HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 5'-O-Acetyl-2',3'-dideoxy-3'-fluorouridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 2',3'-Dideoxy-3'-fluorouridine | HCID 162450 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 5'-O-Acetyl-2',3'-dideoxy-3'-fluorouridine | HCID 13121580 | — |
Reaction Steps
Acetic anhydride (1.2 ml, 13 mmol) was added to a solution of 2',3'-dideoxy-3'-fluorouridine (1 g, 4.34 mmol) in dry pyridine (10 ml) and the mixture was stirred at room temperature for 24 hours. Ethanol (2 ml) was added and the mixture was evaporated to dryness. Residual pyridine was removed by coevaporation with portions of ethanol and the final residue purified by silica gel column chromatography eluting with 5% MeOH/CH2Cl2 to give the title compound which was isolated following trituration with ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05157114 |
| Source dataset | uspto-grants-1992_10 |
| ORD ID | ord-4e3af2f14c7b4ada8a2d95fee6fde7aa |
| Source note | uspto-grants-1992_10 |