IP Library Granted Patent US 9,776,960
Granted Patent B2
US 9,776,960 · App. 14/836,869 · Granted Oct 3, 2017

Compounds and uses thereof for the modulation of hemoglobin

Inventors: Qing Xu (South San Francisco, CA); Zhe Li (South San Francisco, CA)
Assignee: Global Blood Therapeutics, Inc.
C07D207/08C07C271/16C07D207/34C07D207/48C07D211/16C07D211/22C07D211/60C07D211/78C07D213/81C07D241/04C07D265/30C07D279/12C07D309/08C07D309/28C07D333/38C07D335/02C07D401/06C07D401/12C07D403/06
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 9,776,960
App. No.
14/836,869
Granted
Oct 3, 2017
Kind
B2
Abstract

Provide herein are compounds and pharmaceutical compositions suitable as modulators of hemoglobin, methods and intermediates for their preparation, and methods for their use in treating disorders mediated by hemoglobin and disorders that would benefit from tissue and/or cellular oxygenation.

Claims (30)

1. A compound of Formula (II):

or a tautomer thereof, or pharmaceutically acceptable salt of each of thereof, wherein

R 3 is C 1 -C 6 alkyl, C 3 -C 8 cycloalkyl, C 1 -C 6 alkoxy, C 3 -C 8 cycloalkoxy, or —NR 1 R 2 ;

each R 1 and R 2 independently is hydrogen, C 1 -C 6 alkyl, C 3 -C 8 cycloalkyl, C 6 -C 10 aryl, 4-10 membered heterocyclyl or 5-10 membered heteroaryl, each containing up to 5 ring heteroatoms, wherein the heteroatom is selected from the group consisting of O, N, S, and oxidized forms of N and S, wherein each C 1 -C 6 alkyl, C 3 -C 8 cycloalkyl, 4-10 membered heterocyclyl, C 6 -C 10 aryl or 5-10 membered heteroaryl is optionally substituted with 1-3 substituents independently selected from halo, C 1 -C 6 alkyl optionally substituted with 1-5 halo, C 1 -C 6 alkoxy, hydroxy, and oxo, or R 1 and R 2 together with the nitrogen atom they are attached to form a 4-7 membered heterocyclyl optionally substituted with 1-3 substituents independently selected from halo, C 1 -C 6 alkyl optionally substituted with 1-5 halo, C 1 -C 6 alkoxy, hydroxy, and oxo;

ring B is a 5-6 membered heteroaryl having 1-3 nitrogen atoms or oxidized forms of N, wherein the 5-6 membered heteroaryl is optionally substituted with 1-3 substituents independently selected from halo, C 1 -C 6 alkyl optionally substituted with 1-5 halo, C 1 -C 6 alkoxy, hydroxy, oxo, COR 15 , and CO 2 R 15 ;

R 15 is C 1 -C 6 alkyl, C 3 -C 6 cycloalkyl, C 6 -C 10 aryl, 5-10 membered heteroaryl or a 4-10 membered heterocyclyl containing up to 5 ring heteroatoms, wherein the heteroatom is selected from the group consisting of O, N, S, and oxidized forms of N and S;

Y is —CH 2 —;

Z is —O— or —CH 2 —;

wherein Y is α or β substituted relative to —COR 3 ;

ring C is pyridinyl, wherein the pyridinyl is optionally substituted with 1-3 substituents independently selected from halo, C 1 -C 6 alkyl optionally substituted with 1-5 halo, C 1 -C 6 alkoxy, and hydroxyl;

wherein Z and —CHO are ortho to each other;

R 4 is OH, halo, C 1 -C 6 alkoxy optionally substituted with 1-5 halo, or C 3 -C 6 cycloalkoxy; and

R 4 and CHO are ortho to each other.

