REACTION OF SUBSTITUTED 2-ALLYLTHIOPYRIMIDIN-4(3H)-ONES WITH SULFENYL CHLORIDES

Authors

  • A. I. Vaskevich Institute of Organic Chemistry, National Academy of Sciences of Ukraine, Kiev
  • Yu. I. Gevaza Institute of Organic Chemistry, National Academy of Sciences of Ukraine, Kiev
  • R. I. Vaskevich Institute of Organic Chemistry, National Academy of Sciences of Ukraine, Kiev
  • V. I. Staninets Institute of Organic Chemistry, National Academy of Sciences of Ukraine, Kiev

Keywords:

allylthiopyrimidines, 2-benzothiazolyl sulfenyl chloride, p-nitrobenzosulfenyl chloride, thiazolidinopyrimidine, thiazolidinothienopyrimidines, thiazolidinoquinazolone

Abstract

Reaction of substituted 2-allyl-thiopyrimidin-4(3H)-ones with p-nitrobenzosulfenyl chloride gives the products of addition at the allyl moiety, while the reaction with 2-benzothiazolyl sulfenyl chloride yields thiazolidinopyrimidines with an angular structure.

How to Cite
Vaskevich, A. I.; Gevaza, Yu. I.; Vaskevich, R. I.; Staninets, V. I. Chem. Heterocycl. Compd. 2004, 40, 1087. [Khim. Geterotsikl. Soedin. 2004, 1251.]

For this article in the English edition, see DOI 10.1023/B:COHC.0000046702.48941.53

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Published

2004-08-25

Issue

No. 8 (2004)

Section

Original Papers