IP Library Granted Patent US 10,029,988
Granted Patent B2
US 10,029,988 · App. 14/773,472 · Granted Jul 24, 2018

HDAC inhibitors

Inventors: Vincent Jacques (Somerville, MA); James R. Rusche (Framingham, MA)
Assignee: BIOMARIN PHARMACEUTICAL INC.
C07D231/56C07D401/06
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 10,029,988
App. No.
14/773,472
Granted
Jul 24, 2018
Kind
B2
Abstract

Disclosed herein are compounds of formula (I), and methods of inhibiting histone deacetylase (“HDAC”) enzymes (e.g., HDAC1, HDAC2, and HDAC3) using compounds of formula (I).

Claims (107)

1. A compound having formula (I), or a pharmaceutically acceptable salt thereof:

wherein:

R 1 —X is attached to only one of the ring nitrogen atoms;

X is:

(i) —Y—[C(R a ) 2 ] a -A-[C(R b ) 2 ] b —B—;

(ii) direct bond; or

(iii) C═O, C(R j ) 2 —C(═O), C(═O)—C(R j ) 2 , SO 2 —NR k , NR k —SO 2 , C(═O)NR k or NR k —C(═O);

wherein:

Y is bond, CR c ═CR d , O, NR e , or S(O) m ;

each of A and B is, independently, a bond, O, NR f , or S(O) m ;

a is 1, 2, or 3;

b is 0, 1, 2, or 3;

m is 0, 1, or 2;

each occurrence of R a and R b is independently selected from H, F, OH, C1-C6 alkyl, C3-C6 cycloalkyl, NH 2 , OCO—(C1-C6 alkyl), OCO—(C3-C6 cycloalkyl), C1-C6 alkoxy, C1-C6 fluoroalkoxy, and cyano; or

one or more of the following can apply with respect to R a and R b :

any two R a , together with the carbons to which each is attached, together form C3-C6 cycloalkyl or heterocyclyl including 3-6 ring atoms, in which one of the heterocyclyl ring atoms is selected from O, S(O) m , and NR g ; or

one R a and one R b , together with the carbons to which each is attached, form C3-C6 cycloalkyl or heterocyclyl including 3-6 ring atoms, in which one of the heterocyclyl ring atoms is selected from O; S(O)m and NR g ; or

any two R b , together with the carbons to which each is attached, form C3-C6 cycloalkyl or heterocyclyl including 3-6 ring atoms, in which one of the ring atoms is selected from O; S(O)m and NR g ;

each of R c and R d is independently selected from H, F, OH, C1-6 alkyl, C3-C5 cycloalkyl, NH 2 , OCO—(C1-C6 alkyl), OCO—(C3-C5 cycloalkyl), C1-C6 alkoxy, C1-6 fluoroalkoxy, and cyano;

or R c and R d , together with the carbons to which each is attached form a C5-C7 cycloalkyl or heterocyclyl including 3-6 ring atoms, in which from 1-2 of the heterocyclyl ring atoms are independently selected from O, S(O) m and NR g′ ;

each occurrence of R e , R f , R g and R g′ is independently selected from H, C1-6 alkyl, —C(═O)H, —C(═O)R h , C(═O)O(C1-C6 alkyl), C(═O)N(R i ) 2 , and SO 2 —R h ; wherein R h is selected from C1-C6 alkyl, CH 2 -(heteroaryl including 5-10 ring atoms), CH 2 —(C6-C10 aryl), and C6-C10 aryl; and each occurrence of R i is independently selected from H, C1-C6 alkyl, CH 2 -(heteroaryl including 5-10 ring atoms), CH 2 —(C6-C10 aryl), and C6-C10 aryl;

each occurrence of R j is independently selected from H, F, OH, C1-6 alkyl, C3-C6 cycloalkyl, NH 2 , OCO—(C1-C6 alkyl), OCO—(C3-C6 cycloalkyl), C1-C6 alkoxy, C1-C6 fluoroalkoxy, and cyano;

