IP Library Granted Patent US 10,570,106
Granted Patent B2
US 10,570,106 · App. 16/412,212 · Granted Feb 25, 2020

MAGL inhibitors

Inventors: Cheryl A. Grice (Encinitas, CA); Daniel J. Buzard (San Diego, CA); Michael B. Shaghafi (San Diego, CA)
Assignee: LUNDBECK LA JOLLA RESEARCH CENTER, INC.
C07D295/185C07D213/55C07D241/12C07D263/32C07D305/08
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Quick Facts
Patent No.
US 10,570,106
App. No.
16/412,212
Granted
Feb 25, 2020
Kind
B2
Abstract

Provided herein are piperazine carbamates and pharmaceutical compositions comprising said compounds. The subject compounds and compositions are useful as modulators of MAGL. Furthermore, the subject compounds and compositions are useful for the treatment of pain.

Claims (41)

1. A compound having the structure of Formula (I):

wherein:

R 1 is H or C 1-6 alkyl;

R 2 is C 1-6 alkyl;

R 3 is H or C 1-6 alkyl;

R 4 and R 5 are independently selected from H and C 1-6 alkyl;

each R 6 is independently selected from C 1-6 alkyl, halogen, —CN, C 1-6 haloalkyl, —C(O)NR 8 R 9 , C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, —C 1-6 alkyl(C 2-9 heterocycloalkyl), and C 2-9 heteroaryl, wherein C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, —C 1-6 alkyl(C 2-9 heterocycloalkyl), and C 2-9 heteroaryl are optionally substituted with one, two, or three groups independently selected from halogen, C 1-6 alkyl, C 1-6 haloalkyl, and C 1-6 alkoxy;

each R 7 is independently selected from H, C 1-6 alkyl, C 1-6 haloalkyl, and C 3-6 cycloalkyl;

each R 8 and R 9 is each independently selected from H, C 1-6 alkyl, C 3-6 cycloalkyl, aryl, and heteroaryl; or R 8 and R 9 , together with the nitrogen to which they are attached, form a heterocycloalkyl ring optionally substituted with one, two, or three R 10 ;

each R 10 is independently selected from halogen, C 1-6 alkyl, C 1-6 haloalkyl, oxo, —CN, and C 3-6 cycloalkyl;

n is 1; and

p is 0;

or a pharmaceutically acceptable salt or solvate thereof.

2. The compound of claim 1 , or a pharmaceutically acceptable salt or solvate thereof, wherein R 3 is C 1-6 alkyl.

3. The compound of claim 2 , or a pharmaceutically acceptable salt or solvate thereof, wherein R 2 is —CH 3 and R 3 is —CH 3 .

4. The compound of claim 1 , or a pharmaceutically acceptable salt or solvate thereof, wherein each R 6 is independently selected from C 1-6 alkyl, halogen, —CN, C 1-6 haloalkyl, —OR 7 , C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, and C 2-9 heteroaryl, wherein C 3-6 cycloalkyl, C 2-9 heterocycloalkyl, and C 2-9 heteroaryl are optionally substituted with one or two groups independently selected from halogen, C 1-6 alkyl, C 1-6 haloalkyl, and C 1-6 alkoxy.

5. The compound of claim 4 , or a pharmaceutically acceptable salt or solvate thereof, wherein each R 6 is independently selected from C 1-6 alkyl, halogen, —CN, C 1-6 haloalkyl, —OR′, and C 3-6 cycloalkyl.

6. The compound of claim 5 , or a pharmaceutically acceptable salt or solvate thereof, wherein each R 7 is independently selected from C 1-6 alkyl and C 1-6 haloalkyl.

7. The compound of claim 5 , or a pharmaceutically acceptable salt or solvate thereof, wherein each R 6 is independently selected from C 1-6 alkyl, halogen, —CN, and C 1-6 haloalkyl.

8. The compound of claim 7 , or a pharmaceutically acceptable salt or solvate thereof, wherein each R 6 is independently selected from halogen and C 1-6 haloalkyl.

9. The compound of claim 1 , or a pharmaceutically acceptable salt or solvate thereof, wherein R 1 is H.

10. The compound of claim 1 selected from:

or a pharmaceutically acceptable salt or solvate thereof.

11. The compound of claim 1 that is:

or a pharmaceutically acceptable salt or solvate thereof.

12. The compound of claim 1 that is:

or a pharmaceutically acceptable salt or solvate thereof.

13. The compound of claim 1 that is:

or a pharmaceutically acceptable salt or solvate thereof.

14. The compound of claim 1 that is:

or a pharmaceutically acceptable salt or solvate thereof.

15. The compound of claim 1 that is:

or a pharmaceutically acceptable salt or solvate thereof.

16. The compound of claim 1 that is:

or a pharmaceutically acceptable salt or solvate thereof.

17. The compound of claim 1 that is:

or a pharmaceutically acceptable salt or solvate thereof.

18. The compound of claim 1 that is:

or a pharmaceutically acceptable salt or solvate thereof.

19. A pharmaceutical composition comprising a compound of claim 1 , or a pharmaceutically acceptable salt or solvate thereof, and at least one pharmaceutically acceptable excipient.

20. A method of treating pain, epilepsy/seizure disorder, multiple sclerosis, neuromyelitis optica (NMO), Tourette syndrome, Alzheimer's disease, abdominal pain associated with irritable bowel syndrome, or attention deficit and hyperactivity disorder (ADHD) 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.

Assignments (6)
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 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 30, 2019
From: GRICE, CHERYL A.; BUZARD, DANIEL J.; SHAGHAFI, MICHAEL B.
To: ABIDE THERAPEUTICS, INC.
Reel/Frame 051385/0567 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 20, 2019
From: GRICE, CHERYL A.; BUZARD, DANIEL J.; SHAGHAFI, MICHAEL B.
To: ABIDE THERAPEUTICS, INC.
Reel/Frame 051398/0128 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 19, 2019
From: GRICE, CHERYL A.; BUZARD, DANIEL J.; SHAGHAFI, MICHAEL B.
To: LUNDBECK LA JOLLA RESEARCH CENTER, INC.
Reel/Frame 051330/0807 →
CHANGE OF NAME Recorded Sep 16, 2019
From: ABIDE THERAPEUTICS, INC.
To: LUNDBECK LA JOLLA RESEARCH CENTER, INC.
Reel/Frame 050383/0373 →
Continuity (2)
Provisional Application 62671985 · May 15, 2018
Related Publication 20190352273A1 · Nov 21, 2019
Cited By (1)
US 12,286,421