反应 #640591

ord-59f9ba7eac6147c1bcf39b005c2b4c53

反应方程式

NCCN
ethylenediamine
O=C(Cl)c1cc(F)c(F)cc1F
2,4,5-trifluorobenzoylchloride
CC#N
acetonitrile
N=C1N(Cc2cc(F)c(F)cc2F)CCN1Cc1cc(F)c(F)cc1F
title compound
N=C1N(Cc2cc(F)c(F)cc2F)CCN1Cc1cc(F)c(F)cc1F
1,3-Bis-(2,4,5-trifluorobenzyl)imidazolidin-2-ylideneamine

反应条件

详细条件
See reaction.notes.procedure_details.

实验过程

The title compound was prepared in three steps as described in Procedure D. In the first step, ethylenediamine was reacted in acetonitrile with 2,4,5-trifluorobenzoylchloride (2 eq) in the presence of TEA to give the N,N′-dibenzoylated ethylenediamine upon aqueous work-up. After the last step (reaction with cyanogen bromide, performed at 200° C. for 60 min using MW heating), the precipitated solid was filtered off and recrystallized to give the title compound as the hydrogen bromide salt. MS (ES+) m/z 374 ([M+1]+, 100); HR-MS: 374.1086 ([M+1]+, C17H14F6N3; calc. 374.10919).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08048877B2uspto-grants-2011_11