Reacción #5166

Ecuación de reacción

1-bromo-2-fluoroethane

sodium iodide

sodium bicarbonate

(2S, 4S)-2-carbamoyl-4-(4-methoxybenzylthio)pyrrolidine

sodium bicarbonate

→

(2S, 4S)-2-Carbamoyl-4-(4-methoxybenzylthio)-1-(2-fluoroethyl)pyrrolidine

Disolventes

dimethylformamide

Condiciones de reacción

Tratamiento posterior

1. 1
   Temperaturacooling
2. 2
   workup.WAITat 40° C. for 20 hours
3. 3
   Extracciónextracted with ethyl acetate
4. 4
   LavadoThe extract was washed with a saturated aqueous solution of sodium chloride
5. 5
   Secadodried over anhydrous magnesium sulfate
6. 6
   OtroThe solvent was then removed by distillation under reduced pressure
7. 7
   Otromelting of 122°-123° C.
8. 8
   Otrowere obtained as a powder from those fractions
9. 9
   Lavadoeluted with ethyl acetate

Procedimiento

0.4 ml of 1-bromo-2-fluoroethane, 3.83 g of sodium iodide and 0.38 g of sodium bicarbonate were added to a solution of 1.2 g of (2S, 4S)-2-carbamoyl-4-(4-methoxybenzylthio)pyrrolidine dissolved in 12 ml of dry dimethylformamide, whilst ice-cooling, and the mixture was stirred at room temperature for 20 minutes and then at 40° C. for 20 hours. At the end of this time, the reaction mixture was poured into a saturated aqueous solution of sodium bicarbonate and extracted with ethyl acetate. The extract was washed with a saturated 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 subjected to column chromatography through silica gel (Katayama Chemicals Industries Co., silica gel 60K070). 838 mg of the title compound, melting of 122°-123° C., were obtained as a powder from those fractions eluted with ethyl acetate.

Fuente