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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 259558Generated: October 29, 2026

2-(2-Nitrophenyl)oxazolo[5,4-b]pyridine → 2-(2-Aminophenyl)oxazolo[5,4-b]pyridine

https://huagongshe.com/reaction/259558

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(2-Nitrophenyl)oxazolo[5,4-b]pyridineHCID 12461420—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product2-(2-Aminophenyl)oxazolo[5,4-b]pyridineHCID 12461421—

Reaction Steps

A mixture of 700 mg. of 2-(2-nitrophenyl)oxazolo[ 5,4-b]pyridine in 50 ml. of ethanol was hydrogenated over 150 mg. of 5% palladium on carbon catalyst. The catalyst was removed by filtration and the solvent was concentrated to dryness. The residue was recrystallized from chloroform-petroleum ether to give 2-(2-aminophenyl)oxazolo[ 5,4-b]pyridine, m.p. 142°-144° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04038396
Source datasetuspto-grants-1977_07
ORD IDord-392a9a4ecd5d4a4b9e74a49444ec3132
Source noteuspto-grants-1977_07