4.5 Article

Electrochemical Oxidation of Desipramine Drug in the Presence of 4,6-Dimethylpyrimidine-2-thiol Nucleophile in Aqueous Acidic Medium

期刊

ELECTROANALYSIS
卷 27, 期 7, 页码 1693-1698

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WILEY-V C H VERLAG GMBH
DOI: 10.1002/elan.201400574

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Desipramine (DES); 4,6-dimethylpyrimidine-2-thiol(DMPT); Cyclic voltammetry; Electrochemical mechanism; Dibenzazepine compounds

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Electrochemical oxidation of desipramine (DES) has been studied in the presence of 4,6-dimethylpyrimidine-2-thiol (DMPT) as nucleophile in acidic medium by means of cyclic voltammetry, controlled-potential electrolysis and spectroscopic data, as diagnostic techniques. Voltammetric studies of electro-oxidation of desipramine were realized in a range of pH1.0 to 8.0 in the absence and presence of DMPT. The results indicate the participation of the product of electrochemical oxidation of desipramine in the reaction with DMPT with ECEC electrochemical mechanism. However, the voltammetry and coulometry results imply existence of a catalytic (EC) electrochemical mechanism in parallel with ECEC electrochemical mechanism. The product has been characterized by IR, H-1 NMR, (CNMR)-C-13 and MS methods.

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