Reacción #58740

ord-bc54799095de4bcbb89492a23bc17671

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    workup.WAITAfter 18 h
  2. 2
    Extracciónthe reaction is extracted with ethyl acetate (100 mL)
  3. 3
    Lavadowashed with 1 N NaHCO3 (50 mL) and H2O(3×50 mL)
  4. 4
    OtroThe organic layer is dried
  5. 5
    Concentraciónconcentrated
  6. 6
    Otrochromatographed on SiO2

Procedimiento

To a suspension of NaH (1.5 mmol) in DMF is added 3-piperidin-1-yl-propan-1-ol (1.1 mmol). After 30 min, 2-bromo-5-piperidin-1-ylmethyl-pyridine (1 mmol) is added to the mixture. After 18 h, the reaction is extracted with ethyl acetate (100 mL) and washed with 1 N NaHCO3 (50 mL) and H2O(3×50 mL). The organic layer is dried, concentrated, and chromatographed on SiO2 to provide the title compound.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07423147B2uspto-grants-2008_09