Synthesis of Tetrazolo, Triazolo and Quinazolino Annulated Analogues of the Privileged Nucleus of Pyrrolo-[1, 5]-Benzothiazepines of Medicinal Interest

Journal Title: International Journal of Scientific Research and Reviews - Year 2013, Vol 2, Issue 2

Abstract

The nucleophilic displacement of 2-iminothiomethylether derivative of pyrrolo-1,5- benzothiazepines was elegantly exploited in its reaction with bidentate nucleophiles such as NH2-NH2 (followed by reaction with HNO2), acetahydrazide, isatoic anhydride, amino benzonitrile to allow the facile annulation of this molecule with triazole, tetrazole and quinazoline nucleus.

Authors and Affiliations

Priyanka Rani , D. Kishore

Keywords

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  • EP ID EP110124
  • DOI -
  • Views 164
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How To Cite

Priyanka Rani, D. Kishore (2013). Synthesis of Tetrazolo, Triazolo and Quinazolino Annulated Analogues of the Privileged Nucleus of Pyrrolo-[1, 5]-Benzothiazepines of Medicinal Interest. International Journal of Scientific Research and Reviews, 2(2), 85-93. https://europub.co.uk/articles/-A-110124