تفاعل #2472245

ord-ad5852ce168a4a75bf361f76635f421d

المذيبات

ظروف التفاعل

درجة الحرارة
0°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةto warm to ambient temperature
  2. 2
    workup.STIRRINGstirred for 96 h
  3. 3
    استخلاصthe mixture was extracted with ethyl acetate (3×30 mL)
  4. 4
    غسيلThe combined organic extracts were washed with brine (2×30 mL)
  5. 5
    تجفيفdried over anhydrous sodium sulfate
  6. 6
    ترشيحfiltered
  7. 7
    تركيزconcentrated in vacuo
  8. 8
    أخرىPurification of the residue by column chromatography
  9. 9
    غسيلeluted with a 0% to 35% gradient of ethyl acetate in hexanes

الإجراء التجريبي

To a solution of 2,2-difluoro-1,3-benzodioxol-5-ol (Jacobus et al., WO 2004/4048320) (1.15 g, 6.60 mmol) in anhydrous tetrahydrofuran at 0° C. was added isopropylmagnesium chloride (2 M solution in tetrahydrofuran, 3.3 mL, 6.6 mmol). The reaction mixture was stirred at 0° C. for 0.5 h and 1-{[5-(trifluoromethyl)furan-2-yl]methyl}-1H-indole-2,3-dione (1.95 g, 6.60 mmol) was added. The reaction mixture was allowed to warm to ambient temperature and stirred for 96 h. A saturated aqueous solution of ammonium chloride (30 mL) was added and the mixture was extracted with ethyl acetate (3×30 mL). The combined organic extracts were washed with brine (2×30 mL), dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. Purification of the residue by column chromatography eluted with a 0% to 35% gradient of ethyl acetate in hexanes afforded 3-(2,2-difluoro-6-hydroxy-1,3-benzodioxol-5-yl)-3-hydroxy-1-{[5-(trifluoromethyl)furan-2-yl]methyl}-1,3-dihydro-2H-indol-2-one (2.54 g, 73%) as a pale orange solid: MS (ES+) 451.3 (M−17).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08263606B2uspto-grants-2012_09