Abstract
When 2-amino-1-alkylbenzoimidazoles react with alkyl chloroacetates and β-chloroethyl benzoates, alkylation is at the N hetero-atom. The resultant salts on treatment with alkalies give 1, 3-substituted 2-iminobenzoimidazolines (2-imino-2, 3-dihydrobenzimidazoles).
This is a preview of subscription content, log in via an institution to check access.
Similar content being viewed by others
References
A. M. Simonov and A. F. Pozharskii, KhGS, 203, 1965.
N. D. Vitkevich and A. M. Simonov, ZhOKh, 30, 2868, 1960.
A. M. Simonov and Yu. M. Yutilov, ZhOKh, 32, 2670, 1962.
West German Patent 1069634, 1959; C. A., 55, 21147, 1961.
Yu. M. Yutilov, Transactions of the 4th Scientific Conference of Fellows of Rostov University, 110, 1962.
A. M. Simonov and N. D. Vitkevich, ZhOKh, 30, 590, 1960.
V. P. Denisenko and A. I. Lopushanskii, ZhOKh, 32, 734, 1962.
Author information
Authors and Affiliations
Additional information
For Part XVII, see [1].
Rights and permissions
About this article
Cite this article
Yutilov, Y.M., Anisimova, V.A. & Simonov, A.M. Research on benzoimidazole derivatives. Chem Heterocycl Compd 1, 278–280 (1966). https://doi.org/10.1007/BF00473611
Issue Date:
DOI: https://doi.org/10.1007/BF00473611