首页> 外国专利> Su00ecntese beta L - 2 '- deu00f3xi - nucleosu00ecdeos

Su00ecntese beta L - 2 '- deu00f3xi - nucleosu00ecdeos

机译:SU00哦cn特色beta l - 2 '- 的U00发3喜 - 你UCL EOSU00EC的OS

摘要

"Su00ecntese 225 - L - 2 39 - deu00f3xi - nucleosu00ecdeos".An improved process for the preparation of nucleoside 2 39 - modified and 2 39 - deu00f3xi nucleoside, such as 225 - L - 2 39 - deu00f3xi thymidine (LDT) is provided.In particular, the improved process is directed to the synthesis of a 2 39 - deu00f3xinucleosu00eddeo which can use different materials of initiation.But that goes on through the intermediary of chlorine - sugar or via an intermediary of 2,2 '- anhydro 39 1 furanosil - nucleobase.Where an intermediary base 2.2 39 anhydro 1 - furanosila is used, a reducing agent, such as red - A1, and a capture agent, such as 15 - crown - 5 - ether.That causes a substitution reaction and formation of the product intramolecular nucleoside desired in good yields are employed.An alternative process of this invention uses an intermediary base 2.2 39 anhydro - furanosila without a capture agent to provide 2 39 - deu00f3xinucleosu00eddeo in good yields.The compounds made according to the present invention can be used as intermediates in the preparation of other nucleoside analogues, or can be used directly as antiviral agents or antiNeoplastic.
机译:“ S ecntese <225-L-2 <39-de u00f3xi-核苷”。一种改进的制备2 <39-修饰的和2 <39-de 核苷酸的核苷的方法,例如<提供了225-L-2 <39-脱氧胸腺嘧啶核苷(LDT),特别是改进方法涉及2 <39-脱氧胸苷的合成,该合成可以使用不同的引发材料。通过氯-糖或2,2'-脱水39> 1呋喃硅-核碱基的中间体继续进行,如果使用2.2 <39>脱水1-呋喃西拉的中间体,则使用还原剂,例如红色- A1和捕获剂,例如15-冠-5-醚。它引起取代反应并以高收率形成所需的产物分子内核苷。本发明的另一种方法是使用中间体碱2.2 <39>无水呋喃西拉,无需捕获剂,可提供2 <39-de u00f3xinucleos u00eddeo s。根据本发明制备的化合物可以用作制备其他核苷类似物的中间体,或者可以直接用作抗病毒剂或抗肿瘤药物。

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