Reaction between 4-hydroxy- and 4-methoxyhexahydropyrimidine-2-thiones and secondary and tertiary arylamines

Authors

  • А. Д. Шуталев M. V. Lomonosov State Academy of Fine Chemical Technology, Moscow 117571
  • С. Г. Алексеева M. V. Lomonosov State Academy of Fine Chemical Technology, Moscow 117571

Abstract

It is shown that the reaction between both 4-hydroxy- and 4-methoxyhexahydropyrimidine-2-thiones and N,N-dimethylaniline, N-methylaniline and N-methylanthranilic acid in 50% acetic acid proceeds regio- and stereoselectively, resulting in the formation of the corresponding 4-aryl-substituted hexahydropyrimidine-2-thiones.

How to Cite
Shutalev, A. D.; Alekseeva, S. G. Chem. Heterocycl. Compd. 1995, 31, 326. [Khim. Geterotsikl. Soedin. 1995, 377.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF01373551

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Published

1995-03-25

Issue

No. 3 (1995)

Section

Original Papers