Abstract
3-Chloro-1-benzothiophene-2-carbonyl chloride 1 was reacted with glycine in acetone to give 3-chloro-1- benzothiophen-2-yl-carbonylaminoacetic acid 2. Various aldehydes on treatment with compound 2 in acetic anhydride to gave 1,3-oxazol-5-ones 3a-d. These oxazolones was treated with aromatic amines or hydrazides to get various imidazol-4-ones 4a-t or 5a-1. Oxazolones 3a-d was also treated with aromatic hydrazines, expansion of five member oxazole ring to six member triazine ring occurs to yield 1,2,4-triazin-6-ones 6a-h. The structures of all the synthesized compounds were confirmed by spectral data and had been screened for antibacterial activity. Copyright © 2005 KCSNET.
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Naganagowda, G., & Petsom, A. (2011). Synthesis and antimicrobial activity of oxazolone, imidazolone and triazine derivatives containing benzothiophene. Bulletin of the Korean Chemical Society, 32(11), 3914–3922. https://doi.org/10.5012/bkcs.2011.32.11.3914
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