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Synthesis of New Quinazolin-4-(3H)-one Derivatives and Evaluation of Their Biological Activities

机译:新的喹唑啉-4-(3H) - 一种衍生物的合成及其生物活性的评估

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摘要

A new series of quinazolin-4-ones are conveniently synthesized in a one-pot procedure from anthranilamide derivatives and aldehydes using p-toluenesulfonic acid as a catalyst.The aim of inserting azo pyridyl and 4-amino benzamide groups in the structure of quinazolin-4-one derivatives is to achieve skeletal appearance with more antibacterial and antifungal properties.Therefore,the biological activities of the synthetic compounds were studied.The results revealed that almost all compounds exhibit antimicrobial activities.
机译:使用p-甲苯二磺酸作为催化剂,将一系列新系列的喹啉唑蛋白-4-酮从蒽胺衍生物和醛中方便合成。 4个衍生物是实现具有更多抗菌和抗真菌特性的骨骼外观。因此,研究了合成化合物的生物学活性。结果表明,几乎所有化合物都表现出抗菌活性。

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