HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 427235Generated: October 25, 2026
Idoxuridine → 5-[3-(2-Trifluoroacetamidoethoxy)propynyl]-2'-deoxyuridine
https://huagongshe.com/reaction/427235
Participants
| Role | Name | HCID | Charge |
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| Reactant | Idoxuridine | HCID 5905 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Iodide Ion | HCID 30165 | — |
| Reactant | 3-(2-Trifluoroacetamidoethoxy)propyne | HCID 16742621 | — |
| Catalyst | Copper | HCID 23978 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 5-[3-(2-Trifluoroacetamidoethoxy)propynyl]-2'-deoxyuridine | HCID 21309568 | — |
Reaction Steps
A mixture of 5-iodo-2′-deoxyuridine (3.54 g, 10 mmol), copper(l) iodide (0.19 g, 1 mmol) and tetrakis(triphenylphosphine)palladium(O) (0.58 g, 0.5 mmol) is dried in vacuo at 60° for 3 hours and placed under argon. A suspension of the mixture in dry DMF (20 ml) is stirred under argon and treated with dry triethylamine (1.7 ml, 12 mmol) followed by 3-(2-Trifluoroacetamidoethoxy)propyne (3.17 g, 16 mmol). The mixture is cooled at room temperature water bath and stirred for 17 hours. The mixture is treated with 2% acetic acid (100 ml), the catalyst is removed by filtration and washed with 50% methanol. The filtrates are combined and passed onto a LiChroprep RP-18 column (5×25 cm), the column is washed, then eluted with 1% acetic acid in 50% (v/v) methanol. The fractions with the main produce are combined, evaporated, and dried in vacuo. The resultant foam is stirred with 150 ml of ether to give crystalline product; yield 3.6 g (85%); m.p. 145-152°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06312953B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-85feaa8332e7463292c5a31712716730 |
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| Source note | uspto-grants-2001_11 |
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