反应 #640533

ord-8b9f34435be842cf8a5fb4b6184f2648

反应方程式

COc1cc(C(=O)Cn2c(-c3nonc3N)nc3ccccc32)ccc1O
4-[1-(3-methoxy-4-hydroxyphenacyl)-1H-benzimidazol-2-yl]-furazan-3-ylamine
CCN(C(C)C)C(C)C
DIPEA
COCCl
methoxymethyl chloride
COCOc1ccc(C(=O)Cn2c(-c3nonc3N)nc3ccccc32)cc1OC
title compound
COCOc1ccc(C(=O)Cn2c(-c3nonc3N)nc3ccccc32)cc1OC
4-[1-(3-Methoxy-4-methoxymethoxy-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
    洗涤washed with water
  2. 2
    干燥dried over sodium sulphate
  3. 3
    过滤Filtration of the sodium sulphate and concentration of the filtrate under reduced pressure

实验过程

A mixture of 4-[1-(3-methoxy-4-hydroxyphenacyl)-1H-benzimidazol-2-yl]-furazan-3-ylamine (0.10 g, 0.27 mmol), DIPEA and methoxymethyl chloride in dry DMF is stirred at room temperature for 14 hours. The reaction mixture is diluted with ethyl acetate, washed with water and dried over sodium sulphate. Filtration of the sodium sulphate and concentration of the filtrate under reduced pressure gives the title compound as colorless, pure solid, m.p. 190° C.

来源

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