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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2364919Generated: November 2, 2026

Idoxuridine → HCID 67117307, compound

https://huagongshe.com/reaction/2364919

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIdoxuridineHCID 5905—
ReactantChloroformHCID 6212—
ReactantTributylamineHCID 7622—
Reactant1-HepteneHCID 11610—
Catalystpalladium(II) acetateHCID 167845—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 67117307HCID 6711730797%

Reaction Steps

5-iodo-2′-deoxyuridine (1) (500 mg, 1.41 mmol) was dissolved in DMF (2.5 ml) and dioxane (2.5 ml), and palladium acetate (31 mg, 0.14 mmol) was added thereto to obtain a suspension. Tributylamine (340 μl, 1.41 mmol) and 1-heptene (5 ml, 3.53 mmol) were further added, and the reaction was carried out at 100° C. for 20 minutes by heating by microwaves. After confirming at least 90% decrease in the reaction materials by TLC (CHCl3:MeOH=9:1), the obtained sample was purified by using a silica gel column with a development solvent of CHCl3:MeOH=9:1. HU was found to be 445 mg, 1.36 mmol and the yield was 97%. The target compound was determined by 1H NMR for identification. In addition, mass analysis was carried out based on MALDI-TOF MS, and it was identified as the target compound (calcd. for C16H25N2O5 [M+H]+325.179, found 325.801).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697357B2
Source datasetuspto-grants-2014_04
ORD IDord-dc2c871dcdba41d385dd097d271213f8
Source noteuspto-grants-2014_04