Реакция #655446

Уравнение реакции

Potassium thioacetate

(3R,5S)-1-allyloxycarbonyl-5-[1-hydroxy-1-(imidazo[5,1-b]thiazol-3-yl)methyl]-3-methanesulfonyloxypyrrolidine

→

title compound

Выход 72.7%

(3S,5S)-3-Acetylthio-1-allyloxycarbonyl-5-[1-hydroxy-1-(imidazo[5,1-b]thiazol-3-yl)methyl]pyrrolidine

Выход 72.7%

Растворители

ethyl acetate

DMF

toluene

Условия реакции

Обработка

1. 1
   Промывкаwashed twice with semi-saturated saline
2. 2
   Сушкаthe organic layer is dried over magnesium sulfate
3. 3
   Фильтрацияfiltered
4. 4
   ДругоеThe solvent is removed by evaporation under reduced pressure
5. 5
   Другоеthe residue is dried under reduced pressure by means of a vacuum pump
6. 6
   ДругоеThe dark red oil is purified by flash column chromatography on silica gel (ethyl acetate)

Методика

Potassium thioacetate (134 mg) is added to a solution of 314 mg of (3R,5S)-1-allyloxycarbonyl-5-[1-hydroxy-1-(imidazo[5,1-b]thiazol-3-yl)methyl]-3-methanesulfonyloxypyrrolidine (stereoisomer A) in a mixture of 4 ml of dry DMF and 2 ml of dry toluene, and the mixture is stirred in an argon atmosphere at a bath temperature of 70° C. for 22 hr. The mixture is diluted with 60 ml of ethyl acetate and washed twice with semi-saturated saline, and the organic layer is dried over magnesium sulfate and filtered. The solvent is removed by evaporation under reduced pressure, and the residue is dried under reduced pressure by means of a vacuum pump. The dark red oil is purified by flash column chromatography on silica gel (ethyl acetate) to give 217 mg of the title compound as a slightly red amorphous material.

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