Reacción #162415
ord-a7af190c10b84e4a9ea49a32115a1280
Ecuación de reacción
Reactivos
Condiciones de reacción
Tratamiento posterior
- 1workup.ADDITIONUpon completion of the addition
- 2workup.WAITat −20° C. for 1.5 h
- 3Temperaturawas maintained below at −15° C.
- 4workup.STIRRINGto stir at room temperature overnight
- 5TemperaturaThe solution was cooled to 0° C.
- 6Otrowas quenched by the addition of 1 M HCl
- 7workup.ADDITIONSolid Na2CO3 was then added
- 8ExtracciónThe solution was extracted with ethyl acetate three times
- 9Lavadothe combined organic solutions were washed with water (3×) and brine
- 10OtroThe organic layer was dried
- 11Filtraciónfiltered
- 12Otrovolatiles evaporated
- 13OtroThe residue was purified by silica gel chromatography (50% ethyl acetate/hexanes)
Procedimiento
A solution of tert-butyl pyridin-3-ylcarbamate (17.7 g, 91.1 mmol) in THF (300 mL) was cooled to −78° C. and treated with 1.70 M tert-butyllithium in pentane (129 mL). Upon completion of the addition, the reaction was stirred at −78° C. for an additional 15 min and then at −20° C. for 1.5 h. 1-piperidinecarboxaldehyde (30.4 mL, 0.273 mol) was added while the temperature was maintained below at −15° C., and then the mixture was allowed to stir at room temperature overnight. The solution was cooled to 0° C. and was quenched by the addition of 1 M HCl to bring the pH to 2. Solid Na2CO3 was then added to adjust the pH to 7. The solution was extracted with ethyl acetate three times, and the combined organic solutions were washed with water (3×) and brine. The organic layer was dried, filtered, and volatiles evaporated. The residue was purified by silica gel chromatography (50% ethyl acetate/hexanes) to give the desired product as a yellow solid (12.2 g, 60%). LCMS for C11H15N2O3(M+H)+: m/z=223.1.