Synthesis and steric structure of 4-arylaminohexahydropyrimidine-2-thiones

Authors

  • А. Д. Шуталев M. V. Lomonosov State Academy of Fine Chemical Technology, Moscow 117571
  • М. T. Пагаев M. V. Lomonosov State Academy of Fine Chemical Technology, Moscow 117571
  • Л. А. Игнатова M. V. Lomonosov State Academy of Fine Chemical Technology, Moscow 117571

Abstract

Reaction of 4-hydroxy- and 4methoxyhexahydropyrirnidine-2-thiones and 6-methyl-1,2,3,6-tetrahydropyrimidine-2-thione with primary amines occurs readily in the presence of acidic or basic catalysts to give 4-arylaminohexahydropyrimidine-2-thiones both regio- and stereoselectively. It was shown that reaction stereoselectivity depends on the structure of the starting materials and on the reaction conditions. The steric structures of the products synthesized has been studied.

How to Cite
Shutalev, A. D.; Pagaev, M. T.; Ignatova, L. A. Chem. Heterocycl. Compd. 1994, 30, 943. [Khim. Geterotsikl. Soedin. 1994, 1093.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF01165034

Published

1994-08-25

Issue

Section

Original Papers