A compound of Formula (I), or a pharmaceutically acceptable salt or solvate thereof,
wherein,
R
1
and R
2
each independently represent H, halogen, CF
3
, C
1-3
alkyl or C
1-3
alkoxy;
R
3
represents C
1-6
alkyl, C
3-6
cycloalkyl, phenyl (optionally substituted by one or more substituents each independently selected from R
a
) or Het (optionally substituted by one or more substituents each independently selected from OH, oxo, or C
1-4
alkyl);
R
4
represents H or C
1-3
alkyl;
R
5
represents C
1-6
alkyl (optionally substituted by one or more substituents each independently selected from R
b
), C
3-6
cycloalkyl (optionally substituted by one or more substituents each independently selected from oxo or OH), or Het
2
(optionally substituted by one or more substituents each independently selected from R
d
); oxygen atom or 1 sulphur atom, or (c) 1 oxygen atom or 1 sulphur atom, (optionally substituted by one or more substituents each independently selected from OH, oxo or C
1-4
alkyl); and
R
6
represents C
1-3
alkyl (optionally substituted by one or more substituents each independently selected from R
f
), C
3-5
cycloalkyl (optionally substituted by one or more halogen), CN or halogen; where R
f
represents halogen or phenyl: and compositions, processes for the preparation, and uses thereof, e.g. in the treatment of endometriosis or uterine fibroids
A compound of Formula (I), or a pharmaceutically acceptable salt or solvate thereof,
wherein,
R
1
, R
2
, R
3
, R
4
, R
5
and R
6
are as defined herein: and compositions, processes for the preparation, and uses thereof, e.g. in the treatment of endometriosis or uterine fibroids.
A compound of Formula (I), or a pharmaceutically acceptable salt or solvate thereof,
wherein,
R1 and R2 each independently represent H, halogen, CF3, C1-3 alkyl or C1-3 alkoxy;
R3 represents C1-6 alkyl, C3-6 cycloalkyl, phenyl (optionally substituted by one or more substituents each independently selected from Ra) or Het (optionally substituted by one or more substituents each independently selected from OH, oxo, or C1-4 alkyl);
R4 represents H or C1-3 alkyl;
R5 represents C1-6 alkyl (optionally substituted by one or more substituents each independently selected from Rb), C3-6 cycloalkyl (optionally substituted by one or more substituents each independently selected from oxo or OH), or Het2 (optionally substituted by one or more substituents each independently selected from Rd); oxygen atom or 1 sulphur atom, or (c) 1 oxygen atom or 1 sulphur atom, (optionally substituted by one or more substituents each independently selected from OH, oxo or C1-4 alkyl); and
R6 represents C1-3 alkyl (optionally substituted by one or more substituents each independently selected from Rf), C3-5 cycloalkyl (optionally substituted by one or more halogen), CN or halogen; where Rf represents halogen or phenyl: and compositions, processes for the preparation, and uses thereof, e.g. in the treatment of endometriosis or uterine fibroids.
[EN] AMIDE COMPOUNDS USEFUL IN THERAPY<br/>[FR] COMPOSÉS AMIDES UTILES EN THÉRAPIE
申请人:PFIZER LTD
公开号:WO2010032200A1
公开(公告)日:2010-03-25
A compound of Formula (I), or a pharmaceutically acceptable salt or solvate thereof, (I) wherein, R1 and R2 each independently represent H, halogen, CF3, C1-3 alkyl or C1-3 alkoxy; R3 represents C1-6 alkyl, C3-6 cycloalkyl, phenyl (optionally substituted by one or more substituents each independently selected from Ra) or Het (optionally substituted by one or more substituents each independently selected from OH, oxo, or C1-4 alkyl); R4 represents H or C1-3 alkyl; R5 represents C1-6 alkyl (optionally substituted by one or more substituents each independently selected from Rb), C3-6 cycloalkyl (optionally substituted by one or more substituents each independently selected from oxo or OH), or Het2 (optionally substituted by one or more substituents each independently selected from Rd); oxygen atom or 1 sulphur atom, or (c) 1 oxygen atom or 1 sulphur atom, (optionally substituted by one or more substituents each independently selected from OH, oxo or C1-4 alkyl); and R6 represents C1-3 alkyl (optionally substituted by one or more substituents each independently selected from Rf), C3-5 cycloalkyl (optionally substituted by one or more halogen), CN or halogen; where Rf represents halogen or phenyl: and compositions, processes for the preparation, and uses thereof, e.g. in the treatment of endometriosis or uterine fibroids.