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首页> 外文期刊>Der Pharma Chemica: journal for medicinal chemistry, pharmaceutical chemistry and computational chemistry >Synthesis and evaluation of new polysubstituted quinazoline derivatives as potential antimicrobial agents
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Synthesis and evaluation of new polysubstituted quinazoline derivatives as potential antimicrobial agents

机译:新型多取代喹唑啉衍生物作为潜在抗菌剂的合成与评价

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A new series of polysubstituted quinazoline derivatives has been furnished as a product of N-acylation, O-acylation and/or O-alkylation of the corresponding 2-methylquinazolinones; based on using the principles of lactam-lactim dynamic equilibrium phenomena and the role of solvent polarity in shifting such equilibrium. The reaction of the prepared polysubstituted quinazolines with different nitrogen, carbon, and sulphur nucleophiles has produced derivatives of 4-heteroaryl-quinazoline derivatives and interesting moieties such as oxadiazoles, triazoles, fused triazolo-thiadiazole, thiazole, furyl, and pyrazole were introduced at the 4-position of the quinazoline skeleton. Some of the synthesized compounds are tested for its antimicrobial activity.
机译:已经提供了一系列新的多取代的喹唑啉衍生物,其是相应的2-甲基喹唑啉酮的N-酰化,O-酰化和/或O-烷基化的产物。基于内酰胺-内酰胺动态平衡现象的原理以及溶剂极性在改变这种平衡中的作用。制备的多取代喹唑啉与不同的氮,碳和硫亲核试剂反应生成了4-杂芳基-喹唑啉衍生物,并在此引入了有趣的部分,例如恶二唑,三唑,稠合的三唑-噻二唑,噻唑,呋喃基和吡唑。喹唑啉骨架的4位。测试了一些合成的化合物的抗微生物活性。

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