发明名称 PROCEDIMIENTO PARA LA PREPARACION DE DERIVADOS DE CARBACICLINA
摘要 <p>1. Carbacyclin derivatives of the general formula I : see diagramm : EP0098794,P18,F1 wherein R1 is the group OR2 , in which R2 is hydrogen alkyl of 1-4 C-atoms, cycloalkyl of 5-6 C-atoms, phenyl, 1-naphthyl or 2-naphthyl, the group see diagramm : EP0098794,P18,F2 in which aryl is phenyl, 1-naphtyl or 2-naphtyl, each of which is substituted by phenyl, C1 -C2 -alkoxy, chloro or bromo, or R1 is a 5 or 6 membered heterocyclic group with an N-, O- or S-atom, or R1 is the group NHR3 , in which R3 is an organic, carboxylic or sulphonic acid ester group or is the group R2 , A is a -CH2 -CH2 -, trans-CH=CH- or -C-=C-group, W is a free or functionally modified hydroxymethylene group or a free or functionally modified see diagramm : EP0098794,P18,F3 where the OH group may be in the alpha- or beta-configuration, D is the group see diagramm : EP0098794,P18,F4 a straight-chain saturated alkylene group of 1-5 C-atoms or a branched, saturated or a straigth-chain or branche unsaturated alkylen, group of 2-5 C-atoms which can optionally be subsituted by fluorine atoms, n is the number 1, 2 or 3, E is a direct bond, a -C-=C- group or a -CR6 =CR7 - group, where R6 is hydrogen or a C1-4 -alkyl group and R7 is hydrogen, C1-4 -alkyl, chlorine or bromine, R4 is an alkyl group of 1-10 C-atoms, a cycloalkyl group of 3-6 C-atoms, phenyl or 5 or 6 membered heterocyclic group with an N-, O- or S-atom, R5 is a free or functionally modified hydroxy group, and when R2 is hydrogen, its salts with physiologically acceptable bases.</p>
申请公布号 ES523782(D0) 申请公布日期 1984.04.01
申请号 ES19820005237 申请日期 1983.07.01
申请人 SCHERING AG. 发明人
分类号 C07C69/708;A61K31/225;A61K31/35;A61K31/351;A61K31/557;A61P7/02;A61P9/12;A61P11/08;C07C51/00;C07C51/367;C07C59/125;C07C59/62;C07C67/00;C07C67/31;C07C231/00;C07C231/02;C07C231/12;C07C235/06;C07C235/08;C07C235/88;C07C405/00;C07D309/12;C07D317/72;(IPC1-7):07C59/135;07C69/708;07C103/737;61K31/557 主分类号 C07C69/708
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