Реакция #84051

ord-6992c5cb27204b3e83ffb979c478ad2b

Уравнение реакции

O=C(O)c1c(F)c(F)c(O)c(F)c1F
polymeric support resin
O=C(O)c1c(F)c(F)c(O)c(F)c1F
4-Hydroxy-2,3,5,6-tetrafluorobenzoic acid
Cl.O=C(O)CC1CN2CCC1CC2
1-azabicyclo[2.2.2]oct-3-ylacetic acid hydrochloride
CC(C)N=C=NC(C)C
N,N′-diisopropylcarbodiimide
O=C(CC1CN2CCC1CC2)Oc1c(F)c(F)c(C(=O)O)c(F)c1F
polymer-bound title compound
O=C(CC1CN2CCC1CC2)Oc1c(F)c(F)c(C(=O)O)c(F)c1F
(2-(1-Azabicyclo[2.2.2]oct-3-yl)acetoxy}-2,3,5,6-tetrafluorobenzoic acid

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ФильтрацияThe resin is filtered off with suction
  2. 2
    Промывкаwashed twice each with 20 ml each of DMF, THF and DCM
  3. 3
    Другоеdried under high vacuum

Методика

2 g of the polymeric support resin from Example 8A (loading about 1.36 mmol/g, 2.72 mmol) are suspended in 20 ml of DMF and shaken with 1.23 g (5.98 mmol) of 1-azabicyclo[2.2.2]oct-3-ylacetic acid hydrochloride and 130 mg (1.09 mmol) of DMAP for 10 min. Then 1.06 ml (6.80 mmol) of N,N′-diisopropylcarbodiimide are added, and the mixture is shaken overnight. The resin is filtered off with suction, washed twice each with 20 ml each of DMF, THF and DCM and dried under high vacuum. 2.318 g of the polymer-bound title compound are obtained.

Источник

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