IP Library Granted Patent US 7,820,707
Granted Patent B2
US 7,820,707 · App. 11/771,198 · Granted Oct 26, 2010

Heterocyclic derivatives

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Quick Facts
Patent No.
US 7,820,707
App. No.
11/771,198
Granted
Oct 26, 2010
Kind
B2
Abstract

The present invention relates to a heterocyclic derivative according to formula I wherein the variables are defined as in the specification, or to a pharmaceutically acceptable salt or solvate thereof. The present invention also relates to a pharmaceutical composition comprising said heterocyclic derivatives and to their use in therapy, for instance in the treatment or prevention of psychiatric diseases where an enhancement of synaptic responses mediated by AMPA receptors is required, including schizophrenia, depression and Alzheimer's disease.

Claims (39)

1. A heterocyclic derivative according to formula I

wherein

R 1 is C 1-4 alkyl or CN, said C 1-4 alkyl being optionally substituted with 1-3 halogens;

R 2 is C 1-4 alkyl, C 1-4 alkyloxy, or C 1-5 acyl, said C 1-4 alkyl being optionally substituted with a substituent selected from OH, C 1-4 alkyloxy and NR 7 R 8 or R 2 together with R 3 forms a 5 to 7 membered unsaturated carbocyclic ring optionally comprising a N;

R 3 is H or methyl optionally substituted with hydroxy or 1-3 halogens or R 3 together with R 2 forms a 5 to 7 membered unsaturated carbocyclic ring optionally comprising a N;

R 4 is hydroxymethyl, CO 2 H or CONR 9 R 10 ;

R 5 and R 6 are independently H, C 1-4 alkyl or C 3-8 cycloalkyl or R 5 together with R 6 forms a 5 or 6 membered unsaturated carbocyclic ring optionally comprising a heteroatonnic moiety selected from O and NR 11 ;

R 7 and R 8 are independently H, C 1-6 alkyl or C 3-8 cycloalkyl, said C 1-6 alkyl being optionally substituted with hydroxy, C 1-4 alkyloxy or 1-3 halogens; or R 7 and R 8 together with the N to which they are bonded form a 3-6 membered saturated heterocyclic ring;

R 9 is H or C 1-4 alkyl optionally substituted with 1-3 groups selected from hydroxy, C 1-6 alkyloxy, NR 12 R 13 , CONR 14 R 15 and Y, wherein Y is a 5-6 membered heteroaryl comprising 1-2 heteroatoms selected from 0, N and S, or wherein Y is C 3-8 cycloalkyl optionally comprising 1-2 heteroatomic moieties selected from O, S, SO 2 and NR 16 , Y being optionally substituted with 1-2 substituents selected from C 1-4 alkyl, CH 2 OH and CH 2 NR 17 R 18 ;

or R 9 is C 3-8 cycloalkyl comprising a heteroatomic moiety selected from O, S and NR 16 ;

or R 9 and R 10 together with the N to which they are bonded form a 5-6 membered saturated heterocyclic ring optionally comprising a heteroatomic moiety selected from O and NR 16 ;

R 10 is H or methyl with the proviso that when R 9 is methyl R 10 must be C 1-4 alkyl or

R 10 and R 9 together with the N to which they are bonded form a 5-6 membered saturated heterocyclic ring optionally comprising a heteroatomic moiety selected from O and NR 16 ;

R 11 is H or methyl;

R 12 is H or C 1-4 alkyl or R 12 and R 13 together with the N to which they are bonded form a 5-6 membered saturated heterocyclic ring optionally comprising a heteroatomic moiety selected from O, S and NR 19 ;

R 13 is H, C 1-4 alkyl, CO 2 R 20 or SO 2 R 20 or R 13 and R 12 together with the N to which they are bonded form a 5-6 membered saturated heterocyclic ring optionally comprising a heteroatomic moiety selected from O, S and NR 19 ;

R 14 -R 19 are independently H or C 1-4 alkyl;

R 20 is C 1-4 alkyl; and

m is 1-4;

with the proviso that when R 1 is CF 3 , R 2 together with R 3 forms a 6 membered unsaturated carbocyclic ring and R 5 together with R 6 forms a 6 membered unsaturated carbocyclic ring, R 4 cannot be CONH 2 ;

or a pharmaceutically acceptable salt thereof.

