Reacción #45592

ord-b341d755573047dcac0d67357cf083fb

Condiciones de reacción

Temperatura
90°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    TemperaturaAfter cooling to room temperature
  2. 2
    Extracciónfollowed by extraction three times with ethyl acetate
  3. 3
    Lavadothe organic layer was washed with saturated brine
  4. 4
    Secadodried over anhydrous magnesium sulfate
  5. 5
    FiltraciónAfter filtration and concentration under reduced pressure
  6. 6
    Concentraciónthe eluate with chloroform:methanol (50:1) was concentrated under reduced pressure
  7. 7
    workup.DISSOLUTIONthe residue was dissolved in ethyl acetate
  8. 8
    Lavadowashed twice with saturated brine
  9. 9
    Secadodried over anhydrous magnesium sulfate
  10. 10
    FiltraciónAfter 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.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07737166B2uspto-grants-2010_06