HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 2'-Amino-2'-deoxy-5-iodouridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2'-Azido-2'-deoxy-5-iodouridine | HCID 86751178 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2'-Amino-2'-deoxy-5-iodouridine | HCID 69459168 | 78% |
Reaction Steps
To a solution of 5-iodo,2'-azido,2'-deoxyuridine (2.48 g, 6.3 mmoles) in dioxane (33 ml) is added triphenylphosphine (5.8 g, 22 mmoles, 3.5 eq.) and the mixture is stirred at room temperature for 1 h, during which time a white precipitate forms. The precipitate is collected and washed three times with diethyl ether (3×50 ml). The filtrate is evaporated to dryness, taken up in a minimum amount of dioxane, and stored at -20° C. for 48 h. The precipitate is collected and washed with diethyl ether. The combined precipitates gave 1.81 g of 5-iodo,2'-amino,2'-deoxyuridine (78% yield). The spectral properties agreed with those reported in the literature (Verheyden et al. (1971) supra).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05958691 |
| Source dataset | uspto-grants-1999_09 |
| ORD ID | ord-0b9671f6ef774eb186dc6ad71abbf198 |
| Source note | uspto-grants-1999_09 |