IP Library Granted Patent US 9,771,341
Granted Patent B2
US 9,771,341 · App. 15/072,229 · Granted Sep 26, 2017

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 9,771,341
App. No.
15/072,229
Granted
Sep 26, 2017
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 (31)

1. A compound of Formula (I):

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;

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

2. The compound of claim 1 , or a solvate, hydrate, N-oxide, stereoisomer, or pharmaceutically acceptable salt thereof, wherein R 1 is halogen, —OR 3 , or C 1-6 alkyl optionally substituted by halogen.

3. The compound of claim 2 , or a solvate, hydrate, N-oxide, stereoisomer, or pharmaceutically acceptable salt thereof, 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 compound of claim 3 , or a solvate, hydrate, N-oxide, stereoisomer, or pharmaceutically acceptable salt thereof, 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 compound of claim 4 , or a solvate, hydrate, N-oxide, stereoisomer, or pharmaceutically acceptable salt thereof, 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 compound of claim 5 , or a solvate, hydrate, N-oxide, stereoisomer, or pharmaceutically acceptable salt thereof, 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 compound of claim 5 , or a solvate, hydrate, N-oxide, stereoisomer, or pharmaceutically acceptable salt thereof, 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 compound of claim 5 , or a solvate, hydrate, N-oxide, stereoisomer, or pharmaceutically acceptable salt thereof, 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 compound of claim 5 , or a solvate, hydrate, N-oxide, stereoisomer, or pharmaceutically acceptable salt thereof, wherein R 1 is halogen, —CH 3 , —CF 3 , —OCH 3 , or —OCF 3 .

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

11. The compound of claim 1 , or a solvate, hydrate, N-oxide, or pharmaceutically acceptable salt thereof, wherein the compound is

12. The compound of claim 1 , or a solvate, hydrate, N-oxide, stereoisomer, or pharmaceutically acceptable salt thereof, wherein the compound is

13. The compound of claim 1 , or a solvate, hydrate, N-oxide, stereoisomer, or pharmaceutically acceptable salt thereof, wherein the compound is

14. A compound selected from:

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

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

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 May 10, 2016
From: CISAR, JUSTIN S.; GRICE, CHERYL A.; JONES, TODD K.; WEBER, OLIVIA D.; WANG, DONG-HUI
To: ABIDE THERAPEUTICS, INC.
Reel/Frame 038665/0077 →
Continuity (2)
Provisional Application 62135072 · Mar 18, 2015
Related Publication 20160272602A1 · Sep 22, 2016