IP Library Granted Patent US 10,435,393
Granted Patent B2
US 10,435,393 · App. 14/791,017 · Granted Oct 8, 2019

Compounds and uses thereof for the modulation of hemoglobin

Inventors: Qing Xu (South San Francisco, CA); Zhe Li (South San Francisco, CA); Brian W. Metcalf (South San Francisco, CA)
Assignee: Global Blood Therapeutics, Inc.
C07D405/04A61K8/494A61K8/4906A61K8/4913A61K8/4926C07D401/04C07D403/04C07D409/04C07D413/04C07D417/04
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Quick Facts
Patent No.
US 10,435,393
App. No.
14/791,017
Granted
Oct 8, 2019
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 (25)

1. A compound of Formula (I):

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

ring A is a heteroaryl selected from the group consisting of furanyl, imidazolyl, oxadiazolyl, oxazolyl, pyrazolyl, and pyridinyl, wherein the heteroaryl is optionally substituted with 1-3 substituents independently selected from the group consisting of halo, OH, C 1 -C 6 alkyl, and C 1 -C 6 alkoxy, wherein the C 1 -C 6 alkyl is optionally substituted with 1-5 halo;

wherein ring A is α substituted relative to the Y substituent;

ring B is a heterocycle selected from the group consisting of oxazolinyl, piperidinyl, piperazinyl, pyrrolidinyl, morpholino, tetrahydropyridinyl, tetrahydrofuranyl, dihydropyranyl, and tetrahydropyranyl, wherein the heterocycle is optionally substituted with a substituent selected from the group consisting of halo, OH, C 1 -C 6 alkyl, COR 15 , and COOR 15 ; wherein R 15 is C 1 -C 6 alkyl;

Y—Z is —CH 2 O—, wherein the left hand side is joined with ring B;

R 5 is hydrogen, C 1 -C 6 alkyl, wherein the C 1 -C 6 alkyl is optionally substituted with 1-5 halo;

each R 6 is independently selected from the group consisting of halo, C 1 -C 6 alkyl, C 1 -C 6 alkoxy, and C 1 -C 6 alkylthio, wherein the C 1 -C 6 alkyl is optionally substituted with 1-5 halo; and

p is 0, 1, 2, or 3.

2. The compound of claim 1 , or a tautomer thereof, or a pharmaceutically acceptable salt of each thereof, wherein p is 0.

3. The compound of claim 1 , or a tautomer thereof, or a pharmaceutically acceptable salt of each thereof, wherein ring A is pyrazolyl optionally substituted with a C 1 -C 6 alkyl or C 1 -C 6 alkoxy.

4. The compound of claim 1 , or a tautomer thereof, or a pharmaceutically acceptable salt of each thereof, wherein ring A is pyrazolyl substituted with a C 1 -C 6 alkyl.

5. The compound of claim 1 , or a tautomer thereof, or a pharmaceutically acceptable salt of each thereof, wherein ring B is a heterocycle selected from the group consisting of piperidinyl, pyrrolidinyl, morpholino, tetrahydropyridinyl, dihydropyranyl, and tetrahydropyranyl, wherein the heterocycle is optionally substituted with one substituent selected from the group consisting of methyl and —COCH 3 .

6. The compound of claim 1 , or a tautomer thereof, or a pharmaceutically acceptable salt of each thereof, wherein ring B is a heterocycle selected from the group consisting of piperidinyl, tetrahydropyridinyl, dihydropyranyl, and tetrahydropyranyl, wherein the heterocycle is optionally substituted with one substituent selected from the group consisting of methyl and —COCH 3 .

7. A pharmaceutical composition comprising a compound of claim 1 , or a tautomer thereof, or a pharmaceutically acceptable salt of each thereof, and at least one pharmaceutically acceptable excipient.

8. A method for increasing oxygen affinity of hemoglobin S in a subject in need thereof, the method comprising administering to the subject a compound of claim 1 , or a tautomer thereof, or a pharmaceutically acceptable salt of each thereof.

9. A method for treating sickle cell disease comprising administering to a subject in need thereof a compound of claim 1 , or a tautomer thereof, or a pharmaceutically acceptable salt of each thereof.

10. A compound selected from:

wherein

is a double or a single bond;

R 14 is C 1 -C 6 alkyl, C 3 -C 8 cycloalkyl, COR 15 , or COOR 15 ;

wherein R 15 is C 1 -C 6 alkyl;

or an N oxide thereof, or a tautomer thereof, or a pharmaceutically acceptable salt of each thereof.

11. A compound of the formula

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

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 12, 2018
From: XU, QING; LI, ZHE; METCALF, BRIAN W.
To: GLOBAL BLOOD THERAPEUTICS, INC.
Reel/Frame 047753/0165 →
Continuity (2)
Continuation 13815776 · Mar 15, 2013
Related Publication 20160152602A1 · Jun 2, 2016