反应 #2200625

ord-4ce666697c28468b8aacdbdb1f96750a

反应方程式

Cc1cn(-c2ccc([N+](=O)[O-])cc2C#N)cn1
2-(4-methyl-imidazol-1-yl)-5-nitro-benzonitrile
C=[N+](C)C.[I-]
Eschenmoser's salt
Cc1ncn(-c2ccc([N+](=O)[O-])cc2C#N)c1CN(C)C
title compound
收率 35.0%
Cc1ncn(-c2ccc([N+](=O)[O-])cc2C#N)c1CN(C)C
2-(5-Dimethylaminomethyl-4-methyl-imidazol-1-yl)-5-nitro-benzonitrile
收率 35.0%

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, 2-(4-methyl-imidazol-1-yl)-5-nitro-benzonitrile (+regioisomer) was reacted with Eschenmoser's salt in DMF for 16 h at 90° C. Evaporation of the solvent, aqueous workup and chromatography afforded the title compound as a yellow oil that was sufficiently pure to be used in the next step (yield: 35%). MS: m/e=286.1 [M+H]+.

来源

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