IP Library Granted Patent US 10,030,006
Granted Patent B2
US 10,030,006 · App. 15/035,610 · Granted Jul 24, 2018

Coumarin based Hsp90 inhibitors with urea and ether substituents

Inventors: Brian S. J. Blagg (Lawrence, KS); Huiping Zhao (Lawrence, KS)
Assignee: UNIVERSITY OF KANSAS
C07D405/12A61K31/352A61K31/4025A61K31/453A61K31/496A61K31/5377A61K45/06C07D311/16C07D405/14C07D413/12G16H50/50
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Quick Facts
Patent No.
US 10,030,006
App. No.
15/035,610
Granted
Jul 24, 2018
Kind
B2
Abstract

Compounds of the formulas: wherein: R 1 -R 4 , X 1 , Y 1 , and A are as defined herein are provided. Pharmaceutical compositions of the compounds are also provided. In some aspects, these compounds are are useful for the treatment of a disease or disorder. In some embodiments, the disease or disorder is a proliferative disease such as cancer.

Claims (48)

1. A compound of the formula:

wherein:

R 1 and R 2 are each independently selected from hydrogen, alkyl (C≤12) , or substituted alkyl (C≤12) ;

R 3 is hydrogen, alkyl (C≤12) , aralkyl (C≤12) , substituted alkyl (C≤12) , or substituted aralkyl (C≤12) ; or R 3 and Y 1 are taken together as defined below;

R 4 is hydrogen, alkyl (C≤12) , alkoxy (C≤12) , substituted alkyl (C≤12) , or substituted alkoxy (C≤12) ;

X 1 is -alkanediyl (C≤8) -heterocycloalkyl (C≤12) , -alkanediyl (C≤8) -amino (C≤12) , -alkanediyl (C≤8) -alkylamino (C≤12) , -alkanediyl (C≤8) -dialkylamino (C≤12) , heterocycloalkyl (C≤12) , or a substituted version of any of these groups; and

Y 1 is alkyl (C≤12) , cycloalkyl (C≤12) , adamantyl (C≤18) , aryl (C≤18) , aralkyl (C≤18) , acyl (C≤12) , -alkanediyl (C≤8) -cycloalkyl (C≤12) , -arenediyl (C≤12) -alkene (C≤8) , -arenediyl (C≤12) -aryl (C≤12) , -arenediyl (C≤12) -aralkyl (C≤12) , -arenediyl (C≤12) -aryloxy (C≤12) , or a substituted version of any of these groups; or R 3 and Y 1 are taken together and are alkanediyl (C≤8) , alkylaminodiyl (C≤8) , alkoxydiyl (C≤8) , or a substituted version of any of these groups; or

wherein the compound is not selected from:

or a pharmaceutically acceptable salt thereof.

2. The compound of claim 1 further defined as:

wherein:

R 1 and R 2 are each independently selected from hydrogen, alkyl (C≤12) , or substituted alkyl (C≤12) ;

R 3 is hydrogen, alkyl (C≤12) , aralkyl (C≤12) , substituted alkyl (C≤12) , or substituted aralkyl (C≤12) ; or R 3 and Y 1 are taken together as defined below;

X 1 is -alkanediyl (C≤8) -heterocycloalkyl (C≤12) , -alkanediyl (C≤8) -amino (C≤12) , -alkanediyl (C≤8) -alkylamino (C≤12) , -alkanediyl (C≤8) -dialkylamino (C≤12) , heterocycloalkyl (C≤12) , or a substituted version of any of these groups; and

Y 1 is alkyl (C≤12) , cycloalkyl (C≤12) , adamantyl (C≤18) , aryl (C≤18) , aralkyl (C≤18) , acyl (C≤12) , -alkanediyl (C≤8) -cycloalkyl (C≤12) , -arenediyl (C≤12) -alkene (C≤8) , -arenediyl (C≤12) -aryl (C≤12) , -arenediyl (C≤12) -aralkyl (C≤12) , -arenediyl (C≤12) -aryloxy (C≤12) , or a substituted version of any of these groups; or R 3 and Y 1 are taken together and are alkanediyl (C≤8) , alkylaminodiyl (C≤8) , alkoxydiyl (C≤8) , or a substituted version of any of these groups; or

or a pharmaceutically acceptable salt thereof.

3. The compound of claim 1 further defined as:

wherein:

R 2 is hydrogen, alkyl (C≤12) , or substituted alkyl (C≤12) ;

R 3 is hydrogen, alkyl (C≤12) , aralkyl (C≤12) , substituted alkyl (C≤12) , or substituted aralkyl (C≤12) ; or R 3 and Y 1 are taken together as defined below;

X 1 is -alkanediyl (C≤8) -heterocycloalkyl (C≤12) , -alkanediyl (C≤8) -amino (C≤12) , -alkanediyl (C≤8) -alkylamino (C≤12) , -alkanediyl (C≤8) -dialkylamino (C≤12) , heterocycloalkyl (C≤12) , or a substituted version of any of these groups; and

Y 1 is alkyl (C≤12) , cycloalkyl (C≤12) , adamantyl (C≤18) , aryl (C≤18) , aralkyl (C≤18) , acyl (C≤12) , -alkanediyl (C≤8) -cycloalkyl (C≤12) , -arenediyl (C≤12) -alkene (C≤8) , -arenediyl (C≤12) -aryl (C≤12) , -arenediyl (C≤12) -aralkyl (C≤12) , -arenediyl (C≤12) -aryloxy (C≤12) , or a substituted version of any of these groups; or R 3 and Y 1 are taken together and are alkanediyl (C≤8) , alkylaminodiyl (C≤18) , alkoxydiyl (C≤8) , or a substituted version of any of these groups; or

or a pharmaceutically acceptable salt thereof.

