IP Library Granted Patent US 10,676,437
Granted Patent B2
US 10,676,437 · App. 16/218,759 · Granted Jun 9, 2020

Fluorinated 4-(substituted amino)phenyl carbamate derivatives

Inventors: Takeru Furuya (Cambridge, MA); Ben C. Askew (Marshfield, MA); D. Scott Edwards (Bedford, MA)
Assignee: SciFluor Life Sciences, Inc.
C07D211/44A61P25/08C07C233/07C07C233/43C07D217/02
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Quick Facts
Patent No.
US 10,676,437
App. No.
16/218,759
Granted
Jun 9, 2020
Kind
B2
Abstract

The application relates to 4-(substituted amino)phenyl carbamate derivatives, or pharmaceutically acceptable salts or solvates thereof, as KCNQ2/3 potassium channel modulators, and methods of their uses.

Claims (40)

1. A compound of formula A:

or a pharmaceutically acceptable salt or solvate thereof, wherein:

X 1 and X 9 are each independently methyl or ethyl;

X 4 is H, C 1 -C 4 alkyl, C 2 -C 6 alkenyl, or C 2 -C 6 alkynyl;

X 5 is phenyl-(CX 8 X 8 ) m , wherein the phenyl is optionally substituted with one or more substituents independently selected from deuterium, F, SF 5 , C 1 -C 4 alkyl, C 1 -C 4 alkyl substituted with one or more F, C 1 -C 4 alkoxy, and C 1 -C 4 alkoxy substituted with one or more F; or

X 4 and X 5 , together with the nitrogen atom to which they are attached, form a 5- to 7-membered heterocyclic ring comprising 1 or 2 heteroatoms selected from N, O, and S, wherein the heterocyclic ring is optionally substituted with one or more substituents independently selected from deuterium, F, SF 5 , C 1 -C 4 alkyl, C 1 -C 4 alkyl substituted with one or more F, C 1 -C 4 alkoxy, and C 1 -C 4 alkoxy substituted with one or more F, or two substituents attached to adjacent carbon atoms on the heterocyclic ring, together with the carbon atoms to which they are attached, form a phenyl optionally substituted with one or more substituents independently selected from deuterium, F, SF 5 , C 1 -C 4 alkyl, C 1 -C 4 alkyl substituted with one or more F, C 1 -C 4 alkoxy, and C 1 -C 4 alkoxy substituted with one or more F;

each X 5 is independently H, deuterium, F, C 1 -C 4 alkyl, or C 1 -C 4 alkyl substituted with one or more F; and

m is 1, 2, or 3.

2. The compound of claim 1 , being of formula Ia or Ib:

or a pharmaceutically acceptable salt or solvate thereof.

3. The compound of claim 1 , wherein X 4 is H.

4. The compound of claim 1 , wherein X 4 is C 1 -C 4 alkyl, C 2 -C 6 alkenyl, or C 2 -C 6 alkynyl.

5. The compound of claim 1 , wherein X 5 is phenyl-(CX 8 X 8 ), phenyl-(CX 8 X 8 ) 2 , or phenyl-(CX 8 X 8 ) 3 , wherein the phenyl is optionally substituted with one or more substituents independently selected from deuterium, F, SF 5 , C 1 -C 4 alkyl, C 1 -C 4 alkyl substituted with one or more F, C 1 -C 4 alkoxy, and C 1 -C 4 alkoxy substituted with one or more F.

6. The compound of claim 5 , wherein X 5 is phenyl-(CX 8 X 8 ).

7. The compound of claim 5 , wherein the phenyl is substituted with one or more substituents independently selected from F, CF 3 , and OCF 3 .

8. The compound of claim 1 , wherein X 4 and X 5 , together with the nitrogen atom to which they are attached, form a 5- to 7-membered heterocyclic ring comprising 1 or 2 heteroatoms selected from N, O, and S, wherein the heterocyclic ring is optionally substituted with one or more substituents independently selected from deuterium, F, SF 5 , C 1 -C 4 alkyl, C 1 -C 4 alkyl substituted with one or more F, C 1 -C 4 alkoxy, and C 1 -C 4 alkoxy substituted with one or more F.

