SYNTHESIS AND HYDROXYLATION OF 1-ALKYL- AND 7-ALKYL-1,3,7-TRIAZAPYRENIUM SALTS

Authors

  • С. В. Писаренко Stavropol State University, Stavropol 355009
  • О. П. Демидов Stavropol State University, Stavropol 355009
  • А. В. Аксенов Stavropol State University, Stavropol 355009
  • И. В. Боровлев Stavropol State University, Stavropol 355009

DOI:

https://doi.org/10.1007/6724

Keywords:

1, 3, 7-triazapyrenes, 7-triazapyrenium salts, hydroxylation, quaternization

Abstract

The regioselectivity of quaternization of 1,3,5-triazapyrenes by alkyl halides has been studied. Oxidative hydroxylation of 1-alkyl- and  7-alkyl-1,3,7-triazapyrenium salts gives 1-alkyl-1,2-dihydro-1,3,7-triazapyren-2-ones or 7-alkyl-6,7-dihydro-1,3,7-triazapyren-6-ones  respectively. In the absence of an oxidant the hydroxylation of the 1-alkyl-1,3,7-triazapyrenium salts leads to a hydrolytic cleavage of the heterocycle.

How to Cite
Pisarenko, S. V.; Demidov, O. P.; Aksenov, A. V.; Borovlev, I. V.  Chem. Heterocycl. Compd. 2009, 45, 580. [Khim. Geterotsikl. Soedin. 2009, 735.]

For this article in the English edition see DOI 10.1007/s10593-009-0295-6

 

Published

2022-04-14

Issue

Section

Original Papers