HuagongsheHuagongshe Chemistry Print Report · For research reference only
Idoxuridine → 5-(4-Phthalimidobut-1-yn-1-yl)-2'-deoxvuridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Idoxuridine | HCID 5905 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-(3-Butynyl)phthalimide | HCID 11171619 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-(4-Phthalimidobut-1-yn-1-yl)-2'-deoxvuridine | HCID 54351651 | 78.8% |
Reaction Steps
5-Iodo-2′-deoxyuridine (354 mg, 1 mmol) was dissolved in 10 mL of dimethylformamide. Cuprous iodide (76 mg, 0.4 mmol), tetrakis(triphenylphosphine)palladium(0) (230 mg, 0.2 mmol), and triethylamine (200 mg, 2.0 mmol) were added. 4-Phthalimidobut-1-yne (300 mg, 1.5 mmol) was added all at once and the reaction kept at 60° C. for three hours. The clear yellow reaction was then evaporated and methylene chloride was added. Scratching of the flask induced crystallization of nearly all of the product which was filtered and recrystallized from 95% ethanol to give 335 mg (78%) of title compound as fine, feathery needles.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06312953B1 |
| Source dataset | uspto-grants-2001_11 |
| ORD ID | ord-f3a3093a298f454490b24bcc0574b785 |
| Source note | uspto-grants-2001_11 |