IP Library Granted Patent US 7,414,043
Granted Patent B2
US 7,414,043 · App. 10/458,735 · Granted Aug 19, 2008

9-α-substituted estratrienes as selectively active estrogens

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Quick Facts
Patent No.
US 7,414,043
App. No.
10/458,735
Granted
Aug 19, 2008
Kind
B2
Abstract

This invention describes the new 9α-substituted estratrienes of general formula I in which R 3 , R 7 , R 7′ , R 13 , R 16 as well as R 17 and R 17′ have the meanings that are indicated in the description and R 9 means a straight-chain or branched-chain, optionally partially or completely halogenated alkenyl radical with 2 to 6 carbon atoms, an ethinyl or prop-1-inyl radical, as pharmaceutical active ingredients that exhibit in vitro a higher affinity to estrogen receptor preparations from rat prostates than to estrogen receptor preparations from rat uteri and in vivo preferably a preferential action on the ovary in comparison to the uterus, their production, their therapeutic use and pharmaceutical dispensing forms that contain the new compounds. The invention also describes the use of these compounds for treating estrogen-deficiency-induced diseases and conditions.

Claims (81)

1. A 9α-Substituted estra-1,3,5(10)-triene compound of formula I

wherein

R 3 is hydrogen or R 18 ,

R 18 is a straight-chain or branched-chain, saturated or unsaturated hydrocarbon radical with up to 6 carbon atoms, a trifluoromethyl group, an optionally substituted aryl, heteroaryl or aralkyl radical, an acyl radical COR 19 , or R 20 SO 2 ,

R 19 is an optionally substituted, straight-chain or branched-chain hydrocarbon radical with up to 10 carbon atoms that is saturated or unsaturated in up to three places and is optionally partially or completely halogenated,

R 20 is R 21 R 22 N,

R 21 and R 22 are, independently of one another, a hydrogen atom, a C 1 -C 5 -alkyl radical, or C(O)R 23 ,

R 23 is an optionally substituted, straight-chain or branched-chain hydrocarbon radical with up to 10 carbon atoms that is saturated or unsaturated in up to three places and is optionally partially or completely halogenated, an optionally substituted C 3 -C 7 -cycloalkyl radical, an optionally substituted C 4 -C 15 -cycloalkylalkyl radical or an optionally substituted aryl, heteroaryl or aralkyl radical, or, together with the N atom, a polymethylenimino radical with 4 to 6 C atoms or a morpholino radical,

R 17 and R 17′ are, in each case independently of one another, a hydrogen atom or a halogen atom,

R 9 is a straight-chain or branched-chain alkenyl or alkinyl radical with 2 to 6 carbon atoms, which is optionally partially or completely fluorinated, or an ethinyl or prop-1-inyl radical,

R 13 is a methyl group or an ethyl group,

R 16 is a hydroxy group or R 18 O—, R 20 SO 2 —O— or OC(O)R 23 , and

R 17 and R 17′ are, in each case independently of one another, a hydrogen atom or a halogen Atom,

or a pharmaceutically acceptable salt thereof.

2. A compound of formula I according to claim 1 , in which R 3 is a hydrogen atom.

3. A compound of formula I according to claim 1 , in which

R 7 is a hydrogen atom or an α-position fluorine atom,

R 9 is a vinyl, ethinyl or prop-1-inyl group,

R 16 is a hydroxy group, and

R 17 is a hydrogen atom or an α-position fluorine atom.

