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Travoprost method of preparation

机译:Travoprost的制备方法

摘要

The present invention is a process for preparing travoprost of formula (I), wherein the compound of formula (II) is stereoselectively reduced and the resulting compound of formula (III) is crystallized if desired, Reduction of the lactone group of the compound of (III), removal of the p-phenylbenzoyl protecting group of the compound of formula (IV) thus obtained and the triol of formula (V) If so, it relates to a method of crystallization followed by conversion to an acid of formula (VI) by Wittig reaction and esterification.
机译:本发明是制备式(I)的曲普前列素的方法,其中式(II)的化合物被立体选择性地还原,并且如果需要的话,使所得的式(III)的化合物结晶,还原式(I)的化合物的内酯基。 III),除去由此获得的式(IV)的化合物的对苯基苯甲酰基保护基和式(V)的三醇。如果是的话,则涉及结晶方法,随后转化为式(VI)的酸通过维蒂希反应和酯化反应。

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