反应 #640534

ord-0949f1abb4a34ca9835d5fb145ec27a9

反应方程式

COc1cc(C(=O)Cn2c(-c3nonc3N)nc3ccccc32)ccc1OCc1ccccc1
4-[1-(3-methoxy-4-benzyloxyphenacyl)-1H-benzimidazol-2-yl]-furazan-3-ylamine
COc1cc(C(=O)Cn2c(-c3nonc3N)nc3ccccc32)ccc1O
title compound
COc1cc(C(=O)Cn2c(-c3nonc3N)nc3ccccc32)ccc1O
4-[1-(3-Methoxy-4-hydroxyphenacyl)-1H-benzimidazol-2-yl]-furazan-3-yl-amine

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    过滤The catalyst is filtered
  2. 2
    其他the filtrate is evaporated to dryness

实验过程

To a solution of 4-[1-(3-methoxy-4-benzyloxyphenacyl)-1H-benzimidazol-2-yl]-furazan-3-ylamine (1.00 g) in THF (20 ml) is added palladium on carbon (10%, 0.2 g). The mixture is stirred under a hydrogen atmosphere for 1 hour. The catalyst is filtered and the filtrate is evaporated to dryness to give the title compound in pure form, m.p. 265° C. (This compound is also listed as Example 74 in Table 1.)

来源

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