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Voriconazole intermediate and method for synthesizing voriconazole

机译:伏立康唑中间体和伏立康唑的合成方法

摘要

The present invention provides a novel method for synthesizing a voriconazole intermediate condensate represented by Formula II or an acid addition salt thereof, wherein the voriconazole intermediate condensate is represented by Compound Formula III and Formula IV as shown in Reaction Scheme 1. It is obtained by preparing. In the synthesis method provided in the present invention, by adjusting the preparation form, the reaction conditions can be made mild and controllable, the generation of impurities A can be reduced, and the use of lead poison metal is avoided, and Can eliminate the risk of residual chemicals. This makes the product more pure and has great industrial application value. [Reaction Formula 1] [Chemical 1]
机译:本发明提供了一种合成式II所示的伏立康唑中间体缩合物或其酸加成盐的新方法,其中该伏立康唑中间体缩合物由化合物式III和式IV表示,如反应方案1所示。 。在本发明提供的合成方法中,通过调节制备形式,可以使反应条件温和可控,可以减少杂质A的产生,避免了铅有毒金属的使用,并消除了危险。残留化学物质。这使产品更加纯净,具有很大的工业应用价值。 [反应式1] [化学1]

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