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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 477169Generated: October 29, 2026

Trifluridine → HCID 14722799, compound

https://huagongshe.com/reaction/477169

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluridineHCID 6256—
ReactantHCID 19792576HCID 19792576—
ReactantHCID 54403406HCID 54403406—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 14722799HCID 14722799—
ProductHCID 14722801HCID 14722801—

Reaction Conditions

Temperature60 °C

Reaction Steps

1.00 Gram of 2'-deoxy-5-trifluoromethyluridine was dissolved in 15 ml of 1,4-dioxane. Thereto were added 2.50 g of bis-(α,α-dimethylbenzyloxy)methane and 38 mg of toluenesulfonic acid anhydride. They were heated to 60° C. and stirred for 3.5 hours. The reaction mixture was subjected to evaporation. The residue was subjected to silica gel column chromatography wherein a developing solvent of chloroform-methanol (20:1) was first used for preliminary separation and then a developing solvent of benzene-acetone (10:1) was used, to obtain 0.40 g (yield: 29.2%) of hygroscopic and amorphous 2'-deoxy-5'-O-(α,α-dimethylbenzyl)-5-trifluoromethyluridine (compound 22) and 0.28 g (yield: 20.4%) of hygroscopic and amorphous 2'-deoxy-3'-O-(α,α-dimethylbenzyl)-5-trifluoromethyluridine (compound 23).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04886877
Source datasetuspto-grants-1989_12
ORD IDord-d55036830e7d4fad91b850966dfbf35f
Source noteuspto-grants-1989_12