or R j —C—R j together form C3-C6 cycloalkyl or heterocyclyl including 3-6 ring atoms, in which one of the heterocyclyl ring atoms is selected from O; S(O)m and NR j′ ;

each occurrence of R j′ and R k is independently selected from H, C1-C6 alkyl, —C(═O)H, —C(═O)R m , C(═O)O(C1-C6 alkyl), C(═O)N(R n ) 2 , and SO 2 —R m , wherein R m is selected from C1-C6 alkyl, CH 2 -(heteroaryl including 5-10 ring atoms), CH 2 —(C6-C10 aryl), and C6-C10 aryl; and each occurrence of R n is independently selected from H, C1-C6 alkyl, CH 2 -(heteroaryl including 5-10 ring atoms), CH 2 —(C6-C10 aryl), and C6-C10 aryl, and wherein the aryl and heteroaryl portion in R m and R n can be optionally substituted with 1-3 independently selected substituents F, C1-C6 alkyl, fluoro C1-C6 alkyl, C3-C6 cycloalkyl, C1-C6 alkoxy, C1-C6 fluoroalkoxy, or cyano;

further wherein:

(a) when each of A and B is a bond, and b is 0, then X has the following formula:

—Y—[C(R a ) 2 ] a —;

(b) when b is 0 or 1, then A and B cannot both be heteroatoms; and

(c) when A or B serves as the point of connection of X to the nitrogen ring atoms, then A or B cannot be a heteroatom;

R1 is:

(i) monocyclic or bicyclic heteroaryl including from 5-10 ring atoms, which is optionally substituted with from 1-3 R o ; wherein from 1-4 of the ring atoms are a heteroatom independently selected from 0, N, N—H, N—R o , and S;

(ii) C6-C10 aryl, which is optionally substituted with from 1-3 R o ;

(iii) C3-C10 cycloalkyl or C3-C10 cycloalkenyl, each of which is optionally substituted with from 1-6 R o ; or

(iv) hydrogen;

R4 is H or R o and each occurrence of R o is independently selected from the group consisting of halogen; C1-C6 alkyl; fluoro(C1-C6)alkyl; hydroxyl; hydroxy(C 1 -C 4 )alkyl; C1-C6 alkoxy; fluoro(C1-C6)alkoxy; (C1-C6 alkyl)C(O)—; (C1-C6 alkyl)NH—; (C1-C6 alkyl) 2 N—; —N*(R o′ ) 2 , wherein R o′ —N*—R o′ together form a saturated ring having 5 or 6 ring atoms, in which 1 or 2 ring atoms are optionally a heteroatom independently selected from NH, N(C1-C6alkyl), O, or S; formyl; formyl(C 1 -C 4 ) alkyl; cyano; cyano(C 1 -C 4 ) alkyl; benzyl; benzyloxy; (heterocyclyl)—(C0-C6) alkyl, wherein the heterocyclyl portion includes 5 or 6 ring atoms, in which 1 or 2 of the ring atoms are a heteroatom independently selected from NH, N(alkyl), O, or S; phenyl; heteroaryl including from 5-6 ring atoms, wherein from 1-4 of the ring atoms are a heteroatom independently selected from O, N, N—H, N—R o″ , and S, each of which is optionally substituted with from 1-3 R o″ ; SO 2 —(C1-C6)alkyl; SO—(C1-C6)alkyl; and nitro;

each occurrence of R o″ is independently selected from the group consisting of halogen; C1-C6 alkyl; fluoro(C1-C6)alkyl; hydroxyl; hydroxy(C 1 -C 4 )alkyl; C1-C6 alkoxy; fluoro(C1-C6)alkoxy; (C1-C6 alkyl)C(O)—; (C1-C6 alkyl)NH—; (C1-C6 alkyl) 2 N—; formyl; formyl(C 1 -C 4 ) alkyl; cyano; cyano(C 1 -C 4 ) alkyl; benzyl; benzyloxy; (heterocyclyl)—(C0-C6) alkyl, wherein the heterocyclyl portion includes 5 or 6 ring atoms, in which 1 or 2 of the ring atoms are a heteroatom independently selected from NH, N(C1-C6alkyl), O, or S; phenyl; heteroaryl including from 5-6 ring atoms, wherein from 1-4 of the ring atoms are a heteroatom independently selected from O, N, N—H, N—(C1-C6 alkyl), and S; SO 2 —(C1-C6)alkyl; SO—(C1-C6)alkyl; and nitro;

