Reacción #2339836
ord-ab38fd919bbe41b688208f54298c7a37
Ecuación de reacción
Reactivos
Disolventes
Condiciones de reacción
Condiciones detalladas
See reaction.notes.procedure_details.
Tratamiento posterior
- 1OtroAfter removal of the catalyst
- 2Filtraciónby filtration
- 3Otrothe solution was evaporated in vacuo to a pale yellow HCl salt of the product
- 4OtroThe free base is obtained
- 5ExtracciónThe aqueous is then extracted with Et2O several times
- 6Secadothe extracts dried (MgSO4)
- 7Otroevaporated to an oil
Procedimiento
2-Phenylpyridine, Intermediate 14, (4.0 g, 25.81 mmol), and concentrated HCl (3 mL) in EtOH (15 mL) were treated with platinum oxide and subjected to catalytic hydrogenation (˜1 atm, balloon), at room temperature for 72 hours. After removal of the catalyst by filtration, the solution was evaporated in vacuo to a pale yellow HCl salt of the product. The free base is obtained by treating the residue with 10% aqueous sodium hydroxide. The aqueous is then extracted with Et2O several times and the extracts dried (MgSO4) and evaporated to an oil to give the title compound.