Russian Chemical Bulletin

, Volume 46, Issue 6, pp 1178–1179 | Cite as

Synthesis of acetonylmalonaldehyde and its interaction with aminoazoles

  • M. M. Vartanyan
  • O. L. Eliseev
  • Kh. R. Skov
  • R. A. Karakhanov
Brief Communications

Abstract

Acetonylmalonaldehyde (1) was obtained for the first time by hydrolysis of 2,5-dimethoxy-5-methyltetrahydrofuran-3-carbaldehyde. The interaction of1 with 3-amino-5-methylpyrazole, 3-amino-1,2,4-triazole, 2-aminobenzimidazole, and 5-aminotetrazole results in the formation of functionally substituted azolopyrimidines.

Key words

tetrahydrofurans, hydrolysis acetonylmalonaldehyde, aminoazoles, reaction 

References

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Copyright information

© Plenum Publishing Corporation 1997

Authors and Affiliations

  • M. M. Vartanyan
    • 1
  • O. L. Eliseev
    • 1
  • Kh. R. Skov
    • 2
  • R. A. Karakhanov
    • 3
  1. 1.N. D. Zelinsky Institute of Organic ChemistryRussian Academy of SciencesMoscowRussian Federation
  2. 2.Hexagon CompanyCopenhagenDenmark
  3. 3.I. M. Gubkin State Academy of Oil and GasMoscowRussian Federation

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