Reacción #624990

ord-e02538c3a50a4034a532478a866e6957

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.STIRRINGThe reaction was stirred overnight before it
  2. 2
    Concentraciónwas concentrated
  3. 3
    Otrodirectly purified by reverse-phase column chromatography
  4. 4
    Lavadoeluting with 0 to 40% acetonitrile/water

Procedimiento

To a DCM (1 mL) solution of (R)-5-(2-(5-fluoropyridin-3-yl)pyrrolidin-1-yl)pyrazolo[1,5-a]pyrimidin-3-amine (25 mg, 0.084 mmol) was added CDI (27 mg, 0.17 mmol) at ambient temperature in one portion. After stirring for two hours, (S)-pyrrolidin-3-ol (15 mg, 0.17 mmol) was added in one portion. The reaction was stirred overnight before it was concentrated and directly purified by reverse-phase column chromatography, eluting with 0 to 40% acetonitrile/water to yield the final product as a solid (27 mg, 78% yield). MS (apci) m/z=412.2 (M+H).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08865698B2uspto-grants-2014_10