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Synthesis and In-vitro Antifungal Evaluation of 5- Pyrazolones

机译:5-吡唑啉酮的合成及体外抗真菌评价

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摘要

A series of 4-chloro-3-methyl-N-(substituted phenyl)-5-oxo-4,5-dihydro-1H-pyrazole-1- carbothioamidewere synthesized using earmark reaction of thiosemicarbazides and ethyl-2-chloroacetoacetate in DMF. All structures of the synthesized compounds were distinguished on the basis of IR, 1H-NMR, 13C-NMR and also elemental analysis. Synthesized Compounds were examined their potent antifungal activity using disc diffusion technique against three fungal pathogens viz Aspergillus niger, Candida albicans and Curvularia. Fluconazole were used as standard drug respectively. All compounds exhibited good to moderate activity.
机译:利用硫代氨基脲与-2-氯乙酰乙酸乙酯在DMF中的专一反应,合成了一系列4-氯-3-甲基-N-(取代苯基)-5-氧代-4,5-二氢-1H-吡唑-1-碳硫酰胺。基于IR,1 H-NMR,13 C-NMR以及元素分析来区分合成的化合物的所有结构。使用圆盘扩散技术检查了合成的化合物对三种真菌病原菌(即黑曲霉,白色念珠菌和弯曲菌)的有效抗真菌活性。氟康唑分别用作标准药物。所有化合物均表现出良好至中等的活性。

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