تفاعل #2200625

ord-4ce666697c28468b8aacdbdb1f96750a

معادلة التفاعل

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
المردود 35.0%
Cc1ncn(-c2ccc([N+](=O)[O-])cc2C#N)c1CN(C)C
2-(5-Dimethylaminomethyl-4-methyl-imidazol-1-yl)-5-nitro-benzonitrile
المردود 35.0%

الكواشف

لا شيء

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىEvaporation of the solvent, aqueous workup and chromatography

الإجراء التجريبي

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]+.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07432256B2uspto-grants-2008_10