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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2303Generated: October 23, 2026

2-{6-Azido-5-(4-methylphenyl)pyrimidin-4-yloxy}ethanol → 2-{6-Amino-5-(4-methylphenyl)-pyrimidin-4-yloxy}ethanol

https://huagongshe.com/en/reaction/2303

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-{6-Azido-5-(4-methylphenyl)pyrimidin-4-yloxy}ethanolHCID 11807790—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
Product2-{6-Amino-5-(4-methylphenyl)-pyrimidin-4-yloxy}ethanolHCID 1111829789.7%

Reaction Steps

A mixture of 2-{6-azido-5-(4-methylphenyl)pyrimidin-4-yloxy}-ethanol (19.6 g), 10% palladium-carbon (50% moist) (4.0 g) and ethanol (240 ml) is subjected to catalytic hydrogenation at room temperature under hydrogen atmosphere (1 atm) for one hour. The catalyst is removed by filtration, and the filtrate is concentrated under reduced pressure. The residue is recrystallized from ethyl acetate/n-hexane to give 2-{6-amino-5-(4-methylphenyl)pyrimidin-4-yloxy}ethanol (15.9 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05728706
Source datasetuspto-grants-1998_03
ORD IDord-5cec6056ae4c4169bd4252bc117b2be6
Source noteuspto-grants-1998_03