반응 #640528

ord-3b63fa6ef70b423f86b073431b91d64e

반응 방정식

Nc1nonc1-c1nc2ccccc2[nH]1
4-(1H-benzimidazol-2-yl)-furazan-3-ylamine
O=C([O-])[O-].[K+].[K+]
potassium carbonate
O=C(C=Cc1ccccc1)CCl
1-chloro-4-phenyl-but-3-en-2-one
Nc1nonc1-c1nc2ccccc2n1CC(=O)/C=C/c1ccccc1
title compound
Nc1nonc1-c1nc2ccccc2n1CC(=O)/C=C/c1ccccc1
E-1-[2-(4-Aminofurazan-3-yl)-benzimidazol-1-yl]-4-phenyl-but-3-en-2-one

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    세척washed with water
  2. 2
    건조dried over sodium sulphate
  3. 3
    여과Filtration of the sodium sulphate, concentration of the filtrate under reduced pressure and chromatography of the residue on silicagel

실험 절차

A suspension of 4-(1H-benzimidazol-2-yl)-furazan-3-ylamine (0.275 g, 1.37 mmol), potassium carbonate (0.472 g, 3.42 mmol) and 1-chloro-4-phenyl-but-3-en-2-one (0.297 g, 1.64 mmol) in DMF (5 ml) is stirred at room temperature for 16 hours. The reaction mixture is diluted with ethyl acetate, washed with water and dried over sodium sulphate. Filtration of the sodium sulphate, concentration of the filtrate under reduced pressure and chromatography of the residue on silicagel using hexane-ethyl acetate as eluent gives the title compound as a yellowish solid, m.p. 176-180° C.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: USRE042890E1uspto-grants-2011_11