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A novel approach to quinazolin-4(3H)-one via quinazoline oxidation: an improved synthesis of 4-anilinoquinazolines

机译:一种经由喹唑啉氧化的喹唑啉-4(3H)-的新方法:一种改进的4-苯胺基喹唑啉合成方法

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摘要

A novel strategy to prepare 4-anilinoquinazoline derivatives based on the oxidation of the quinazoline ring is described. Quinazoline oxidation has been investigated and improved, thus leading to an efficient and high yielding method to quinazolin-4(3H)-ones. Efficiency of this approach has been evaluated synthesizing four well known tyrosine kinase inhibitors and comparing the obtained yields with those achievable through conventional synthetic methods.
机译:描述了一种基于喹唑啉环氧化制备4-苯胺基喹唑啉衍生物的新策略。喹唑啉氧化已得到研究和改进,从而导致了一种高效,高产率的喹唑啉-4(3H)-酮合成方法。已经评估了合成四种众所周知的酪氨酸激酶抑制剂并将这种获得的产率与通过常规合成方法可获得的产率进行比较的方法的效率。

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