R5 is selected from the group consisting of: hydrogen, halogen; C1-06 alkyl; fluoro(C1-C6)alkyl; hydroxyl; hydroxy(C 1 -C 4 )alkyl; (C1-C6 alkyl)C(O)—; formyl; formyl(C 1 -C 4 ) alkyl; cyano; cyano(C 1 -C 4 ) alkyl; benzyl; (heterocyclyl)-(C0-C6)alkyl, wherein the heterocyclyl portion includes 5 or 6 ring atoms, in which 1 or 2 of the ring atoms are a heteroatom independently selected from NH, N(C1-C6alkyl), O, or S; phenyl; heteroaryl including from 5-6 ring atoms, wherein from 1-4 of the ring atoms are a heteroatom independently selected from O, N, N—H, and S; SO 2 —(C1-C6)alkyl; SO—(C1-C6)alkyl; and nitro;

R2 is selected from H, F, CI, CF 3 , CF 2 CF 3 , CH 2 CF 3 , OCF 3 , OCHF 2 , phenyl; or phenyl substituted with 1-3 R o ; and

R3 is H, F, or Cl.

2. The compound or salt of claim 1 , wherein X is —Y—[C(R a ) 2 ] a -A-[C(R b ) 2 ] b —B—.

3. The compound or salt according to claim 1 , wherein X is CH 2 .

4. The compound or salt according to claim 1 , wherein X is (CH 2 ) 2-4 .

5. The compound or salt according to claim 1 , wherein X is —CH═CH—C(R a ) 2 —or —CH═CHC(R a ) 2 C(R a ) 2 —.

6. The compound or salt according to claim 1 , wherein X is —O—(CH 2 ) 2-3 or —N(CH 3 )—(CH 2 ) 2-3 .

7. The compound or salt according to claim 1 , wherein X is a bond.

8. The compound or salt according to claim 1 , wherein R2 is hydrogen, and R3 is F or Cl.

9. The compound or salt according to claim 1 , wherein:

X is:

(i) —Y—[C(R a ) 2 ] a -A-[C(R b ) 2 ] b —B—;

(ii) direct bond; or

(iii) C═O, C(R j ) 2 —C(═O), C(═O)—C(R j ) 2 , SO 2 —NR k , NR k —SO 2 , C(═O)NR k or NR k —C(═O);

R1 is:

(i) monocyclic or bicyclic heteroaryl including from 5-10 ring atoms, which is optionally substituted with from 1-3 R o ; wherein from 1-4 of the ring atoms are a heteroatom independently selected from O, N, N—H, N—R o , and S;

(ii) C6-C10 aryl, which is optionally substituted with from 1-3 R o ;

(iii) C3-C10 cycloalkyl or C3-C10 cycloalkenyl, each of which is optionally substituted with from 1-3 R o ; or

(iv) hydrogen;

R o is independently selected from the group consisting of halogen; C1-C6 alkyl; fluoro(C1-C6)alkyl; hydroxyl; hydroxy(C 1 -C 4 )alkyl; C1-C6 alkoxy; fluoro(C1-C6)alkoxy; (C1-C6 alkyl)C(O)—; (C1-C6 alkyl)NH—; (C1-C6 alkyl) 2 N—; —N*(R o′ ) 2 , wherein R o′ —N*—R o′ together form a saturated ring having 5 or 6 ring atoms, in which 1 or 2 ring atoms are optionally a heteroatom independently selected from NH, N(C1-C6alkyl), O, or S; cyano; phenyl; heteroaryl including from 5-6 ring atoms, wherein from 1-4 of the ring atoms are a heteroatom independently selected from O, N, N—H, N—R o″ , and S, each of which is optionally substituted with from 1-3 R o″ ; and SO 2 —(C1-C6)alkyl;

R4 is hydrogen or halo;

R5 is hydrogen; and

(i) each of R2 and R3 is hydrogen; or (ii) R2 is hydrogen, and R3 is fluoro; or (iii) R2 is a substituent other than hydrogen, and R3 is hydrogen.

