IP Library Granted Patent US 9,994,537
Granted Patent B2
US 9,994,537 · App. 15/672,165 · Granted Jun 12, 2018

Piperazine carbamates and methods of making and using same

Inventors: Justin S. Cisar (San Diego, CA); Cheryl A. Grice (Encinitas, CA); Todd K. Jones (Solana Beach, CA); Olivia D. Weber (San Diego, CA); Dong-Hui Wang (San Diego, CA)
Assignee: ABIDE THERAPEUTICS, INC.
C07D295/205C07D207/08C07D207/12C07D207/14C07D207/16C07D211/14C07D211/38C07D211/58C07D211/62C07D265/30C07D295/26C07D401/04C07D403/04C07D417/04C07D471/10C07D487/04C07D498/08
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Quick Facts
Patent No.
US 9,994,537
App. No.
15/672,165
Granted
Jun 12, 2018
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 and/or ABHD6. Furthermore, the subject compounds and compositions are useful for the treatment of pain.

Claims (33)

1. A method of treating pain in a patient in need thereof, comprising administering to the patient a therapeutically effective amount of a compound of Formula (I), or a solvate, hydrate, N-oxide, stereoisomer, or pharmaceutically acceptable salt thereof:

wherein:

R 1 is halogen, —OR 3 , —CN, C 1-6 alkyl optionally substituted by halogen, or —C(O)OR 9 ;

R 2 is —NR 5 R 6 ;

R 3 is selected from H, C 1-6 alkyl, C 1-6 haloalkyl, and C 1-6 aminoalkyl;

R 5 and R 6 , together with the nitrogen to which they are attached, form

(i) a 4-6 membered saturated monocyclic heterocycle; or

(ii) a 7-8 membered bridged heterocyclic ring optionally containing an additional O, N, or S;

wherein the 4-6 membered saturated monocyclic heterocycle is substituted with one or two substituents independently selected from —C(O)OR 9 ; and the 4-6 membered saturated monocyclic heterocycle optionally contains an additional O, N, or S; and

the 7-8 membered bridged heterocyclic ring is optionally substituted with one or two substituents independently selected from halogen, oxo, and C 1-6 alkyl; and

each R 9 is independently selected from H and C 1-6 alkyl.

2. The method of claim 1 , wherein R 1 is halogen, OR 3 , or C 1-6 alkyl optionally substituted by halogen.

3. The method of claim 2 , wherein R 5 and R 6 , together with the nitrogen to which they are attached, form a 4-6 membered saturated monocyclic heterocycle, wherein:

the 4-6 membered saturated monocyclic heterocycle is substituted with one —C(O)OR 9 ; and the 4-6 membered saturated monocyclic heterocycle optionally contains an additional O, N, or S.

4. The method of claim 3 , wherein R 5 and R 6 , together with the nitrogen to which they are attached, form a 4-6 membered saturated monocyclic heterocycle wherein:

the 4-6 membered saturated monocyclic heterocycle is substituted with one —C(O)OR 9 ; and the 4-6 membered saturated monocyclic heterocycle is selected from azetidine, pyrrolidine, piperidine, and morpholine.

5. The method of claim 4 , wherein R 5 and R 6 , together with the nitrogen to which they are attached, form a 4-6 membered saturated monocyclic heterocycle substituted with one —C(O)OR 9 , wherein the 4-6 membered saturated monocyclic heterocycle is selected from pyrrolidine, piperidine, and morpholine.

6. The method of claim 5 , wherein R 5 and R 6 , together with the nitrogen to which they are attached, form a 4-6 membered saturated monocyclic heterocycle substituted with one —C(O)OR 9 , wherein the 4-6 membered saturated monocyclic heterocycle is pyrrolidine.

7. The method of claim 5 , wherein R 5 and R 6 , together with the nitrogen to which they are attached, form a 4-6 membered saturated monocyclic heterocycle substituted with one —C(O)OR 9 , wherein the 4-6 membered saturated monocyclic heterocycle is piperidine.

8. The method of claim 5 , wherein R 5 and R 6 , together with the nitrogen to which they are attached, form a 4-6 membered saturated monocyclic heterocycle substituted with one —C(O)OR 9 , wherein the 4-6 membered saturated monocyclic heterocycle is morpholine.

9. The method of claim 5 , wherein R 1 is halogen, —CH 3 , —CF 3 , —OCH 3 , or —OCF 3 .

10. The method of claim 1 , wherein the compound is

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

11. The method of claim 1 , wherein the compound is

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

12. The method of claim 1 , wherein the compound is

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

13. The method of claim 1 , wherein the compound is

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

14. A method of treating pain in a patient in need thereof, comprising administering to the patient a therapeutically effective amount of a compound selected from:

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

15. The method of claim 1 , wherein the pain is neuropathic pain.

16. The method of claim 14 , wherein the pain is neuropathic 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 →
MERGER Recorded Mar 23, 2021
From: ABIDE THERAPEUTICS, INC.
To: LUNDBECK LA JOLLA RESEARCH CENTER, INC.
Reel/Frame 057434/0784 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 11, 2017
From: CISAR, JUSTIN S.; GRICE, CHERYL A.; JONES, TODD K.; WEBER, OLIVIA D.; WANG, DONG-HUI
To: ABIDE THERAPEUTICS, INC.
Reel/Frame 043538/0741 →
Continuity (3)
Continuation 15072229 · Mar 16, 2016
Provisional Application 62135072 · Mar 18, 2015
Related Publication 20170334874A1 · Nov 23, 2017