A NEW ROUTE FOR THE SYNTHESIS OF 4,5-DIAMINO-6-ARYLSULFANYLPYRIMIDINE DERIVATIVES AND ALSO PURINES ON THEIR BASIS

Authors

  • С. В. Попильниченко Institute of Bioorganic Chemistry and Petrochemistry, National Academy of Sciences of Ukraine
  • Р. Н. Соломянный Institute of Bioorganic Chemistry and Petrochemistry, National Academy of Sciences of Ukraine
  • В. С. Броварец Institute of Bioorganic Chemistry and Petrochemistry, National Academy of Sciences of Ukraine

DOI:

https://doi.org/10.1007/2078

Keywords:

benzamidine, 4, 5-diamino-6-arylsulfanylpyrimidines, purine bases, thiophenols, heterocyclization

Abstract

5-Acylamino-4-amino-6-arylsulfanylpyrimidines were formed by the reaction 3-arylsulfanyl-2-acylamino-3-chloroacrylonitriles with benzamidine. The products were converted into new derivatives of 6-arylsulfanylsubstituted purine bases by treatment with polyphosphoric acid.

How to Cite
Popil’nichenko, C. V.; Solomyannyj, R. N.; Brovarets, V. S. Chem. Heterocycl. Compd. 2011, 47(4), 492. [Khim. Geterotsikl. Soedin. 2011, 597.]

For this article in the English edition see DOI 10.1007/s10593-011-0786-0

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Published

2014-11-28

Issue

No. 4 (2011)

Section

Original Papers