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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2204318Generated: November 2, 2026

Ammonium Chloride → 5-amino-3-chloro-1-(4-methoxy-benzyl)-1H-pyridin-2-one

https://huagongshe.com/reaction/2204318

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant3-chloro-1-(4-methoxy-benzyl)-5-nitro-1H-pyridin-2-oneHCID 86703125—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
Product5-amino-3-chloro-1-(4-methoxy-benzyl)-1H-pyridin-2-oneHCID 86703124—

Reaction Steps

A saturated aqueous solution of NH4Cl (99 mL) was added to a solution of 3-chloro-1-(4-methoxy-benzyl)-5-nitro-1H-pyridin-2-one (Step O5) (6.8 g, 23.0 mmol) in EtOH (300 mL). After stirring for 15 min, iron powder (6.4 g, 115 mmol) was added and the resulting mixture was heated to reflux, stirred for 1 h, cooled to rt and concentrated. The residue was diluted with EtOH and the mixture was filtered through a pad of celite. The filtrate was concentrated. The residue was purified by silica gel column chromatography (CH2Cl2/MeOH, 100:0→96.5:3.5). ESI-MS: tR=0.61 min, [M+H]+ 265/267 (LC-MS 1); Rf=0.53 (9:1 CH2Cl2/MeOH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365576B2
Source datasetuspto-grants-2016_06
ORD IDord-9cd98a3f32ea481aa19d3d89c6cd98da
Source noteuspto-grants-2016_06