Abstract
A number of 1-alkyl (1, 2-dialkyl)-4-nitro-5-alkyl (aryl, dialkyl) aminoimidazoles are synthesized by reacting 1-alkyl (1, 2-dialkyl)-4-nitro-5-chloroimidazoles with aliphatic, aromatic, and heterocyclic amines. Hydrogenation of 1-ethyl-2-methyl-4-nitro-5-(N-morpholino) imidazole in acetic anhydride gives 1-ethyl-2-methyl -4-diacetylamino-5-(n-morpholino) imidazole, characterized as its picrate.
This is a preview of subscription content, log in via an institution to check access.
Similar content being viewed by others
References
P. M. Kochergin, S. G. Verenikina, and K. S. Bushueva, KhGS [Chemistry of Heterocyclic Compounds], 765, 1965.
H. Schubert and D. Heydenhauss, J. Pr. Chem., 22, 304, 1963.
P. M. Kochergin, KhGS [Chemistry of Heterocyclic Compounds], 761, 1965.
P. M. Kochergin and L. S. Bushueva, ZhPKh, 35, 2745, 1962.
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Kochergin, P.M., Verenikina, S.G. Researches on imidazoles. Chem Heterocycl Compd 1, 522–524 (1965). https://doi.org/10.1007/BF00469933
Issue Date:
DOI: https://doi.org/10.1007/BF00469933