Faculty of Science of Girls, King Khaled University, Abha, Saudi Arabia.
Spectrochim Acta A Mol Biomol Spectrosc. 2012 Oct;96:898-905. doi: 10.1016/j.saa.2012.04.068. Epub 2012 May 22.
The reactions of 2-phenyl-4-arylmethylene-2-oxazolin-5-ones (1a, b) and 2-phenyl-4-arylazo-2-oxazolin-5-ones (8a, b) with p-aminoazobenzene derivatives (2a-c) gave the corresponding imidazolone derivatives (4a-f) and triazole derivatives (10a-f), respectively. Also, the reaction of 1a with o-aminophenol to give the imidazolone derivative 5 was studied. The reaction of 1a with 2,4-dinitrophenylhydrazine gave the corresponding 1,2,4-triazine derivatives 14a-c, respectively. The newly synthesized compounds were screened for their antibacterial activity against Gram-positive (Bacillus subtilis and Bacillus thuringiensis), Gram-negative bacteria (Escherichia coli and Pseudomonas aeruginosa) and in vitro antifungal potential against Fusarium oxysporum and Botrytis fabae fungal strains. The results revealed that the investigated compounds exhibited antibacterial and a significant antifungal activity.
2-苯基-4-亚芳基甲叉-2-噁唑啉-5-酮(1a、b)和 2-苯基-4-芳基偶氮-2-噁唑啉-5-酮(8a、b)与对氨基偶氮苯衍生物(2a-c)的反应分别得到相应的咪唑啉酮衍生物(4a-f)和三唑衍生物(10a-f)。此外,还研究了 1a 与邻氨基酚反应生成咪唑啉酮衍生物 5 的反应。1a 与 2,4-二硝基苯肼的反应分别得到相应的 1,2,4-三嗪衍生物 14a-c。对新合成的化合物进行了革兰氏阳性菌(枯草芽孢杆菌和苏云金芽孢杆菌)、革兰氏阴性菌(大肠杆菌和铜绿假单胞菌)的抗菌活性筛选,并在体外对尖孢镰刀菌和灰葡萄孢菌真菌菌株进行了抗真菌潜力筛选。结果表明,所研究的化合物表现出抗菌和显著的抗真菌活性。