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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 276830Generated: October 26, 2026

Ammonium Chloride → 6-Amino-4-(3-bromo-phenylamino)-[1,8]naphthyridine-3-carbonitrile

https://huagongshe.com/reaction/276830

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant4-(3-Bromo-phenylamino)-6-nitro-[1,8]naphthyridine-3-carbonitrileHCID 9929272—
CatalystIronHCID 23925—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product6-Amino-4-(3-bromo-phenylamino)-[1,8]naphthyridine-3-carbonitrileHCID 994981378%

Reaction Steps

A mixture of 11.2 g (30.3 mmol) of 4-(3-bromo-phenylamino)-6-nitro-[1.8]naphthyridine-3-carbonitrile, 5.1 g (90.8 mmol) of powdered iron, and 8.1 g (151 mmol) of ammonium chloride was mechanically stirred at reflux in a mixture of 330 ml water and 560 ml methanol for 40 min. The liquid layer was decanted from the solids and diluted with ethyl acetate, saturated sodium bicarbonate, and brine. This mixture was extract multiple times with ethyl acetate (final volume 3500 ml). The combined extracts were dried with magnesium sulfate and filter through a short column of silica gel. The solvent was removed and the residue was stirred with ether. The solid was collected and dried give 8.04 g of the title compound as an orange solid: mass spectrum (electrospray, m/e): M+H 340, 342.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06355636B1
Source datasetuspto-grants-2002_03
ORD IDord-978eac5f84814ad7ad64916ca55555f3
Source noteuspto-grants-2002_03