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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 37276Generated: October 25, 2026

Dimethylformamide → 4-Methanesulfonyloxy-1-(4-nitrobenzyloxycarbonyl)pyrrolidine

https://huagongshe.com/reaction/37276

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantAzane;hydrateHCID 12896473—
Reactant(2S,4R)-2-(4-carboxythiazol-2-yl)-4-methanesulfonyloxy-1-(4-nitrobenzyloxycarbonyl) pyrrolidineHCID 18638791—
SolventTetrahydrofuranHCID 8028—
Product4-Methanesulfonyloxy-1-(4-nitrobenzyloxycarbonyl)pyrrolidineHCID 22242888124.5%

Reaction Steps

To a mixture of dimethylformamide (0.45 ml) and tetrahydrofuran (10 ml) was dropwise added phosphorus oxychloride (0.46 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-(4-carboxythiazol-2-yl) -4-methanesulfonyloxy-1-(4-nitrobenzyloxycarbonyl) pyrrolidine (1.54 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 (15 ml) at 0°-10° C. with stirring. The mixture was stirred at the same condition for 2 hours. Tetrahydrofuran was removed under reduced pressure to give a residue, which was extracted with ethyl acetate. The organic layer was dried over magnesium sulfate and concentrated under reduced pressure to give (2S, 4R)-2-(4-carbamoylthiazol)-2-yl) -4-methanesulfonyloxy-1-(4-nitrobenzyloxycarbonyl)pyrrolidine (1.4 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05420122
Source datasetuspto-grants-1995_05
ORD IDord-e47ef4e0559c40acb2ec7e2e9b0dc4e6
Source noteuspto-grants-1995_05