Reaktion #43731

ord-31a4ca9a7ba84f0c9334d5980e253fdb

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    FiltrationThe reaction mixture is filtered through kieselguhr
  2. 2
    Sonstigethe solvent is removed
  3. 3
    WaschenThe resulting solution is washed with 1N aqueous sodium hydroxide solution
  4. 4
    TrocknenThe organic phase is dried over sodium sulfate
  5. 5
    Sonstigethe solvent is then removed under reduced pressure
  6. 6
    workup.DISSOLUTIONThe resulting solid is dissolved in a little THF
  7. 7
    workup.ADDITIONan excess of 1N HCl in diethyl ether is added
  8. 8
    workup.DISTILLATIONThe THF is then distilled off

Vorschrift

129 mg (0.35 mmol) of rac-N-(1-azabicyclo[2.2.2]oct-3-yl)-5-nitro-1-benzothiophene-2-carboxamide hydrochloride are dissolved in a mixture of 5 ml of acetic acid and 3 ml of water. 114.7 mg (1.75 mmol) of zinc are added, and the mixture is stirred at RT for 5 h. The reaction mixture is filtered through kieselguhr, the solvent is removed and the residue is taken up in dichloromethane. The resulting solution is washed with 1N aqueous sodium hydroxide solution. The organic phase is dried over sodium sulfate and the solvent is then removed under reduced pressure. The resulting solid is dissolved in a little THF, and an excess of 1N HCl in diethyl ether is added. The THF is then distilled off. 103 mg (80% of theory) of the title compound are isolated.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07732477B2uspto-grants-2010_06