Synthesis and biological evaluation some new of 7-hydroxy-4-methylcoumarin derivative
Journal Title: Asian Pacific Journal of Health Sciences - Year 2017, Vol 4, Issue 4
Abstract
7-hydroxy-4-methylcoumarin derivatives were synthesized. The title compounds (M1-M5) were obtained by the reaction of 7-hydroxy-4-methylcoumarin with ethyl chloroacetate in the presence of potassium carbonate in acetone afforded ethyl-2-(4-methyl-2-oxo-2H-chromen-7-yloxy)acetate, which react with hydrazine hydrate in ethanol afforded 2-(4-methyl-2-oxo-2H-chromen-7-yloxy) acetohydrazide, on further reaction with various acetophenones in the presence of glacial acetic acid in absolute alcohol gave 2-(4-methyl-2-oxo-2H-chromen-7-yloxy)-N’-substituted acetohydrazides (M1-M5). The structures of target compounds (M1-M5) were established on the basis of infrared and 1H-nuclear magnetic resonance spectral analysis. Target compounds (M1-M5) were screened for their antimicrobial activity and showing significant antimicrobial activity as compared to standard drug.
Authors and Affiliations
Aniruddh Dev Singh,
Keywords
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- EP ID EP525498
- DOI 10.21276/apjhs.2017.4.4.21
- Views 143
- Downloads 0
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