Purines, pyrimidines, and condensed systems based on these compounds. 13. Transformation of fervenulin-1-oxide to 8-alkylaminotheophyllines under the action of alkylamines

Authors

  • A. B. Гулевская Rostov State University, Rostov-on-Don 344090
  • А. Ф. Пожарский Rostov State University, Rostov-on-Don 344090
  • C. B. Швидченко Rostov State University, Rostov-on-Don 344090

Abstract

Fervenulin-1-oxide undergoes reactions with secondary alkylamines in which the triazine ring is ruptured and 8-alkylaminotheophyllines are formed. The final product of the interaction of fervenulin-1-oxide with primary amines or with liquid ammonia is 1,3-dimethyl-5-imino-6-hydroximinouracil.

How to Cite
Gulevskaya, A. V.; Pozharskii, A. F.; Shvidchenko, S. V. Chem. Heterocycl. Compd. 1994, 30, 1087. [Khim. Geterotsikl. Soedin. 1994, 1253.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF01171171

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Published

1994-09-25

Issue

No. 9 (1994)

Section

Original Papers