Chemistry of Heterocyclic Compounds

, Volume 28, Issue 5, pp 559–566 | Cite as

Reaction of quinazoline derivatives with quaternary salts of heterocyclic bases

  • S. P. Gromov
  • M. A. Razinkin


The formation of carbocyanine and styryl dyes from quinazoline derivatives and quaternary salts of heterocyclic bases was detected. The intermediate compounds were separated and mechanisms of the reactions were proposed.


Organic Chemistry Intermediate Compound Quinazoline Styryl Quaternary Salt 
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Literature cited

  1. 1.
    S. P. Gromov, D. V. Yashunskii, R. S. Sagitullin, and Yu. G. Bundel', Dokl. Akad. Nauk, 292, 364 (1987).Google Scholar
  2. 2.
    A. Kreutzberger, Arch. Pharm., 299, 897 (1966).Google Scholar
  3. 3.
    D. J. Fry, J. D. Kendall, and A. J. Morgan, UK Patent No. 870,633.Google Scholar
  4. 4.
    M. J. Strauss, Chem. Rev., 70, 667 (1970).Google Scholar
  5. 5.
    H. C. van der Plas, Tetrahedron, 41, 237 (1985).Google Scholar
  6. 6.
    A. E. A. Porter, General Organic Chemistry [Russian translation], Vol. 8, Khimiya, Moscow (1985), p. 118.Google Scholar
  7. 7.
    A. N. Kost, S. P. Gromov, and R. S. Sagitullin, Tetrahedron, 37, 3423 (1981).Google Scholar
  8. 8.
    T. Higashino, Y. Nagano, and E. Hayashi, Chem. Pharm. Bull., 21, 1943 (1973).Google Scholar
  9. 9.
    G. Klopman, Reactivity and Reaction Paths, Wiley, New York (1974) [Russian translation, Mir, Moscow (1977), p. 83].Google Scholar
  10. 10.
    T. L. Pilicheva, O. N. Chupakhin, and I. Ya. Postovskii, Khim. Geterotsikl. Soedin., No. 4, 561 (1975).Google Scholar
  11. 11.
    S. P. Gromov, O. A. Fedorova, M. V. Alfimov, V. V. Tkachev, and L. O. Atovmyan, Dokl. Akad. Nauk, 319, 1141 (1991).Google Scholar
  12. 12.
    T. Higashino, A. Goto, A. Miyashita, and E. Hayashi, Chem. Pharm. Bull., 34, 4352 (1986).Google Scholar
  13. 13.
    K. Venkataraman, Chemistry of Synthetic Dyes, Vol. 2, Academic, New York (1952) [Russian translation, Goskhimizdat, Leningrad (1957), p. 1323].Google Scholar
  14. 14.
    S. P. Gromov, M. V. Fomina, E. N. Ushakov, I. K. Lednev, and M V. Alfimov, Dokl. Akad. Nauk, 314, 1135 (1990).Google Scholar
  15. 15.
    K. Adachi, Yakugaku Zasshi, 77, 507 (1957); Chem. Abstr., 14744i (1957).Google Scholar
  16. 16.
    D. J. Fry, J. D. Kendall, and A. J. Morgan, J. Chem. Soc., 5062 (1960).Google Scholar
  17. 17.
    O. N. Chupakhin, V. N. Charushin, L. M. Naumova, A. I. Rezvukhin, and N. A. Klyuev, Khim. Geterotsikl. Soedin., No. 11, 1549 (1981).Google Scholar
  18. 18.
    W. H. Mills, J. Chem. Soc., 121, 455 (1922).Google Scholar

Copyright information

© Plenum Publishing Corporation 1992

Authors and Affiliations

  • S. P. Gromov
    • 1
  • M. A. Razinkin
    • 1
  1. 1.N. N. Semenov Institute of Chemical PhysicsRussian Academy of SciencesMoscow

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