Thio‐Induced Organophosphate Breakdown Promoted by Methimazole: an Experimental and Theoretical Study

The drug methimazole has two non-equivalent nucleophilic centers: sulfur and imidazole. It was studied in a dephosphorylation reaction with an organophosphate that has three possible electrophilic sites. Results show the preference for the nucleophilic aromatic attack via the anionic sulfur atom. This sheds lights towards the mechanistic understanding of reactions targeted for the neutralization of toxic agents such as organophosphates.

Abstract

Investigating the reactivity of small nucleophilic scaffolds is a strategic approach for the design of new catalysts aiming at effective detoxification processes of organophosphorus compounds. The drug methimazole (MMZ) is an interesting candidate featuring two non-equivalent nucleophilic centers. Herein, phosphoryl transfer reactions mediated by MMZ were assessed by means of spectrophotometric kinetic studies, mass spectrometry (MS) analyses, and density functional theory (DFT) calculations using the multi-electrophilic compound O,O-diethyl 2,4-dinitrophenyl phosphate (DEDNPP). MMZ anion acts primarily as an S-nucleophile, exhibiting a nucleophilic activity comparable to that of certain oximes featuring alpha-effect. Selective nucleophilic aromatic substitution was observed, consistent with the DFT prediction of a low energy barrier. Overall, the results bring important advances regarding the mechanistic understanding of nucleophilic dephosphorylation reactions, which comprises a strategic tool for neutralizing toxic organophosphates, hence promoting chemical security.

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