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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1416941Generated: October 27, 2026

Ammonium formate → Ethyl 8-aminoquinoline-3-carboxylate

https://huagongshe.com/reaction/1416941

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium formateHCID 2723923—
ReactantEthyl 4-chloro-8-nitroquinoline-3-carboxylateHCID 11196760—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductEthyl 8-aminoquinoline-3-carboxylateHCID 2125012858%

Reaction Steps

Ammonium formate was added to a vigorously stirred mixture of 4-chloro-3-ethoxycarbonyl-8-nitro-quinoline (5.6 g), ethanol (1000 ml) and 10% palladium on carbon catalyst (2 g). The mixture was stirred at ambient temperature for 1 hour, filtered through a pad of celite and the pad washed with dichloromethane. The combined filtrate and washings were evaporated to dryness. The residue so obtained was purified by flash chromatography on silica using chloroform as eluant to give 3-ethoxycarbonyl-8-amino-quinoline in 58% yield, mp 94-96° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05916898
Source datasetuspto-grants-1999_06
ORD IDord-7a1ce72d16c0489c89aba36e3aff8d0b
Source noteuspto-grants-1999_06