4. A compound of formula I according to claim 1 , in which R 16 is R 18 —O— or R 20 SO 2 —O—.

5. A compound of formula I according to claim 1 , which is

9α-Vinyl-estra-1,3,5(10)-triene-3,16α-diol

9α-Allyl-estra-1,3,5(10)-triene-3,16α-diol

18a-Homo-9α-vinyl-estra-1,3,5(10)-triene-3,16α-diol

18a-Homo-9α-allyl-estra-1,3,5(10)-triene-3,16α-diol

3-Methoxy-9α-vinyl-estra-1,3,5(10)-trien-16α-ol

9α-Allyl-3-methoxy-estra-1,3,5(10)-trien-16α-ol

18a-Homo-3-methoxy-9α-vinyl-estra-1,3,5(10)-trien-16α-ol

18a-Homo-9α-allyl-3-methoxy-estra-1,3,5(10)-trien-16α-ol

9α-(2′,2′-Difluorovinyl)-estra-1,3,5(10)-triene-3,16α-diol

9α-(2′,2′-Difluorovinyl)-3-methoxy-estra-1,3,5(10)-trien-16α-ol

16α-Hydroxy-9α-vinyl-estra-1,3,5(10)-trien-3yl-sulfamate

9α-Allyl-16α-hydroxy-estra-1,3,5(10)-trien-3yl-sulfamate

18a-Homo-16α-hydroxy-9α-vinyl-estra-1,3,5(10)-trien-3yl-sulfamate

18a-Homo-9α-allyl-16α-hydroxy-estra-1,3,5(10)-trien-3yl-sulfamate

9α-Vinyl-estra-1,3,5(10)-triene-3,16α-diyl-disulfamate

9α-Allyl-estra-1,3,5(10)-triene-3,16α-diyl-disulfamate

18a-Homo-9α-vinyl-estra-1,3,5(10)-triene-3,16α-diyl-disulfamate

18a-Homo-9α-allyl-estra-1,3,5(10)-triene-3,16α-diyl-disulfamate

16α-Hydroxy-9α-vinyl-estra-1,3,5(10)-trien-3yl-(N-acetyl)-sulfamate

9α-Allyl-16α-hydroxy-estra-1,3,5(10)-trien-3yl-(N-acetyl)-sulfamate

18a-Homo-16α-hydroxy-9α-vinyl-estra-1,3,5(10)-trien-3yl-(N-acetyl)-sulfamate

18a-Homo-9α-allyl-16α-hydroxy-estra-1,3,5(10)-trien-3yl-(N-acetyl)-sulfamate

9α-(Prop-(Z)-enyl)-estra-1,3,5(10)-triene-3,16α-diol

9α-(n-Propyl)-estra-1,3,5(10)-triene-3,16α-diol

9α-Ethinyl-estra-1,3,5(10)-triene-3,16α-diol

9α-Vinyl-estra-1,3,5(10)-triene-3,16α-diol-diacetate

18a-Homo-9α-vinyl-estra-1,3,5(10)-triene-3,16α-diol-diacetate

16α-Valeroyloxy-9α-vinyl-estra-1,3,5(10)-trien-3-ol

16α-Acetoxy-9α-vinyl-estra-1,3,5(10)-trien-3-ol

18a-Homo-16α-acetoxy-9α-vinyl-estra-1,3,5(10)-trien-3-ol

7α-Fluoro-9α-vinyl-estra-1,3,5(10)-triene-3,16α-diol

7α-Fluoro-9α-allyl-estra-1,3,5(10)-triene-3,16α-diol

17β-Fluoro-9α-vinyl-estra-1,3,5(10)-triene-3,16α-diol

17β-Fluoro-9α-allyl-estra-1,3,5(10)-triene-3,16α-diol

18a-Homo-7α-fluoro-9α-vinyl-estra-1,3,5(10)-triene-3,16α-diol

18a-Homo-7α-fluoro-9α-allyl-estra-1,3,5(10)-triene-3,16α-diol

18a-Homo-17β-fluoro-9α-vinyl-estra-1,3,5(10)-triene-3,16α-diol or

18a-Homo-17β-fluoro-9α-allyl-estra-1,3,5(10)-triene-3,16α-diol.

6. A compound of formula I according to claim 5 , which is 17β-Fluoro-9α-vinyl-estra- 1,3,5(10)-triene-3,16α-diol.

7. A pharmaceutical composition comprising a compound according to claim 1 and a pharmaceutically compatible vehicle.

8. A pharmaceutical composition comprising a compound according to claim 5 and a pharmaceutically compatible vehicle.

9. A method for in vitro treatment of female infertility comprising administering to a female in need thereof an effective amount of a pharmaceutical composition according to claim 7 .

10. A method for in vivo treatment of female infertility comprising administering to a female in need thereof an effective amount of a pharmaceutical composition according to claim 7 .

11. A method for hormone replacement therapy comprising administering to a patient in need of replacement of estrogen, an effective amount of a pharmaceutical composition according to claim 7 .

12. A method according to claim 11 further comprising administering to said patient a selective estrogen receptor modulator or raloxifene.

13. A method for therapy of prostate hyperplasia comprising administering to a patient in need thereof an effective amount of a pharmaceutical composition according to claim 7 , an antiestrogen and a selective estrogen receptor modulator.

14. A method for treating rheumatoid arthritis comprising administering to a patient in need thereof an effective amount of a pharmaceutical composition according to claim 6 .

15. A method for treating multiple sclerosis comprising administering to a patient in need thereof an effective amount of a pharmaceutical composition according to claim 7 .

16. A method for treatment of prostate hyperplasia comprising administering to a patient in need thereof an effective amount of a pharmaceutical composition according to claim 7 .

17. A method for treatment of a perimenopausal or postmenopausal symptom selected from hot flashes, sleep disturbances, irritability, mood swings, incontinence and vaginal atrophy, comprising administering to a patient in need thereof an effective amount of a pharmaceutical composition according to claim 7 .

18. A method according to claim 17 , wherein hot flashes are treated.

19. A method according to claim 17 , wherein sleep disturbances are treated.

20. A method according to claim 17 , wherein irritability is treated.

21. A method according to claim 17 , wherein mood swings are treated.

22. A method according to claim 17 , wherein incontinence is treated.

23. A method according to claim 17 , wherein vaginal atrophy is treated.

24. A method for treatment of prostate hyperplasia comprising administering to a patient in need thereof an effective amount of a pharmaceutical composition according to claim 8 .

25. A method for in vitro treatment of female infertility or for in vivo treatment of female infertility or for hormone replacement therapy comprising administering to a female in need thereof an effective amount of a pharmaceutical composition comprising a compound according to claim 6 and a pharmaceutically compatible vehicle.

26. A method for treatment of prostate hyperplasia; rheumatoid arthritis; multiple sclerosis; a perimenospausal or postmenopausal symptom selected from hot flashes, sleep disturbances, irritability, mood swings, incontinence, and vaginal atrophy, comprising administering to a patient in need thereof an effective amount of a pharmaceutical composition comprising a compound according to claim 6 and a pharmaceutically compatible vehicle.

Assignments (2)
CHANGE OF NAME Recorded Jul 1, 2013
From: BAYER PHARMA AKTIENGESELLSCHAFT
To: BAYER INTELLECTUAL PROPERTY GMBH
Reel/Frame 030719/0474 →
CHANGE OF NAME Recorded Nov 11, 2012
From: BAYER SCHERING PHARMA AKTIENGESELLSCHAFT
To: BAYER PHARMA AKTIENGESELLSCHAFT
Reel/Frame 029277/0286 →