SYNTHESIS AND PROPERTIES OF METHYL HYDROPYRIMIDINEACETATES

Authors

  • К. Брокайте Kaunas Technological University, Kaunas LT-50524
  • В. Мицкявичюс Kaunas Technological University, Kaunas LT-50524
  • Г. Микульскене Institute of Biochemistry, Vilnius LT-08622

DOI:

https://doi.org/10.1007/7467

Keywords:

1-aryldihydro-2, 4(1H, 3H)-pyrimidinedione, benzimidazoles, hydropyrimidineacetic acids, alkylation, condensation, NMR, IR, mass spectrometry

Abstract

The alkylation of 1-aryl-substituted dihydro-2,4(1H,3H)-pyrimidinediones  with methyl 2-bromoacetate has been studied followed by hydrolysis and condensation of the products with o-phenylenediamine. The compounds have been identified by NMR, and IR spectrometry  and mass spectrometry.  Structural characteristics in the 1H and 13C NMR spectra of the synthesized are discussed.

How to Cite
Brokaite, K.; Mickevičius, V.; Mikulskiene, G.  Chem. Heterocycl. Compd. 2007, 43, 926. [Khim. Geterotsikl. Soedin. 2007, 1095.]

For this article in the English edition see DOI 10.1007/s10593-007-0146-2


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Published

2023-02-16

Issue

No. 7 (2007)

Section

Original Papers