IP Library Granted Patent US 10,385,057
Granted Patent B2
US 10,385,057 · App. 15/777,199 · Granted Aug 20, 2019

Pyrazole compounds and methods of making and using same

Inventors: Cheryl A. Grice (Encinitas, CA); Todd K. Jones (Solana Beach, CA); Katharine K. Duncan (San Diego, CA); Olivia D. Weber (San Diego, CA); Justin S. Cisar (San Diego, CA); Jeffrey E. Merit (San Diego, CA)
Assignee: LUNDBECK LA JOLLA RESEARCH CENTER, INC.
C07D487/04C07D401/14C07D403/06C07D403/14C07D417/14C07D487/10C07D519/00
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Quick Facts
Patent No.
US 10,385,057
App. No.
15/777,199
Granted
Aug 20, 2019
Kind
B2
Abstract

Provided herein are pyrazole compounds and pharmaceutical compositions comprising said compounds. The subject compounds and compositions are useful as modulators of MAGL and/or FAAH. Furthermore, the subject compounds and compositions are useful for the treatment of, for example, pain.

Claims (60)

1. A compound of Formula (I):

wherein:

R 1 is H, —CF 3 , C 1-6 alkyl, —CN, halogen, optionally substituted phenyl, —CO 2 R 11 , or —C(O)NR 12 R 13 ;

R 2 is H or optionally substituted phenyl;

R 3 is H, halogen, —OR 6 , C 1-6 alkyl, C 1-6 haloalkyl, optionally substituted heterocycloalkyl, optionally substituted C 1-6 alkyl-heterocycloalkyl, optionally substituted phenyl, or optionally substituted heteroaryl;

R 4 is H, halogen, C 1-6 alkyl, C 1-6 haloalkyl, or phenyl; or

R 3 and R 4 are combined to form a heterocycloalkyl ring;

R 5 is H, halogen or C 1-6 alkyl;

R 6 is H, C 1-6 alkyl, optionally substituted phenyl, optionally substituted C 1-6 alkyl-phenyl, optionally substituted heteroaryl, optionally substituted heterocycloalkyl, or —C 1-6 alkylC(O)NR 9 R 10 ;

R 9 and R 10 are each independently H, or C 1-6 alkyl; or R 9 and R 10 together with the nitrogen to which they are attached are combined to form a heterocycloalkyl ring;

R 11 is H or C 1-6 alkyl; and

R 12 and R 13 are each independently H, C 1-6 alkyl, or C 3-8 cycloalkyl; or R 12 and R 13 together with the nitrogen to which they are attached are combined to form a 4-, 5-, 6-, 7-, or 8-member heterocycloalkyl ring, optionally substituted with C 1-6 alkyl or C 3-8 cycloalkyl;

or a solvate, hydrate, tautomer, N-oxide, or pharmaceutically acceptable salt thereof.

2. A compound of Formula (II):

wherein:

R 1 is H, —CF 3 , C 1-6 alkyl, cyano, halogen, optionally substituted phenyl, —CO 2 R 11 , or —C(O)NR 12 R 13 ;

R 2 is H or optionally substituted phenyl;

R 3 is H, halogen, —OR 6 , C 1-6 alkyl, C 1-6 haloalkyl, optionally substituted heterocycloalkyl, optionally substituted C 1-6 alkyl-heterocycloalkyl, optionally substituted phenyl, or optionally substituted heteroaryl;

R 4 is H, halogen, C 1-6 alkyl, C 1-6 haloalkyl, or phenyl; or

R 3 and R 4 are combined to form a heterocycloalkyl ring;

R 5 is H, halogen or C 1-6 alkyl;

R 6 is H, C 1-6 alkyl, optionally substituted phenyl, optionally substituted C 1-6 alkyl-phenyl, optionally substituted heteroaryl, optionally substituted heterocycloalkyl, or —C 1-6 alkylC(O)NR 9 R 10 ;

