تفاعل #45592

ord-b341d755573047dcac0d67357cf083fb

المذيبات

ظروف التفاعل

درجة الحرارة
90°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةAfter cooling to room temperature
  2. 2
    استخلاصfollowed by extraction three times with ethyl acetate
  3. 3
    غسيلthe organic layer was washed with saturated brine
  4. 4
    تجفيفdried over anhydrous magnesium sulfate
  5. 5
    ترشيحAfter filtration and concentration under reduced pressure
  6. 6
    تركيزthe eluate with chloroform:methanol (50:1) was concentrated under reduced pressure
  7. 7
    workup.DISSOLUTIONthe residue was dissolved in ethyl acetate
  8. 8
    غسيلwashed twice with saturated brine
  9. 9
    تجفيفdried over anhydrous magnesium sulfate
  10. 10
    ترشيحAfter filtration and concentration tinder reduced pressure

الإجراء التجريبي

(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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07737166B2uspto-grants-2010_06