IP Library Granted Patent US 10,519,134
Granted Patent B2
US 10,519,134 · App. 15/777,198 · Granted Dec 31, 2019

Pyrazole compounds and methods of making and using same

Inventors: Olivia D. Weber (San Diego, CA); Michael B. Shaghafi (San Diego, CA); Cheryl A. Grice (Encinitas, CA); Todd K. Jones (Solana Beach, CA)
Assignee: LUNDBECK LA JOLLA RESEARCH CENTER, INC.
C07D401/14A61P25/04C07D413/14C07D487/10C07D491/08
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Quick Facts
Patent No.
US 10,519,134
App. No.
15/777,198
Granted
Dec 31, 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 ABHD6. Furthermore, the subject compounds and compositions are useful for the treatment of, for example, pain.

Claims (49)

1. A compound of Formula (III):

wherein:

R 1 is —N(R 2 )C(O)R 15 or —N(H)SO 2 R 15 ;

R 2 is H or C 1-6 alkyl;

R 3 is H or optionally substituted phenyl;

R 4 is H, halogen, —OR′, C 1-6 alkyl, C 2-6 alkynyl, C 1-6 haloalkyl, C 3-6 cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted C 1-6 alkyl-heterocycloalkyl, optionally substituted phenyl, optionally substituted heteroaryl, —CO 2 H, or —C(O)NR 8 R 9 ;

R 5 is H, halogen, —CN, C 1-6 alkyl, C 1-6 haloalkyl, or phenyl; or

R 4 and R 5 are combined to form an optionally substituted heterocycloalkyl ring or an optionally substituted heteroaryl ring;

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

R 7 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 10 R 11 ;

R 8 and R 9 are each independently H, or C 1-6 alkyl; or R 8 and R 9 together with the nitrogen to which they are attached are combined to form an optionally substituted heterocycloalkyl ring;

R 10 and R 11 are each independently H, or C 1-6 alkyl; or R 10 and R 11 together with the nitrogen to which they are attached are combined to form a heterocycloalkyl ring; and

R 15 is optionally substituted C 1-6 alkyl;

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

2. A compound of Formula (IV):

wherein:

R 1 is —N(R 2 )C(O)R 15 or —N(H)SO 2 R 15 ;

R 2 is H or C 1-6 alkyl;

R 3 is H or optionally substituted phenyl;

R 4 is H, halogen, —OR 7 , C 1-6 alkyl, C 2-6 alkynyl, C 1-6 haloalkyl, C 3-6 cycloalkyl, optionally substituted heterocycloalkyl, optionally substituted C 1-6 alkyl-heterocycloalkyl, optionally substituted phenyl, optionally substituted heteroaryl, —CO 2 H, or —C(O)NR 8 R 9 ;

R 5 is H, halogen, —CN, C 1-6 alkyl, C 1-6 haloalkyl, or phenyl; or

R 4 and R 5 are combined to form an optionally substituted heterocycloalkyl ring or an optionally substituted heteroaryl ring;

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

R 7 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 10 R 11 ;

R 8 and R 9 are each independently H, or C 1-6 alkyl; or R 8 and R 9 together with the nitrogen to which they are attached are combined to form an optionally substituted heterocycloalkyl ring;

R 10 and R 11 are each independently H, or C 1-6 alkyl; or R 10 and R 11 together with the nitrogen to which they are attached are combined to form a heterocycloalkyl ring;

R 12 is H or C 1-6 alkyl;

R 13 is H or C 1-6 alkyl; and

R 15 is optionally substituted C 1-6 alkyl;

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

3. The compound of claim 1 , or a solvate, hydrate, tautomer, N-oxide, or pharmaceutically acceptable salt thereof, wherein R 4 is optionally substituted heterocycloalkyl and the heterocycloalkyl is a 4-6 membered monocyclic heterocycloalkyl, a 8-9 membered bicyclic heterocycloalkyl, a 7-8 membered bridged heterocycloalkyl, a 5,5 fused heterocycloalkyl, or an 8-11 membered spirocyclic heterocycloalkyl.

