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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1358063Generated: October 25, 2026

Methanol → Doxifluridine

https://huagongshe.com/reaction/1358063

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantTributylstannaneHCID 5948—
Reactant5'-Deoxy-5'-iodo-5-fluorouridineHCID 10872387—
SolventTolueneHCID 1140—
ProductDoxifluridineHCID 18343—

Reaction Steps

When the reduction is carried out by using tributyltin hydride, the reaction takes place by dissolving 5′-deoxy-5′-iodo-5-fluorouridine in an alcohol, for example methanol, the reducing agent being added as a solution in an organic solvent, for example in toluene, and the mixture is heated at reflux in the presence of α,α′-azoisobutyro nitrile in catalytic amount. After 1÷3 hours the reduction is complete and, after evaporation of the solvent, the 5′-deoxy-5-fluorouridine thus obtained is recovered according to conventional methods.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06593467B2
Source datasetuspto-grants-2003_07
ORD IDord-e4e4832fa8694f1daf899ed2aee7ad27
Source noteuspto-grants-2003_07