IP Library Granted Patent US 9,388,197
Granted Patent B2
US 9,388,197 · App. 14/762,692 · Granted Jul 12, 2016

Heterocyclic amide derivatives as P2X7 receptor antagonists

Inventors: Kurt Hilpert (Allschwil, CH); Francis Hubler (Allschwil, CH); Dorte Renneberg (Allschwil, CH); Simon Stamm (Allschwil, CH)
Assignee: ACTELION PHARMACEUTICALS LTD.
C07D513/04C07D277/60C07D277/64C07D277/66C07D277/68C07D277/82
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,388,197
App. No.
14/762,692
Granted
Jul 12, 2016
Kind
B2
Abstract

The invention relates to heterocyclic amide derivatives of formula (I), wherein R 1 , R 2 , R 3 , R 4 , R 5 , n, m, p and X are as defined in the description, their preparation and their use as pharmaceutically active compounds.

Claims (137)

1. A compound of the formula (I),

wherein

n represents 1, 2 or 3;

m represents 0, 1 or 2;

p represents 0, 1 or 2;

X represents —O— or —CH 2 —;

R 1 represents hydrogen, (C 1 -C 2 )alkyl or hydroxy-(C 1 -C 2 )alkyl and R 2 represents hydrogen or halogen; or R 1 and R 2 together represent a —CH 2 CH 2 — or a —CH 2 CH 2 CH 2 — group;

each R 3 independently represents (C 1 -C 4 )alkyl, (C 3 -C 6 )cycloalkyl, (C 1 -C 4 )alkoxy, hydroxy-(C 1 -C 3 )alkyl, hydroxy-(C 2 -C 3 )alkoxy, hydroxy-(C 2 -C 3 )alkoxy-(C 1 -C 2 )alkyl, (C 1 -C 2 )alkoxy-(C 1 -C 2 )alkyl, (C 1 -C 3 )fluoroalkyl, (C 1 -C 3 )fluoroalkoxy, cyano, halogen or phenoxy;

R 4 represents hydrogen, (C 1 -C 4 )alkyl, (C 1 -C 3 )fluoroalkyl, amino, halogen or phenyl; and

R 5 represents hydrogen or methyl;

or a salt of such a compound.

2. The compound of formula (I) according to claim 1 , that is a compound of formula (Ixo),

wherein

n represents 1, 2 or 3;

m represents 0, 1 or 2;

p represents 1 or 2;

R 1 represents hydrogen, (C 1 -C 2 )alkyl or hydroxy-(C 1 -C 2 )alkyl and R 2 represents hydrogen or halogen; or R 1 and R 2 together represent a —CH 2 CH 2 — or a —CH 2 CH 2 CH 2 — group;

each R 3 independently represents (C 1 -C 4 )alkyl, (C 3 -C 6 )cycloalkyl, (C 1 -C 4 )alkoxy, hydroxy-(C 1 -C 3 )alkyl, hydroxy-(C 2 -C 3 )alkoxy, hydroxy-(C 2 -C 3 )alkoxy-(C 1 -C 2 )alkyl, (C 1 -C 2 )alkoxy-(C 1 -C 2 )alkyl, (C 1 -C 3 )fluoroalkyl, (C 1 -C 3 )fluoroalkoxy, cyano, halogen or phenoxy; and

R 5 represents hydrogen or methyl;

or a salt of such a compound.

3. The compound of formula (I) according to claim 1 , wherein

m represents 0;

or a salt of such a compound.

4. The compound of formula (I) according to claim 1 , wherein

p represents 2;

or a salt of such a compound.

5. The compound of formula (I) according to claim 1 , wherein

R 1 represents hydrogen and R 2 represents chloro;

or a salt of such a compound.

6. The compound of formula (I) according to claim 1 , wherein

R 1 and R 2 together represent a —CH 2 CH 2 — group;

or a salt of such a compound.

