反应 #2200621

ord-b55bfc4ddda74493b8792d91965a3fbf

反应方程式

COc1ccc(-n2cnc(C)c2)c(C#N)c1
5-methoxy-2-(4-methyl-imidazol-1-yl)-benzonitrile
C=[N+](C)C.[I-]
Eschenmoser's salt
COc1ccc(-n2cnc(C)c2CN(C)C)c(C#N)c1
title compound
收率 83.0%
COc1ccc(-n2cnc(C)c2CN(C)C)c(C#N)c1
2-(5-Dimethylaminomethyl-4-methyl-imidazol-1-yl)-5-methoxy-benzonitrile
收率 83.0%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他Evaporation of the solvent, aqueous workup and chromatography

实验过程

In analogy to example 5b, 5-methoxy-2-(4-methyl-imidazol-1-yl)-benzonitrile was reacted with Eschenmoser's salt in DMF for 16 h at 70° C. Evaporation of the solvent, aqueous workup and chromatography afforded the title compound as an oil (yield: 83%). MS: m/e=271.4 [M+H]+.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07432256B2uspto-grants-2008_10