Abstract
The action of benzyl alcohol on 2-aminobenzimidazoles in the presence of alkali has given a high yield of a number of 2-benzylaminobenzimidazoles which have been converted subsequently into 2-dibenzylaminobenzimidazoles and 2-benzyliminobenzimidazolines.
Similar content being viewed by others
References
V. M. Mar'yanovskii, A. F. Pozharskii, and A. M. Simonov, KhGS [Chemistry of Heterocyclic Compounds], 6, 216, 1970.
A. F. Pozharskii, E. A. Zvezdina, and A. M. Simonov, Tetrah. Lett., 23, 2219, 1967.
Y. Sprinzak, J. Am. Chem. Soc., 78, 3207, 1956.
A. Hunger, J. Kebrle, A. Rossi, and K. Hoffmann, Helv. Chim. Acta, 44, 1273, 1961.
Y. F. Duffin and J. D. Kendall, J. Chem. Soc., 361, 1956.
Yu. N. Sheinker, A. M. Simonov, Yu. M. Yutilov, V. N. Sheinker, and E. I. Perel'shtein, ZhOrKh, 2, 917, 1966.
N. P. Bednyagina and I. Ya. Postovskii, ZhOKh, 5, 1431, 1960.
Dictionary of Organic Compounds 3, [Russian translation], IL, Moscow, 798, 1949.
Author information
Authors and Affiliations
Additional information
For part IV, see ¦1¦.
Rights and permissions
About this article
Cite this article
Zvezdina, É.A., Pozharskii, A.F. & Sokolov, V.I. Imidazole derivatives containing potentially labile groupings attached to an N-atom. Chem Heterocycl Compd 6, 389–391 (1970). https://doi.org/10.1007/BF00471250
Issue Date:
DOI: https://doi.org/10.1007/BF00471250