10. The compound or salt according to claim 1 , wherein:

X is —Y—[C(R a ) 2 ] a -A-[C(R b ) 2 ] b —B—;

R1 is:

(i) monocyclic or bicyclic heteroaryl including from 5-10 ring atoms, which is optionally substituted with from 1-3 R o ; wherein from 1-4 of the ring atoms are a heteroatom independently selected from O, N, N—H, N—R o , and S;

(ii) C6-C10 aryl, which is optionally substituted with from 1-3 R o ; or

(iii) C3-C10 cycloalkyl or C3-C10 cycloalkenyl, each of which is optionally substituted with from 1-3 R o ; or

(iv) hydrogen;

R o is independently selected from the group consisting of halogen; C1-C6 alkyl; fluoro(C1-C6)alkyl; hydroxyl; hydroxy(C1-C4)alkyl; C1-C6 alkoxy; fluoro(C1-C6)alkoxy; (C1-C6 alkyl)C(O)—; (C1-C6 alkyl)NH—; (C1-C6 alkyl) 2 N—; —N*(R o′ ) 2 , wherein R o′ —N*—R o′ together form a saturated ring having 5 or 6 ring atoms, in which 1 or 2 ring atoms are optionally a heteroatom independently selected from NH, N(C1-C6alkyl), 0, or S; cyano; phenyl; heteroaryl including from 5-6 ring atoms, wherein from 1-4 of the ring atoms are a heteroatom independently selected from O, N, N—H, N—R o″ , and S, each of which is optionally substituted with from 1-3 R o″ ; and SO 2 —(C1-C6)alkyl;

R4 is hydrogen or halo;

R5 is hydrogen; and

(i) each of R2 and R3 is hydrogen; or (ii) R2 is hydrogen, and R3 is fluoro; or (iii) R2 is a substituent other than hydrogen, and R3 is hydrogen.

11. The compound or salt according to claim 1 , wherein:

X is —Y—[C(R a ) 2 ] a -A-[C(R b ) 2 ] b —B—;

R1 is C3-C10cycloalkyl or C3-C10 cycloalkenyl, optionally substituted with from 1-3 R o ;

R o is independently selected from the group consisting of: halogen; C1-C6 alkyl; fluoro(C1-C6)alkyl; hydroxyl; hydroxy(C 1 -C 4 )alkyl; C1-C6 alkoxy; fluoro(C1-C6)alkoxy; (C1-C6 alkyl)NH—; (C1-C6 alkyl) 2 N—; cyano; and SO 2 —(C1-C6)alkyl.;

R4 is hydrogen or halo;

R5 is hydrogen; and

(i) each of R2 and R3 is hydrogen; or (ii) R2 is hydrogen, and R3 is fluoro; or (iii) R2 is a substituent other than hydrogen, and R3 is hydrogen.

12. The compound or salt according to claim 1 , wherein:

X is —Y—[C(R a ) 2 ] a -A-[C(R b ) 2 ] b —B—;

R1 is monocyclic or bicyclic heteroaryl including from 5-10 ring atoms, optionally substituted with from 1-3 R o ; wherein from 1-4 of the ring atoms are a heteroatom independently selected from O, N, N—H, N—R o , and S;

R o is independently selected from the group consisting of: halogen; C1-C6 alkyl; fluoro(C1-C6)alkyl; hydroxyl; hydroxy(C 1 -C 4 )alkyl; C1-C6 alkoxy; fluoro(C1-C6)alkoxy; (C1-C6 alkyl)NH—; (C1-C6 alkyl) 2 N—; cyano; and SO 2 —(C1-C6)alkyl;

R4 is hydrogen or halo;

R5 is hydrogen; and

(i) each of R2 and R3 is hydrogen; or (ii) R2 is hydrogen, and R3 is fluoro; or (iii) R2 is a substituent other than hydrogen, and R3 is hydrogen.

