反应 #640522

ord-bdc05eaa34b34a0ab1fd3859f5f40060

反应方程式

Nc1nonc1-c1nc2ccccc2[nH]1
4-(1H-benzimidazol-2-yl)-furazan-3-ylamine
O=C([O-])[O-].[K+].[K+]
potassium carbonate
ICOc1ccccc1
iodomethoxy benzene
Nc1nonc1-c1nc2ccccc2n1COc1ccccc1
title compound
Nc1nonc1-c1nc2ccccc2n1COc1ccccc1
4-(1-Phenoxymethyl-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Evaporation of the solvent under reduced pressure
  2. 2
    其他partitioning of the resulting residue between water and ethyl acetate
  3. 3
    干燥by drying of the organic solution over sodium sulphate and chromatography of the residue

实验过程

To a solution of 4-(1H-benzimidazol-2-yl)-furazan-3-ylamine (0.10 g, 0.497 mmol) is added potassium carbonate (0.172 g, 1.24 mmol) and iodomethoxy benzene (0.128 g, 0.546 mmol). The mixture is stirred over night. Evaporation of the solvent under reduced pressure and partitioning of the resulting residue between water and ethyl acetate followed by drying of the organic solution over sodium sulphate and chromatography of the residue gives the title compound as a colorless solid, m.p. 171-173° C.

来源

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