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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2313Generated: October 27, 2026

2-(6-Azidopyrimidin-4-yloxy)ethanol → 2-((6-Aminopyrimidin-4-yl)oxy)ethanol

https://huagongshe.com/reaction/2313

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(6-Azidopyrimidin-4-yloxy)ethanolHCID 18931071—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
Product2-((6-Aminopyrimidin-4-yl)oxy)ethanolHCID 1893106979%

Reaction Steps

A mixture of 2-(6-azidopyrimidin-4-yloxy)ethanol (1.64 g), 10% palladium-carbon (0.25 g) and ethanol (20 ml) is subjected to catalytic hydrogenation at room temperature for one hour under hydrogen atmosphere (1 atm). The catalyst is removed by filtration, and the filtrate is concentrated. The residue is recrystallized from ethanol/diethyl ether to give 2-(6-aminopyrimidin-4-yloxy)ethanol (1.11 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05728706
Source datasetuspto-grants-1998_03
ORD IDord-fa1f51d360144913905861053111ec80
Source noteuspto-grants-1998_03