4. The compound of claim 3 , or a solvate, hydrate, tautomer, N-oxide, or pharmaceutically acceptable salt thereof, wherein R 4 is optionally substituted with one or two groups selected from halogen, hydroxy, C 1-6 alkyl, —C 1-6 alkyl-OH, C 1-6 fluoroalkyl, C 3-6 cycloalkyl, heteroaryl, —CO 2 H, —C 1-6 alkyl-CO 2 H, —C(O)C 1-6 alkyl, —C(O)C 1-6 alkyl-OH, —N(H)C(O)C 1-6 alkyl, —C(O)NH 2 , —C(O)N(H)(C 1-6 alkyl), —C(O)N(C 1-6 alkyl) 2 , —C(O)C 2-7 heterocycloalkyl, and —S(O) 2 C 1-6 alkyl.

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

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

7. The compound of claim 1 , or a solvate, hydrate, tautomer, N-oxide, or pharmaceutically acceptable salt thereof, wherein R 4 is optionally substituted heteroaryl and the heteroaryl is a 5-6 membered heteroaryl ring.

8. The compound of claim 7 , or a solvate, hydrate, tautomer, N-oxide, or pharmaceutically acceptable salt thereof, wherein R 4 is a 5-6 membered heteroaryl ring optionally substituted with one or two groups selected from halogen, hydroxy, C 1-6 alkyl, C 1-6 fluoroalkyl, C 3-6 cycloalkyl, —CO 2 H, —C 1-6 alkyl-CO 2 H, and —C(O)NH 2 .

9. The compound of claim 8 , or a solvate, hydrate, tautomer, N-oxide, or pharmaceutically acceptable salt thereof, wherein R 4 is

10. The compound of claim 1 , or a solvate, hydrate, tautomer, N-oxide, or pharmaceutically acceptable salt thereof, wherein R 5 is halogen.

11. The compound of claim 1 , or a solvate, hydrate, tautomer, N-oxide, or pharmaceutically acceptable salt thereof, wherein R 5 is C 1-6 haloalkyl.

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

13. The compound of claim 1 , or a solvate, hydrate, tautomer, N-oxide, or pharmaceutically acceptable salt thereof, wherein R 1 is —N(R 2 )C(O)R 15 .

14. The compound of claim 13 , or a solvate, hydrate, tautomer, N-oxide, or pharmaceutically acceptable salt thereof, wherein R 2 is H and R 15 is unsubstituted C 1-6 alkyl.

15. The compound of claim 1 , or a solvate, hydrate, tautomer, N-oxide, or pharmaceutically acceptable salt thereof, wherein R 1 is —N(H)SO 2 R 15 .

16. The compound of claim 15 , or a solvate, hydrate, tautomer, N-oxide, or pharmaceutically acceptable salt thereof, wherein R 15 is unsubstituted C 1-6 alkyl.

17. A compound selected from:

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

18. A pharmaceutical composition comprising a compound of claim 1 , or a solvate, hydrate, tautomer, N-oxide, or a pharmaceutically acceptable salt thereof, and at least one pharmaceutically acceptable excipient.

19. A method of treating pain in a patient in need thereof, comprising administering to the patient a therapeutically effective amount of a compound of claim 1 , or a pharmaceutically acceptable salt or solvate thereof.

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 1 , or a pharmaceutically acceptable salt or solvate thereof, wherein the disease or disorder is selected from multiple sclerosis, Alzheimer's disease, inflammatory bowel disease, epilepsy/seizure disorder, neuromyelitis optica (NMO), Tourette syndrome, persistent motor tic disorder, persistent vocal tic disorder, and abdominal pain associated with irritable bowel syndrome.

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 Aug 29, 2019
From: ABIDE THERAPEUTICS, INC.
To: LUNDBECK LA JOLLA RESEARCH CENTER, INC.
Reel/Frame 050216/0627 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 2, 2018
From: WEBER, OLIVIA D.; SHAGHAFI, MICHAEL B.; GRICE, CHERYL A.; JONES, TODD K.
To: ABIDE THERAPEUTICS, INC.
Reel/Frame 046690/0039 →
Continuity (2)
Provisional Application 62258371 · Nov 20, 2015
Related Publication 20190256494A1 · Aug 22, 2019
Cited By (1)
US 12,258,340