Reacción #792174
ord-6e206051077f4a788d0f3e7729061cd6
Ecuación de reacción
Reactantes
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1OtroThe reaction mixture thinned to form a pale green, nearly clear solution
- 2Otroto form a pale yellow suspension
- 3Temperaturathe reaction mixture was heated
- 4Temperaturaat gentle reflux for 3.5 hours
- 5TemperaturaAfter cooling
- 6Otroa precipitate of white solid was removed by filtration
- 7workup.ADDITIONThe filtrate was diluted with water (400 mL)
- 8Extracciónextracted three times with ethyl ether (700 mL total)
- 9Otroprecipitation of an off-white solid (3.75 g), which
- 10Filtraciónwas collected by filtration
- 11ConcentraciónThe ether mother liquor was further concentrated
Procedimiento
To a suspension of ethyl 2-(3-chloro-2-pyridinyl)-5-oxo-3-pyrazolidinecarboxylate (i.e. product of Example 12, Step A) (27 g, 100 mmol) stirred in dry acetonitrile (200 mL) was added sulfuric acid (20 g, 200 mmol) in one portion. The reaction mixture thinned to form a pale green, nearly clear solution before thickening again to form a pale yellow suspension. Potassium persulfate (33 g, 120 mmol) was added in one portion, and then the reaction mixture was heated at gentle reflux for 3.5 hours. After cooling using an ice bath, a precipitate of white solid was removed by filtration and discarded. The filtrate was diluted with water (400 mL) and then extracted three times with ethyl ether (700 mL total). Concentration of the combined ether extracts to a reduced volume (75 mL) caused precipitation of an off-white solid (3.75 g), which was collected by filtration. The ether mother liquor was further concentrated to yield a second crop of an off-white precipitate (4.2 g), which was also collected by filtration. An off-white solid also precipitated from the aqueous phase; this solid (4.5 g) was collected by filtration to provide a combined total of 12.45 g of the title compound.