7. The compound of formula (I) according to claim 1 , wherein

a first R 3 group is attached in para-position relative to the R 1 -bearing carbon atom and represents chloro; and

a second R 3 group is absent, or is attached in ortho-position relative to the R 1 -bearing carbon atom and represents methyl, cyclopropyl, methoxy, hydroxy-methyl, 2-hydroxy-ethoxy, (2-hydroxy-ethoxy)-methyl, methoxy-methyl, chloro or bromo;

or a salt of such a compound.

8. The compound of formula (I) according to claim 1 , wherein

R 4 represents hydrogen;

or a salt of such a compound.

9. The compound of formula (I) according to claim 1 , wherein

R 5 represents hydrogen;

or a salt of such a compound.

10. The compound of formula (I) according to claim 1 , selected from the group consisting of:

N-(4-chlorobenzyl)-5,6-dihydrofuro[2,3-d]thiazole-6-carboxamide;

N-(2,4-dichlorobenzyl)-5,6-dihydrofuro[2,3-d]thiazole-6-carboxamide;

N-(2-chloro-4-fluorobenzyl)-5,6-dihydrofuro[2,3-d]thiazole-6-carboxamide;

N-(3,4-dichlorobenzyl)-5,6-dihydrofuro[2,3-d]thiazole-6-carboxamide;

N-(2-bromo-4,6-dichlorobenzyl)-5,6-dihydrofuro[2,3-d]thiazole-6-carboxamide;

N-(2,4-dichloro-6-methylbenzyl)-5,6-dihydrofuro[2,3-d]thiazole-6-carboxamide;

N-(2,4-dichlorophenethyl)-5,6-dihydrofuro[2,3-d]thiazole-6-carboxamide;

N-(3-(2,4-dichlorophenyl)propyl)-5,6-dihydrofuro[2,3-d]thiazole-6-carboxamide;

N-(1-(2,4-dichlorophenyl)-2-hydroxyethyl)-5,6-dihydrofuro[2,3-d]thiazole-6-carboxamide;

N-(2,4-dichloro-6-(hydroxymethyl)benzyl)-5,6-dihydrofuro[2,3-d]thiazole-6-carboxamide;

N-(5,7-dichloro-2,3-dihydro-1H-inden-1-yl)-5,6-dihydrofuro[2,3-d]thiazole-6-carboxamide;

N-(2,4-dichloro-6-cyclopropylbenzyl)-5,6-dihydrofuro[2,3-d]thiazole-6-carboxamide;

N-(2-chloro-3-(trifluoromethyl)benzyl)-5,6-dihydrofuro[2,3-d]thiazole-6-carboxamide;

N-(3-chloro-2-(trifluoromethyl)benzyl)-5,6-dihydrofuro[2,3-d]thiazole-6-carboxamide;

N-(2,4-dichloro-6-((2-hydroxyethoxy)methyl)benzyl)-5,6-dihydrofuro[2,3-d]thiazole-6-carboxamide;

N-(4-phenoxybenzyl)-5,6-dihydrofuro[2,3-d]thiazole-6-carboxamide;

N-(2,4-dichlorobenzyl)-5,6-dihydro-4H-cyclopenta[d]thiazole-6-carboxamide;

N-(2-chloro-4-fluorobenzyl)-5,6-dihydro-4H-cyclopenta[d]thiazole-6-carboxamide;

N-(2-bromo-4,6-dichlorobenzyl)-5,6-dihydro-4H-cyclopenta[d]thiazole-6-carboxamide;

N-(2,4-dichloro-6-methylbenzyl)-5,6-dihydro-4H-cyclopenta[d]thiazole-6-carboxamide;

N-(2,4-dichlorophenethyl)-5,6-dihydro-4H-cyclopenta[d]thiazole-6-carboxamide;

N-(2-chloro-3-cyanobenzyl)-5,6-dihydro-4H-cyclopenta[d]thiazole-6-carboxamide;

N-(3-(2,4-dichlorophenyl)propyl)-5,6-dihydro-4H-cyclopenta[d]thiazole-6-carboxamide;

