Design, synthesis, spectral analysis, antibabacterial activity of n-(3-chloro-2- oxo-4-arylazetidin-1-yl)-3 hydroxybenzofuran-2- carboxamide derivatives
DOI:
https://doi.org/10.61096/ijpar.v5.iss4.2016.518-524Keywords:
Carbohydrazide, Synthesis, 1H NMR, 13C NMR, ESI MASS, Antibacterial activity.Abstract
3-hydroxybenzofuran-2-carbohydrazide undergoes facile condensation with aromatic aldehydes to afford the corresponding N-rylidene-3-hydroxybenzofuran-2-carbohydrazide in good yields. Cyclo condensation of compounds with chloro acetyl chloride yields N-(3-chloro-2-oxo-4-arylazetidin-1-yl)-3 hydroxybenzofuran-2- carboxamide. The structures of these compounds were established on the basis of analytical and spectral data. The newly synthesized compounds were evaluated for their antibacteri al activity.