Synthesis and Biological Activity of N-Substituted-3-chloro-2-azetidinones

Molecules

关键词: 2-Aminobenzothiazole;    azetidinones;    antibacterial activity.;   

DOI  :  10.3390/12112467

来源: DOAJ

【 摘 要 】

2-Aminobenzothiazole-6-carboxylic acid (1), on condensation with chloroacetylchloride yielded 2-(2-chloroacetylamino)benzothiazole-6-carboxylic acid (2), which onamination with hydrazine hydrate yielded in turn 2-(2-hydrazinoacetylamino)benzo-thiazole-6-carboxylic acid (3). Compound 3, on condensation with various aromaticaldehydes afforded a series of 2-{2-[N’-(arylidene)hydrazino]acetylamino}benzothiazole-6-carboxylic acids 4a-h, which upon dehydrative annulation in the presence ofchloroacetyl chloride and triethylamine yielded 2-{2-[3-chloro-2-(aryl)-4-oxoazetidin-1-ylamino]-acetylamino}benzothiazole-6-carboxylic acids 5a-h. The synthesized compounds4a-h and 5a-h were screened for their antibacterial activity against four microorganisms:Staphylococcus aureus (Gram positive), Bacillus subtilis (Gram positive), Psuedomonasaeruginosa (Gram negative) and Escherichia coli (Gram negative). They were found toexhibit good to moderate antibacterial activity. The antifungal activity of these compoundswere also tested against three different fungal species. None of them were active againstthe species tested.

【 授权许可】

Unknown