HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 84063Generated: October 29, 2026
Water → 5'-O-(Bis(4-methoxyphenyl)(phenyl)methyl)-2'-deoxy-2'-fluorouridine
https://huagongshe.com/reaction/84063
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 1,1'-(Chlorophenylmethylene)bis(4-methoxybenzene) | HCID 96831 | — |
| Reactant | 2'Fluoro-2'-deoxyuridine | HCID 150851 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 5'-O-(Bis(4-methoxyphenyl)(phenyl)methyl)-2'-deoxy-2'-fluorouridine | HCID 7073186 | 126.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08846885B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-40e4a7d6907d4433a85732a382139631 |
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| Source note | uspto-grants-2014_09 |
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