease, stroke, head trauma and other chronic neurodegenerative diseases, Bipolar Disease, affective disorders, depression, schizophrenia or cognitive disorders. 
   
   
       51 . A method of prevention and/or treatment according to  claim 42  wherein said condition is selected from: predemented states, Mild Cognitive Impairment, Age-Associated Memory Impairment, Age-Related Cognitive Decline, Cognitive Impairment No Dementia, mild cognitive decline, mild neurocognitive decline, Late-Life Forgetfulness, memory impairment and cognitive impairment, vascular dementia, dementia with Lewy bodies or Frontotemporal dementia. 
   
   
       52 . A method according to  claim 50  wherein the condition is Bipolar Disease.