Reacción #217684

Ecuación de reacción

trimethylphosphine tetrahydrofuran

(1R,2S,3R,5R,6R)-2-azido-3-(3,4-dichlorobenzylsulfanyl)-6-fluoro-bicyclo[3.1.0]hexane-2,6-dicarboxylic acid diethyl ester

sodium hydrogen carbonate

→

(1R,2S,3R,5R,6R)-2-amino-3-(3,4-dichlorobenzylsulfanyl)-6-fluoro-bicyclo[3.1.0]hexane-2,6-dicarboxylic acid diethyl ester

Rendimiento 87.8%

Disolventes

tetrahydrofuran

water

diethyl ether

Condiciones de reacción

Tratamiento posterior

1. 1
   OtroAfter separation
2. 2
   Lavadothe organic layers were washed with a saturated aqueous solution of sodium chloride
3. 3
   Secadodried over anhydrous sodium sulfate
4. 4
   FiltraciónThe desiccant was filtered off
5. 5
   Concentraciónthe filtrate was concentrated under reduced pressure
6. 6
   workup.ADDITIONThe residue was diluted with chloroform
7. 7
   workup.ADDITIONsilica gel (Wako gel C200 (made by Wako Pharmaceutical Industries Ltd.)) was added
8. 8
   ConcentraciónThe mixture was concentrated under reduced pressure
9. 9
   workup.WAITleft
10. 10
    workup.WAITto stand for 18 hours at room temperature
11. 11
    Otropurified by column chromatography (silica gel: Wako gel C200 (made by Wako Pure Chemical Industries Ltd.), eluent: hexane-ethyl acetate=2:1)

Procedimiento

7.7 mL of a solution of 1M trimethylphosphine/tetrahydrofuran was added to 3.35 g of (1R,2S,3R,5R,6R)-2-azido-3-(3,4-dichlorobenzylsulfanyl)-6-fluoro-bicyclo[3.1.0]hexane-2,6-dicarboxylic acid diethyl ester dissolved in 100 mL of tetrahydrofuran and 10 mL of water, and the mixture was stirred for 1 hour at room temperature. The mixture was diluted with 200 mL of diethyl ether, and after 50 mL of a saturated aqueous solution of sodium hydrogen carbonate was added thereto, the mixture was stirred for 1.5 hours at room temperature. After separation, the organic layers were washed with a saturated aqueous solution of sodium chloride and then dried over anhydrous sodium sulfate. The desiccant was filtered off, and the filtrate was concentrated under reduced pressure. The residue was diluted with chloroform, and then silica gel (Wako gel C200 (made by Wako Pharmaceutical Industries Ltd.)) was added thereto. The mixture was concentrated under reduced pressure, left to stand for 18 hours at room temperature, and then purified by column chromatography (silica gel: Wako gel C200 (made by Wako Pure Chemical Industries Ltd.), eluent: hexane-ethyl acetate=2:1), thereby yielding 2.78 g of (1R,2S,3R,5R,6R)-2-amino-3-(3,4-dichlorobenzylsulfanyl)-6-fluoro-bicyclo[3.1.0]hexane-2,6-dicarboxylic acid diethyl ester.

Fuente