9. The compound of claim 8 , wherein the heterocyclic ring is substituted with one or more substituents independently selected from CH 3 and OCH 3 .

10. The compound of claim 8 , wherein the heterocyclic ring is pyrrolidinyl, tetrahydrofuranyl, tetrahydrothiophenyl, oxazolidinyl, isoxazolidinyl, thiazolidinyl, isothiazolidinyl, piperidinyl, piperazinyl, tetrahydropyranyl, tetrahydrothiapyranyl, dioxanyl, morpholinyl, oxazinanyl, thiazinanyl, or oxathianyl.

11. The compound of claim 1 , wherein X 4 and X 5 , together with the nitrogen atom to which they are attached, form a 5- to 7-membered heterocyclic ring substituted with two or more substituents, wherein two substituents attached to adjacent carbon atoms on the heterocyclic ring, together with the carbon atoms to which they are attached, form a phenyl optionally substituted with one or more substituents independently selected from deuterium, F, SF 5 , C 1 -C 4 alkyl, C 1 -C 4 alkyl substituted with one or more F, C 1 -C 4 alkoxy, and C 1 -C 4 alkoxy substituted with one or more F.

12. The compound of claim 11 , wherein X 4 and X 5 , together with the nitrogen atom to which they are attached, form a heterocyclic ring selected from

wherein the nitrogen atom is the nitrogen atom bonded to X 4 and X 5 .

13. The compound of claim 1 , being of formula IIa or IIb:

or a pharmaceutically acceptable salt or solvate thereof, wherein:

X 4 is H, C 1 -C 4 alkyl, C 2 -C 6 alkenyl, or C 2 -C 6 alkynyl;

t1 is 1, 2, 3, 4, or 5;

each Z 1 is independently selected from deuterium, F, SF 5 , C 1 -C 4 alkyl, C 1 -C 4 alkyl substituted with one or more F, C 1 -C 4 alkoxy, and C 1 -C 4 alkoxy substituted with one or more F; and

m is 1, 2, or 3.

14. The compound of claim 1 , being of formula IIIa or IIIb:

or a pharmaceutically acceptable salt or solvate thereof, wherein:

q is 1, 2, or 3;

t2 is 1, 2, 3, or 4; and

each Z 2 is independently selected from deuterium, F, SF 5 , C 1 -C 4 alkyl, C 1 -C 4 alkyl substituted with one or more F, C 1 -C 4 alkoxy, and C 1 -C 4 alkoxy substituted with one or more F.

15. The compound of claim 1 , being of formula IVa or IVb:

or a pharmaceutically acceptable salt or solvate thereof, wherein:

r is 1, 2, or 3;

t3 is 1, 2, 3, or 4; and

each Z 3 is independently selected from deuterium, F, SF 5 , C 1 -C 4 alkyl, C 1 -C 4 alkyl substituted with one or more F, C 1 -C 4 alkoxy, and C 1 -C 4 alkoxy substituted with one or more F.

16. The compound of claim 1 , being selected from the groups consisting of

and pharmaceutically acceptable salts and solvates thereof.

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

Assignments (2)
CHANGE OF NAME Recorded Aug 13, 2024
From: SCIFLUOR LIFE SCIENCES, INC.
To: OCUTERRA THERAPEUTICS, INC.
Reel/Frame 068585/0362 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 14, 2019
From: FURUYA, TAKERU; ASKEW, BEN C.; EDWARDS, D. SCOTT
To: SCIFLUOR LIFE SCIENCES, INC.
Reel/Frame 047986/0627 →
Continuity (2)
Provisional Application 62597979 · Dec 13, 2017
Related Publication 20190177274A1 · Jun 13, 2019