Synthesis of 2-[{2-(1-Acyl-3-aryl-4,5-dihydro-1H­-pyrazol-5-yl)phenoxy}methyl]-5-aryl-1,3,4-oxadiazoles and related compounds as potential pesticides

Abstract

Cyclization of substituted chalkones 3a,b with hydrazine hydrate followed by acylation of the resulting 3-aryl-4,5-dihydro-5-(2-hydroxyphenyl)-1 H -pyrazoles ( 4a,b ) with alkanoic acids furnished 1-acyl-3-aryl-4,5-dihydro-5-(2-hydroxyphenyl)-1 H -pyrazoles ( 5a-d ). The compounds 5a-d are also directly prepared by refluxing 3a,b with hydrazine hydrate in alkanoic acids. Alkylation of 5a-d with ethyl chloroacetate have been yielded the corresponding aryloxyacetates 6a-d . Aminolysis of the ester 6a-d have resulted in the formation of corresponding substituted aryloxyacetamides 7a-l . Hydrazinolysis of esters 6a-d with hydrazine hydrate followed by cyclization of the resulting aryloxyacetic acid hydrazides 8a-d with aromatic acids in refluxing POCl 3 have afforded the title compounds 9a-t . The compounds 3-9 have been evaluated for their in vitro growth-inhibitory activity against four fungal pests, Alternaria helianthus, Colletotrichum falcatum, fusarium oxysporum and Rhizoctonia solani . Many of the compounds have displayed promising activity at different concentrations ranging from 313 – 100 mg L -1 .