发明名称 Camptothecin analogs and methods of preparation thereof
摘要 A compound has the formulain racemic form, enantiomerically enriched form or enantiomerically pure form. R6 is preferably -Si(R8R9R10) or -(R7)Si(R8R9R10), wherein R7 is an alkylene group, an alkenylene group, or an alkynylene group; and R8, R9 and R10 are independently a C1-10 alkyl group, a C2-10 alkenyl group, a C2-10 alkynyl group, an aryl group or a -(CH2)NR11 group, wherein N is an integer within the range of 1 through 10 and R11 is a hydroxy group, alkoxy group, an amino group, an alkylamino group, a dialkylamino group, a halogen atom, a cyano group, -SRc or a nitro group. R1-R can be broadly substituted. R5 is preferably a C1-10 alkyl group, an alkenyl group, an alkynyl group, or a benzyl group. R13 is preferably H, F or -CH3. R16 is R16 is -C(O)Rf or H. The E-ring (the lactone ring) may be opened. A method of synthesis of compound (1) and intermediates in the synthesis thereof are provided.
申请公布号 US6207832(B1) 申请公布日期 2001.03.27
申请号 US19990290019 申请日期 1999.04.09
申请人 UNIVERSITY OF PITTSBURGH 发明人 CURRAN DENNIS P.;DAVID BOM;BURKE THOMAS G.
分类号 A61K31/4375;A61P35/00;A61P35/02;A61P43/00;C07D471/14;C07D491/04;C07D491/044;C07D491/22;C07F7/08;(IPC1-7):C07D491/14 主分类号 A61K31/4375
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