| Literature DB >> 18096350 |
Elisabetta Brenna1, Samuele Frigoli, Giovanni Fronza, Claudio Fuganti, Stefano Serra.
Abstract
Two impurities showing structures 5 and 6 were isolated and characterised by means of NMR analysis, during the optimisation of a synthetic procedure to tazarotene. Impurity 5, i.e. ethyl 6-((4,4-dimethyl-4H-thiochromen-6-yl)ethynyl)nicotinate, was a by-product of the reduction of the intermediate sulfoxide 7 with PCl(3). Impurity 6, i.e. 1,4-bis(4,4-dimethylthiochroman-6-yl)buta-1,3-diyne, was due to a side reaction of the Sonogashira coupling.Entities:
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Year: 2007 PMID: 18096350 DOI: 10.1016/j.jpba.2007.11.004
Source DB: PubMed Journal: J Pharm Biomed Anal ISSN: 0731-7085 Impact factor: 3.935