IP Library Granted Patent US 9,193,714
Granted Patent B2
US 9,193,714 · App. 14/364,974 · Granted Nov 24, 2015

Fluorinated estrogen receptor modulators and uses thereof

Inventors: Nicholas D. Smith (San Diego, CA); Steven P. Govek (San Diego, CA); Mehmet Kahraman (La Jolla, CA); Johnny Y. Nagasawa (San Diego, CA); Andiliy G. Lai (San Diego, CA); Celine Bonnefous (San Diego, CA)
Assignee: SERAGON PHARMACEUTICALS, INC.
C07D405/12C07D311/58C07D311/70C07D405/14C07D413/12
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Quick Facts
Patent No.
US 9,193,714
App. No.
14/364,974
Granted
Nov 24, 2015
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 as 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 (36)

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

wherein,

R 1 is H, C 1 -C 6 alkyl, or C 1 -C 6 fluoroalkyl;

R 23 is —CH 2 F;

t is 1;

R 5 is H, halogen, —CN, —OH, —OR 11 , —NHR 11 , —NR 11 R 12 , SR 11 , —S(═O)R 12 , —S(O) 2 R 12 , C 1 -C 6 alkyl, C 1 -C 6 fluoroalkyl, C 1 -C 6 fluoroalkoxy, C 1 -C 6 alkoxy, or C 1 -C 6 heteroalkyl;

each R 6 is independently selected from H, halogen, —CN, —OH, —OR 11 , —SR 11 , —S(═O)R 12 , —S(═O) 2 R 12 , C 1 -C 6 alkyl, C 1 -C 6 fluoroalkyl, C 1 -C 6 fluoroalkoxy, C 1 -C 6 alkoxy, and C 1 -C 6 heteroalkyl;

each R 10 is independently selected from H, halogen, —CN, —OH, —OR 11 , —SR 11 , —S(═O)R 12 , —S(═O) 2 R 12 , C 1 -C 6 alkyl, C 1 -C 6 fluoroalkyl, C 1 -C 6 fluoroalkoxy, C 1 -C 6 alkoxy, and C 1 -C 6 heteroalkyl;

each R 11 is independently selected from H, —C(═O)R 12 , —C(═O)OR 12 , —C(═O)NHR 12 , C 1 -C 6 alkyl, C 1 -C 6 heteroalkyl, 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);

each R 12 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);

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

n is 0, 1, or 2.

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

R 1 is H or C 1 -C 6 alkyl.

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

R 5 is —OH;

each R 10 is independently selected from H, halogen, —CN, —OH, —S(═O)R 12 , —S(═O) 2 R 12 , C 1 -C 6 alkyl, C 1 -C 6 fluoroalkyl, C 1 -C 6 fluoroalkoxy, C 1 -C 6 alkoxy, and C 1 -C 6 heteroalkyl; and

R 11 is H.

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

R 1 is H, or —CH 3 .

5. The compound of claim 1 , or a pharmaceutically acceptable salt, or solvate thereof, wherein the compound has one of the following structures:

6. The compound of claim 5 , or a pharmaceutically acceptable salt, or solvate thereof, wherein:

R 5 is —OH;

each R 6 is independently selected from H and halogen;

each R 10 is independently selected from H and halogen; and

R 11 is H.

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

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

9. The compound of claim 1 , wherein the compound has one of the following structures:

or a pharmaceutically acceptable salt, or solvate thereof.

10. The compound of claim 1 , wherein the compound has one of the following structures:

or a pharmaceutically acceptable salt, or solvate thereof.

11. A pharmaceutical composition comprising a compound of claim 1 , or a pharmaceutically acceptable salt, or solvate thereof, and at least one pharmaceutically acceptable inactive ingredient.

12. The pharmaceutical composition of claim 11 , wherein the pharmaceutical composition is formulated for intravenous injection, subcutaneous injection, oral administration, or topical administration.

13. The pharmaceutical composition of claim 11 , 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.

14. A method for treating cancer in a mammal comprising administering to the mammal a compound of claim 1 , or a pharmaceutically acceptable salt, or solvate thereof, wherein the cancer is breast cancer, cervical cancer, colorectal cancer, lung cancer, ovarian cancer, endometrial cancer, prostate cancer, or uterine cancer.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 2, 2014
From: SMITH, NICHOLAS D.; GOVEK, STEVEN P.; KAHRAMAN, MEHMET; NAGASAWA, JOHNNY Y.; LAI, ANDILIY G.; BONNEFOUS, CELINE
To: SERAGON PHARMACEUTICALS, INC.
Reel/Frame 033234/0501 →
Continuity (2)
Provisional Application 61570756 · Dec 14, 2011
Related Publication 20150005286A1 · Jan 1, 2015