Literature DB >> 27915196

Identification and characterization of a new dapoxetine impurity by NMR: Transformation of N-oxide by Cope elimination.

András Darcsi1, Ákos Rácz2, Szabolcs Béni3.   

Abstract

Unknown impurity associated with the degradation process of dapoxetine base was isolated. The structure elucidation of this new compound using accurate mass data, IR and NMR spectroscopy is presented herein. The unambiguous resonance assignment concluded to the formation of geometrical isomers of cinnamyloxynaphtalenes via Cope elimination of dapoxetin-N-oxide, the major oxidative and metabolic degradation product of dapoxetine. An efficient and simple synthetic approach has also been developed for the synthesis of dapoxetine-N-oxide for the first time and cinnamyloxynaphtalene in order to confirm the proposed degradation pathway and structures of the degradation products. It was observed that the main degradation product of dapoxetine base when exposed to air is 1-(2E)-cinnamyloxynaphthalene, while its Z isomer was also confirmed as a minor impurity.
Copyright © 2016 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Degradation product; Drug analysis geometric (E/Z) isomer; Hofmann elimination; Impurity profiling; Metabolism; Priligy

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Year:  2016        PMID: 27915196     DOI: 10.1016/j.jpba.2016.11.029

Source DB:  PubMed          Journal:  J Pharm Biomed Anal        ISSN: 0731-7085            Impact factor:   3.935


  1 in total

1.  Synthesis of (±)-Setigerumine I: Biosynthetic Origins of the Elusive Racemic Papaveraceae Isoxazolidine Alkaloids*.

Authors:  Ana V Serna; László Kürti; Juha H Siitonen
Journal:  Angew Chem Int Ed Engl       Date:  2021-11-18       Impact factor: 15.336

  1 in total

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