IP Library Granted Patent US 10,329,286
Granted Patent B2
US 10,329,286 · App. 15/619,675 · Granted Jun 25, 2019

FXR (NR1H4) modulating compounds

Inventors: Peter A. Blomgren (Issaquah, WA); Kevin S. Currie (North Bend, WA); Julie Farand (San Mateo, CA); Christian Gege (Mauer, DE); Jeffrey E. Kropf (Issaquah, WA); Jianjun Xu (Seattle, WA)
Assignee: Gilead Sciences, Inc.
C07D413/14C07D401/14
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Quick Facts
Patent No.
US 10,329,286
App. No.
15/619,675
Granted
Jun 25, 2019
Kind
B2
Abstract

The present disclosure relates generally to compounds which bind to the NR1H4 receptor (FXR) and act as agonists of FXR. The disclosure further relates to the use of the compounds for the preparation of a medicament for the treatment of diseases and/or conditions through binding of said nuclear receptor by said compounds and to a process for the synthesis of said compounds.

Claims (23)

1. A compound according to Formula (I):

wherein:

Q is phenylene optionally substituted with one or two substituents selected from halogen, methyl, —CH 2 F, —CHF 2 , and —CF 3 ;

Z is:

L is a bond;

X is CH or C—CH 3 ;

R 1 is C 1-4 -alkyl or C 3-6 -cycloalkyl;

R 3 is halogen, C 1-4 -alkyl, halo-C 1-4 -alkyl, C 1-4 -alkoxy, or halo-C 1-4 -alkoxy;

R 4 is hydroxyl, C 1-6 -alkoxy, halo-C 1-6 -alkoxy, or NR 5 R 6 ;

R 5 is hydrogen, C 1-6 -alkyl, or halo-C 1-6 -alkyl;

R 6 is hydrogen or C 1-6 -alkyl, wherein said C 1-6 -alkyl is optionally substituted with 1 to 6 substituents independently selected from halogen, —SO 3 H, and —CO 2 H;

R 7 and R 8 are independently selected from halogen, C 1-3 -alkoxy, and fluoro-C 1-3 -alkoxy; and

n is 0 or 1;

or a pharmaceutically acceptable salt, a stereoisomer, a mixture of stereoisomers, or a tautomer thereof.

2. The compound of claim 1 , wherein R 4 is hydroxyl; or a pharmaceutically acceptable salt, a stereoisomer, a mixture of stereoisomers, or a tautomer thereof.

3. The compound of claim 1 , wherein Q is phenylene substituted with one chloro; or a pharmaceutically acceptable salt, a stereoisomer, a mixture of stereoisomers, or a tautomer thereof.

4. The compound of claim 1 , wherein R 1 is cyclopropyl; or a pharmaceutically acceptable salt, a stereoisomer, a mixture of stereoisomers, or a tautomer thereof.

5. The compound of claim 1 , wherein

is:

or a pharmaceutically acceptable salt, a stereoisomer, a mixture of stereoisomers, or a tautomer thereof.

6. A compound selected from the group consisting of:

or a pharmaceutically acceptable salt, a stereoisomer, a mixture of stereoisomers, or a tautomer thereof.

7. A pharmaceutical composition comprising a compound of claim 1 , or a pharmaceutically acceptable salt, a stereoisomer, a mixture of stereoisomers, or a tautomer thereof, and a pharmaceutically acceptable excipient.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 28, 2017
From: BLOMGREN, PETER A.; CURRIE, KEVIN S.; FARAND, JULIE; KROPF, JEFFREY E.; XU, JIANJUN
To: GILEAD SCIENCES, INC.
Reel/Frame 043126/0054 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 28, 2017
From: GEGE, CHRISTIAN
To: PHENEX PHARMACEUTICALS AG
Reel/Frame 043126/0229 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 28, 2017
From: PHENEX PHARMACEUTICALS AG
To: GILEAD SCIENCES, INC.
Reel/Frame 043126/0660 →
Continuity (2)
Provisional Application 62349479 · Jun 13, 2016
Related Publication 20170355693A1 · Dec 14, 2017