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Electrochemical <i>N</i> -Demethylation of 14-Hydroxy Morphinans: Sustainable Access to Opioid Antagonists

Gabriel Glotz, C. Oliver Kappe, David Cantillo

2020Organic Letters26 citationsDOIOpen Access PDF

Abstract

The most challenging step in the preparation of many opioid antagonists is the selective N-demethylation of a 14-hydroxymorphinan precursor. This process is carried out on a large scale using stoichiometric amounts of hazardous chemicals like cyanogen bromide or chloroformates. We have developed a mild reagent- and catalyst-free procedure for the N-demethylation step based on the anodic oxidation of the tertiary amine. The ensuing intermediates can be readily hydrolyzed to the target nor-opioids in very good yields.

Topics & Concepts

ChemistryDemethylationReagentAmine gas treatingCombinatorial chemistryElectrochemistryBromideCatalysisHydrolysisOrganic chemistryBiochemistryGene expressionElectrodePhysical chemistryDNA methylationGeneRadical Photochemical ReactionsSynthesis and Catalytic ReactionsSulfur-Based Synthesis Techniques
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