Reaktion #1760747

ord-51665185760c4980a144e588644e73c2

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Temperaturthe resulting mixture was heated
  2. 2
    Temperaturto reflux for 2 hours
  3. 3
    Temperaturthe resulting mixture was heated
  4. 4
    Temperaturto reflux for 6 hours
  5. 5
    TemperaturAfter the reaction mixture was cooled to room temperature
  6. 6
    SonstigeThe organic layer was separated
  7. 7
    Trocknendried over anhydrous magnesium sulfate
  8. 8
    Waschenafter washed with a saturated sodium chloride aqueous solution
  9. 9
    Sonstigethe solvent was evaporated under reduced pressure
  10. 10
    SonstigeThe obtained residue was purified with silica gel column chromatography [PSQ100B (spherical) manufactured by Fuji Silysia Chemical Ltd., eluent; hexane:ethyl acetate=10:1]

Vorschrift

86 mg of 4-phenylpiperidine, 0.22 g of cesium carbonate, 2.4 mg of tris(dibenzylideneacetone)dipalladium(0), 1.2 mg of palladium acetate and 6.3 mg of 2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl were added to 3.0 mL of toluene solution containing 0.10 g of tert-butyl 2-(benzamido)-4-bromobenzoate, and the resulting mixture was heated to reflux for 2 hours. After the reaction mixture was cooled to room temperature, 2.4 mg of tris(dibenzylideneacetone)dipalladium(0), 1.2 mg of palladium acetate and 6.3 mg of 2-dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl were added and the resulting mixture was heated to reflux for 6 hours. After the reaction mixture was cooled to room temperature, ethyl acetate and 10% citric acid aqueous solution were added. The organic layer was separated and dried over anhydrous magnesium sulfate after washed with a saturated sodium chloride aqueous solution, and the solvent was evaporated under reduced pressure. The obtained residue was purified with silica gel column chromatography [PSQ100B (spherical) manufactured by Fuji Silysia Chemical Ltd., eluent; hexane:ethyl acetate=10:1] to obtain tert-butyl 2-(benzamido)-4-(4-phenylpiperidin-1-yl)benzoate as pale yellow solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07999132B2uspto-grants-2011_08