Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 427233Generated: October 25, 2026

Idoxuridine → 5-(4-Phthalimidobut-1-yn-1-yl)-2'-deoxvuridine

https://huagongshe.com/reaction/427233

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIdoxuridineHCID 5905—
ReactantTriethylamineHCID 8471—
ReactantN-(3-Butynyl)phthalimideHCID 11171619—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
Product5-(4-Phthalimidobut-1-yn-1-yl)-2'-deoxvuridineHCID 5435165178.8%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06312953B1
Source datasetuspto-grants-2001_11
ORD IDord-f3a3093a298f454490b24bcc0574b785
Source noteuspto-grants-2001_11