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Eco Friendly Synthesis and Potent Antimicrobial Activities of Pyrazoles and Isoxazoles
Authors: BHOYAR A. D. , PARIHAR R.T. , RAJPUT P.R
Number of views: 511
Condensation of 2-substituted-3,5-dichloroacetophenones 2a-c obtained from
the condensation of 2-hydroxy-3,5-dichloroacetophenone 1 and benzoyl chloride were
dissolved in NaOH , on treatment under baker venkatraman transformation in presence
of KOH with pyridine gives 1-(2-hydroxy-3,5- dichlorophenyl )-3-substituted-1,3-
propanedione 3a-c. Then converted into 3–aroyl-6,8-dichloroflavanones 4a-i by using
different aromatic aldehyde in the presence of ethanol, Piperidine. The condensation of
4a-i with crystal of iodine in DMF solvent gives 3-aroylflavone 5a-i. The condensation of
5a-i and phenylhydrazinehydrochlorides, piperidine in DMF gives 4-aroyl-3,5-
diarylpyrazoles 6a-i and condensation of 5a- i and hydroxylaminehydrochlorides gives 4-
aroyl–3,5diarylisoxazoles 7a –i. The above compounds are screened for their
antimicrobial activities and have been found to exhibit significant antibacterial and
antifungal activities. The zones of inhibition measured in term of mm.