Reacción #1069133
ord-03883153fa7247be8260b1669ed3fb2e
Ecuación de reacción
Reactantes
Reactivos
Condiciones de reacción
Tratamiento posterior
- 1workup.STIRRINGAfter being stirred at the same temperature for 30 minutes
- 2workup.STIRRINGdropwise at -20° C. and the mixture was stirred at -20° C. to 10° C. for 2 hours
- 3Otroevaporated in vacuo
- 4workup.ADDITIONA saturated sodium bicarbonate solution was added to the residue
- 5Extracciónextracted twice with chloroform (50 ml)
- 6ExtracciónThe combined extract
- 7Lavadowas washed with saturated brine (50 ml)
- 8Secadodried over magnesium sulfate
- 9Otroevaporated in vacuo
- 10OtroThe residue was chromatographed on silica gel (40 g) with chloroform as an eluent
- 11workup.ADDITIONThe fractions containing the object compound
- 12Otroevaporated in vacuo
Procedimiento
Isobutyl chloroformate (1.04 g) was added dropwise to a mixture of 3-(2-phenylpyrazolo[1,5-a]pyridin-3-yl)acrylic acid (trans isomer) (2.0 g) and triethylamine (0.766 g) in methylene chloride (40 ml) and tetrahydrofuran (10 ml) at -20° C. with stirring. After being stirred at the same temperature for 30 minutes, a solution of 2-ethylpiperidine (0.942 g) in tetrahydrofuran (10 ml) was added thereto dropwise at -20° C. and the mixture was stirred at -20° C. to 10° C. for 2 hours. The mixture was warmed to room temperature and evaporated in vacuo. A saturated sodium bicarbonate solution was added to the residue and extracted twice with chloroform (50 ml). The combined extract was washed with saturated brine (50 ml), dried over magnesium sulfate and evaporated in vacuo. The residue was chromatographed on silica gel (40 g) with chloroform as an eluent. The fractions containing the object compound were combined and evaporated in vacuo to give 1-[3-(2-phenylpyrazolo[1,5-a]pyridin-3-yl)acryloyl]-2-ethylpiperidine (trans isomer) (1.30 g) as an oil.