Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 329838Generated: October 31, 2026

Ethanol hydrochloride → 5'-O-{N-(N-lysylalanyl)isoleucyl}-5-fluorouridine dihydrochloride

https://huagongshe.com/reaction/329838

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanol hydrochlorideHCID 21887872—
Reactant5'-O-[N-{N-(Nalpha,Nepsilon-di benzyloxycarbonyllysyl)alanyl}isoleucyl]-5-fluorouridineHCID 67896792—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
Product5'-O-{N-(N-lysylalanyl)isoleucyl}-5-fluorouridine dihydrochlorideHCID 1863734099%

Reaction Steps

0.94 Gram (1.11 mmol) of the ester obtained as described above was dissolved in ethanol (100 ml) and methanol (20 ml), and 0.40 g of 10% palladium-carbon and 0.50 g (4.93 mmol) of 36% hydrogen chloride-ethanol were added. The mixture was stirred in a stream of hydrogen under normal pressure for 2 hours at room temperature. The catalyst was filtered off and the filtrate was concentrated under reduced pressure. The residue was washed with ether (20 ml) to obtain 0.71 g (99%) of the desired 5'-O-{N-(N-lysylalanyl)isoleucyl}-5-fluorouridine dihydrochloride as a colorless powdery solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04892939
Source datasetuspto-grants-1990_01
ORD IDord-a684b95c5bfc41e9adf65dff0b86e3b3
Source noteuspto-grants-1990_01