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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 572120Generated: November 3, 2026

Triethylamine → 8-Chloro-2-(pyridin-3-yl)-1,4-dihydroquinoline-3-carboxylic acid ethyl ester

https://huagongshe.com/reaction/572120

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Chloro-6-iodoanilineHCID 13218925—
ReactantEthyl-2-(hydroxy(pyridin-3-yl)methyl)acrylateHCID 15812391—
Catalystpalladium(II) acetateHCID 167845—
SolventAcetonitrileHCID 6342—
Product8-Chloro-2-(pyridin-3-yl)-1,4-dihydroquinoline-3-carboxylic acid ethyl esterHCID 6669190287%

Reaction Conditions

Temperature70 °C

Reaction Steps

A degassed mixture of 2-[(hydroxy)(pyridin-3-yl)methyl]acrylic acid ethyl ester (8.2 g, 39.6 mmol), 6-chloro-2-iodoaniline (10.0 g, 39.5 mmol), triethylamine (9 mL, 122 mmol) and palladium(II) acetate (300 mg) in acetonitrile (80 mL) was heated at 70° C. overnight. The mixture was cooled to room temperature and partitioned between ethyl acetate (200 mL) and water (100 mL). The aqueous layer was separated and the organic layer was washed with brine (50 mL), filtered, dried (phase separator) and concentrated in vacuo to give a crude solid. This was washed with a minimum of ice-cold diethyl ether to yield 8-chloro-2-(pyridin-3-yl)-1,4-dihydroquinoline-3-carboxylic acid ethyl ester (10.8 g, 87%) as a white solid. δH (CDCl3) 8.73 (m, 2H), 8.04 (m, 1H), 7.66 (dd, J 7.9, 5.5 Hz, 1H), 7.18 (m, 1H), 7.05 (m, 1H), 6.94 (m, 1H), 6.29 (s, 1H), 3.99 (m, 4H), 1.04 (t, J 7.1 Hz, 3H). LCMS (ES+) 315.0 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029392B2
Source datasetuspto-grants-2015_05
ORD IDord-980a07723755405a8843db84202ab62d
Source noteuspto-grants-2015_05