Abstract
By reactions of 1-methyl-4-nitro-5-chlorimidazole with 4-nitrophenol, α- and β-naphthols, and 8-hydroxyquinoline, a number of 1-methyl-4-nitro-5-aryl(heteryl)oxyimidazoles have been obtained. With aminophenols, under analogous conditions, 1-methyl-4-nitro-5-hydroxyphenylaminoimidazoles have been obtained.
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 and V. A. Lifanov, Khim. Geterotsikl. Soedin., No. 4, 490 (1994).
A. Mroczkeiwicz, Acta Pol. Pharm.,41, 397 (1984); Chem. Abstr.,102, 166701 (1985).
S. S. Berg and V. Petrov, J. Chem. Soc., 784 (1952).
Drugs of the Future, Vol. 6 (1981), p. 538.
R. Nietzki, Chem. Ber.,28, 2973 (1896).
L. J. Bellamy, The Infra-Red Spectra of Complex Molecules, 2nd ed., Methuen, London (1958).
Additional information
For Communication 95, see [1].
Novokuznetsk Scientific-Research Chemical-Pharmaceutical Institute, Novokuznetsk 654034, Russia. Center for Medicinal Chemistry, All-Russian Scientific-Research Chemical-Pharmaceutical Institute, Moscow 119815. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 3, pp. 327–329, March, 1998.
Rights and permissions
About this article
Cite this article
Reznichenko, L.A., Gireva, R.N., Kochergin, P.M. et al. Research in the imidazole series. 96. Reaction of 1-methyl-4-nitro-5-chlorimidazole with phenols, naphthols, and 8-hydroxyquinoline. Chem Heterocycl Compd 34, 294–296 (1998). https://doi.org/10.1007/BF02290719
Received:
Issue Date:
DOI: https://doi.org/10.1007/BF02290719