Reaction of polychloroacetaldehyde arylsulfonylimines with 2-amino-6H-1,3-thiazine-6-thiones and 2-amino-4-phenyl-6H-1,3-thiazin-6-one


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Abstract

2-Amino-4-R-6H-1,3-thiazine-6-thiones and 2-amino-4-phenyl-6H-1,3-thiazin-6-one react with highly electrophilic N-arylsulfonylimines of chloral and phenyldichloroacetic aldehyde at the exocyclic amino group affording in good yields products of nucleophilic addition to the azomethine group of imines: N-[2-polychloro-1-(6-thioxo-4-R-6H-1,3-thiazin-2-ylamino)ethyl]- or -[2-polychloro-1-(6-oxo-4-phenyl-6H-1,3-thiazin-2-ylamino)ethyl]arenesulfonamides.

About the authors

A. R. Kaliev

Favorskii Irkutsk Institute of Chemistry, Siberian Branch

Email: i_roz@irioch.irk.ru
Russian Federation, ul. Favorskogo 1, Irkutsk, 664033

V. Yu. Serykh

Favorskii Irkutsk Institute of Chemistry, Siberian Branch

Email: i_roz@irioch.irk.ru
Russian Federation, ul. Favorskogo 1, Irkutsk, 664033

G. G. Levkovskaya

Favorskii Irkutsk Institute of Chemistry, Siberian Branch

Email: i_roz@irioch.irk.ru
Russian Federation, ul. Favorskogo 1, Irkutsk, 664033

V. I. Potkin

Institute of Physical Organic Chemistry

Email: i_roz@irioch.irk.ru
Belarus, Minsk

S. K. Petkevich

Favorskii Irkutsk Institute of Chemistry, Siberian Branch

Email: i_roz@irioch.irk.ru
Russian Federation, ul. Favorskogo 1, Irkutsk, 664033

I. B. Rozentsveig

Favorskii Irkutsk Institute of Chemistry, Siberian Branch

Author for correspondence.
Email: i_roz@irioch.irk.ru
Russian Federation, ul. Favorskogo 1, Irkutsk, 664033

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