4. The compound of claim 1 further defined as:

wherein:

R 3 is hydrogen, alkyl (C≤12) , aralkyl (C≤12) , substituted alkyl (C≤12) , or substituted aralkyl (C≤12) ; or R 3 and Y 1 are taken together as defined below;

X 1 is -alkanediyl (C≤8) -heterocycloalkyl (C≤12) , -alkanediyl (C≤8) -amino (C≤12) , -alkanediyl (C≤8) -alkylamino (C≤12) , -alkanediyl (C≤8) -dialkylamino (C≤12) , heterocycloalkyl (C≤12) , or a substituted version of any of these groups; and

Y 1 is alkyl (C≤12) , cycloalkyl (C≤12) , adamantyl (C≤18) , aryl (C≤18) , aralkyl (C≤18) , acyl (C≤12) , -alkanediyl (C≤8) -cycloalkyl (C≤12) , -arenediyl (C≤12) -alkene (C≤8) , -arenediyl (C≤12) -aryl (C≤12) , -arenediyl (C≤12) -aralkyl (C≤12) , -arenediyl (C≤12) -aryloxy (C≤12) , or a substituted version of any of these groups; or R 3 and Y 1 are taken together and are alkanediyl (C≤8) , alkylaminodiyl (C≤8) , alkoxydiyl (C≤8) , or a substituted version of any of these groups; or

or a pharmaceutically acceptable salt thereof.

5. The compound of claim 1 further defined as:

wherein:

R 3 is hydrogen, alkyl (C≤12) , substituted alkyl (C≤12) , aralkyl (C≤12) , or substituted aralkyl (C≤12) ; or R 3 and Y 1 are taken together as defined below;

X 1 is heterocycloalkyl (C≤12) or substituted heterocycloalkyl (C≤12) ; and

Y 1 is alkyl (C≤12) , cycloalkyl (C≤12) , adamantyl (C≤18) , aryl (C≤18) , aralkyl (C≤18) , acyl (C≤12) , -alkanediyl (C≤8) -cycloalkyl (C≤12) , -arenediyl (C≤12) -alkene (C≤8) , -arenediyl (C≤12) -aryl (C≤12) , -arenediyl (C≤12) -aralkyl (C≤12) , -arenediyl (C≤12) -aryloxy (C≤12) , or a substituted version of any of these groups; or R 3 and Y 1 are taken together and are alkanediyl (C≤8) , alkylaminodiyl (C≤8) , alkoxydiyl (C≤8) , or a substituted version of any of these groups; or

or a pharmaceutically acceptable salt thereof.

6. The compound of claim 1 , wherein R 3 is hydrogen.

7. The compound of claim 1 , wherein R 3 is alkyl (C≤6) .

8. The compound of claim 1 , wherein X 1 is heterocycloalkyl (C≤8) or substituted heterocycloalkyl (C≤8) .

9. The compound of claim 8 , wherein X 1 is:

10. The compound of claim 1 , wherein Y 1 is aryl (C≤18) or substituted aryl (C≤18) .

11. The compound of claim 10 , wherein Y 1 is aryl (C≤12) .

12. The compound of claim 10 , wherein Y 1 is biphenyl (C≤12) .

13. The compound of claim 10 , wherein Y 1 is substituted aryl (C≤12) .

14. The compound of claim 10 , wherein Y 1 is substituted biphenyl (C≤18) .

15. The compound of claim 1 , wherein Y 1 is aralkyl (C≤18) or substituted aralky (C≤18) .

16. The compound of claim 1 , wherein the compound is further defined as:

or a pharmaceutically acceptable salt thereof.

17. A pharmaceutical composition comprising a compound of claim 1 and an excipient.

Assignments (5)
RELEASE OF SECURITY INTEREST Recorded Apr 9, 2025
From: BIOPHARMA CREDIT PLC
To: REATA PHARMACEUTICALS HOLDINGS, LLC; REATA PHARMACEUTICALS GLOBAL, INC.; REATA PHARMACEUTICALS, INC.
Reel/Frame 070793/0130 →
RELEASE OF SECURITY INTEREST Recorded Apr 9, 2025
From: BIOPHARMA CREDIT PLC
To: REATA PHARMACEUTICALS HOLDINGS, LLC; REATA PHARMACEUTICALS GLOBAL, INC.; REATA PHARMACEUTICALS, INC.
Reel/Frame 070793/0228 →
AMENDED AND RESTATED PATENT SECURITY AGREEMENT Recorded Jul 12, 2023
From: REATA PHARMACEUTICALS HOLDINGS, LLC; REATA PHARMACEUTICALS GLOBAL, INC.; REATA PHARMACEUTICALS, INC.
To: BIOPHARMA CREDIT PLC
Reel/Frame 064264/0557 →
PATENT SECURITY AGREEMENT Recorded May 18, 2023
From: REATA PHARMACEUTICALS HOLDINGS, LLC; REATA PHARMACEUTICALS GLOBAL, INC.; REATA PHARMACEUTICALS, INC.
To: BIOPHARMA CREDIT PLC
Reel/Frame 063697/0461 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 26, 2016
From: BLAGG, BRIAN S.J.; ZHAO, HUIPING
To: UNIVERSITY OF KANSAS
Reel/Frame 039550/0206 →
Continuity (2)
Provisional Application 61902517 · Nov 11, 2013
Related Publication 20160289217A1 · Oct 6, 2016
Cited By (3)
US 50,319 US 12,595,278 US 12,679,860