Reacción #84051

ord-6992c5cb27204b3e83ffb979c478ad2b

Ecuación de reacción

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

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    FiltraciónThe resin is filtered off with suction
  2. 2
    Lavadowashed twice each with 20 ml each of DMF, THF and DCM
  3. 3
    Otrodried under high vacuum

Procedimiento

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.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US09433614B2uspto-grants-2016_09