Articles written in Journal of Chemical Sciences
Volume 98 Issue 3 March 1987 pp 221-228 Organic
The reduction of 7-chloro-1,3-dihydro-1-methyl-5-phenyl-2H-1,4-benzodiazepine-2-one at the dropping mercury electrode has been investigated. The process is diffusion controlled; furthermore, the reduction wave enables the quantitative determination of the drug both in acid and basic media. The reagent captures two electrons and two hydrogen ions. A disproportionation reaction of the hydrazo-compound takes place, and amines are the final reduction products.
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