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.
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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.
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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
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DOI: https://doi.org/10.1007/BF02290719