Réaction #5200

ord-bf4b72bd1c12477f9a2610f9db0493f3

Équation de réaction

[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

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Traitement

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

Mode opératoire

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.

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US05242914uspto-grants-1993_09