Journal of Pharmaceutical Research International

A series of substituted 4-{1-aza-2-[(aryl) amino)]}-3-methyl-2-pyrazolin-5-ones has been synthesized and evaluated for their biological activity. The title compounds (4a-l) were prepared by the diazotization of substituted anilines (1a-l) to form substituted phenyl hydrazine derivatives (2a-l) which synthesized substituted 4-{1-aza-2-[(aryl) amino)]}-3-methyl-2-pyrazolin-5-ones (4a-l) by Michael addition reaction, which is a nucleophilic addition of enolate anion to the carbon-carbon double bond of a α, β–unsaturated carboxylic acid derivatives. Twelve different pyrazolinone derivatives (4a to 4l) were synthesized. Structural assignments of these compounds have been made by elemental analysis, FTIR, ¹HNMR and Mass spectral data and the purity of the compounds was determined by TLC. The antifeedant activity of the newly isolated heterocyclic compounds was evaluated against agriculture pest Achoea janata. Compound 4d found to be very effective as antifeedant while rest of the compounds showed a moderate to good degree of antifeedant activity.