Reacción #62281
ord-02594a7a820b48c7a022f86fea160b3e
Ecuación de reacción
Reactantes
Reactivos
Ninguno
Disolventes
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1Extracciónextracted with ethyl acetate
- 2Lavadowashed with water
- 3Secadodried over magnesium sulfate
- 4OtroAfter evaporating
- 5Otrothe residue was purified
- 6Otroseparated 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.