반응 #5200

ord-bf4b72bd1c12477f9a2610f9db0493f3

반응 방정식

[Cl-].[Na+]
sodium chloride
CCI
ethyl iodide
O=C([O-])O.[Na+]
sodium bicarbonate
CNC(=O)[C@@H]1C[C@H](SCc2ccc(OC)cc2)CN1
(2S, 4S)-4-(4-methoxybenzylthio)-2-methylcarbamoylpyrrolidine
CCN1C[C@@H](SCc2ccc(OC)cc2)C[C@H]1C(=O)NC
title compound
CCN1C[C@@H](SCc2ccc(OC)cc2)C[C@H]1C(=O)NC
(2S, 4S)-1-Ethyl-4-(4-methoxybenzylthio)-2-methylcarbamoylpyrrolidine

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.WAITat room temperature for 5 hours
  2. 2
    추출extracted with ethyl acetate
  3. 3
    세척The extract was washed with an aqueous solution of sodium chloride
  4. 4
    건조dried over anhydrous magnesium sulfate
  5. 5
    기타after which the solvent was removed by distillation under reduced pressure
  6. 6
    기타The residue was purified by column chromatography (eluted with ethyl acetate)

실험 절차

0.71 ml of ethyl iodide and 742 mg of sodium bicarbonate were added to a solution of 2.25 g of (2S, 4S)-4-(4-methoxybenzylthio)-2-methylcarbamoylpyrrolidine dissolved in 20 ml of dry dimethylformamide, and the mixture was stirred at 0° to 5° C. for 1 hour and then at room temperature for 5 hours. 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, after which the solvent was removed by distillation under reduced pressure. The residue was purified by column chromatography (eluted with ethyl acetate), to afford 1.87 g of the title compound as colorless crystals, melting at 68°-70° C.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05242914uspto-grants-1993_09