发明名称 PROCEDIMIENTO DE PREPARAR COMPUESTOS AMIDICOS
摘要 <p>Compounds of the structure: <IMAGE> wherein R1, R2, R3, R4, R5, and R6 are hydrogen, alkyl, alkenyl, alkynyl, phenyl-alkyl, or cycloalkyl, n is an integer from 0 to 4 inclusive, M is alkenyl, alkynyl, cycloalkyl, cycloalkyl-alkyl, polycycloalkyl, polycyclo-alkyl-alkyl, aryl, aralkyl, heteroaryl, heteroaryl-alkyl, hetero-cycloalkyl, hetero-cycloalkyl-alkyl, alkoxyalkyl, alkylthioalkyl, alkylamino-alkyl, dialkylamino-alkyl, fused aryl-cycloalkyl, fused aryl-cycloalkyl-alkyl, fused heteroaryl-cycloalkyl, or fused heteroaryl-cycloalkyl-alkyl, Y is hydroxy, alkoxy, amino, or substituted amino, aminoalkanoyl, aryloxy, aminoalkoxy, or hydroxyalkoxy, and R7 is hydrogen, alkanoyl, carboxylalkanoyl, hydroxyalkanoyl, amino-alkanoyl, cyano, amidino, carbalkoxy, ZS, or <IMAGE> wherein Z is hydrogen, alkyl, hyroxyalkyl, aminoalkyl or the radical <IMAGE> wherein R1, R2, R3, R4, R5, R6, n, M and Y are as described above; and where Y is hydroxy their non-toxic, pharmaceutically acceptable alkali metal, alkaline earth metal, and amine salts.</p>
申请公布号 ES494165(D0) 申请公布日期 1981.08.01
申请号 ES19650004941 申请日期 1980.07.11
申请人 USV PHARMACEUTICAL CORPORATION 发明人
分类号 A61K31/16;A61K31/165;A61K31/19;A61K31/195;A61K31/21;A61K31/215;A61K31/22;A61P9/00;A61P9/12;A61P43/00;C07C67/00;C07C313/00;C07C323/60;C07C325/00;C07C327/20;C07C327/22;C07C327/32;C07C329/14;C07C329/16;C07C335/32;C07D207/08;C07D211/26;C07D213/38;C07D213/40;C07D213/75;C07D215/38;C07D217/22;C07D219/14;C07D235/30;C07D239/42;C07D277/46;C07D307/22;C07D307/52;C07D307/66;C07D307/82;C07D309/14;C07D317/66;C07D319/18;C07D333/20;C07D333/36;C07D333/48;(IPC1-7):07C149/41;61K31/10 主分类号 A61K31/16
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