Reacción #57996

ord-14f61712884949cfaf2783c6c5b1ae07

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Otroto give
  2. 2
    Otroprecipitates which
  3. 3
    workup.ADDITIONwas broken up by the addition of water (20 ml)
  4. 4
    FiltraciónThe solid was filtered
  5. 5
    workup.DISSOLUTIONthe cake was dissolved in ethyl acetate
  6. 6
    OtroThe residual water was removed by pipette and hexane
  7. 7
    workup.ADDITIONwas added

Procedimiento

Methyl 4-(2-aminoethylsulfanyl)benzoate hydrochloride (0.248 g, 1.00 mmol), was combined with benzofuran-2-carboxylic acid (0.162 g, 1.00 mmol) and HBTU (0.379 g, 1.00 mmol) in DMF (5 ml) at room temperature. Triethylamine (0.307 ml, 2.2 mmol) was added and the reaction mixture was stirred at room temperature overnight. Saturated aqueous NaHCO3 (15 ml) was added to give precipitates which was broken up by the addition of water (20 ml). The solid was filtered and the cake was dissolved in ethyl acetate. The residual water was removed by pipette and hexane was added to give methyl 4-{2-[(benzofuran-2-yl-carbonyl)-amino]ethylsulfanyl}benzoate (0.138 g) as a gum which was used in the next step without further purification.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07420089B2uspto-grants-2008_09