Реакция #640516

ord-3183b4f3c424424c9aae9d495ef6789c

Уравнение реакции

O=C(CBr)c1ccccc1
Phenacylbromid
Nc1nonc1-c1nc2ccccc2[nH]1
4-(1H-benzimidazol-2-yl)-furazan-3-ylamine
O=C([O-])[O-].[K+].[K+]
potassium carbonate
Nc1nonc1-c1nc2ccccc2n1CC(=O)c1ccccc1
title compound
Nc1nonc1-c1nc2ccccc2n1CC(=O)c1ccccc1
4-(1-Phenacyl-1H-benzimidazol-2-yl)-furazan-3-ylamine

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеat room temperature
  2. 2
    Промывкаthe organic phase is washed repeatedly with brine
  3. 3
    ДругоеDrying of the solvent
  4. 4
    Фильтрацияfiltering
  5. 5
    Другоеevaporation of the solvent under reduced pressure

Методика

Phenacylbromid (0.1 g, 0.49 mmol) is added to an efficiently stirred suspension of 4-(1H-benzimidazol-2-yl)-furazan-3-ylamine (0.1 g, 0.4 mmol) [A. V. Sergievskii, O. A. Krasnoshek, S. F. Mel'nikova, I. V. Tselinskii, Russian Journal of Organic Chemistry, 2002, 38, 915-917] and potassium carbonate (0.172 g, 1.24 mmol) in dry DMF (5 ml) at room temperature. After 4 hours the reaction mixture is diluted with ethyl acetate and the organic phase is washed repeatedly with brine. Drying of the solvent, filtering and evaporation of the solvent under reduced pressure gives the title compound in crude form. The title compound is obtained in pure form by chromatography over silicagel, m.p. 202-204° C.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: USRE042890E1uspto-grants-2011_11