HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine, hydrofluoride (1:1) → 2'Fluoro-2'-deoxyuridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine, hydrofluoride (1:1) | HCID 64774 | — |
| Reactant | 2,2'-Anhydrouridine | HCID 806138 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2'Fluoro-2'-deoxyuridine | HCID 150851 | 75% |
Reaction Steps
2,2'-Cyclouridine is treated with a solution of 70% hydrogen fluoride/pyridine in dioxane at 120° C. for ten hours to provide after solvent removal a 75% yield of 2'-deoxy-2'-fluorouridine. The 5'-DMT and 3'-cyanoethoxydiisopropyl-phosphoramidite derivitized nucleoside is obtained by standard literature procedures [Gait, Ed., Oligonucleotide Synthesis. A Practical Approach, IRL Press, Washington, D.C. (1984)], or according to the procedure of Example 4-a.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05898031 |
| Source dataset | uspto-grants-1999_04 |
| ORD ID | ord-67084895f5eb4df3bee0151b009e2230 |
| Source note | uspto-grants-1999_04 |