IP Library Granted Patent US 8,703,810
Granted Patent B2
US 8,703,810 · App. 13/702,394 · Granted Apr 22, 2014

Estrogen receptor modulators and uses thereof

Inventors: Mehmet Kahraman (La Jolla, CA); Steven P. Govek (San Diego, CA); Johnny Y. Nagasawa (San Diego, CA); Nicholas D. Smith (San Diego, CA)
Assignee: Seragon Pharmaceuticals, Inc.
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Quick Facts
Patent No.
US 8,703,810
App. No.
13/702,394
Granted
Apr 22, 2014
Kind
B2
Abstract

Described herein are compounds that are estrogen receptor modulators. Also described are pharmaceutical compositions and medicaments that include the compounds described herein, as well methods of using such estrogen receptor modulators, alone and in combination with other compounds, for treating diseases or conditions that are mediated or dependent upon estrogen receptors.

Claims (137)

1. A compound of Formula (VI), or a pharmaceutically acceptable salt thereof:

wherein,

R 1 is H, F, C 1 -C 4 alkyl, or C 1 -C 4 fluoroalkyl;

R 3 is H, halogen, C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, or C 1 -C 4 fluoroalkyl;

each R 4 is independently selected from H, halogen, —CN, —OH, —OR 9 , —SR 9 , —S(═O)R 10 , —S(═O) 2 R 10 , —C(═O)R 10 , C(═O)OH, —C(═O)OR 10 , —C(═O)NHR 10 , —C(═O)N(R 10 ) 2 , substituted or unsubstituted C 1 -C 6 alkyl, substituted or unsubstituted C 1 -C 6 fluoroalkyl, substituted or unsubstituted C 1 -C 6 -fluoroalkoxy, substituted or unsubstituted C 1 -C 6 alkoxy, and substituted or unsubstituted C 1 -C 6 heteroalkyl;

each R 5 is independently selected from H, halogen, —CN, —OH, —OR 9 , —SR 9 , —S(═O)R 10 , —S(═O) 2 R 10 , substituted or unsubstituted C 1 -C 6 alkyl, substituted or unsubstituted C 1 -C 6 fluoroalkyl, substituted or unsubstituted C 1 -C 6 -fluoroalkoxy, substituted or unsubstituted C 1 -C 6 alkoxy, and substituted or unsubstituted C 1 -C 6 heteroalkyl;

each R 6 is independently selected from H, halogen, —CN, —OH, —OR 9 , —SR 9 , —S(═O)R 10 , —S(═O) 2 R 10 , substituted or unsubstituted C 1 -C 6 alkyl, substituted or unsubstituted C 1 -C 6 fluoroalkyl, substituted or unsubstituted C 1 -C 6 -fluoroalkoxy, substituted or unsubstituted C 1 -C 6 alkoxy, and substituted or unsubstituted C 1 -C 6 heteroalkyl;

is azetidinyl or pyrrolidinyl;

R 7 is H or C 1 -C 4 alkyl;

each R 8 is independently selected from F, Cl, —CN, —OH, —OR 9 , —SR 9 , —S(═O)R 10 , —S(═O) 2 R 10 , substituted or unsubstituted C 1 -C 6 alkyl, substituted or unsubstituted C 1 -C 6 fluoroalkyl, substituted or unsubstituted C 1 -C 6 fluoroalkoxy, substituted or unsubstituted C 1 -C 6 alkoxy, and substituted or unsubstituted C 1 -C 6 heteroalkyl;

or 1 R 8 is taken together with R 1 along with the intervening atoms joining R 8 to R 1 to form a 5-, 6-, or 7-membered ring;

each R 9 is independently selected from H, —C(═O)R 10 , —C(═O)OR 10 , —C(═O)NHR 10 , substituted or unsubstituted C 1 -C 6 alkyl, substituted or unsubstituted C 1 -C 6 heteroalkyl, substituted or unsubstituted C 1 -C 6 fluoroalkyl, substituted or unsubstituted C 3 -C 10 cycloalkyl, substituted or unsubstituted C 2 -C 10 heterocycloalkyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, —C 1 -C 2 alkylene-(substituted or unsubstituted C 3 -C 10 cycloalkyl), —C 1 -C 2 alkylene-(substituted or unsubstituted C 2 -C 10 heterocycloalkyl), —C 1 -C 2 alkylene-(substituted or unsubstituted aryl), and —C 1 -C 2 alkylene-(substituted or unsubstituted heteroaryl); or

each R 10 is independently selected from substituted or unsubstituted C 1 -C 6 alkyl, substituted or unsubstituted C 1 -C 6 heteroalkyl, substituted or unsubstituted C 1 -C 6 fluoroalkyl, substituted or unsubstituted C 3 -C 10 cycloalkyl, substituted or unsubstituted C 2 -C 10 heterocycloalkyl, substituted or unsubstituted aryl, substituted or unsubstituted heteroaryl, —C 1 -C 2 alkylene-(substituted or unsubstituted C 3 -C 10 cycloalkyl), —C 1 -C 2 alkylene-(substituted or unsubstituted C 2 -C 10 heterocycloalkyl), —C 1 -C 2 alkylene-(substituted or unsubstituted aryl), and —C 1 -C 2 alkylene-(substituted or unsubstituted heteroaryl);

