Réaction #5175

Équation de réaction

sodium bicarbonate

dioxane

hydrogen chloride

(2S, 4S)-1-(t-butoxycarbonyl)-2-(N,N-dimethylcarbamoyl)-4-(4-methoxybenzylthio)pyrrolidine

→

title compound

Rendement 56.7%

(2S, 4S)-2-(N,N-Dimethylcarbamoyl)-4-(4-methoxybenzylthio)pyrrolidine

Rendement 56.7%

Solvants

ethyl acetate

Conditions de réaction

Traitement

1. 1
   Extractionit was extracted with ethyl acetate
2. 2
   LavageThe extract was washed with an aqueous solution of sodium chloride
3. 3
   Séchagedried over anhydrous magnesium sulfate
4. 4
   AutreThe solvent was then removed by distillation under reduced pressure
5. 5
   Autrethe residue was purified by column chromatography through silica gel (
6. 6
   Lavageeluted with a 1:2 by volume mixture of ethyl acetate and methanol),

Mode opératoire

1 ml of a 4N dioxane solution of hydrogen chloride was added, whilst ice-cooling, to a solution of 385 mg of (2S, 4S)-1-(t-butoxycarbonyl)-2-(N,N-dimethylcarbamoyl)-4-(4-methoxybenzylthio)pyrrolidine [prepared as described in step (3) above] dissolved in 1 ml of ethyl acetate, and the mixture was stirred at room temperature for 1.5 hours. At the end of this time, the reaction mixture was poured into a saturated aqueous solution of sodium bicarbonate to make it weakly basic, and it was 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 1:2 by volume mixture of ethyl acetate and methanol), to afford 163 mg of the title compound as an oil.

Source