Reacción #44237
ord-2a38b22f978247a88c8d9e78908eb208
Ecuación de reacción
Reactantes
Reactivos
Condiciones de reacción
Tratamiento posterior
- 1Temperaturaheated at 80° C. for 16 hours
- 2workup.STIRRINGwith stirring
- 3TemperaturaThe reaction mixture was cooled to room temperature
- 4FiltraciónThe precipitate was filtered off
- 5Lavadowashed with EtOAc
- 6LavadoThe filtrate was washed with water
- 7OtroThe organic layer was separated
- 8Extracciónthe aqueous layer was extracted with EtOAc
- 9SecadoThe combined organic layers were dried over MgSO4
- 10Filtraciónfiltered
- 11Concentraciónconcentrated
- 12Otroto give the crude material that
- 13Otrowas purified by silica gel flash column chromatography (100% CH2Cl2 to 1% MeOH in CH2Cl2)
Procedimiento
A mixture solution of methyl 4-chloro-1-methyl-6-oxo-1,6-dihydropyridazine-3-carboxylate (72 mg, 0.35 mmol), 2-fluoro-4-methylthioaniline (69 mg, 0.44 mmol), Pd(OAc)2 (10 mg, 0.044 mmol), BINAP (40 mg, 0.064 mmol), and Cs2CO3 (197 mg, 0.60 mmol) in toluene (1.5 mL) was sealed in a vial under N2 atmosphere. It was stirred for 10 minutes at room temperature and then heated at 80° C. for 16 hours with stirring. The reaction mixture was cooled to room temperature and diluted with EtOAc. The precipitate was filtered off and washed with EtOAc. The filtrate was washed with water. The organic layer was separated and the aqueous layer was extracted with EtOAc. The combined organic layers were dried over MgSO4, filtered, concentrated to give the crude material that was purified by silica gel flash column chromatography (100% CH2Cl2 to 1% MeOH in CH2Cl2) followed by additional silica gel flash column chromatography (10 to 15 to 20% EtOAc in CH2Cl2) to afford 48 mg (42%) of the desired product.