IP Library › Granted Patent US 9,611,220
Granted Patent B2
US 9,611,220 · App. 14/472,059 · Granted Apr 4, 2017

Inhibitors of histone demethylases

Inventors: Marc Labelle (Basking Ridge, NJ); Thomas Boesen (Københaven Ø, DK); Mukund Mehrotra (Winnipeg, CA); Qasim Khan (Winnipeg, CA); Farman Ullah (Winnipeg, CA)
Assignee: Gilead Sciences, Inc.
C07D213/79A61K31/44A61K31/443A61K31/444A61K31/4439A61K31/4545A61K31/496C07D401/06C07D401/12C07D405/12C07D413/12
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Quick Facts
Patent No.
US 9,611,220
App. No.
14/472,059
Granted
Apr 4, 2017
Kind
B2
Abstract

The present application discloses compounds capable of modulating the activity of histone demethylases (HDMEs), which are useful for prevention and/or treatment of diseases in which genomic dysregulation is involved in the pathogenesis, such as e.g. cancer. The present application also discloses pharmaceutical compositions comprising said compounds and the use of such compounds as a medicament. The compounds take the form

Claims (22)

1. A compound of Formula (I)

wherein

A is —CH 2 C(O)—;

Y is —NR 6 R 7 ; p 1 R 1 is —H;

Z is selected from a single bond, C 1-4 alkylene, heterocyclylene and C 3-6 cycloalkylene;

each R 4 is independently selected from C 1-6 alkyl, C 1-4 fluoroalkyl, C 1-4 hydroxyalkyl, C 1-4 alkoxy, C 3-10 cycloalkyl, —N(R 10 ) 2 , carbamoyl, and —OH;

each R 5 is independently selected from C 1-6 alkyl, C 1-4 fluoroalkyl, C 1-4 hydroxyalkyl, C 1-4 alkoxy, C 3-6 cycloalkyl, —CN, —F, —Cl, —Br, carbamoyl and —OH;

each of R 6 and R 7 is independently selected from —H, C 1-8 alkyl, C 1-4 fluoroalkyl, C 1-4 hydroxyalkyl, C 2-8 alkenyl, C 2-8 alkynyl, C 3-10 cycloalkyl, —Z-heterocyclyl, —Z-heteroaryl and —Z-aryl, wherein alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclyl, heteroaryl and aryl may optionally be substituted with one or more independently selected R 8 ;

each R 8 is independently selected from C 1-6 alkyl, C 1-4 fluoroalkyl, C 1-4 hydroxyalkyl, C 2-6 alkenyl, C 2-6 alkynyl, C 3-10 cycloalkyl, —Z-heterocyclyl, —Z-heteroaryl, —Z-aryl, —Z—NR 10 R 11 , —Z—C(═O)—NR 10 R 11 , —Z—OR 9 , halogen, —CN, —Z—SR 9 , —Z—SOR 9 , —Z—SO 2 R 9 and —Z—COOR 9 , wherein alkyl, alkenyl, alkynyl, cycloalkyl, heterocyclyl, heteroaryl and aryl may optionally be substituted with one or more selected from C 1-4 alkyl, C 1-4 fluoroalkyl, C 1-4 hydroxyalkyl, C 3-6 cycloalkyl, —Z-heterocyclyl, —Z-heteroaryl, —Z-aryl, —Z—NR 10 R 11 ,—Z—C(═O)—NR 10 R 11 ,—Z—OR 9 , halogen, —CN, —Z—SR 9 , —Z—SOR 9 , —Z—SO 2 R 9 and —Z—COOR 9 ; wherein any heterocyclyl may be further substituted with one or more R 4 as defined above, and wherein any heteroaryl and any aryl may be further substituted with one or more R 5 as defined above;

each R 9 is independently selected from —H, C 1-8 alkyl, C 1-4 fluoroalkyl, C 1-4 hydroxyalkyl, C 2-8 alkenyl, C 2-8 alkynyl, C 3-10 cycloalkyl, —Z-heterocyclyl, —Z-aryl, and —Z— heteroaryl, wherein any heterocyclyl may be substituted with one or more R 4 as defined above, and wherein any heteroaryl and any aryl may be substituted with one or more R 5 as defined above; and

each of R 10 and R 11 is independently selected from —H, C 1-6 alkyl, C 1-4 fluoroalkyl, C 1-4 hydroxyalkyl, C 2-8 alkenyl, C 2-8 alkynyl, C 3-10 cycloalkyl, heterocyclyl, heteroaryl, and aryl, wherein any heterocyclyl may be substituted with one or more R 4 as defined above, and wherein any heteroaryl and any aryl may be substituted with one or more R 5 as defined above;

or a pharmaceutically acceptable salt thereof.

2. The compound of claim 1 , wherein Y is

wherein n is from 1 to 3.

3. The compound of claim 1 , wherein Y is

wherein n is from 1 to 3 and each m independently is from 0 to 2.

4. The compound of claim 1 , wherein the compound is

or a pharmaceutically acceptable salt thereof.

5. The pharmaceutically acceptable salt of the compound of claim 1 , wherein the pharmaceutically acceptable salt is selected from succinic, maleic, acetic, fumaric, citric, tartaric, benzoic, trifluoroacetic, malic, lactic, formic, propionic, glycolic, gluconic, camphorsulfuric, isothionic, mucic, gentisic, isonicotinic, saccharic, glucuronic, furoic, glutamic, ascorbic, anthranilic, salicylic, phenylacetic, mandelic, embonic (pamoic), ethanesulfonic, pantothenic, stearic, sulfinilic, alginic, galacturonic, benzenesulfonic, p-toluenesulfonic, oxalic, methanesulfonic and naphthalenesulfonic acid salt.

6. A pharmaceutical composition comprising a compound of claim 1 and one or more pharmaceutically acceptable excipients, diluents or carriers.

7. The pharmaceutical composition according to claim 6 , further comprising one or more active substances.

8. The pharmaceutically acceptable salt of claim 5 , wherein the pharmaceutically acceptable salt is the oxalic acid salt.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 12, 2016
From: EPITHERAPEUTICS, APS
To: GILEAD SCIENCES, INC.
Reel/Frame 039997/0367 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 20, 2015
From: LABELLE, MARC; BOESEN, THOMAS; MEHROTRA, MUKUND; KHAN, QASIM; ULLAH, FARMAN
To: EPITHERAPEUTICS APS
Reel/Frame 034755/0752 →
Priority Claims (2)
DK 2012 00599 · Oct 2, 2012 · national
DK 2013 70112 · Feb 27, 2013 · national
Continuity (4)
Continuation 14381558
Provisional Application 61708806 · Oct 2, 2012
Provisional Application 61770050 · Feb 27, 2013
Related Publication 20140371195A1 · Dec 18, 2014