反应 #640589

ord-e83eb20cb7d14388bd92d7273355ee1f

反应方程式

N#CBr
cyanogen bromide
N[C@@H]1CCCC[C@H]1N
(±)-trans-1,2-cyclohexanediamine
O=Cc1ccc(F)c(F)c1
3,4-difluorobenzaldehyde
N=C1N(Cc2ccc(F)c(F)c2)[C@@H]2CCCC[C@H]2N1Cc1ccc(F)c(F)c1
title compound
N=C1N(Cc2ccc(F)c(F)c2)[C@@H]2CCCC[C@H]2N1Cc1ccc(F)c(F)c1
(±)-trans-1,3-Bis-(3,4-difluoro-benzyl)octahydro-benzoimidazol-2-ylideneamine

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他the reaction mixture was evaporated to dryness
  2. 2
    洗涤the crude product washed with ether
  3. 3
    其他recrystallized from MeOH

实验过程

The title compound was prepared from (±)-trans-1,2-cyclohexanediamine and 3,4-difluorobenzaldehyde by Procedure C. After reacting with cyanogen bromide, the reaction mixture was evaporated to dryness and the crude product washed with ether and recrystallized from MeOH to give the title compound as the hydrogen bromide salt (mp 238-240° C.). MS (ES+) m/z 392 ([M+1]+, 100).

来源

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