N-(1-(2,4-dichlorophenyl)-2-hydroxyethyl)-5,6-dihydro-4H-cyclopenta[d]thiazole-6-carboxamide;

N-(2,4-dichloro-6-(hydroxymethyl)benzyl)-5,6-dihydro-4H-cyclopenta[d]thiazole-6-carboxamide;

N-(2,4-dichloro-6-methoxybenzyl)-5,6-dihydro-4H-cyclopenta[d]thiazole-6-carboxamide;

N-(5,7-dichloro-2,3-dihydro-1H-inden-1-yl)-5,6-dihydro-4H-cyclopenta[d]thiazole-6-carboxamide;

N-(2-chloro-3-(trifluoromethyl)benzyl)-5,6-dihydro-4H-cyclopenta[d]thiazole-6-carboxamide;

N-(3-fluoro-4-(trifluoromethoxy)benzyl)-5,6-dihydro-4H-cyclopenta[d]thiazole-6-carboxamide;

N-(4-chlorobenzyl)-N-methyl-6,7-dihydro-5H-pyrano[2,3-d]thiazole-7-carboxamide;

N-(2,4-dichlorobenzyl)-6,7-dihydro-5H-pyrano[2,3-d]thiazole-7-carboxamide;

N-(2-chloro-4-fluorobenzyl)-6,7-dihydro-5H-pyrano[2,3-d]thiazole-7-carboxamide;

N-(2,3-dichlorobenzyl)-6,7-dihydro-5H-pyrano[2,3-d]thiazole-7-carboxamide;

N-(2,4-dichloro-6-methylbenzyl)-6,7-dihydro-5H-pyrano[2,3-d]thiazole-7-carboxamide;

N-(2,4-dichlorophenethyl)-6,7-dihydro-5H-pyrano[2,3-d]thiazole-7-carboxamide;

N-(2-chloro-3-cyanobenzyl)-6,7-dihydro-5H-pyrano[2,3-d]thiazole-7-carboxamide;

N-(4-(trifluoromethyl)benzyl)-6,7-dihydro-5H-pyrano[2,3-d]thiazole-7-carboxamide;

N-(3-(2,4-dichlorophenyl)propyl)-6,7-dihydro-5H-pyrano[2,3-d]thiazole-7-carboxamide;

N-((S)-1-(2,4-dichlorophenyl)-2-hydroxyethyl)-6,7-dihydro-5H-pyrano[2,3-d]thiazole-7-carboxamide;

N-(2,4-dichloro-6-(hydroxymethyl)benzyl)-6,7-dihydro-5H-pyrano[2,3-d]thiazole-7-carboxamide;

N-((S)-5,7-dichloro-2,3-dihydro-1H-inden-1-yl)-6,7-dihydro-5H-pyrano[2,3-d]thiazole-7-carboxamide;

N-(2-chloro-3-(trifluoromethyl)benzyl)-6,7-dihydro-5H-pyrano[2,3-d]thiazole-7-carboxamide;

N-(2,4-dichloro-6-(2-hydroxyethoxy)benzyl)-6,7-dihydro-5H-pyrano[2,3-d]thiazole-7-carboxamide;

N-(3-fluoro-4-(trifluoromethoxy)benzyl)-6,7-dihydro-5H-pyrano[2,3-d]thiazole-7-carboxamide;

N-(4-phenoxybenzyl)-6,7-dihydro-5H-pyrano[2,3-d]thiazole-7-carboxamide;

N-(4-chlorobenzyl)-4,5,6,7-tetrahydrobenzo[d]thiazole-7-carboxamide;

N-(4-chlorobenzyl)-N-methyl-4,5,6,7-tetrahydrobenzo[d]thiazole-7-carboxamide;

N-(3-chloro-2-methylbenzyl)-4,5,6,7-tetrahydrobenzo[d]thiazole-7-carboxamide;

2-amino-N-(2,4-dichlorobenzyl)-4,5,6,7-tetrahydrobenzo[d]thiazole-7-carboxamide;