R 9 and R 10 are each independently H, or C 1-6 alkyl; or R 9 and R 10 together with the nitrogen to which they are attached are combined to form a heterocycloalkyl ring;

R 1 is H or C 1-6 alkyl;

R 12 and R 13 are each independently H, C 1-6 alkyl, or C 3-8 cycloalkyl; or R 12 and R 13 together with the nitrogen to which they are attached are combined to form a 4-, 5-, 6-, 7-, or 8-member heterocycloalkyl ring, optionally substituted with C 1-6 alkyl or C 3-8 cycloalkyl, and optionally containing another heteroatom selected from N, S or O;

R 14 is H or C 1-6 alkyl; and

R 15 is H or C 1-6 alkyl;

or a solvate, hydrate, tautomer, N-oxide, stereoisomer, or pharmaceutically acceptable salt thereof.

3. A compound of Formula (III):

wherein:

R 1 is H, —CF 3 , C 1-6 alkyl, cyano, halogen, optionally substituted phenyl, —CO 2 R 11 , or —C(O)NR 12 R 13 ;

R 2 is H or optionally substituted phenyl;

R 3 is H, halogen, —OR 6 , C 1-6 alkyl, C 1-6 haloalkyl, optionally substituted heterocycloalkyl, optionally substituted C 1-6 alkyl-heterocycloalkyl, optionally substituted phenyl, or optionally substituted heteroaryl;

R 4 is H, halogen, C 1-6 alkyl, C 1-6 haloalkyl, or phenyl; or

R 3 and R 4 are combined to form a heterocycloalkyl ring;

R 5 is H, halogen or C 1-6 alkyl;

R 6 is H, C 1-6 alkyl, optionally substituted phenyl, optionally substituted C 1-6 alkyl-phenyl, optionally substituted heteroaryl, optionally substituted heterocycloalkyl, or —C 1-6 alkylC(O)NR 9 R 10 ;

R 9 and R 10 are each independently H, or C 1-6 alkyl; or R 9 and R 10 together with the nitrogen to which they are attached are combined to form a heterocycloalkyl ring;

R 11 is H or C 1-6 alkyl;

R 12 and R 13 are each independently H, C 1-6 alkyl, or C 3-8 cycloalkyl; or R 12 and R 13 together with the nitrogen to which they are attached are combined to form a 4-, 5-, 6-, 7-, or 8-member heterocycloalkyl ring, optionally substituted with C 1-6 alkyl or C 3-8 cycloalkyl, and optionally containing another heteroatom selected from N, S or O; and

R 16 is H, C 1-6 alkyl, or —C(O)C 1-6 alkyl;

or a solvate, hydrate, tautomer, N-oxide, stereoisomer, or pharmaceutically acceptable salt thereof.

4. The compound of claim 3 , or a solvate, hydrate, tautomer, N-oxide, or pharmaceutically acceptable salt thereof, wherein R 3 is optionally substituted heterocycloalkyl.

5. The compound of claim 4 , or a solvate, hydrate, tautomer, N-oxide, or pharmaceutically acceptable salt thereof, wherein R 3 is

6. The compound of claim 3 , or a solvate, hydrate, tautomer, N-oxide, or pharmaceutically acceptable salt thereof, wherein R 3 is optionally substituted heteroaryl and the heteroaryl is a 5-6 membered heteroaryl ring.

7. The compound of claim 6 , or a solvate, hydrate, tautomer, N-oxide, or pharmaceutically acceptable salt thereof, wherein R 3 is

8. The compound of claim 3 , or a solvate, hydrate, tautomer, N-oxide, or pharmaceutically acceptable salt thereof, wherein R 3 is halogen.

9. The compound of claim 3 , or a solvate, hydrate, tautomer, N-oxide, or pharmaceutically acceptable salt thereof, wherein R 3 is C 1-6 haloalkyl.

