Piperazine carbamates and methods of making and using same
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.
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.