N-(2,4-dichlorobenzyl)-2-methyl-4,5,6,7-tetrahydrobenzo[d]thiazole-7-carboxamide;

2-bromo-N-(2,4-dichlorobenzyl)-4,5,6,7-tetrahydrobenzo[d]thiazole-7-carboxamide;

N-(2,4-dichlorobenzyl)-4,5,6,7-tetrahydrobenzo[d]thiazole-7-carboxamide;

N-(2-chloro-4-fluorobenzyl)-4,5,6,7-tetrahydrobenzo[d]thiazole-7-carboxamide;

N-(2,3-dichlorobenzyl)-4,5,6,7-tetrahydrobenzo[d]thiazole-7-carboxamide;

N-(2,3-dihydro-1H-inden-1-yl)-4,5,6,7-tetrahydrobenzo[d]thiazole-7-carboxamide;

N-((R)-1-(2,4-dichlorophenyl)ethyl)-4,5,6,7-tetrahydrobenzo[d]thiazole-7-carboxamide;

N-(2,4-dichloro-6-methylbenzyl)-2-phenyl-4,5,6,7-tetrahydrobenzo[d]thiazole-7-carboxamide;

N-(2,4-dichloro-6-methylbenzyl)-2-(trifluoromethyl)-4,5,6,7-tetrahydrobenzo[d]thiazole-7-carboxamide;

2-amino-N-(2,4-dichloro-6-methylbenzyl)-4,5,6,7-tetrahydrobenzo[d]thiazole-7-carboxamide;

N-(2,4-dichloro-6-methylbenzyl)-2-methyl-4,5,6,7-tetrahydrobenzo[d]thiazole-7-carboxamide;

2-bromo-N-(2,4-dichloro-6-methylbenzyl)-4,5,6,7-tetrahydrobenzo[d]thiazole-7-carboxamide;

N-(2,4-dichloro-6-methylbenzyl)-4,5,6,7-tetrahydrobenzo[d]thiazole-7-carboxamide;

N-(2,4-dichlorophenethyl)-4,5,6,7-tetrahydrobenzo[d]thiazole-7-carboxamide;

N-((S)-1-(2,4-dichlorophenyl)-2-hydroxyethyl)-4,5,6,7-tetrahydrobenzo[d]thiazole-7-carboxamide;

N-(2,4-dichloro-6-(hydroxymethyl)benzyl)-4,5,6,7-tetrahydrobenzo[d]thiazole-7-carboxamide;

2-bromo-N-(2-chloro-3-(trifluoromethyl)benzyl)-4,5,6,7-tetrahydrobenzo[d]thiazole-7-carboxamide;

N-(2-chloro-3-(trifluoromethyl)benzyl)-4,5,6,7-tetrahydrobenzo[d]thiazole-7-carboxamide;

N-(2,4-dichloro-6-(methoxymethyl)benzyl)-4,5,6,7-tetrahydrobenzo[d]thiazole-7-carboxamide;

N-(3-fluoro-4-(trifluoromethoxy)benzyl)-4,5,6,7-tetrahydrobenzo[d]thiazole-7-carboxamide;

N-(4-phenoxybenzyl)-4,5,6,7-tetrahydrobenzo[d]thiazole-7-carboxamide;

2-amino-N-(2,4-dichlorobenzyl)-5,6,7,8-tetrahydro-4H-cyclohepta[d]thiazole-8-carboxamide;

N-(2,4-dichlorobenzyl)-5,6,7,8-tetrahydro-4H-cyclohepta[d]thiazole-8-carboxamide;

2-amino-N-(2,4-dichloro-6-methylbenzyl)-5,6,7,8-tetrahydro-4H-cyclohepta[d]thiazole-8-carboxamide;

N-(2,4-dichloro-6-methylbenzyl)-5,6,7,8-tetrahydro-4H-cyclohepta[d]thiazole-8-carboxamide;

(R)—N—((S)-1-(2,4-dichlorophenyl)-2-hydroxyethyl)-5,6,7,8-tetrahydro-4H-cyclohepta[d]thiazole-8-carboxamide; and

(S)—N—((S)-1-(2,4-dichlorophenyl)-2-hydroxyethyl)-5,6,7,8-tetrahydro-4H-cyclohepta[d]thiazole-8-carboxamide;

or a salt of such a compound.

