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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1944274Generated: October 25, 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/1944274

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 numberUS08394830B2
Source datasetuspto-grants-2013_03
ORD IDord-7a98662dabdb42859fbdac59c9b25ae3
Source noteuspto-grants-2013_03