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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1597072Generated: October 30, 2026

5-Fluorouracil → HCID 10675385, compound

https://huagongshe.com/reaction/1597072

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 numberUS06291670B1
Source datasetuspto-grants-2001_09
ORD IDord-03f0102b7a0f47cc934b819f6a4f85c8
Source noteuspto-grants-2001_09