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Abstract
2-Hydroxy acetophenones on treatment with 6-methyl-2-(1H-pyrazol-1-yl) quinoline-3-carbaldehyde by conventional and ultrasonication methods gave the corresponding chalcones. These chalcones were transformed into chromones and 1, 5-benzothizepines by using DMSO/I2 and 2-aminothiophenol respectively. Compounds 3b and 3e have shown better antibacterial activity against Gentamycin and Tetracycline. Similarly 2e have also been shown moderate antifungal activity against Ketoconazole taken as reference drug.