2. The compound of claim 1 , wherein ring B is substituted with 1-3substituents independently selected from halo, C 1 -C 6 alkyl, COR 15 , and CO 2 R 15 ; and

R 15 is C 1 -C 6 alkyl, C 6 -C 10 aryl, 5-10 membered heteroaryl or a 4-10 membered heterocyclyl containing up to 5 ring heteroatoms, wherein the heteroatom is selected from the group consisting of O, N, S, and oxidized forms of N;

each R 1 and R 2 independently is hydrogen, C 1 -C 6 alkyl, or C 3 -C 8 cycloalkyl, wherein each cycloalkyl is optionally substituted with 1-3 C 1 -C 6 alkyl groups, or R 1 and R 2 together with the nitrogen atom they are attached to form 4-7 membered heterocyclyl optionally substituted with 1-3 C 1 -C 6 alkyl groups.

3. A composition comprising a compound of claim 1 and at least one pharmaceutically acceptable excipient.

4. A method for increasing oxygen affinity of hemoglobin S in a subject, the method comprising administering to a subject in need thereof a therapeutically effective amount of a compound of claim 1 .

5. A method for treating oxygen deficiency associated with sickle cell disease or acute respiratory distress syndrome, the method comprising administering to a subject in need thereof a therapeutically effective amount of a compound of claim 1 .

6. A method for increasing oxygen affinity of hemoglobin S in a subject, the method comprising administering to a subject in need thereof a therapeutically effective amount of a composition of claim 3 .

7. A method for treating oxygen deficiency associated with sickle cell disease or acute respiratory distress syndrome, the method comprising administering to a subject in need thereof a therapeutically effective amount of a composition of claim 3 .

8. The compound of claim 1 , wherein the compound is:

or a pharmaceutically acceptable salt thereof.

9. A composition comprising a compound of claim 8 and at least one pharmaceutically acceptable excipient.

10. A method for increasing oxygen affinity of hemoglobin S in a subject, the method comprising administering to a subject in need thereof a therapeutically effective amount of a compound of claim 8 .

11. A method for treating oxygen deficiency associated with sickle cell disease or acute respiratory distress syndrome, the method comprising administering to a subject in need thereof a therapeutically effective amount of a compound of claim 8 .

12. A method for increasing oxygen affinity of hemoglobin S in a subject, the method comprising administering to a subject in need thereof a therapeutically effective amount of a composition of claim 9 .

13. A method for treating oxygen deficiency associated with sickle cell disease or acute respiratory distress syndrome, the method comprising administering to a subject in need thereof a therapeutically effective amount of a composition of claim 9 .

14. A method for treating sickle cell disease or acute respiratory distress syndrome, the method comprising administering to a subject in need thereof a therapeutically effective amount of a compound of claim 1 .

15. A method for treating sickle cell disease or acute respiratory distress syndrome, the method comprising administering to a subject in need thereof a therapeutically effective amount of a compound of claim 8 .

Assignments (5)
RELEASE OF SECURITY INTEREST Recorded Oct 6, 2022
From: BIOPHARMA CREDIT PLC, AS COLLATERAL AGENT
To: GLOBAL BLOOD THERAPEUTICS, INC.
Reel/Frame 061620/0186 →
SECOND AMENDED AND RESTATED PATENT SECURITY AGREEMENT Recorded Dec 22, 2021
From: GLOBAL BLOOD THERAPEUTICS, INC.
To: BIOPHARMA CREDIT PLC
Reel/Frame 058575/0921 →
AMENDED AND RESTATED PATENT SECURITY AGREEMENT Recorded Dec 9, 2020
From: GLOBAL BLOOD THERAPEUTICS, INC.
To: BIOPHARMA CREDIT PLC
Reel/Frame 054664/0871 →
SECURITY INTEREST Recorded Dec 20, 2019
From: GLOBAL BLOOD THERAPEUTICS, INC.
To: BIOPHARMA CREDIT PLC
Reel/Frame 051396/0312 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 11, 2015
From: XU, QING; LI, ZHE
To: GLOBAL BLOOD THERAPEUTICS, INC.
Reel/Frame 037270/0044 →
Continuity (3)
Continuation 14599341 · Jan 16, 2015
Continuation 13815735 · Mar 15, 2013
Related Publication 20160083348A1 · Mar 24, 2016