Research in the imidazole series. 96. Reaction of 1-methyl-4-nitro-5-chlorimidazole with phenols, naphthols, and 8-hydroxyquinoline

Authors

  • Л. А. Рeзниченко Novokuznetsk Scientific-Research Chemical-Pharmaceutical Institute, Novokuznetsk 654034
  • P. Н. Гирева Novokuznetsk Scientific-Research Chemical-Pharmaceutical Institute, Novokuznetsk 654034
  • П. М. Кочергин Center for Medicinal Chemistry, All-Russian Scientific-Research Chemical-Pharmaceutical Institute, Moscow 119815
  • E. B. Александрова Center for Medicinal Chemistry, All-Russian Scientific-Research Chemical-Pharmaceutical Institute, Moscow 119815

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.

How to Cite
Reznichenko, L. A.; Gireva, R. N.; Kochergin, P. M.; Aleksandrova, E. V. Chem. Heterocycl. Compd. 1998, 34, 294. [Khim. Geterotsikl. Soedin. 1998, 34, 327.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF02290719

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Published

1998-03-25

Issue

No. 3 (1998)

Section

Original Papers