IP Library Granted Patent US 7,323,587
Granted Patent B2
US 7,323,587 · App. 11/152,891 · Granted Jan 29, 2008

Selective estrogen receptor modulators

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Quick Facts
Patent No.
US 7,323,587
App. No.
11/152,891
Granted
Jan 29, 2008
Kind
B2
Abstract

The present invention provides, inter alia, triphenylethylene derivatives, such as, 3-{4-[6-(3-Methoxy-phenyl)-8,9-dihydro-7H-benzocyclohepten-5-yl]-phenyl}-acrylic acid, as selective estrogen receptor modulators. Also provided are methods for treating estrogen stimulated diseases in mammals including, but not limited to, for example, breast, uterine, ovarian, prostate and colon cancer; osteoporosis; endometriosis; uterine fibroid; Alzheimer's disease; macular degeneration; urinary incontinence; and type II diabetes, as well as, pharmaceutical compositions comprising at least one compound of the present invention.

Claims (42)

1. A compound of Formula (I):

or pharmaceutically acceptable salt form thereof,

wherein R 1 is

R 2 and R 3 , together with the atoms to which they are attached, form a seven-membered ring structure where the atoms forming the ring are carbon atoms;

R 4 is selected from H, OH, C 1-8 alkyl, OC 1-8 alkyl, and halo;

R 5 is selected from H, OH, CN, nitro, C 1-8 alkyl, OC 1-8 alkyl, and halo;

R 6 is selected from H, OH, CN, OC 1-8 alkyl, methyl, ethyl, propyl and butyl;

X is selected from the group consisting of O, or NH, wherein when X is O, R 6 is other than OH; and

the bond represented by a broken line and a solid line is an optional double bond.

2. A compound of Formula (I):

or pharmaceutically acceptable salt form thereof,

wherein R 1 is

R 2 and R 3 , together with the atoms to which they are attached, form a seven-membered ring structure where one or more of the atoms forming the ring are oxygen;

R 4 is selected from H, OH, C 1-8 alkyl, OC 1-8 alkyl, and halo;

R 5 is selected from H, OH, CN, nitro, C 1-8 alkyl, OC 1-8 alkyl, and halo;

R 6 is selected from H, OH, CN, OC 1-8 alkyl, methyl, ethyl, propyl and butyl;

X is selected from the group consisting of O, or NH, wherein when X is O, R 6 is other than OH; and

the bond represented by a broken line and a solid line is an optional double bond.

3. A compound according to claim 1 , wherein R 1 is —C(═O) OH.

4. A compound according to claim 3 , wherein the bond represented by a broken line and a solid line is a double bond.

5. A compound according to claim 1 , wherein R 4 and R 5 are each independently H.

6. A compound according to claim 1 , wherein R 4 is OH and R 5 is H.

7. A compound according to claim 1 , wherein R 4 is OCH 3 and R 5 is H.

8. A compound according to claim 1 , wherein R 4 is OH and R 5 is OH.

9. A compound according to claim 1 , wherein R 4 is H and R 5 is OH.

10. A compound selected from:

a) 3-{4-[6-(3-Methoxy-phenyl)-8,9-dihydro-7H-benzocyclohepten-5-yl]-phenyl}-acrylic acid;

b) 3-{4-[6-(4-Methoxy-phenyl)-8,9-dihydro-7H-benzocyclohepten-5-yl]-phenyl}-acrylic acid;

c) 3-{4-[6-(3-Hydroxy-phenyl)-8,9-dihydro-7H-benzocyclohepten-5-yl]-phenyl}-acrylic acid;

d) 3-{4-[6-(4-Hydroxy-phenyl)-8,9-dihydro-7H-benzocyclohepten-5-yl]-phenyl}-acrylic acid;

f) 3-[4-(6-Phenyl-6,7,8,9-tetrahydro-5H-benzocyclohepten-5-yl)-phenyl]-acrylic acid;

g) 3-[4-(2-Hydroxy-6-phenyl-8,9-dihydro-7H-benzocyclohepten-5-yl)-phenyl]-acrylic acid;

h) 3-{4-[2-Hydroxy-6-(3-hydroxy-phenyl)-8,9-dihydro-7H-benzocyclohepten-5-yl]-phenyl}-acrylic acid;

i) 3-{4-[2-Hydroxy-6-(4-hydroxy-phenyl)-8,9-dihydro-7H-benzocyclohepten-5-yl]-phenyl}-acrylic acid;

r) 3-[4-(3-Phenyl-2H-chromen-4-yl)-phenyl]-acrylic acid;

s) 3-[4-(2-Phenyl-3,4-dihydro-naphthalen-1-yl)-phenyl]-acrylic acid;

t) 3-[4-(2-Phenyl-1,2,3,4-tetrahydro-naphthalen-1-yl)-phenyl]-acrylic acid; and

u) 3-[4-(6-Phenyl-8,9-dihydro-7H-benzocyclohepten-5-yl)-phenyl]-acrylic acid.

11. 3-[4-(6-Phenyl-8,9-dihydro-7H-benzocyclohepten-5-yl)-phenyl]-propionic acid, or a pharmaceutical acceptable salt form.

12. A pharmaceutical composition comprising at least one pharmaceutically acceptable carrier in combination with a therapeutically effective amount of at least one compound of claim 1 .

13. A method of treating breast, uterine, ovarian, prostate, or colon cancer; osteoporosis; endometriosis; uterine fibroid; Alzheimer's disease; macular degeneration; or urinary incontinence, comprising:

administering to a host in need of such treatment a therapeutically effective amount of at least one compound of claim 1 .