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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703550Generated: October 30, 2026

Isophthaloyl chloride → 5'-O-acetyl-3-[3-(4-benzoyloxy-5-chloro-2-pyridyloxycarbonyl)benzoyl]-3'-O-benzyl-2'-deoxy-5-fluorouridine

https://huagongshe.com/reaction/703550

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsophthaloyl chlorideHCID 7451—
ReactantTriethylamineHCID 8471—
Reactant5'-O-acetyl-3'-O-benzyl-2'-deoxy-5-fluorouridineHCID 13687484—
Reactant5-Chloro-2-oxo-1,2-dihydropyridin-4-yl benzoateHCID 14049646—
Solvent1,4-DioxaneHCID 31275—
Product5'-O-acetyl-3-[3-(4-benzoyloxy-5-chloro-2-pyridyloxycarbonyl)benzoyl]-3'-O-benzyl-2'-deoxy-5-fluorouridineHCID 1863481437.4%

Reaction Steps

To a solution of 0.60 g of 5'-O-acetyl-3'-O-benzyl-2'-deoxy-5-fluorouridine in 30 ml of dry dioxane were added 0.42 g of isophthaloyl chloride and 1.11 ml of triethylamine, and the mixture was refluxed for 2 hours. Then 0.60 g of 4-benzoyloxy-5-chloro-2(1H)-pyridone and 1.11 ml of triethyl amine were added and the resulting mixture was refluxed for 1 hour. The precipitate thus formed was filtered off, and the filtrate was concentrated. The residue was placed on a silica gel column and eluted with 40% ethyl acetate-benzene, giving 0.45 g of the title compound in a yield of 37%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04983609
Source datasetuspto-grants-1991_01
ORD IDord-ba9781ca37d84e488918675ad90467f5
Source noteuspto-grants-1991_01