Dimethylformamide → (2S,4R)-2-(carbamylmethyloxymethyl)-4-hydroxy-1-(4-nitrobenzyloxycarbonyl)pyrrolidine

To a mixture of dimethylformamide (1.50 ml) and tetrahydrofuran (10 ml) was dropwise added phosphorus oxychloride (1.50 ml) at -5°~5° C. and the mixture was stirred at the same temperature for 30 minutes. To the mixture was added a solution of (2S,4R)-2-carboxymethyloxymethyl-4-hydroxy-1-(4-nitrobenzyloxycarbonyl)pyrrolidine (2.30 g) in tetrahydrofuran (20 ml) at -5°~5° C., followed by stirring at the same temperature for 30 minutes. The mixture was dropwise added to concentrated ammonia water (30 ml) at 0°-10° C. with stirring. The mixture was stirred at the same condition for 2 hours. Tetrahydrofuran was evaporated under reduced pressure to give a mixture. The mixture was extracted with ethyl acetate (50 ml×3). The ethyl acetate layer was dried over magnesium sulfate and concentrated under reduced pressure to give a syrup. The syrup was subjected to a column chromatography on silica gel (20 g) and eluted with a mixture of methanol and chloroform (3:97 V/V) to give (2S,4R)-2-(carbamoylmethyloxymethyl)-4-hydroxy-1-(4-nitrobenzyloxycarbonyl)pyrrolidine (1.43 g).

1. customat -5°~5° C.
2. stirringby stirring at the same temperature for 30 minutes
3. stirringwith stirring
4. stirringThe mixture was stirred at the same condition for 2 hours
5. customTetrahydrofuran was evaporated under reduced pressure
6. customto give a mixture
7. extractionThe mixture was extracted with ethyl acetate (50 ml×3)
8. dry with materialThe ethyl acetate layer was dried over magnesium sulfate
9. concentrationconcentrated under reduced pressure
10. customto give a syrup
11. washeluted with a mixture of methanol and chloroform (3:97 V/V)

ORD record

ord-8167c848f860439f99c75490a788a377

Source dataset

uspto-grants-1991_10

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US05061804