N-arylation of 1-aminobenzimidazole

Authors

  • А. Ф. Пожарский Rostov State University, Rostov-on-Don 344090
  • O. В. Дябло Rostov State University, Rostov-on-Don 344090
  • В. В. Кузьменко Rostov State University, Rostov-on-Don 344090
  • E. А. Евграфова Rostov State University, Rostov-on-Don 344090

Abstract

By treatment of the sodium (potassium) salt of 1-formylaminobenzimidazole in acetone or DMF with picryl chloride. 2,4-dinitrochlorobenzene, 2- and 4-nitrochlorobenzenes, we obtained the corresponding 1-aryl-aminobenzimidazoles. This is the first case of direct arylation of the amino group in N-aminobenzimidazole.

How to Cite
Pozharskii, A. F.; Dyablo, O. V.; Kuz'menko, V. V.; Evgrafova, E. A. Chem. Heterocycl. Compd. 1996, 32, 1156. [Khim. Geterotsikl. Soedin. 1996, 1347.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF01169226

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Published

1996-10-25

Issue

No. 10 (1996)

Section

Original Papers