Реакция #84050

ord-b3b1aaa0e07f4281b55d14c723e1b6a1

Уравнение реакции

Oc1c(F)c(F)c(F)c(F)c1F
pentafluorophenol
ClCCCl
EDC
Cl.O=C(O)CC1CN2CCC1CC2
1-azabicyclo[2.2.2]oct-3-ylacetic acid hydrochloride
Cl.O=C(CC1CN2CCC1CC2)Oc1c(F)c(F)c(F)c(F)c1F
Pentafluorophenyl (1-azabicyclo[2.2.2]oct-3-yl)acetate hydrochloride

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    КонцентрированиеThe contents of the flask are concentrated in vacuo
  2. 2
    Другоеdried under high vacuum
  3. 3
    ДругоеThe resulting crude product is employed without further purification in the following stages

Методика

358 mg (1.94 mmol) of pentafluorophenol, 120.5 mg (0.63 mmol) of EDC and 1 drop of N,N-diisopropylethylamine are added to a solution of 100 mg (0.49 mmol) of 1-azabicyclo[2.2.2]oct-3-ylacetic acid hydrochloride in 4 ml of dichloromethane at 0° C. The mixture is stirred at room temperature for 18 h. The contents of the flask are concentrated in vacuo and dried under high vacuum. The resulting crude product is employed without further purification in the following stages.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US09433614B2uspto-grants-2016_09