11. A pharmaceutical composition containing, as active principle the compound of formula (I) according to claim 1 , or a pharmaceutically acceptable salt thereof, and at least one therapeutically inert excipient.

12. A pharmaceutical composition containing, as active principle, a compound of formula (I) according to claim 10 , or a pharmaceutically acceptable salt thereof, and at least one therapeutically inert excipient.

13. A method for the treatment of a disease selected from spinal cord injury, stroke, Alzheimer's disease, epilepsy, amyotrophic lateral sclerosis, pain, rheumatoid arthritis, asthma, chronic obstructive pulmonary disease, lung emphysema, glomerulonephritis, irritable bowel syndrome, psoriasis, atopic dermatitis, Crohn's disease, ulcerative colitis, diabetes mellitus, osteoporosis, and ischemic heart disease, comprising administering to a subject a pharmaceutically active amount of a compound according to claim 1 , or a pharmaceutically acceptable salt thereof.

14. A method for the treatment of a disease selected from spinal cord injury, stroke, Alzheimer's disease, epilepsy, amyotrophic lateral sclerosis, pain, rheumatoid arthritis, asthma, chronic obstructive pulmonary disease, lung emphysema, glomerulonephritis, irritable bowel syndrome, psoriasis, atopic dermatitis, Crohn's disease, ulcerative colitis, diabetes mellitus, osteoporosis, and ischemic heart disease, comprising administering to a subject a pharmaceutically active amount of a compound according to claim 10 , or a pharmaceutically acceptable salt thereof.

15. The compound of formula (I) according to claim 2 , wherein

m represents 0;

or a salt of such a compound.

16. The compound of formula (I) according to claim 15 , wherein

R 1 represents hydrogen and R 2 represents chloro;

or a salt of such a compound.

17. The compound of formula (I) according to claim 15 , wherein

R 1 and R 2 together represent a —CH 2 CH 2 — group;

or a salt of such a compound.

18. The compound of formula (I) according to claim 15 , wherein

R 5 represents hydrogen;

or a salt of such a compound.

19. The method of claim 13 , wherein the disease is selected from spinal cord injury, Alzheimer's disease, amyotrophic lateral sclerosis, pain, rheumatoid arthritis, asthma, chronic obstructive pulmonary disease, lung emphysema, glomerulonephritis, irritable bowel syndrome, psoriasis, atopic dermatitis, Crohn's disease, ulcerative colitis, diabetes mellitus, and osteoporosis.

Assignments (4)
CORRECTIVE ASSIGNMENT TO CORRECT THE ASSIGNEE ADDRESS PREVIOUSLY RECORDED AT REEL: 042464 FRAME: 0407. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Jun 28, 2017
From: ACTELION PHARMACEUTICALS LTD
To: IDORSIA PHARMACEUTICALS LTD
Reel/Frame 043017/0022 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 13, 2017
From: ACTELION PHARMACEUTICALS LTD
To: IDORSIA PHARMACEUTICALS LTD
Reel/Frame 042464/0407 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 29, 2015
From: HILPERT, KURT; HUBLER, FRANCIS; RENNEBERG, DORTE; STAMM, SIMON
To: ACTELION PHARMACEUTICALS LTD.
Reel/Frame 036677/0808 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 22, 2015
From: HILPERT, KURT; HUBLER, FRANCIS; RENNEBERG, DORTE; STAMM, SIMON
To: ACTELION PHARMACEUTICALS LTD.
Reel/Frame 036155/0712 →
Priority Claims (1)
EP 13152217 · Jan 22, 2013 · regional
Continuity (1)
Related Publication 20150361096A1 · Dec 17, 2015