تفاعل #2200623

ord-32a187cb0a57488fa31135a7ac3801eb

معادلة التفاعل

Cc1cn(-c2ccc(C(F)(F)F)cc2C#N)cn1
5-trifluoromethyl-2-(4-methyl-imidazol-1-yl)-benzonitrile
C=[N+](C)C.[I-]
Eschenmoser's salt
Cc1ncn(-c2ccc(C(F)(F)F)cc2C#N)c1CN(C)C
title compound
المردود 53.0%
Cc1ncn(-c2ccc(C(F)(F)F)cc2C#N)c1CN(C)C
5-Trifluoromethyl-2-(5-dimethylaminomethyl-4-methyl-imidazol-1-yl)-benzonitrile
المردود 53.0%

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, 5-trifluoromethyl-2-(4-methyl-imidazol-1-yl)-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: 53%). MS: m/e=309.3 [M+H]+.

المصدر

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