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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIdoxuridineHCID 5905—
ReactantTriethylamineHCID 8471—
ReactantIodide IonHCID 30165—
Reactant3-(2-Trifluoroacetamidoethoxy)propyneHCID 16742621—
CatalystCopperHCID 23978—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventAcetic AcidHCID 176—
Product5-[3-(2-Trifluoroacetamidoethoxy)propynyl]-2'-deoxyuridineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06312953B1
Source datasetuspto-grants-2001_11
ORD IDord-85feaa8332e7463292c5a31712716730
Source noteuspto-grants-2001_11