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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2217793Generated: October 26, 2026

Phosphorus oxychloride → 2,6-Dichloroquinolin-5-amine

https://huagongshe.com/reaction/2217793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantAmmonium ChlorideHCID 25517—
Reactant6-Chloro-5-nitroquinoline 1-oxideHCID 68809094—
CatalystIronHCID 23925—
SolventWater ethanolHCID 19096565—
Product2,6-Dichloroquinolin-5-amineHCID 24820374—

Reaction Steps

6-Chloro-5-nitroquinoline 1-oxide (4 g) was added to phosphorus oxychloride (15 mL) at 0° C. The solution was allowed to warm to room temperature and stirred for 12 hours. The excess phosphorus oxychloride was evaporated in vacuo and the residue dissolved in water (100 mL)/dichloromethane (100 mL). The layers were separated and the aqueous layer extracted with dichloromethane (2×50 mL). The combined extracts were dried over anhydrous magnesium sulfate, filtered and concentrated to give an oil. The residue was dissolved in ethanol/water (1:1, 80 mL), ammonium chloride (2.8 g) and iron (2.8 g) added. The mixture was stirred at 65° C. for 4 hours, cooled to room temperature and filtered. The resulting solid was suspended in dimethylsulfoxide (50 mL), methanol (50 mL) and aqueous hydrochloric acid added (2M, 100 mL). The resulting solid was removed by filtration and then treated with ether (50 mL) and isohexane (50 mL). Evaporation of the mixture afforded the sub-title compound as a solid (1 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07408065B2
Source datasetuspto-grants-2008_08
ORD IDord-012e23d57d324f71be509a76c9285fee
Source noteuspto-grants-2008_08