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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1088282Generated: November 2, 2026

4,6-Dimethyl-2-(4-nitrobenzyloxycarbonylthio)pyrimidine → (2R,4R)-1-p-nitrobenzyloxycarbonyl-2-(4-t-butoxycarbonylbutyl)-4-t-butyldimethylsilyloxypyrrolidine

https://huagongshe.com/reaction/1088282

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,6-Dimethyl-2-(4-nitrobenzyloxycarbonylthio)pyrimidineHCID 13504316—
Reactant(2R,4R)-2-(4-t-butoxycarbonylbutyl)-4-t-butyldimethylsilyloxypyrrolidineHCID 15671521—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Product(2R,4R)-1-p-nitrobenzyloxycarbonyl-2-(4-t-butoxycarbonylbutyl)-4-t-butyldimethylsilyloxypyrrolidineHCID 15671522—

Reaction Steps

S-p-Nitrobenzyloxycarbonyl-4,6-dimethyl-2-mercaptopyrimidine (719 mg) was added to 770 mg of (2R,4R)-2-(4-t-butoxycarbonylbutyl)-4-t-butyldimethylsilyloxypyrrolidine in 7 ml of tetrahydrofuran and stirred at room temperature for 2 hours. The reaction mixture was diluted with ethyl acetate, washed successively with brine, dilute hydrochloric acid and brine, dried over anhydrous sodium sulfate and distilled to remove the solvent. The residue was purified by silica gel chromatography to obtain (2R,4R)-1-p-nitrobenzyloxycarbonyl-2-(4-t-butoxycarbonylbutyl)-4-t-butyldimethylsilyloxypyrrolidine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04962103
Source datasetuspto-grants-1990_10
ORD IDord-7dde82a565624ae0977c5122641c87fc
Source noteuspto-grants-1990_10