IP Library Granted Patent US 8,729,274
Granted Patent B2
US 8,729,274 · App. 13/255,630 · Granted May 20, 2014

Tricyclic heterocyclic derivatives

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Quick Facts
Patent No.
US 8,729,274
App. No.
13/255,630
Granted
May 20, 2014
Kind
B2
Abstract

The present invention relates to a tricyclic 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 pharmaceutical compositions comprising said tricyclic heterocyclic derivatives and to their use in therapy, for instance in the treatment or prevention of serotonin mediated disorders, such as obesity.

Claims (33)

1. A tricyclic heterocyclic derivative according to Formula I

wherein

m is 1 and n is 0;

R 1 is H;

R 2 is H, C 3-5 cycloalkyl or C 3-5 cycloalkylC 1-2 alkyl said C 1-4 alkyl, C 3-5 cycloalkyl and C 3-5 cycloalkylC 1-2 alkyl each being optionally substituted with one or more halogens;

R 3 is C 1-4 alkyl, hydroxyC 1-2 alkyl or C 1-2 alkyloxyC 1-2 alkyl said C 1-4 alkyl and C 1-2 alkyloxyC 1-2 alkyl each being optionally substituted with one or more halogens;

L 1 is C═O or CR 4 R 5 ;

L 2 is CR 4′ R 5′ ;

R 4 , R 4′ , R 5 and R 5′ are each independently H, F, C 1-4 alkyl, C 2-4 alkenyl, C 2-4 alkynyl, hydroxy, C 1-4 alkyloxy, C 1-2 alkyloxyC 1-2 alkyl, C 3-5 cycloalkyl or C 3-5 cycloalkylC 1-2 alkyl said C 1-4 alkyl, C 3-5 cycloalkyl and C 3-5 cycloalkylC 1-2 alkyl each being optionally substituted with one or more halogens or

one of R 4 and R 4′ together with one of R 5 and R 5′ along with the atoms to which they are bonded form a 3-6 membered ring optionally comprising a heteroatom selected from O, S and NR 4 ″, wherein R 4 ″ is H, C 1-4 alkyl, COC 1-4 alkyl or SO 2 C 1-4 alkyl;

Y 1 is N or CR 6 ;

Y 2 is N or CR 7 ;

Y 3 is N or CR 8 ;

Y 4 is N or CR 9 with the proviso that no more than two of Y 1 -Y 4 can be N simultaneously;

R 6 is H, C 1-6 alkyl, C 2-6 alkenyl, C 3-7 cycloalkyl, or halogen, said C 1-6 alkyl, and C 2-6 alkenyl being optionally substituted with one or more halogens;

R 7 is H, C 1-6 alkyl, C 3-7 cycloalkyl, C 6-10 arylC 1-2 alkyloxy or halogen, said C 1-6 alkyl, and C 6-10 arylC 1-2 alkyloxy being optionally substituted with one or more halogens;

R 8 is H, C 1-6 alkyl, C 3-7 cycloalkyl, C 6-10 arylC 1-2 alkyloxy or halogen, said C 1-6 alkyl, and C 6-10 arylC 1-2 alkyloxy being optionally substituted with one or more halogens;

R 9 is H, with the proviso that R 6 -R 9 cannot simultaneously be H;

R 10 and R 11 are each independently H or C 1-6 alkyl; and

R 12 is C 1-6 alkyl;

or a pharmaceutically acceptable salt thereof.

2. The tricyclic heterocyclic derivative according to claim 1 , wherein R 2 is H.

3. The tricyclic heterocyclic derivative according to claim 1 , wherein R 3 is methyl, ethyl, fluoromethyl, hydroxymethyl, difluoromethyl or trifluoromethyl.

4. The tricyclic heterocyclic derivative according to claim 1 , wherein L 1 is CH 2 and L 2 is CH 2 .

5. The tricyclic heterocyclic derivative according to claim 1 , wherein Y 1 is CR 6 , Y 2 is CR 7 , Y 3 is CR 8 and Y 4 is CR 9 .

6. The tricyclic heterocyclic derivative according to claim 1 , wherein R 6 is H, F, difluoromethyl, trifluoromethyl, chloro, bromo, cyclopropyl or 2-methylpropyl.

7. The tricyclic heterocyclic derivative according to claim 1 , wherein R 7 is H, methyl, trifluoromethyl, ethyl, propyl, cyclopropyl, 2-methylpropyl, bromo or chloro.

8. The tricyclic heterocyclic derivative according to claim 1 , wherein R 8 is H, methyl, trifluoromethyl, ethyl, or cyclopropyl.

9. A tricyclic heterocyclic derivative selected from:

or a pharmaceutically acceptable salt.

10. A pharmaceutical composition comprising a tricyclic heterocyclic derivative according to claim 1 or a pharmaceutically acceptable salt thereof in admixture with one or more pharmaceutically acceptable excipient.

11. A pharmaceutical composition comprising a tricyclic heterocyclic derivative according to claim 9 or a pharmaceutically acceptable salt thereof in admixture with one or more pharmaceutically acceptable excipient.

12. A method of treating a serotonin mediated disorder, wherein the disorder is selected from the group consisting of obesity, diabetes (type I and type II), diabetic complications, atherosclerosis, impaired glucose tolerance and dyslipidemia, anxiety, depression, obsessive compulsive disorder, panic disorder, psychosis, schizophrenia, sleep disorder, sexual disorder and social phobias; cephalic pain; and migraine and gastrointestinal disorders, the method comprising administering to a patient in need thereof a therapeutically effective amount of a tricyclic heterocyclic derivative according to claim 1 or a pharmaceutically acceptable salt thereof.

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 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 1, 2012
From: DAVIES, KENETH; KIYOI, TAKAO; MISTRY, ASHVINKUMAR DHIRUBHAI; RAY, PETER CHRISTOPHER; REID, MARK; WISHART, GRANT
To: N. V. ORGANON
Reel/Frame 027629/0783 →
MERGER Recorded Dec 1, 2011
From: N.V. ORGANON
To: MSD OSS B.V.
Reel/Frame 027307/0482 →