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首页> 外文期刊>Journal of Heterocyclic Chemistry: The International Journal of Heterocyclic Chemistry >Synthesis of some novel pyrazoline-thiazole hybrids and their antimicrobial activities
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Synthesis of some novel pyrazoline-thiazole hybrids and their antimicrobial activities

机译:一些新型吡唑啉 - 噻唑杂交种及其抗菌活性的合成

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摘要

A series of novel thiazolyl pyrazolines 7a-h, 9a-f, and 11a-f have been synthesized by the reaction of thioamide derivatives 5a,b with 1-aryl-2-bromoethanones 6a-d, chloroacetones 8a-c, and hydrazonoyl chlorides 10a-c. Additionally, pyrazoles 15a-c and 20 were prepared starting from enaminone 13. These newly synthesized compounds were screened for their in vitro antibacterial activity against four bacterial species. Compound 11b showed a moderate activity against Klebsiella pneumoniae. Compounds 7c and 11c revealed a moderate activity against Pseudomonas aeruginosa. In addition, the antifungal activity of the newly synthesized compounds was determined against five fungal strains. Compounds 7e, 7g, and 11e showed a good activity against Aspergillus flavus and Penicillium expansum.
机译:通过用1-芳基-2-溴乙酮6a-d,氯酰丙酮8a-c和肼氯酰氯的硫代胺衍生物5a,b的反应合成了一系列新的噻唑吡唑啉7a-h,9a-f和11a-f。 10A-C。 另外,从烯氨基酮13开始制备吡唑15A-C和20.这些新合成的化合物筛选其对四种细菌种类的体外抗菌活性。 化合物11b显示对抗克雷斯氏菌肺炎的适度活性。 化合物7c和11c揭示了对铜绿假单胞菌的适度活性。 此外,对新合成的化合物的抗真菌活性针对五种真菌菌株测定。 化合物7e,7g和11e显示出对曲霉和小钙的良好活性。

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