Acylated benzothiazinesulfoneamides: Synthesis and molecular structure

O. A. Tevs; Ya. V. Veremeichik; D. N. Shurpik; O. A. Lodochnikova; V. V. Plemenkov

doi:10.1134/S1070363216080120

Acylated benzothiazinesulfoneamides: Synthesis and molecular structure

Autores: Tevs O.¹, Veremeichik Y.¹, Shurpik D.², Lodochnikova O.³, Plemenkov V.¹
Afiliações:
1. Kant Baltic Federal University
2. Kazan (Volga Region) Federal University
3. Arbuzov Institute of Organic and Physical Chemistry, Kazan Scientific Centre
Edição: Volume 86, Nº 8 (2016)
Páginas: 1850-1853
Seção: Article
URL: https://journals.rcsi.science/1070-3632/article/view/215930
DOI: https://doi.org/10.1134/S1070363216080120
ID: 215930

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Resumo

1,2,3,4,4a,10b-Hexahydro-1,4-methano-6H-dibenzo[c,e]-5,6-thiazine-5,5-dioxide has been converted into the corresponding N-acyl derivatives via the reaction with acid chlorides and anhydrides. X-Ray diffraction data have revealed the presence of an intramolecular С–H···O=S hydrogen bond in the molecules of the obtained compounds.