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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2206357Generated: November 2, 2026

Water → 5'-O-(Bis(4-methoxyphenyl)(phenyl)methyl)-2'-deoxy-2'-fluorouridine

https://huagongshe.com/reaction/2206357

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
Reactant1,1'-(Chlorophenylmethylene)bis(4-methoxybenzene)HCID 96831—
Reactant2'Fluoro-2'-deoxyuridineHCID 150851—
SolventPyridineHCID 1049—
Product5'-O-(Bis(4-methoxyphenyl)(phenyl)methyl)-2'-deoxy-2'-fluorouridineHCID 7073186126.7%

Reaction Steps

An operation of dissolving 2′-Deoxy-2′-fluorouridine (3.00 g, 12.2 mmol) in dry pyridine, followed by concentration under reduced pressure was repeated 3 times to perform dehydrative azeotropic distillation. Thereafter, under an argon atmosphere, the reaction mixture was dissolved in dry pyridine (120 ml), 4,4′-dimethoxytrityl chloride (4.55 g, 13.4 mmol) was added, and the mixture was stirred at room temperature for 3 hr. The completion of the reaction was confirmed, and ethyl acetate (150 ml) and water (60 ml) were added to the reaction mixture to allow layer separation. The organic layer was washed 3 times with 5% aqueous sodium hydrogen carbonate solution (20 ml), washed with water (20 ml) and saturated brine (20 ml), and the obtained organic layer was dried over sodium sulfate. The solvent in the filtrate was evaporated and the obtained residue was purified by silica gel column chromatography (hexane:ethyl acetate=50:50-0/100 (v/v), containing 1% triethylamine). The object fractions were collected and concentrated to give the title compound (8.48 g, quant).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09371353B2
Source datasetuspto-grants-2016_06
ORD IDord-26c56df0c31a4b11884ba25efa0dba40
Source noteuspto-grants-2016_06