IP Library Granted Patent US 8,168,672
Granted Patent B2
US 8,168,672 · App. 12/698,472 · Granted May 1, 2012

Thioamide derivatives as progesterone receptor modulators

Assignee: Wyeth
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Quick Facts
Patent No.
US 8,168,672
App. No.
12/698,472
Granted
May 1, 2012
Kind
B2
Abstract

Thioamide compounds, and specifically, thioamide pyrrole compounds, and preparation thereof are provided. These thioamide compounds can be used as progesterone receptor modulators, in contraception, and in the treatment of progesterone-related maladies.

Claims (48)

1. A method for hormone replacement therapy, treating hormone-dependent neoplastic disease, or synchronizing estrus, said method comprising administering to a mammal in need thereof a compound of formula I of the following structure:

wherein:

R 1 and R 2 are, independently, H, C 1 to C 6 alkyl, or substituted C 1 to C 6 alkyl;

or R 1 and R 2 are fused to form a ring comprising —CH 2 (CH 2 ) n CH 2 —, —CH 2 CH 2 C(CH 3 ) 2 CH 2 CH 2 —, —O(CH 2 ) p CH 2 —, —O(CH 2 ) q O—, —CH 2 CH 2 OCH 2 CH 2 —, or —CH 2 CH 2 NR 6 CH 2 CH 2 —;

n is 1 to 5;

p is 1 to 4;

q is 1 to 4;

R 3 is H, OH, NH 2 , CN, halogen, C 1 to C 6 alkyl, substituted C 1 to C 6 alkyl, C 2 to C 6 alkenyl, substituted C 2 to C 6 alkenyl, C 2 to C 6 alkynyl, substituted C 2 to C 6 alkynyl, or COR A ;

R A is H, C 1 to C 6 alkyl, substituted C 1 to C 6 alkyl, C 1 to C 6 alkoxy, substituted C 1 to C 6 alkoxy, C 1 to C 6 aminoalkyl, or substituted C 1 to C 6 aminoalkyl;

R 4 is H, C 1 to C 6 alkyl, substituted C 1 to C 6 alkyl, C 1 to C 6 alkoxy, substituted C 1 to C 6 alkoxy, C 1 to C 6 aminoalkyl, or substituted C 1 to C 6 aminoalkyl;

R 5 is C 1 to C 6 alkyl, substituted C 1 to C 6 alkyl, or COR A ;

R 6 is H or C 1 to C 6 alkyl;

X is O or S;

Q is O or S;

or a pharmaceutically acceptable salt thereof.

2. The method according to claim 1 , further comprising administering an estrogen, progestin, estrone, androgen, estrogen receptor agonist, or selective estrogen receptor modulator.

3. A method for contraception, hormone replacement therapy, treating hormone-dependent neoplastic disease, or synchronizing estrus, said method comprising administering to a mammal in need thereof a compound of formula I of the following structure:

wherein:

R 1 and R 2 are, independently, H, C 1 to C 6 alkyl, or substituted C 1 to C 6 alkyl;

or R 1 and R 2 are fused to form a ring comprising —CH 2 (CH 2 ) n CH 2 —, —CH 2 CH 2 C(CH 3 ) 2 CH 2 CH 2 —, —O(CH 2 ) p CH 2 —, —O(CH 2 ) p —, —CH 2 CH 2 OCH 2 CH 2 —, or —CH 2 CH 2 NR 6 CH 2 CH 2 —;

n is 1 to 5;

p is 1 to 4;

q is 1 to 4;

R 3 is H, OH, NH 2 , CN, halogen, C 1 to C 6 alkyl, substituted C 1 to C 6 alkyl, C 2 to C 6 alkenyl, substituted C 2 to C 6 alkenyl, C 2 to C 6 alkynyl, substituted C 2 to C 6 alkynyl, or COR A ;

R A is H, C 1 to C 6 alkyl, substituted C 1 to C 6 alkyl, C 1 to C 6 alkoxy, substituted C 1 to C 6 alkoxy, C 1 to C 6 aminoalkyl, or substituted C 1 to C 6 aminoalkyl;

R 4 is H, C 1 to C 6 alkyl, substituted C 1 to C 6 alkyl, C 1 to C 6 alkoxy, substituted C 1 to C 6 alkoxy, C 1 to C 6 aminoalkyl, or substituted C 1 to C 6 aminoalkyl;

R 5 is C 1 to C 6 alkyl, substituted C 1 to C 6 alkyl, or COR A ;

R 6 is H or C 1 to C 6 alkyl;

X is absent;

Q is O or S;

or a pharmaceutically acceptable salt thereof.

4. The method according to claim 3 , further comprising administering an estrogen, progestin, estrone, androgen, estrogen receptor agonist, or selective estrogen receptor modulator.

5. A method for contraception, hormone replacement therapy, treating hormone-dependent neoplastic disease, or synchronizing estrus, said method comprising administering to a mammal in need thereof a compound of formula I of the following structure:

wherein:

R 1 and R 2 are, independently, H, C 1 to C 6 alkyl, or substituted C 1 to C 6 alkyl;

or R 1 and R 2 are fused to form a ring comprising —CH 2 (CH 2 ) n CH 2 —, —CH 2 CH 2 C(CH 3 ) 2 CH 2 CH 2 —, —O(CH 2 ) p CH 2 —, —O(CH 2 ) q O—, —CH 2 CH 2 OCH 2 CH 2 —, or —CH 2 CH 2 NR 6 CH 2 CH 2 —;

n is 1 to 5;

p is 1 to 4;

q is 1 to 4;

R 3 is H, OH, NH 2 , CN, halogen, C 1 to C 6 alkyl, substituted C 1 to C 6 alkyl, C 2 to C 6 alkenyl, substituted C 2 to C 6 alkenyl, C 2 to C 6 alkynyl, substituted C 2 to C 6 alkynyl, or COR A ;

R A is H, C 1 to C 6 alkyl, substituted C 1 to C 6 alkyl, C 1 to C 6 alkoxy, substituted C 1 to C 6 alkoxy, C 1 to C 6 aminoalkyl, or substituted C 1 to C 6 aminoalkyl;

R 4 is H, C 1 to C 6 alkyl, substituted C 1 to C 6 alkyl, C 1 to C 6 alkoxy, substituted C 1 to C 6 alkoxy, C 1 to C 6 aminoalkyl, or substituted C 1 to C 6 aminoalkyl;

R 5 is C 1 to C 6 alkyl, substituted C 1 to C 6 alkyl, or COR A ;

R 6 is H or C 1 to C 6 alkyl;

X is O, S or absent;

Q is O or S;

or a pharmaceutically acceptable salt thereof.

6. The method according to claim 5 , further comprising administering an estrogen, progestin, estrone, androgen, estrogen receptor agonist, or selective estrogen receptor modulator.

Assignments (1)
CHANGE OF NAME Recorded Jun 16, 2010
From: WYETH
To: WYETH LLC
Reel/Frame 024541/0922 →
Continuity (5)
Continuation 12369789 · Feb 12, 2009
Division 12044287 · Mar 7, 2008
Division 11100860 · Apr 7, 2005
Provisional Application 60560569 · Apr 8, 2004
Related Publication 20100197645A1 · Aug 5, 2010