发明名称 OPTICALLY PURE CAMPTOTHECIN ANALOGUES, OPTICALLY PURE SYNTHESIS INTERMEDIATE AND METHOD FOR PREPARING THE SAME
摘要 <p>Two optically pure beta-hydroxy lactone camptothecin analogs (+)-5-ethyl-9,10-difluoro-5-hydroxy-4,5,13,15-tetrahydro-1H,3H-oxepino(3',4':6,7)indolizino(1,2-b)quinoline-3,15-dione (I) and (+)-9-chloro-5-ethyl-5-hydroxy-10-methyl-12-(4-methylpiperidinomethyl)-4,5,13,15-tetrahydro-1H,3H-oxepino(3',4':6,7)indolizino(1,2-c)quinoline-2,15-dione (II), as well as one of its salts, (+)-1-(9-chloro-5-ethyl-5-hydroxy-10-methyl-3,15-dioxo-4,5,13,15-tetrahydro-1H,3H-oxepino(3',4':6,7)indolizino(1,2-b)quinoline-12-yl methyl)-4-methyl-hexahydropyridinium chloride (III) and intermediates (M) are new. Optically pure beta-hydroxy lactone camptothecin analogs of formulae (I) and (II), as well as salts of (II) of formulae (III) are new. Independent claims are also included for industrial intermediates of formula (M) and their preparation. R = 1-10C alkyl, especially ethyl.</p>
申请公布号 HRP20000110(A2) 申请公布日期 2001.02.28
申请号 HR2000P000110 申请日期 2000.02.29
申请人 SOCIETE DE CONSEILS DE RECHERCHES ET D'APPLICATIONS SCIENTIFIQUES (S.C.R.A.S.) 发明人 JEAN-BERNARD CAZAUX;OLIVIER LAVERGNE;CHRISTINE LE BRETON;ERIC MANGINOT;DENNIS BIGG
分类号 C07D491/22;A61K31/435;A61K31/4353;A61K31/4375;A61P31/12;A61P33/00;A61P35/00;C07D491/04;C07D491/044;(IPC1-7):C07D491/22 主分类号 C07D491/22
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