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Design, Synthesis, and Antimicrobial Activity of Novel Fluorine-Containing Imidazolones

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Abstract

A simple synthetic protocol have been developed for the preparation of novel N-(4-benzylidene-5-oxo-2-phenyl-4,5-dihydro-1H-imidazol-1-yl)-N′-phenylthiourea derivatives by the reaction of 4-benzylidene-2-phenyl-4,5-dihydro-1,3-oxazol-5-ones with N-(3-chloro-4-fluorophenyl)- and N-[3-(trifluoromethyl)phenyl)hydrazinecarbothioamides. The synthesized imidazolones have been characterized by using different spectroscopic techniques and evaluated for their antimicrobial activity against some bacterial and fungal strains. Imidazolone derivatives containing 2-nitrobenzylidene and 4-methoxybenzylidene substituents were found to be potent against fungal strains Candida albicans and Aspergillus clavatus..

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Funding

Prof. N.C. Desai thanks the UGC for awarding BSR faculty fellowship-2019 (no. F18-1/2011) and financial assistant. The authors also thank the University Grants Commission and Department of Science and Technology (New Delhi) for financial support under the NON-SAP and DST-FIST programs, respectively.

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Desai, N.C., Wadekar, K.R., Mehta, H.K. et al. Design, Synthesis, and Antimicrobial Activity of Novel Fluorine-Containing Imidazolones. Russ J Org Chem 57, 976–985 (2021). https://doi.org/10.1134/S1070428021060142

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