Reacción #45592
ord-b341d755573047dcac0d67357cf083fb
Ecuación de reacción
Reactantes
Reactivos
Disolventes
Condiciones de reacción
Tratamiento posterior
- 1TemperaturaAfter cooling to room temperature
- 2Extracciónfollowed by extraction three times with ethyl acetate
- 3Lavadothe organic layer was washed with saturated brine
- 4Secadodried over anhydrous magnesium sulfate
- 5FiltraciónAfter filtration and concentration under reduced pressure
- 6Concentraciónthe eluate with chloroform:methanol (50:1) was concentrated under reduced pressure
- 7workup.DISSOLUTIONthe residue was dissolved in ethyl acetate
- 8Lavadowashed twice with saturated brine
- 9Secadodried over anhydrous magnesium sulfate
- 10FiltraciónAfter filtration and concentration tinder reduced pressure
Procedimiento
(3S)-3-(Dimethylamino)pyrrolidine (76 μl, 0.60 mmol) was added to a dimethyl sulfoxide (4 ml) solution of 7-fluoro-2-(methoxymethyl)-5-methyl-6-phenyl-1,3-benzoxazole-4-carbonitrile (I-59) (58 mg, 0.20 mmol), followed by stirring at 90° C. for 1 hour. After cooling to room temperature, the above brown oily substance and saturated sodium bicarbonate water were added, followed by extraction three times with ethyl acetate, the organic layer was washed with saturated brine, then dried over anhydrous magnesium sulfate. After filtration and concentration under reduced pressure, the resulting residue was subjected to column chromatography, and the eluate with chloroform:methanol (50:1) was concentrated under reduced pressure, the residue was dissolved in ethyl acetate, washed twice with saturated brine, then dried over anhydrous magnesium sulfate. After filtration and concentration tinder reduced pressure, the entitled compound (39 mg, 17%) was obtained as a brown oily substance.