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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1267313Generated: October 25, 2026

Ethyl Acetate → 5-Amino-2-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]pyridine

https://huagongshe.com/reaction/1267313

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant2-[2-(5-Methyl-2-phenyl-4-oxazolyl)ethoxy)-5-nitropyridineHCID 11067329—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
Product5-Amino-2-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]pyridineHCID 1108772293.7%

Reaction Steps

A mixture of 2-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]-5-nitropyridine (13.4 g), palladium-carbon (5%, 1.5 g) and ethyl acetate (200 ml)-methanol (150 ml) was subjected catalytic hydrogenation at room temperature under one atmospheric pressure. The catalyst was filtered off, and the filtrate was concentrated under reduced pressure. The residual crystals were collected by filtration to obtain 5-amino-2-[2-(5-methyl-2-phenyl-4-oxazolyl)ethoxy]pyridine (11.4 g, 93%). Recrystallization from ethyl acetate-hexane gave brown crystals, m.p.107.0-108.0° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06552058B1
Source datasetuspto-grants-2003_04
ORD IDord-0c1aaefdf7914842988a2268d63fd681
Source noteuspto-grants-2003_04