Chemistry of Heterocyclic Compounds

, Volume 30, Issue 8, pp 972–975 | Cite as

Synthesis and properties ofsym-triazene derivatives 13. Synthesis of 6-substituted 2,4-dialkyl(aryl)thio-sym-triazenes from imino esters of carboxylic acids

  • V. I. Kelarev
  • V. N. Koshelev
  • N. V. Belov
  • O. V. Malova
  • R. A. Karakhanov
Article
  • 30 Downloads

Abstract

6-Substituted 2,4-dialkyl(aryl)thio-sym-triazenes are synthesized by condensation of imino esters of carboxylic acids with thiocyanates.

Keywords

Ester Organic Chemistry Carboxylic Acid Thiocyanate Imino 
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References

  1. 1.
    V. I. Kelarev, V. N. Koshelev, N. V. Belov, O. V. Malova, and R. A. Karakhanov, Khim. Geterotsikl. Soedin., No. 2, 240 (1994).Google Scholar
  2. 2.
    V. I. Kelarev, Dibi Ammar, A. F. Lunin, R. D. Ushakova, A. I. Mikaya, N. V. Petrova, and S. G. Shvekhgeimer, Zh. Org. Khim.,19, 2401 (1983).Google Scholar
  3. 3.
    V. I. Kelarev, F. Yakh'ya Laauad, R. A. Karakhanov, A. F. Lunin, and O. V. Malova, Khim. Geterotsikl. Soedin., No. 1, 107 (1986).Google Scholar
  4. 4.
    V. I. Kelarev, R. A. Karakhanov, M. Bellul', R. L. Ushakova, and A. I. Mikaya, Khim. Geterotsikl. Soedin., No. 5, 674 (1988).Google Scholar
  5. 5.
    V. I. Kelarev, R. A. Karakhanov, A. S. Kokosova, and G. D. Gankin, Khim. Geterotsikl. Soedin., No. 9, 1250 (1992).Google Scholar
  6. 6.
    R. A. Karakhanov, V. I. Kelarev, A. S. Kokosova, V. A. Malyshev, and V. I. Zav'yalov, Zh. Org. Khim.,28, No. 8, 1750 (1992).Google Scholar
  7. 7.
    H. Eilingsfeld and H. Scheherman, Ber. Deut. Chem. Gesell.,100, 1874 (1967).Google Scholar
  8. 8.
    British Pat. 887753; Chem. Abstr.,58, 11502 (1963).Google Scholar
  9. 9.
    C. Grundmann, H. Ulrich, and A. Kreutzberger, Ber. Deut. Chem. Gesell.,86, 181 (1953).Google Scholar
  10. 10.
    A. S. Éstrin, E. G. Sochilin, M. I. Dolgopol'skii, L. A. Baranova, and A. D. Rusenko, Zh. Obshch. Khim.,37; 2247 (1967).Google Scholar
  11. 11.
    A. I. Finkel'shtein and E. N. Boitsov, Usp. Khim.,31, 1496 (1962).Google Scholar
  12. 12.
    A. R. Katritzky (ed.) Physical Methods in the Chemistry of Heterocyclic Compounds [Russian translation], Mir, Moscow-Leningrad (1966), 594.Google Scholar
  13. 13.
    V. V. Ershov, G. A. Nikiforov, and A. A. Volod'kin, Sterically Hindered Phenols, Khimiya, Moscow (1972), p. 38.Google Scholar
  14. 14.
    T. N. Pliev, Dokl. Akad. Nauk SSSR,176, 113 (1967).Google Scholar
  15. 15.
    R. Haque and S. Lilley, Appl. Spectrosc.,26, 309 (1972).Google Scholar
  16. 16.
    T. N. Pliev, Zh. Priklad. Spektrosk.13, 124 (1970).Google Scholar
  17. 17.
    V. I. Kelarev and S. G. Shvekhgeimer, Khim. Geterotsikl. Soedin., No. 4, 645 (l980).Google Scholar
  18. 18.
    H. Watanabe, Y. Kikugawa, and S. Yamada, Chem. Pharm. Bull.,21, 465 (1973).Google Scholar
  19. 19.
    A. Banashek and M. N. Shchukina, Zh. Obshch. Khim.,30, 3328 (1960).Google Scholar
  20. 20.
    V. A. Vinokurov, V. I. Kelarev, G. R. Aliev, V. N. Koshelev, E. M. Lisitsyn, and R. A. Karakhanov, Azerb. Khim. Zh., No. 4, 116 (1987).Google Scholar

Copyright information

© Plenum Publishing Corporation 1995

Authors and Affiliations

  • V. I. Kelarev
    • 1
  • V. N. Koshelev
    • 1
  • N. V. Belov
    • 1
  • O. V. Malova
    • 1
  • R. A. Karakhanov
    • 1
  1. 1.Gubkin State Petroleum and Gas AcademyMoscow

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