反应 #2200625
ord-4ce666697c28468b8aacdbdb1f96750a
反应方程式
2-(4-methyl-imidazol-1-yl)-5-nitro-benzonitrile
Eschenmoser's salt
→
title compound
收率 35.0%
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]+.