Y is —O—, —S—, or —NR 11 —; R 11 is H, —C(═O)R 10 , substituted or unsubstituted C 1 -C 6 alkyl, substituted or unsubstituted C 1 -C 6 fluoroalkyl, or substituted or unsubstituted C 1 -C 6 heteroalkyl;

X is —O—, —S—, —CH 2 —, —NH— or —N(C 1 -C 6 alkyl)-;

m is 0, 1, 2, 3 or 4;

n is 0, 1, 2, or 3;

p is 0, 1, 2, 3 or 4;

t is 1, 2, 3 or 4.

2. The compound of claim 1 , or a pharmaceutically acceptable salt thereof, wherein:

R 1 is H or C 1 -C 4 alkyl;

R 3 is C 1 -C 4 alkyl or C 1 -C 4 fluoroalkyl;

each R 4 is independently selected from H, halogen, —CN, —OH, —OR 9 , —SR 9 , —S(═O)R 10 , —S(═O) 2 R 10 , C 1 -C 4 alkyl, C 1 -C 4 fluoroalkyl, C 1 -C 4 -fluoroalkoxy, C 1 -C 4 alkoxy, and C 1 -C 4 heteroalkyl;

each R 5 is independently selected from H, halogen, —OH, C 1 -C 4 alkyl, C 1 -C 4 fluoroalkyl, C 1 -C 4 fluoroalkoxy, C 1 -C 4 alkoxy, and C 1 -C 4 heteroalkyl;

each R 6 is independently selected from H, halogen, —OH, C 1 -C 4 alkyl, C 1 -C 4 fluoroalkyl, C 1 -C 4 fluoroalkoxy, and C 1 -C 4 alkoxy;

R 7 is H or —CH 3 ;

Y is —O— or —S—;

X is —O—, —S—, —CH 2 —, —NH— or —N(CH 3 )—;

p is 0, 1, or 2.

3. The compound of claim 2 , or a pharmaceutically acceptable salt thereof, wherein:

each R 5 is independently selected from H, F, Cl, —OH, —CH 3 , —CF 3 , —OCF 3 and —OCH 3 ;

each R 6 is independently selected from H, F, Cl, —OH, —CH 3 , —CF 3 , —OCF 3 and —OCH 3 ;

R 7 is H;

is azetidinyl, or pyrrolidinyl;

each R 8 is independently selected from F, Cl, —OH, C 1 -C 4 alkyl, C 1 -C 4 fluoroalkyl, C 1 -C 4 fluoroalkoxy, C 1 -C 4 alkoxy, and C 1 -C 4 heteroalkyl.

4. The compound of claim 3 , or a pharmaceutically acceptable salt thereof, wherein:

5. The compound of claim 1 , wherein the compound of Formula (VI) has the structure of Formula (VIII):

or is a pharmaceutically acceptable salt thereof.

6. The compound of claim 1 , wherein the compound of Formula (VI) has the structure of Formula (X):

or is a pharmaceutically acceptable salt thereof.

7. The compound of claim 6 , or a pharmaceutically acceptable salt thereof, wherein:

R 1 is H or —CH 3 ;

R 3 is —CH 3 or —CF 3 ;

each R 8 is independently selected from F, Cl, —OH, —CH 3 , —CH 2 CH 3 , —CH(CH 3 ) 2 , —CF 3 , —CH 2 CF 3 , —OCF 3 , —OCH 2 CF 3 , —OCH 3 , —OCH 2 CH 3 , —CH 2 OCH 3 , —CH 2 OCH 2 CH 3 , and —CH 2 OH;

R 9 is H;

X is —O—.

8. A compound that is:

3-(3-Hydroxyphenyl)-4-methyl-2-(4-((S)-2-((R)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-2H-chromen-6-ol;

(S)-3-(3-Hydroxyphenyl)-4-methyl-2-(4-((S)-2-((R)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-2H-chromen-6-ol

(R)-3-(3-Hydroxyphenyl)-4-methyl-2-(4-((S)-2-((R)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-2H-chromen-6-ol;

3-(3-Hydroxyphenyl)-4-methyl-2-(4-(2-((R)-3-methylpyrrolidin-1-yl)ethoxy)phenyl)-2H-chromen-6-ol;

3-(3-Hydroxyphenyl)-4-methyl-2-(4-((R)-2-((R)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-2H-chromen-6-ol;

