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Synthesis of Polyfunctionally Substituted Fused Pyrimidine Derivatives as Antimicrobial Agents

机译:多官能取代的嘧啶衍生物作为抗菌剂的合成

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摘要

A VARIETY of pyrimidine derivatives 2-4 and annulated pyrimidine derivatives 5-17 have been synthesized via a sequence of heterocyclization reactions of readily available 6-naphthyl - 4-oxo-2-thioxo- l,2,3,4-tetrahydroprimidine-5-carbonitrile (1) with different acidic and basic reagents. The new compounds were synthesized with the aim of studying their antimicrobial activity. The structures of all synthesized compounds were elucidated by elemental analysis and spectroscopic studies.
机译:通过易于获得的6-萘基-4-氧代-2-氧代-2-硫代氧代-1,2,3,4-四氢伯啶-5的一系列杂环反应合成了各种嘧啶衍生物2-4和环状嘧啶衍生物5-17。 -腈(1)具有不同的酸性和碱性试剂。为了研究它们的抗微生物活性,合成了这些新化合物。通过元素分析和光谱研究阐明了所有合成化合物的结构。

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