发明名称
摘要 The present invention provides compounds of formula I <CHEM> wherein R<1> is -H, -OH, -O(C1-C4 alkyl), -OCOC6H5, -OCO(C1-C6 alkyl), or -OSO2(C4-C6 alkyl); R<2> is C1-C6 alkyl or C5-C7 cycloalkyl which is optionally substituted with 1 to 3 substitutents selected from the group consisting of C1-C4 alkyl, C1-C4 alkoxy, hydroxy, amino, nitro, and halo; X is -CH(OH)- or -CH2-; M is -CH2CH2- or -CH=CH-; n is 2 or 3; and R<3> is 1-piperidinyl, 1-pyrrolidinyl, methyl-1-pyrrolidinyl, dimethyl-1-pyrrolidinyl, 4-morpholino, dimethylamino, diethylamino, or 1-hexamethyleneimino; or a pharmaceutically acceptable salt thereof. Also provided are methods of using the compounds of the present invention for the treatment of various medical indications associated with post-menopausal syndrome, uterine fibroid disease, endometriosis, and aortal smooth muscle cell proliferation. The present invention further provides pharmaceutical compositions of compounds of formula I, as well, as intermediate compounds for the preparation thereof.
申请公布号 JPH11510798(A) 申请公布日期 1999.09.21
申请号 JP19970507821 申请日期 1996.07.26
申请人 发明人
分类号 C07D295/08;A61K31/00;A61K31/12;A61K31/40;A61K31/445;A61K31/4453;A61K31/4465;A61K31/535;A61K31/5375;A61K31/695;A61P3/00;A61P3/06;A61P5/24;A61P9/00;A61P9/10;A61P15/00;A61P15/12;A61P19/00;A61P19/10;A61P35/00;C07C39/23;C07C43/205;C07C43/23;C07C49/84;C07D295/092;(IPC1-7):C07C43/23 主分类号 C07D295/08
代理机构 代理人
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