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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1032989Generated: October 27, 2026

Triethylamine → Napthylmethylaminopyridone

https://huagongshe.com/reaction/1032989

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-BromomethylnaphthaleneHCID 70320—
Reactant3-Amino-5-ethyl-6-methyl-1H-pyridin-2-oneHCID 481022—
SolventAcetonitrileHCID 6342—
ProductNapthylmethylaminopyridoneHCID 5389356747.9%

Reaction Steps

A mixture of 3-amino-5-ethyl-6-methyl-2-(1H)-pyridinone (3.0 g, 20 mmol), 2-bromomethylnapthalene (4.4 g, 20 mmol), triethylamine (2.0 g, 20 mmol) in acetonitrile (200 mL) was heated under reflux for 4 hours. The resultant mixture was allowed to cool to room temperature and concentrated under reduced pressure (15 torr). The residue was then subjected to column chromatography on silica gel (300 g, elution with methanol-chloroform, 5:95 v/v). Collection and concentration of appropriate fractions provided 2.4 g (42%) of the napthylmethylaminopyridone.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05308854
Source datasetuspto-grants-1994_05
ORD IDord-eef5d0e6cfba422ca871ffaa9288b788
Source noteuspto-grants-1994_05