Chemistry of Heterocyclic Compounds

, Volume 5, Issue 4, pp 536–539 | Cite as

Reaction of 4-aminouracil with 2-(arylmethylene)indan-1, 3-diones

  • E. I. Stankevich
  • A. Ya. Ozol
  • G. Ya. Dubur
Article
  • 39 Downloads

Abstract

The reaction of the arylmethyleneindanones (I) with 4-aminouracil or its N-methyl derivative (IV) gives new multinuclear nitrogencontaining systems—5-aryl-2,4,6-trioxo-1-R-3-R′-1,2,3,4,5,11-hexahydro-11-azafluoreno[3,2-d]pyrimidines (V), which are oxidized by chromic anhydride to 5-aryl-2,4,6-trioxo-1-R-3-R′-1,2,3,4-tetrahydro-11-azafluoreno[3,2-d]pyrimidines (VI). The UV and IR spectra of the compounds synthesized are given.

Keywords

Organic Chemistry Anhydride Pyrimidine Chromic Anhydride 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.
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References

  1. 1.
    E. I. Stankevich and G. Ya. Vanag, ZhOKh, 32, 1146, 1962.Google Scholar
  2. 2.
    E. I. Stankevich and G. Ya. Vanag, Izv. AN LatvSSR, ser. khim., 283, 1962.Google Scholar
  3. 3.
    E. I. Stankevich and G. Ya. Vanag, ZhOrKh, 1, 815, 1965.Google Scholar
  4. 4.
    Yu. E. Pelcher, O. E. Grinshtein, E. I. Stankevich, and G. Ya. Vanag, KhGS, collection 1, 406, 1967.Google Scholar

Copyright information

© Consultants Bureau 1972

Authors and Affiliations

  • E. I. Stankevich
    • 1
  • A. Ya. Ozol
    • 1
  • G. Ya. Dubur
    • 1
  1. 1.Institute of Organic Synthesis AS LatvSSRRiga

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