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A process for the preparation of cicloalca (4,5) pirrolo (2.3 g) - isoquinolinas
A process for the preparation of cicloalca (4,5) pirrolo (2.3 g) - isoquinolinas
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机译:一种制备西氯洛卡(4,5)皮洛洛(2.3 g)-异喹啉类的方法
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摘要
A process for the preparation of cicloalca / 4.5 / pirrolo / 2.3 g / isoquinolinas. They REACT with a compound of General formula (ii) with Phosphorus pentasulphide.The Compound (i) is obtained, which optionally may refer to the following: (a) to End a relationship isomerizar mixture comprising predominantly isomer after being able to separate the Trans isomer in the mixture. (b) resolution of a racemic mixture obtained in the optical Antipodes.(c) convert the compound obtained in the acid Addition Salt of a pharmaceutically acceptable salt in the respective pharmaceutically acceptable.R is Hydrogen, alkyl or aralquilo; R is Hydrogen, alkyl, aralquilo Cycle, alquenilo alkoxyalkyl esters, alkyl, alkyl, alkyl alquinilo, Thienyl, furil aralquenilo, alkyl, or aryl alqueniloxialquilo, ariloxialquilo, N - imidazolinialquilo; n is 3, 4, 5 or 6.
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机译:制备环氯半乳苷/ 4.5 //吡罗洛/ 2.3 g //异喹啉类的方法。它们与通式(ii)的化合物与五硫化二磷反应。获得的化合物(i),其可任选地涉及以下内容:(a)在能够分离反式后,终止主要包含异构体的关系异构体混合物混合物中的异构体。 (b)在旋光对映体中得到的外消旋混合物的拆分。(c)将在药学上可接受的盐的酸加成盐中得到的化合物转化为相应的药学上可接受的。R为氢,烷基或芳基; R为氢,烷基,芳基环,烷基铝烷氧基烷基酯,烷基,烷基,烷基烷基铝,噻吩基,呋喃基芳基烷基,烷基或芳基烷基铝基喹啉基,芳基铝基奎洛基,N-咪唑啉基基洛基; n为3、4、5或6。
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