IP Library Granted Patent US 9,732,072
Granted Patent B2
US 9,732,072 · App. 14/882,638 · Granted Aug 15, 2017

PRMT5 inhibitors and uses thereof

Inventors: Kenneth W. Duncan (Westwood, MA); Richard Chesworth (Concord, MA); Paula Ann Boriack-Sjodin (Lexington, MA); Michael John Munchhof (Salem, CT)
Assignee: Epizyme, Inc.
C07D413/12C07D209/44C07D401/12C07D401/14C07D403/12C07D403/14C07D405/12C07D405/14C07D407/12
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Quick Facts
Patent No.
US 9,732,072
App. No.
14/882,638
Granted
Aug 15, 2017
Kind
B2
Abstract

Described herein are compounds of Formula (I), pharmaceutically acceptable salts thereof, and pharmaceutical compositions thereof. Compounds of the present invention are useful for inhibiting PRMT5 activity. Methods of using the compounds for treating PRMT5-mediated disorders are also described.

Claims (38)

1. A compound of formula (IV D ):

or a pharmaceutically acceptable salt thereof,

wherein:

R 1 is hydrogen, R z , or —C(O)R z , wherein R z is optionally substituted C 1-6 alkyl;

Ring A is phenyl;

R 4 is -L 1 -Cy D ;

L 1 is a bond, —O—, —S—, —N(R)—, —C(O)—, —C(O)N(R)—, —N(R)C(O)N(R)—, —N(R)C(O)—, —N(R)C(O)O—, —OC(O)N(R)—, —SO 2 —, —SO 2 N(R)—, —N(R)SO 2 —, —OC(O)—, —C(O)O—, or an optionally substituted, straight or branched, C 1-6 aliphatic chain wherein one, two, or three methylene units of L 1 are optionally and independently replaced by —O—, —S—, —N(R)—, —C(O)—, —C(O)N(R)—, —N(R)C(O)N(R)—, —N(R)C(O)—, —N(R)C(O)O—, —OC(O)N(R)—, —SO 2 —, —SO 2 N(R)—, —N(R)SO 2 —, —OC(O)—, or —C(O)O—;

each R is independently hydrogen or optionally substituted C 1-6 aliphatic;

Cy D is an optionally substituted, monocyclic, bicyclic or tricyclic, saturated, partially unsaturated, or aromatic ring having 0-4 heteroatoms independently selected from nitrogen, oxygen, and sulfur;

R 5B , R 6B , R 7B , and R 8B are independently hydrogen, halo, or optionally substituted aliphatic;

each R x is independently selected from the group consisting of halo, —CN, optionally substituted aliphatic, and —OR′;

R′ is hydrogen or optionally substituted aliphatic;

n is 0 or 1; and

m is O.

2. The compound of claim 1 , wherein the compound is of formula (IV D -a):

or a pharmaceutically acceptable salt thereof.

3. The compound of claim 1 , wherein the compound is of formula (IV D -b):

or a pharmaceutically acceptable salt thereof.

4. The compound of claim 1 , wherein the compound is of formula (IV D -c):

or a pharmaceutically acceptable salt thereof.

5. The compound of claim 1 , wherein R 1 is hydrogen.

6. The compound of claim 1 , wherein n is 0.

7. The compound of claim 1 , wherein n is 1.

8. The compound of claim 1 , wherein the compound is of formula (VI D ):

or a pharmaceutically acceptable salt thereof, wherein L D is —O—.

9. The compound of claim 1 , wherein the compound is of formula (VI D -c):

or a pharmaceutically acceptable salt thereof, wherein L D is —O—.

10. The compound of claim 1 , wherein L 1 is a bond.

11. The compound of claim 1 , wherein L 1 is an optionally substituted, straight or branched, C 1-3 aliphatic chain wherein one methylene unit of L 1 is replaced by —N(R)—.

12. The compound of claim 1 , wherein Cy D is an optionally substituted 5- to 6-membered carbocyclic ring.

13. The compound of claim 1 , wherein Cy D is an optionally substituted 9- to 10-membered bicyclic heteroaryl having 1-4 heteroatoms independently selected from nitrogen, oxygen, and sulfur.

14. The compound of claim 13 , wherein Cy D is optionally substituted indazole, optionally substituted quinoline, optionally substituted benzimidazole, optionally substituted benzothiazole, optionally substituted deazapurine, optionally substituted indole, optionally substituted purine, optionally substituted pyrazolopyridine, optionally substituted pyrrolopyridine, optionally substituted pyrrolopyrimidine, optionally substituted imidazopyridine, or optionally substituted imidazopyridine.

15. The compound of claim 1 , wherein the compound is selected from the group consisting of:

and pharmaceutically acceptable salts thereof.

16. A pharmaceutical composition comprising a compound of claim 1 , or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable excipient.

17. A kit or packaged pharmaceutical comprising a compound of claim 1 , or a pharmaceutically acceptable salt thereof, and instructions for use thereof.

18. A pharmaceutical composition comprising a compound of claim 15 , or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable excipient.

19. A kit or packaged pharmaceutical comprising a compound of claim 15 , or a pharmaceutically acceptable salt thereof, and instructions for use thereof.

Assignments (3)
TERMINATION AND RELEASE OF SECURITY INTEREST IN PATENTS AT REEL/FRAME: 051057/0848 Recorded Aug 13, 2022
From: BIOPHARMA CREDIT PLC
To: EPIZYME, INC.
Reel/Frame 061165/0501 →
SECURITY INTEREST Recorded Nov 19, 2019
From: EPIZYME, INC.
To: BIOPHARMA CREDIT PLC
Reel/Frame 051057/0848 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 19, 2015
From: DUNCAN, KENNETH W.; CHESWORTH, RICHARD; BORIACK-SJODIN, PAULA ANN; MUNCHHOF, MICHAEL JOHN
To: EPIZYME, INC.
Reel/Frame 036818/0184 →
Continuity (4)
Continuation 14136691 · Dec 20, 2013
Provisional Application 61785095 · Mar 14, 2013
Provisional Application 61745494 · Dec 21, 2012
Related Publication 20160137631A1 · May 19, 2016