一系列2-苯胺-5-(2-氯苯基)-1,3,4-恶二唑衍生物的合成、表征及生物学评价

S. Kumar, P. Srivastava
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引用次数: 1

摘要

在常温乙酸中,以酰基硫代氨基脲为原料,在铂电极上电化学合成了2-苯基氨基-5-(2-氯苯基)-1,3,4-恶二唑。采用两个方板形式的铂电极作为工作电极和对电极,饱和甘汞电极作为参比电极。化合物的结构经IR、NMR、质谱和元素分析证实。还评估了衍生物的抗菌活性,并与革兰氏阳性肺炎克雷伯菌、大肠杆菌和革兰氏阴性细菌金黄色链球菌和枯草Bascillus的抗菌活性进行了比较。测定了其对黑曲霉、猪瘟孢子菌、褐皮糙皮菌和白色念珠菌的抗真菌活性,并与标准抗真菌药物格里斯沃霉素进行了比较。达卡大学药学院。科学18(1):75-83,2019 (6)
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Syntheses, Characterization and Biological Evaluation of a Series of 2-Phenylamino-5-(2-Chlorophenyl)-1,3,4-Oxadiazole Derivatives
Electrochemical synthesis of 2-phenylamino-5-(2-chlorophenyl)-1,3,4-oxadiazoles have been carried out in good yields at platinum electrode through the electrochemical oxidation of acyl thiosemicarbazide at room temperature in acetic acid. Two platinum electrodes in the form of square plates were used as working as well as counter electrode and saturated calomel electrode was used as reference electrode. The structure of the compounds was confirmed by IR, NMR, mass spectral and elemental analyses. The antibacterial activity of the derivatives was also assessed and compared with data against a series of Gram-positive Klebsiella pneumoniae, Escherichia coli and Gramnegative bacteria Streptococcus aureus and Bascillus subtilis. The antifungal activity was assessed against the fungal strain Aspergillus niger, Crysosporium pannical, Pellicularia solmanicolor and Candida albicans and compared against the standard antifungal drug Griesvofulvin. Dhaka Univ. J. Pharm. Sci. 18(1): 75-83, 2019 (June)
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