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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1082299Generated: October 25, 2026

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

https://huagongshe.com/reaction/1082299

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 numberUS05589478
Source datasetuspto-grants-1996_12
ORD IDord-938db4b6a7e84b90807c1255f7dfd655
Source noteuspto-grants-1996_12