2. The heterocyclic derivative according to claim 1 , wherein R 1 is CF 3 .

3. The heterocyclic derivative according to claim 1 , wherein R 2 is methyl optionally substituted with hydroxy or NR 7 R 8 .

4. The heterocyclic derivative according to claim 1 , wherein R 2 together with R 3 forms a 5 to 7 membered unsaturated carbocyclic ring.

5. The heterocyclic derivative according to claim 1 , wherein R 4 is CONR 9 R 10 and wherein R 9 and R 10 have the previously defined meanings.

6. The heterocyclic derivative according to claim 1 , wherein R 5 together with R 6 forms a 5 to 7 membered unsaturated carbocyclic ring optionally comprising an O.

7. The heterocyclic derivative according to claim 1 , wherein m is 1.

8. A heterocyclic derivative selected from

2-[2-(3-Trifluoromethyl-4,5,6,7-tetrahydro-indazol-1-yl)-acetylamino]-4,5,6,7-tetrahydro-benzo[b]thiophene-3-carboxylic acid (3-hydroxy-propyl)-amide;

2-[2-(3-Trifluoromethyl-4,5,6,7-tetrahydro-indazol-1-yl)-acetylamino]-4,5,6,7-tetrahydro-benzo[b]thiophene-3-carboxylic acid (2-methanesulfonylamino-ethyl)-amide;

2-[2-(3-Trifluoromethyl-4,5,6,7-tetrahydro-indazol-1-yl)-acetylamino]-4,5,6,7-tetrahydro-benzo[b]thiophene-3-carboxylic acid azetidin-3-ylamide;

2-(2-(3-(trifluoromethyl)-4,5-dihydro-1H-indazole-1-yl)acetamido-4,5,6,7-tetrahydrothieno[2,3-c]pyran-3-carboxamide;

2-[2-(4-ethylaminomethyl-3-trifluoromethyl-pyrazol-1-yl)-acetylamino]-4,5,6,7-tetrahydro-benzo[b]thiophene-3-carboxamide;

2-(2-(4-hydroxymethyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl)acetamido)-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxamide;

2-{2-[4-(1-Hydroxy-ethyl)-3-trifluoromethyl-pyrazol-1-yl]-acetylamino}-4,5,6,7-tetrahydro-benzo[b]thiophene-3-carboxamide;

2-[2-(3-tert-Butyl-4-dimethylaminomethyl-pyrazol-1-yl)-acetylamino]-4,5,6,7-tetrahydro-benzo[b]thiophene-3-carboxamide and

N-(2-hydroxyethyl)-2-(2-(4-((methylamino)methyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl)acetamido)-4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxamide and a pharmaceutically acceptable salt thereof.

9. A pharmaceutical composition comprising a heterocyclic derivative according to claim 1 or a pharmaceutically acceptable salt thereof in admixture with a pharmaceutically acceptable auxiliary.

10. A pharmaceutical composition comprising a heterocyclic derivative according to claim 8 or a pharmaceutically acceptable salt thereof in admixture with a pharmaceutically acceptable auxiliary.

Assignments (4)
MERGER Recorded Mar 8, 2013
From: ORGANON BIOSCIENCES NEDERLAND B.V.
To: MERCK SHARP & DOHME B.V.
Reel/Frame 029940/0296 →
MERGER Recorded Mar 7, 2013
From: MSD OSS B.V.
To: ORGANON BIOSCIENCES NEDERLAND B.V.
Reel/Frame 029939/0001 →
MERGER Recorded Dec 1, 2011
From: N.V. ORGANON
To: MSD OSS B.V.
Reel/Frame 027307/0482 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 29, 2007
From: GILLEN, KEVIN JAMES; JAMIESON, CRAIG; MOIR, ELIZABETH MARGARET; RANKOVIC, ZORAN; MACLEAN, JOHN KINNAIRD FERGUSON
To: N.V. ORGANON
Reel/Frame 019499/0027 →