反应 #640516

ord-3183b4f3c424424c9aae9d495ef6789c

反应方程式

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

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他at room temperature
  2. 2
    洗涤the organic phase is washed repeatedly with brine
  3. 3
    其他Drying of the solvent
  4. 4
    过滤filtering
  5. 5
    其他evaporation of the solvent under reduced pressure

实验过程

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.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: USRE042890E1uspto-grants-2011_11