Abstract
The alkylation of 2-chloro-5(6)-nitrobenzimidazole with 2-chloromethylthiirane was studied for the first time. Depending on the conditions, isomeric mixtures of nitro-substituted 2-chloro-1-(thietan-3-yl)benzimidazoles and dihydrothiazolo[3,2-a]benzimidazoles were obtained.
Similar content being viewed by others
REFERENCES
Spasov, A.A., Iezhitsa, I.N., Bugaeva, L.I. and Anisimova, V.A., Khim.-Farm. Zh., 1999, no. 5, pp. 6-18.
Kataev, V.A., Sadykov, R.F., Khaliullin, F.A., Sibiryak, S.V., Alekhin, E.K., and Volkova, S.S., Khim.-Farm. Zh., 1996, no. 7, pp. 22-24.
Fokin, A.V. and Kolomiets, A.F., Khimiya tiiranov (Chemistry of Thiiranes), Moscow: Nauka, 1978.
Khaliullin, F.A., Kataev, V.A., and Strokin, Yu.V., Khim. Geterotsikl. Soedin., 1991, no. 4, pp. 516-518.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Kataev, V.A., Spirikhin, L.V., Khaliullin, A.N. et al. Reaction of 2-Chloro-5(6)-nitrobenzimidazole with Cloromethylthiirane and Isomeric Composition of the Products. Russian Journal of Organic Chemistry 38, 1507–1509 (2002). https://doi.org/10.1023/A:1022516824376
Issue Date:
DOI: https://doi.org/10.1023/A:1022516824376