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Synthesis, DFT study, molecular docking and insecticidal evaluation of some pyrazole-based tetrahydropyrimidine derivatives

Karema N. M. Halim, Sayed K. Ramadan, Sameh A. Rizk, Maher A. El‐Hashash

2020Synthetic Communications39 citationsDOI

Abstract

The building block synthon, 1-(4-(1,3-diphenyl-1H-pyrazol-4-yl)-6-methyl-2-thioxo-1,2,3,4-tetrahydropyrimidin-5-yl)ethan-1-one was efficiently synthesized by Biginelli reaction of 1,3-diphenyl-1H-pyrazole-4-carbaldehdye, acetylacetone, and thiourea and submitted to react with ethyl chloroacetate and chloroacetyl chloride under different conditions to afford some N-heterocycles integrated with pyrazole scaffold. Hydrazinolysis of the pyrimidinethione was studied under different conditions. The insecticidal activity for these compounds, DFT calculations, and docking were run and discussed. Some of them exhibited 100% mortality against Nilaparvata lugens and Mythimna separata.

Topics & Concepts

ChemistryPyrazoleThioureaChloroacetyl chlorideSynthonMythimna separataAcetylacetoneDocking (animal)Ethyl chloroacetateCombinatorial chemistryChlorideOrganic chemistryBiologyNursingLepidoptera genitaliaEcologyMedicineHydrateMulticomponent Synthesis of HeterocyclesSynthesis and biological activitySynthesis and Biological Evaluation