IP Library Granted Patent US 8,883,807
Granted Patent B2
US 8,883,807 · App. 13/884,632 · Granted Nov 11, 2014

Piperidinone carboxamide indane CGRP receptor antagonists

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Quick Facts
Patent No.
US 8,883,807
App. No.
13/884,632
Granted
Nov 11, 2014
Kind
B2
Abstract

The present invention is directed to piperidinone carboxamide indane derivatives which are antagonists of CGRP receptors and useful in the treatment or prevention of diseases in which the CGRP is involved, such as migraine. The invention is also directed to pharmaceutical compositions comprising these compounds and the use of these compounds and compositions in the prevention or treatment of such diseases in which CGRP is involved.

Claims (83)

1. A compound of Formula I:

or a pharmaceutically acceptable salt thereof, wherein:

X is selected from —C(R 8 )═or —N═, wherein R 8 is hydrogen, F or CN;

R 1 is selected from the group consisting of: C 1-4 alkyl, cyclopropylmethyl, cyclobutylmethyl and [1-(trifluoromethyl)cyclopropyl]methyl, each of which is optionally substituted with one or more substituents as allowed by valence independently selected from the group consisting of: F and hydroxy;

R 2 is selected from hydrogen and methyl;

when R 2 is hydrogen then

R 3 is selected from hydrogen, F or Cl;

R 4 is selected from hydrogen, F or Cl;

R 5 is hydrogen;

R 6 is selected from hydrogen or F; and

R 7 is selected from hydrogen, F or Cl;

except that at least two of R 3 , R 4 , R 6 and R 7 must be F or Cl unless R 3 is F in which case R 4 , R 6 and R 7 may all be hydrogen; and if R 4 is Cl then R 7 cannot be Cl;

when R 2 is methyl then

R 3 is selected from hydrogen, methyl, F, Cl, or Br;

R 4 is selected from hydrogen, methyl, F or Cl;

R 5 is selected from hydrogen or F;

R 6 is selected from hydrogen or F; and

R 7 is selected from hydrogen, methyl, F or Cl;

except that if R 5 is F then at least three of R 3 , R 4 , R 6 and R 7 must be F; and if R 4 is methyl or Cl then R 7 cannot be methyl or Cl.

2. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein X is —N═.

3. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein X is —CH═.

4. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein X is —C(CN)═.

5. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein R 1 is C 1-4 alkyl, optionally substituted with 1 to 3 F or hydroxy, or both.

6. The compound of claim 5 , or a pharmaceutically acceptable salt thereof, wherein R 1 is selected from the group consisting of: isopropyl, 2,2,2-trifluoroethyl and 2-methylpropyl.

7. The compound of claim 6 , or a pharmaceutically acceptable salt thereof, wherein R 1 is 2,2,2-trifluoroethyl.

8. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein R 2 is hydrogen.

9. The compound of claim 8 , or a pharmaceutically acceptable salt thereof, wherein at least two of R 3 , R 4 , R 6 and R 7 are F or Cl, except that if R 4 is Cl then R 7 cannot be Cl.

10. The compound of claim 8 , or a pharmaceutically acceptable salt thereof, wherein R 3 is F and R 4 , R 6 and R 7 are hydrogen.

11. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein R 2 is methyl.

12. The compound of claim 11 , or a pharmaceutically acceptable salt thereof, wherein R 5 is F and at least three of R 3 , R 4 , R 6 and R 7 are F.

13. The compound of claim 11 , or a pharmaceutically acceptable salt thereof, wherein R 5 is hydrogen and if R 4 is methyl or Cl then R 7 cannot be methyl or Cl.

14. The compound according to claim 11 , or a pharmaceutically acceptable salt thereof, wherein R 3 is selected from hydrogen, F or Cl; R 4 is selected from hydrogen, F or Cl; R 5 is hydrogen; R 6 is selected from hydrogen or F; and R 7 is selected from hydrogen, F or Cl; except that if R 4 is Cl then R 7 cannot be Cl.

15. A compound of claim 1 , which is selected from the following:

R 2

Ar

H

3,5-difluorophenyl

H

2,3-difluorophenyl

H

2,5-difluorophenyl

H

2,3,5-trifluorophenyl

H

2-chloro-6-fluorophenyl

H

2,6-dichlorophenyl

H

2,3,6-trifluorophenyl

Me

2,3,5,6-tetrafluorophenyl

Me

2,3,6-trifluorophenyl

H

2-fluorophenyl

R 1

Ar

2-methylpropyl

2,3-difluorophenyl

isopropyl

2,3-difluorophenyl

R 2

Ar

Me

phenyl

Me

2,3,5-trifluorophenyl

Me

2,3,6-trifluorophenyl

R 2

Ar

Me

phenyl

Me

2,3,5,6-tetrafluorophenyl

Me

2,3,6-trifluorophenyl

Me

2,3,5-trifluorophenyl

or a pharmaceutically acceptable salt thereof.

16. A pharmaceutical composition which comprises an inert carrier and the compound of claims 1 , or a pharmaceutically acceptable salt thereof.

17. A method of treating headache in a mammalian patient in need of such treatment, which comprises administering to the patient a therapeutically effective amount of the compound of claim 1 , or a pharmaceutically acceptable salt thereof.

18. The method of claim 17 , wherein the headache is migraine headache.

Assignments (2)
MERGER Recorded Aug 8, 2022
From: MERCK SHARP & DOHME CORP.
To: MERCK SHARP & DOHME LLC
Reel/Frame 061102/0145 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 23, 2013
From: BELL, IAN M.; FRALEY, MARK E.; GALLICCHIO, STEVEN N.; GINNETTI, ANTHONY; MITCHELL, HELEN J.; PAONE, DANIEL V.; STAAS, DONNETTE D.; WANG, CHENG; ZARTMAN, C. BLAIR; STEVENSON, HEATHER E.
To: MERCK, SHARP & DOHME, CORP.
Reel/Frame 030852/0676 →