Reacción #8249

ord-d9bb5586c23743ebb695b08c565f0db1

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturacooled to −5°
  2. 2
    Otrothe organic layer separated
  3. 3
    Extracciónthe aqueous layer re-extracted with dichloromethane (2×300 ml)
  4. 4
    Secadodried (magnesium sulfate)
  5. 5
    FiltraciónAfter filtration and evaporation
  6. 6
    Otrothe residue was recrystallised from toluene (400 ml)

Procedimiento

5-Amino-2-(2-methylimidazol-1-yl)fluorobenzene (34.25 g, 0.179 M) was dissolved in dry dichloromethane (600 ml) under nitrogen, and cooled to −5°. Pyridine (17.7 g, 0.224 M) was added, followed by benzyl chloroformate (33.7 g, 0.197 M) over 20 minutes. The mixture was stirred and the temperature allowed to rise to ambient over 16 hours. Aqueous sodium bicarbonate (5%, 250 ml) was added, the organic layer separated, the aqueous layer re-extracted with dichloromethane (2×300 ml), and combined extracts dried (magnesium sulfate). After filtration and evaporation, the residue was recrystallised from toluene (400 ml) to give title product (54.5 g).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07087629B2uspto-grants-2006_08