3-(3-Hydroxyphenyl)-4-methyl-2-(4-(2-((S)-3-methylpyrrolidin-1-yl)ethoxy)phenyl)-2H-chromen-6-ol;

3-(3-hydroxyphenyl)-4-methyl-2-(4-((S)-2-((S)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-2H-chromen-6-ol;

3-(3-hydroxyphenyl)-4-methyl-2-(4-((R)-2-((S)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-2H-chromen-6-ol;

2-(4-((S)-2-(3,3-Dimethylpyrrolidin-1-yl)propoxy)phenyl)-3-(3-hydroxyphenyl)-4-methyl-2H-chromen-6-ol;

2-(4-(2-(3,3-Dimethylpyrrolidin-1-yl)ethoxy)phenyl)-3-(3-hydroxyphenyl)-4-methyl-2H-chromen-6-ol;

3-(3-Hydroxyphenyl)-4-methyl-2-(4-(2-((R)-2-methylpyrrolidin-1-yl)ethoxy)phenyl)-2H-chromen-6-ol;

3-(3-Hydroxyphenyl)-4-methyl-2-(4-((S)-2-((R)-2-methylpyrrolidin-1-yl)propoxy)phenyl)-2H-chromen-6-ol;

3-(3-Hydroxyphenyl)-4-methyl-2-(4-((S)-2-((S)-2-methylpyrrolidin-1-yl)propoxy)phenyl)-2H-chromen-6-ol;

3-(3-Hydroxyphenyl)-4-methyl-2-(4-((S)-2-((R)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-2H-chromen-7-ol;

3-(4-Hydroxyphenyl)-4-methyl-2-(4-((S)-2-((R)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-2H-chromen-7-ol;

4-Methyl-2-(4-((S)-2-((R)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-3-phenyl-2H-chromen-6-ol;

3-(4-Fluorophenyl)-4-methyl-2-(4-((S)-2-((R)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-2H-chromen-6-ol;

(S)-3-(4-Fluorophenyl)-4-methyl-2-(4-((S)-2-((R)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-2H-chromen-6-ol;

(R)-3-(4-Fluorophenyl)-4-methyl-2-(4-((S)-2-((R)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-2H-chromen-6-ol;

3-(4-Hydroxyphenyl)-4-methyl-2-(4-((S)-2-((R)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-2H-chromen-6-ol;

3-(3-Fluorophenyl)-4-methyl-2-(4-((S)-2-((R)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-2H-chromen-6-ol;

3-(3-Fluoro-4-hydroxyphenyl)-4-methyl-2-(4-((S)-2-((R)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-2H-chromen-6-ol;

2-(2-Fluoro-4-((S)-2-((R)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-3-(3-hydroxyphenyl)-4-methyl-2H-chromen-6-ol;

3-(3-Hydroxy-4-methylphenyl)-4-methyl-2-(4-((S)-2-((R)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-2H-chromen-6-ol;

3-(3-Hydroxy-2-methylphenyl)-4-methyl-2-(4-((S)-2-((R)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-2H-chromen-6-ol;

3-(4-Hydroxy-2-methylphenyl)-4-methyl-2-(4-((S)-2-((R)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-2H-chromen-6-ol;

3-(4-Hydroxy-3-methylphenyl)-4-methyl-2-(4-((S)-2-((R)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-2H-chromen-6-ol;

3-(3-Fluoro-5-hydroxyphenyl)-4-methyl-2-(4-((S)-2-((R)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-2H-chromen-6-ol;

3-(4-Chlorophenyl)-4-methyl-2-(4-((S)-2-((R)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-2H-chromen-6-ol;

3-(2-Fluoro-4-hydroxyphenyl)-4-methyl-2-(4-((S)-2-((R)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-2H-chromen-6-ol;

3-(3,4-Difluorophenyl)-4-methyl-2-(4-((S)-2-((R)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-2H-chromen-6-ol;

3-(3,5-Difluoro-4-hydroxyphenyl)-4-methyl-2-(4-((S)-2-((R)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-2H-chromen-6-ol;

3-(2,4-Difluoro-3-hydroxyphenyl)-4-methyl-2-(4-((S)-2-((R)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-2H-chromen-6-ol;

3-(3,4-Difluoro-5-hydroxyphenyl)-4-methyl-2-(4-((S)-2-((R)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-2H-chromen-6-ol;

3-(2-Chloro-4-fluorophenyl)-4-methyl-2-(4-((S)-2-((R)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-2H-chromen-6-ol;

3-(2,4-Difluorophenyl)-4-methyl-2-(4-((S)-2-((R)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-2H-chromen-6-ol;

3-(4-Bromophenyl)-4-methyl-2-(4-((S)-2-((R)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-2H-chromen-6-ol;

