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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2266492Generated: November 1, 2026

HCID 2769565, compound → HCID 68780079, compound

https://huagongshe.com/reaction/2266492

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 2769565HCID 2769565—
ReactantMethyl 2-(3-amino-4-chlorophenoxy)acetateHCID 66717604—
SolventWaterHCID 962—
ProductHCID 68780079HCID 68780079—
ProductHCID 68787407HCID 68787407—

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of (3-amino-4-chlorophenoxy)acetic acid methyl ester (1.5 g), 2-(4-fluorobenzyl)-3-oxobutyric acid ethyl ester (1.7 g) and polyphosphoric acid (15 g) was heated at 100° C. for 3 hours. The mixture was cooled to room temperature, diluted with water and extracted with ethyl acetate. The combined extracts were washed with water and saturated aqueous sodium chloride solution and then dried over magnesium sulfate. The solvent was removed under reduced pressure and the residue purified by column chromatography on silica gel, eluting with a mixture of ethyl acetate and cyclohexane (3:7 by volume) to afford [8-chloro-3-(4-fluorobenzyl)-4-methyl-2-oxo-1,2-dihydroquinolin-5-yloxy]acetic acid methyl ester as a yellow-brown solid, 0.13 g and [8-chloro-3-(4-fluorobenzyl)-2-methyl-4-oxo-1,4-dihydroquinolin-5-yloxy]acetic acid methyl ester as a brown oil, 0.21 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858640B2
Source datasetuspto-grants-2010_12
ORD IDord-fdbfb1306df54530816d303ce07253fb
Source noteuspto-grants-2010_12