Reacción #62281

ord-02594a7a820b48c7a022f86fea160b3e

Disolventes

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Extracciónextracted with ethyl acetate
  2. 2
    Lavadowashed with water
  3. 3
    Secadodried over magnesium sulfate
  4. 4
    OtroAfter evaporating
  5. 5
    Otrothe residue was purified
  6. 6
    Otroseparated by silica gel column chromatography (ethyl acetate:n-hexane=3:1)

Procedimiento

To 10 mL of a solution containing 360 mg of 3-naphthalen-2-yl-1-trityl-1H-pyrazolo[4,3-b]pyridine-5-carbonitrile obtained by Production example 15 in dichloromethane, 3 mL of trifluoroacetic acid was added at room temperature and stirred for 2 hours. The reaction solution was added with aqueous sodium hydrogen carbonate, extracted with ethyl acetate, washed with water, and dried over magnesium sulfate. After evaporating, the residue was purified and separated by silica gel column chromatography (ethyl acetate:n-hexane=3:1), to afford 180 mg of the title compound as a colorless powder.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07429609B2uspto-grants-2008_09