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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1922063Generated: October 26, 2026

(3-Amino-4-fluorophenoxy)acetic acid methyl ester → [2-Ethyl-8-fluoro-4-oxo-3-(4-pyrazol-1-ylbenzyl)-1,4-dihydroquinolin-5-yloxy]acetic acid methyl ester

https://huagongshe.com/reaction/1922063

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3-Amino-4-fluorophenoxy)acetic acid methyl esterHCID 66717607—
Reactant3-Oxo-2-(4-pyrazol-1-ylbenzyl)pentanoic acid ethyl esterHCID 67456360—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product[2-Ethyl-8-fluoro-4-oxo-3-(4-pyrazol-1-ylbenzyl)-1,4-dihydroquinolin-5-yloxy]acetic acid methyl esterHCID 6745743042.7%

Reaction Conditions

Temperature120 °C

Reaction Steps

A solution of (3-amino-4-fluorophenoxy)acetic acid methyl ester (0.42 g) and 3-oxo-2-(4-pyrazol-1-ylbenzyl)pentanoic acid ethyl ester (0.63 g) in 1,4-dioxane (20 mL) was added to polyphosphoric acid (3 g) at 100° C., and the resulting mixture was stirred at 120° C. for 18 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 cyclohexane and ethyl acetate to afford title compound (0.39 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173812B2
Source datasetuspto-grants-2012_05
ORD IDord-adc235f8c47c44719537e8e37a520d9e
Source noteuspto-grants-2012_05