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stereospezifisches procedure for the manufacture of enantiomers of furo replaced: 3 - 3.4 - c) pyridins, enantiomers or mixtures thereof, as well as the received the therapeutic resources
stereospezifisches procedure for the manufacture of enantiomers of furo replaced: 3 - 3.4 - c) pyridins, enantiomers or mixtures thereof, as well as the received the therapeutic resources
The present invention relates to stereospecific processes for the preparation of enantiomers of 3-substituted-furo[3,4-c]pyridine of formula I, wherein R3, R4 and R6 stand for various substituents, comprising the steps of: oxidation of a racemic pyridine derivative of formula II, reduction of the resulting ketone with a reducing agent, sterospecific locking or blocking of the OH group of the enantiomer alcohol, opening of the acetonide ring and cyclization of the resulting compound. IMAGE I IMAGE II The present invention also relates to compounds thus obtained and therapeutical compositions thereof.
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机译:本发明涉及用于制备式I的3-取代的呋喃[3,4-c]吡啶的对映异构体的立体有择方法,其中R3,R4和R6代表各种取代基,包括以下步骤:氧化外消旋体式II的吡啶衍生物,用还原剂还原所得的酮,对映异构体醇的立体特异性锁定或封端,乙交酯环的打开和所得化合物的环化。 <图像> I <图像> II本发明还涉及由此获得的化合物及其治疗组合物。
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