Reacción #164227

ord-4ad19121a6ce4ccf88a864aaf064938e

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    OtroThe suspension is evaporated
  2. 2
    Otrothe white residue is first purified by flash chromatography (DCM/MeOH=9/1 to 8/2)

Procedimiento

(R)-Quinuclidin-3-yl 2-(4-fluorobenzylamino)-2-phenylacetate (C78) (85 mg, 0.23 mmol) is dissolved in ethyl acetate (2.31 mL) and 2-chloro-1-(thiophen-2-yl)ethanone (40.8 mg, 0.25 mmol) is added. The solution is stirred at RT overnight. The suspension is evaporated and the white residue is first purified by flash chromatography (DCM/MeOH=9/1 to 8/2) and then by trituration with Et2O to afford the title compound as an off-white powder (83 mg, 68% yield, chloride salt, mixture of diastereoisomers).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08835682B2uspto-grants-2014_09