Reacción #56221

ord-b306f7b542d648819f0f1e38cfa67467

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Filtraciónfiltered
  2. 2
    Extracciónextracted with water
  3. 3
    ExtracciónThe aqueous phase is extracted with ether
  4. 4
    LavadoThe combined organic phases are washed with saturated aqueous NaHCO3, water and saturated aqueous NaCl
  5. 5
    Secadodried over CaSO4 and solvent
  6. 6
    Otroevaporated

Procedimiento

To a stirred solution of 3-benzylpyrrolyl methanol (1.8 mmol), 2-(5-fluoro-2-benzothienyl)-3-methylbutanoic acid (2.0 mmol) and 4-dimethylaminopyridine (2.0 mmol) in 20 ml of methylene chloride and 2 ml of DMF is added N,N'-dicyclohexylcarbodiimide (2.0 mml). The reaction mixture is stirred, under nitrogen, for about two hours and then filtered and extracted with water. The aqueous phase is extracted with ether. The combined organic phases are washed with saturated aqueous NaHCO3, water and saturated aqueous NaCl, dried over CaSO4 and solvent evaporated to yield 3-benzylpyrrolylmethyl 2-(5-fluoro-2-benzothienyl)-3-methylbutanoate.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US04224330uspto-grants-1980_09