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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2119260Generated: October 31, 2026

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

https://huagongshe.com/reaction/2119260

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 numberUSRE038416E1
Source datasetuspto-grants-2004_02
ORD IDord-954b506e05814b2f94472c6502fcf821
Source noteuspto-grants-2004_02