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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1531688Generated: October 27, 2026

Ammonium formate → Ethyl 8-aminoquinoline-3-carboxylate

https://huagongshe.com/reaction/1531688

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 numberUS06200974B1
Source datasetuspto-grants-2001_03
ORD IDord-721f8a81d01b4203b75e626acbda4ef5
Source noteuspto-grants-2001_03