Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Floxuridine | HCID 5790 | — |
| Reactant | 2-Chloropyridine | HCID 7977 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | HCID 18646874 | HCID 18646874 | — |
| Product | HCID 18646875 | HCID 18646875 | — |
Reaction Steps
A 0.70 g quantity of sodium hydride (60%, dispersion in mineral oil) was added to a solution of 2.00 g of 2'-deoxy-5-fluorouridine in 10 ml of dimethyl sulfoxide. The mixture was stirred at room temperature for 30 minutes. To the mixture was added 0.91 ml of 2-chloropyridine. Then the mixture was stirred at 80° C. for 3 hours. The solvent was distilled off and the residue was dissolved in 50 ml of ethyl acetate and 30 ml of water. The solution was made into a weak acidic solution by addition of 6N-hydrochloric acid. The ethyl acetate layer was separated, washed with water, dried over anhydrous magnesium sulfate and concentrated. The residue was purified by silica gel column chromatography using 1- 2% methanol-chloroform as an eluent, giving 2'-deoxy3',5'-0-di-(2-pyridyl)-5-fluorouridine (Example 46), 2'-deoxy-5-fluoro-3'-O-(2-pyridyl)uridine (Example 47) and 2'-deoxy-5-fluoro- 5'-O-(2-pyridyl)uridine (Example 48).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05047521 |
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| Source dataset | uspto-grants-1991_09 |
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| ORD ID | ord-7cf8f354407a448fae8b7b51b238a0ae |
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| Source note | uspto-grants-1991_09 |
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