反応 #5171

ord-b3ce27b511c44d5bba8fee0419416c71

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    workup.WAITto stand overnight at room temperature
  2. 2
    抽出extracted with ethyl acetate
  3. 3
    洗浄The extract was washed with an aqueous solution of sodium chloride
  4. 4
    乾燥dried over anhydrous magnesium sulfate
  5. 5
    その他The solvent was then removed by distillation under reduced pressure
  6. 6
    その他the residue was purified by column chromatography through silica gel (
  7. 7
    洗浄eluted with a 10:1 by volume mixture of ethyl acetate and methanol),

実験手順

244 μl of methyl iodide and 300 mg of sodium bicarbonate were added, whilst ice-cooling, to a solution of 1.00 g of (2S, 4S)-4-(4-methoxybenzylthio)-2-methylcarbamoylpyrrolidine [prepared as described in step (4) above] dissolved in 6 ml of dry dimethylformamide. The mixture was then stirred at 0° to 5° C. for 1 hour and allowed to stand overnight at room temperature. At the end of this time, the reaction mixture was poured into an aqueous solution of sodium chloride and extracted with ethyl acetate. The extract was washed with an aqueous solution of sodium chloride and dried over anhydrous magnesium sulfate. The solvent was then removed by distillation under reduced pressure, and the residue was purified by column chromatography through silica gel (eluted with a 10:1 by volume mixture of ethyl acetate and methanol), to afford 222 mg of the title compound as colorless crystals, melting at 82°-84° C.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05242914uspto-grants-1993_09