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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2271262Generated: November 3, 2026

5-Fluorouracil → HCID 10675385, compound

https://huagongshe.com/reaction/2271262

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-FluorouracilHCID 3385—
ReactantTrimethylsilyl triflateHCID 65367—
ReactantSodium BicarbonateHCID 516892—
ReactantN,O-bis(trimethylsilyl)acetamideHCID 6913588—
ReactantHCID 12042250HCID 12042250—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 10675385HCID 10675385—

Reaction Steps

Compound 6 (2.00 g, 3.62 mmol) was dissolved in 1,2-dichloroethane (60.0 ml), and 5-fluorouracil (0.71 g, 5.46 mmol) and N,O-bis(trimethylsilyl)acetamide (5.37 ml, 21.7 mmol) were added to the solution, followed by refluxing for one hour. After the reaction mixture was allowed to cool to room temperature, trimethylsilyl trifluoromethanesulfonate (0.85 ml, 4.70 mmol) was added thereto, followed by stirring overnight at 50° C. A saturated aqueous solution of sodium hydrogencarbonate was added to the mixture, and after stirring, the organic layer was dried over anhydrous magnesium sulfate. The residue was purified by means of silica gel column chromatography (silica gel 300 ml, eluent; n-hexane:ethyl acetate=3:1), to thereby yield a colorless viscous compound (Compound 31; 0.80 g, 1.28 mmol, 35.4%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06333315B1
Source datasetuspto-grants-2001_12
ORD IDord-664c38a4a34240d4878784decea552ea
Source noteuspto-grants-2001_12