10. The compound of claim 3 , or a solvate, hydrate, tautomer, N-oxide, or pharmaceutically acceptable salt thereof, wherein R 4 is halogen.

11. The compound of claim 3 , or a solvate, hydrate, tautomer, N-oxide, or pharmaceutically acceptable salt thereof, wherein R 4 is C 1-6 haloalkyl.

12. The compound of claim 3 , or a solvate, hydrate, tautomer, N-oxide, or pharmaceutically acceptable salt thereof, wherein R 5 is H and R 2 is H.

13. The compound of claim 3 , or a solvate, hydrate, tautomer, N-oxide, or pharmaceutically acceptable salt thereof, wherein R 1 is halogen.

14. The compound of claim 3 , or a solvate, hydrate, tautomer, N-oxide, or pharmaceutically acceptable salt thereof, wherein R 1 is —C(O)NR 12 R 13 .

15. The compound of claim 14 , or a solvate, hydrate, tautomer, N-oxide, or pharmaceutically acceptable salt thereof, wherein R 12 and R 13 are each H.

16. The compound of claim 14 , or a solvate, hydrate, tautomer, N-oxide, or pharmaceutically acceptable salt thereof, wherein R 12 and R 13 together with the nitrogen to which they are attached are combined to form a 5- or 6-member heterocycloalkyl ring, optionally substituted with C 1-6 alkyl or C 3-8 cycloalkyl.

17. The compound of claim 16 , or a solvate, hydrate, tautomer, N-oxide, or pharmaceutically acceptable salt thereof, wherein R 12 and R 13 together with the nitrogen to which they are attached are combined to form an unsubstituted pyrrolidine, unsubstituted piperidine, or unsubstituted morpholine ring.

18. A compound selected from:

or a solvate, hydrate, tautomer, N-oxide, or pharmaceutically acceptable salt thereof.

19. A pharmaceutical composition comprising a compound of claim 3 , or a solvate, hydrate, tautomer, N-oxide, or a pharmaceutically acceptable salt thereof, and at least one pharmaceutically acceptable excipient.

20. A method of treating a disease or disorder in a patient comprising administering to the patient in need thereof a therapeutically effective amount of a compound of claim 3 , or a pharmaceutically acceptable salt or solvate thereof, wherein the disease or disorder is selected from epilepsy/seizure disorder, neuromyelitis optica (NMO), Tourette syndrome, persistent motor tic disorder, persistent vocal tic disorder, abdominal pain associated with irritable bowel syndrome, multiple sclerosis, Alzheimer's disease, inflammatory bowel disease, neuropathic pain, and inflammatory pain.

Assignments (4)
CORRECTIVE ASSIGNMENT TO CORRECT THE THE RECEIVING PARTY NAME PREVIOUSLY RECORDED AT REEL: 055679 FRAME: 0885. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Jun 11, 2021
From: LUNDBECK LA JOLLA RESEARCH CENTER, INC.
To: H. LUNDBECK A/S
Reel/Frame 056544/0697 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 23, 2021
From: LUNDBECK LA JOLLA RESEARCH CENTER, INC.
To: H. LUNDBECK A/S.
Reel/Frame 055679/0885 →
CHANGE OF NAME Recorded Jun 21, 2019
From: ABIDE THERAPEUTICS, INC.
To: LUNDBECK LA JOLLA RESEARCH CENTER, INC.
Reel/Frame 049554/0642 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 4, 2018
From: GRICE, CHERYL A.; JONES, TODD K.; WEBER, OLIVIA D.; CISAR, JUSTIN S.; DUNCAN, KATHARINE K.; MERIT, JEFFREY E.
To: ABIDE THERAPEUTICS, INC.
Reel/Frame 047191/0035 →
Continuity (2)
Provisional Application 62258372 · Nov 20, 2015
Related Publication 20180327410A1 · Nov 15, 2018
Cited By (1)
US 12,258,340