4-Methyl-2-(4-((S)-2-((R)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-3-(o-tolyl)-2H-chromen-6-ol;

3-(4-Fluoro-3-hydroxyphenyl)-4-methyl-2-(4-((S)-2-((R)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-2H-chromen-6-ol;

3-(4-Ethynylphenyl)-4-methyl-2-(4-((S)-2-((R)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-2H-chromen-6-ol;

4-Methyl-2-(4-((S)-2-((R)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-3-(4-(methylsulfonyl)phenyl)-2H-chromen-6-ol;

3-(2-Fluoro-3-hydroxyphenyl)-4-methyl-2-(4-((S)-2-((R)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-2H-chromen-6-ol;

5-Fluoro-3-(3-hydroxyphenyl)-4-methyl-2-(4-((S)-2-((R)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-2H-chromen-6-ol;

3-(2-Fluoro-5-hydroxyphenyl)-4-methyl-2-(4-((S)-2-((R)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-2H-chromen-6-ol;

3-(4-Fluorophenyl)-4-methyl-2-(4-((S)-2-((R)-2-methylpyrrolidin-1-yl)propoxy)phenyl)-2H-chromen-6-ol;

2-(4-((S)-2-((R)-3-Fluoropyrrolidin-1-yl)propoxy)phenyl)-3-(3-hydroxyphenyl)-4-methyl-2H-chromen-6-ol;

3-(4-Hydroxyphenyl)-2-(4-((S)-2-((R)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-4-(trifluoromethyl)-2H-chromen-6-ol;

3-(3-Hydroxyphenyl)-2-(4-((S)-2-((R)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-4-(trifluoromethyl)-2H-chromen-6-ol;

3-(3-Hydroxy-4-(trifluoromethyl)phenyl)-4-methyl-2-(4-((S)-2-((R)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-2H-chromen-6-ol; or

3-(4-Hydroxy-3-(trifluoromethyl)phenyl)-4-methyl-2-(4-((S)-2-((R)-3-methylpyrrolidin-1-yl)propoxy)phenyl)-2H-chromen-6-ol;

or a pharmaceutically acceptable salt thereof.

9. A pharmaceutical composition comprising a compound of claim 1 , or a pharmaceutically acceptable salt thereof.

10. The pharmaceutical composition of claim 9 , wherein the pharmaceutical composition is formulated for intravenous injection, subcutaneous injection, oral administration, or topical administration.

11. The pharmaceutical composition of claim 9 , wherein the pharmaceutical composition is a tablet, a pill, a capsule, a liquid, a suspension, a gel, a dispersion, a solution, an emulsion, an ointment, or a lotion.

12. The compound of claim 1 , wherein the compound of Formula (VI) has the structure of Formula (IX):

or is a pharmaceutically acceptable salt thereof.

13. The compound of claim 12 , wherein:

R 1 is H or —CH 3 ;

R 3 is —CH 3 ;

R 4 is —OH;

R 8 is —CH 3 ;

R 9 is H;

X is —O—;

Y is —O—;

n is 0;

m is 1.

14. The compound of claim 5 , wherein:

R 1 is H or —CH 3 ;

R 3 is —CH 3 ;

R 4 is —OH;

R 8 is —CH 3 ;

R 9 is H;

X is —O—;

Y is —O—;

n is 0;

m is 1.

15. The compound of claim 1 , wherein the compound of Formula (VI) has the following structure:

or is a pharmaceutically acceptable salt thereof.

16. The compound of claim 5 , wherein the compound of Formula (VIII) has the following structure:

or is a pharmaceutically acceptable salt thereof.

17. The compound of claim 1 , wherein the compound of Formula (VI) has the following structure:

or is a pharmaceutically acceptable salt thereof.

18. The compound of claim 1 , wherein the compound of Formula (VI) has the following structure:

or is a pharmaceutically acceptable salt thereof.

19. The compound of claim 1 , wherein the compound of Formula (VI) has the following structure:

or is a pharmaceutically acceptable salt thereof.

20. The compound of claim 1 , wherein the compound of Formula (VI) has the following structure:

or is a pharmaceutically acceptable salt thereof.

21. The compound of claim 1 , wherein the compound of Formula (VI) has the following structure:

or is a pharmaceutically acceptable salt thereof.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 16, 2013
From: ARAGON PHARMACEUTICALS, INC.
To: SERAGON PHARMACEUTICALS, INC.
Reel/Frame 031025/0411 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 16, 2013
From: KAHRAMAN, MEHMET; GOVEK, STEVEN P.; NAGASAWA, JOHNNY Y.; SMITH, NICHOLAS D.
To: ARAGON PHARMACEUTICALS, INC.
Reel/Frame 029644/0416 →
Continuity (2)
Provisional Application 61353531 · Jun 10, 2010
Related Publication 20130116232A1 · May 9, 2013