融合吡喃并[3,2-e]四唑并[1,5-c]嘧啶和二氮杂卓的设计、合成和体外抗菌评估。

ISRN Organic Chemistry Pub Date : 2013-08-21 eCollection Date: 2013-01-01 DOI:10.1155/2013/635384
Sankari Kanakaraju, P Sagar Vijay Kumar, Bethanamudi Prasanna, G V P Chandramouli
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引用次数: 0

摘要

通过相应的四唑 2a-f 分别与二硫化碳、苯甲醛和 4-甲氧基苯溴化物缩合,合成了一系列与嘧啶乙酮、嘧啶和二氮杂卓融合的新型含吡喃色烯的四唑 3a-f、4a-f 和 5a-f。化合物 2a-f 是由吡喃并[3,2-c]色烯 1a-f 与叠氮化钠反应得到的。根据元素分析、红外光谱、(1)H NMR、(13)C NMR 和质谱数据,确定了新合成的化合物 2a-f 至 5a-f 的结构。对所有标题化合物都进行了体外抗菌测试和抗真菌筛选,前者针对四种致病菌株,后者针对两种真菌。初步结果表明,其中一些化合物具有良好的活性,值得进一步考虑将其作为潜在的抗菌剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Design, Synthesis, and In Vitro Antimicrobial Evaluation of Fused Pyrano[3,2-e]tetrazolo[1,5-c]pyrimidines and Diazepines.

Design, Synthesis, and In Vitro Antimicrobial Evaluation of Fused Pyrano[3,2-e]tetrazolo[1,5-c]pyrimidines and Diazepines.

A series of novel pyranochromene-containing tetrazoles fused with pyrimidinethiones, pyrimidines, and diazepines 3a-f, 4a-f, and 5a-f were synthesized by condensation of the corresponding tetrazoles 2a-f with carbon disulfide, benzaldehyde, and 4-methoxy phenacyl bromide, respectively. The compound 2a-f was obtained by reaction of pyrano[3,2-c]chromenes 1a-f with sodium azide. The structures of the newly synthesized compounds 2a-f to 5a-f were established on the basis of their elemental analyses, IR, (1)H NMR, (13)C NMR, and mass spectral data. All of the title compounds were subjected to in vitro antibacterial testing against four pathogenic strains and antifungal screening against two fungi. Preliminary results indicate that some of them exhibited promising activities and that they deserve more consideration as potential antimicrobials.

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