13. The compound or salt according to claim 1 , wherein:

X is —Y—[C(R a ) 2 ] a -A-[C(R b ) 2 ] b —B—;

R1 is C6-C10 aryl, optionally substituted with from 1-3 R o ;

R o is independently selected from the group consisting of: halogen; C1-C6 alkyl; fluoro(C1-C6)alkyl; hydroxyl; hydroxy(C 1 -C 4 )alkyl; C1-C6 alkoxy; fluoro(C1-C6)alkoxy; (C1-C6 alkyl)NH—; (C1-C6 alkyl) 2 N—; cyano; and SO 2 —(C1-C6)alkyl;

R4 is hydrogen or halo;

R5 is hydrogen; and

(i) each of R2 and R3 is hydrogen; or (ii) R2 is hydrogen, and R3 is fluoro; or (iii) R2 is a substituent other than hydrogen, and R3 is hydrogen.

14. The compound or salt according to claim 1 , wherein the compound or salt has formula (Ia):

15. The compound or salt according to claim 1 , wherein the compound or salt has formula (Ib):

16. The compound or salt according to claim 9 , wherein X is CH 2 .

17. The compound or salt according to claim 9 , wherein X is (CH 2 ) 2-4 .

18. The compound or salt according to claim 9 , wherein R1 is C3-C6 cycloalkyl, optionally substituted with from 1-3 R o .

19. The compound or salt according to claim 1 , wherein the compound is selected from A1-A16.

20. The compound or salt according to claim 1 , wherein —X—R 1 is CH 2 phenyl, optionally substituted with one or more substituents selected from halo and methyl.

21. The compound or salt according to claim 1 , wherein —XR 1 , is CH 2 pyridyl, optionally substituted with one or more substituents selected from halo and methyl.

22. The compound or salt according to claim 1 , wherein —XR 1 is CH 2 cyclopropyl, optionally substituted with one or more of C1-C3alkyl, C1-C3alkoxy, and halo.

23. The compound or salt according to claim 1 , wherein —XR 1 is CH 2 pyrazolyl, optionally substituted with one or more substituents selected from methyl and halo.

24. The compound or salt according to claim 1 , wherein R 2 is hydrogen and R 3 is F or Cl.

25. A pharmaceutical composition comprising a compound, or pharmaceutically acceptable salt thereof, as claimed in claim 1 and a pharmaceutically acceptable carrier.

26. A method of inhibiting HDAC1, HDAC2, and HDAC3, the method comprising contacting a cell with an effective amount of a compound, or pharmaceutically acceptable salt thereof, as claimed in claim 1 .

27. A method of treating Friedreich's ataxia in a patient in need thereof, the method comprising administering a compound, or pharmaceutically acceptable salt thereof, as claimed in claim 1 to said patient.

28. The compound or salt according to claim 1 , wherein the compound or salt is selected from the group consisting of:

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 2, 2016
From: JACQUES, VINCENT; RUSCHE, JAMES R.
To: BIOMARIN PHARMACEUTICAL INC.
Reel/Frame 038783/0218 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 29, 2016
From: JACQUES, VINCENT; RUSCHE, JAMES R.
To: REPLIGEN CORPORATION
Reel/Frame 038417/0566 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 29, 2016
From: REPLIGEN CORPORATION
To: BIOMARIN PHARMACEUTICAL INC.
Reel/Frame 038417/0742 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 29, 2016
From: JACQUES, VINCENT; RUSCHE, JAMES R.
To: REPLIGEN CORPORATION
Reel/Frame 038572/0860 →
Continuity (3)
Provisional Application 61863235 · Aug 7, 2013
Provisional Application 61800170 · Mar 15, 2013
Related Publication 20160031823A1 · Feb 4, 2016
Cited By (1)
US 12,540,132