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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607327Generated: October 30, 2026

Isophthaloyl chloride → HCID 178476350, compound

https://huagongshe.com/reaction/1607327

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsophthaloyl chlorideHCID 7451—
ReactantTriethylamineHCID 8471—
Reactant5'-O-acetyl-3'-O-benzyl-2'-deoxy-5-fluorouridineHCID 13687484—
Reactant4-Hydroxy-2(1H)-pyridinoneHCID 54696004—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 178476350HCID 17847635030.1%

Reaction Steps

To a solution of 3.00 g of 5'-O-acetyl-3'-O-benzyl-2'-deoxy-5-fluorouridine in 100 ml of dry dioxane were added 2.40 g of isophthaloyl chloride and 8.5 ml of triethylamine, and the mixture was refluxed for 2 hours. Then, to the reaction mixture were added a suspension of 1.77 g of 4-hydroxy-2(1H)-pyridone and 9.60 ml of triethylamine in 100 ml of dry dioxane, and the mixture was refluxed for 2 hours. The insolubles were removed by filtration and the filtrate was concentrated. The residue was dissolved in 100 ml of ethyl acetate, and the solution was washed twice with 30 ml of saturated aqueous solution of sodium chloride. The ethyl acetate layer was dried on anhydrous sodium sulfate and concentrated. The residue was placed on a silica gel column to conduct a gradient elution using chloroform and mixtures of methanol (up to 2%) and chloroform. The fractions corresponding to the title compound were collected and concentrated to dryness, giving 1.48 g of the title compound as a powder in a yield of 30%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04864021
Source datasetuspto-grants-1989_09
ORD IDord-e004b8f04a3c423e8528fb798b090b76
Source noteuspto-grants-1989_09