SOME CHEMICAL PROPERTIES OF 2,3-DIHYDRO-4H-[1,3]THIAZINO[3,2-<i>a</i>]BENZIMIDAZOL-4-ONE AND 2-ARYL-2,3-DIHYDRO-4H-[1,3]THIAZINO[3,2-<i>a</i>]BENZIMIDAZOL-4-ONES

Authors

  • В. Н. Брицун Institute of Organic Chemistry, National Academy of Sciences of Ukraine, Kiev 02094
  • А. Н. Есипенко Institute of Organic Chemistry, National Academy of Sciences of Ukraine, Kiev 02094
  • М. О. Лозинский Institute of Organic Chemistry, National Academy of Sciences of Ukraine, Kiev 02094

DOI:

https://doi.org/10.1007/8037

Keywords:

2-aryl-2, 3-dihydro-4H-[1, 3]thiazino[3, 2-a]benzimidazol-4-ones, 2, 2-a]benzimidazol-4-one, alkylation, amination, oxidation

Abstract

We have studied the reaction of 2,3-dihydro-4H-[1,3]thiazino[3,2-a]benzimidazol-4-one and 2-aryl-2,3-dihydro-4H-[1,3]thiazino[3,2-a]benzimidazol-4-ones with amines,  alkylating reagents, and hydrogen peroxide. We have shown that the presence of an aryl substituent at the 2 position of [1,3-thiazino[3,2-a]benzimidazol-4-ones has a substantial effect on the direction of the reactions.

How to Cite
Britsun, V. N.; Esipenko, A. N.; Lozinskii, M. O.  Chem. Heterocycl. Compd. 2006, 42, 396. [Khim. Geterotsikl. Soedin. 2006, 445.]

For this article in the English edition, see DOI 10.1007/s10593-006-0099-x


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Published

2023-09-12

Issue

No. 3 (2006)

Section

Original Papers