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吡唑基查尔酮合成子在磨盘技术下合成氮杂嘧啶的效用。

Utility of Pyrazolylchalcone Synthon to Synthesize Azolopyrimidines under Grindstone Technology.

作者信息

El-Hashash Maher Abd El-Aziz, Gomha Sobhi Mohamed, El-Arab Elham Ezz

机构信息

Chemistry Department, Faculty of Science, Ain Shams University.

出版信息

Chem Pharm Bull (Tokyo). 2017;65(1):90-96. doi: 10.1248/cpb.c16-00759.

Abstract

A series of pyrazolyl-triazolo[1,5-a]pyrimidines, pyrazolyl-tetrazolo[1,5-a]pyrimidines, pyrazolyl-benzo[4,5]imidazo[1,2-a]pyrimidines and bis-azolopyrimidines were prepared by reaction of pyrazolyl-chalcones or its bis-pyrazolyl-chalcones with the appropriate heterocyclic amines as aminotriazole, aminotetrazole, 2-aminobenzimidazole and 4,6-dimethyl-1H-pyrazolo[3,4-b]pyridin-3-amine by grinding method. The newly synthesized compounds have been characterized on the basis of elemental analysis and spectral data (IR, H- and C-NMR, Mass). Moreover, the newly synthesized products were screened for their in vitro antibacterial activities and the results showed that compounds 5f and 11d exhibited excellent activities compared with penicillin G and streptomycin as reference drugs.

摘要

通过研磨法,使吡唑基查尔酮或其二吡唑基查尔酮与适当的杂环胺(如氨基三唑、氨基四唑、2-氨基苯并咪唑和4,6-二甲基-1H-吡唑并[3,4-b]吡啶-3-胺)反应,制备了一系列吡唑基-三唑并[1,5-a]嘧啶、吡唑基-四唑并[1,5-a]嘧啶、吡唑基-苯并[4,5]咪唑并[1,2-a]嘧啶和双唑基嘧啶。基于元素分析和光谱数据(红外光谱、氢谱和碳谱、质谱)对新合成的化合物进行了表征。此外,对新合成的产物进行了体外抗菌活性筛选,结果表明,与作为参考药物的青霉素G和链霉素相比,化合物5f和11d表现出优异的活性。

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