Synthesis of Hybrid Pharmacophores Based on Adducts of N-Sulfinylaniline and Norbornadiene


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Abstract

Acylation of benzothiazinesulfonamides obtained by the oxidation of N-sulfinylaniline and norbornadiene adducts with acid chlorides and carboxylic anhydrides led to the formation of N-acylated sulfonamide hybrid pharmacophores. Molecular and crystal structure of the acylated products was established by X-ray diffraction method.

About the authors

O. A. Tevs

Kant Baltic Federal University

Email: lod_olga@mail.ru
Russian Federation, Kaliningrad

Ya. V. Veremeychik

Kant Baltic Federal University

Email: lod_olga@mail.ru
Russian Federation, Kaliningrad

O. A. Lodochnikova

A.E. Arbuzov Institute of Organic and Physical Chemistry, FRC Kazan Scientific Center; Butlerov Institute of Chemistry

Author for correspondence.
Email: lod_olga@mail.ru
Russian Federation, ul. Akademika Arbuzova 8, Kazan, Tatarstan, 420088; Kazan, Tatarstan

V. V. Plemenkov

Butlerov Institute of Chemistry

Email: lod_olga@mail.ru
Russian Federation, Kazan, Tatarstan

I. A. Litvinov

A.E. Arbuzov Institute of Organic and Physical Chemistry, FRC Kazan Scientific Center; Tupolev Kazan National Research Technical University (KAI)

Email: lod_olga@mail.ru
Russian Federation, ul. Akademika Arbuzova 8, Kazan, Tatarstan, 420088; Kazan, Tatarstan

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