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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 610182Generated: October 30, 2026

Ethyl 3-(3-chloro-2,4,5-trifluorophenyl)-3-oxopropanoate → Ethyl 8-chloro-6,7-difluoro-1-(3,5-difluoro-6-methylamino-pyridin-2-yl)-4-oxo-1,4-dihydroquinoline-3-carboxylate

https://huagongshe.com/reaction/610182

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-(3-chloro-2,4,5-trifluorophenyl)-3-oxopropanoateHCID 10934859—
Reactant2-Amino-3,5-difluoro-6-(methylamino)pyridineHCID 15896296—
ReactantEthyl 3-ethoxy-2-(3-chloro-2,4,5-trifluorobenzoyl)acrylateHCID 54402571—
SolventChloroformHCID 6212—
ProductEthyl 8-chloro-6,7-difluoro-1-(3,5-difluoro-6-methylamino-pyridin-2-yl)-4-oxo-1,4-dihydroquinoline-3-carboxylateHCID 15896297—

Reaction Conditions

Temperature90 °C

Reaction Steps

To 5 ml of chloroform solution of ethyl 3-ethoxy-2-(3-chloro-2,4,5-trifluorobenzoyl)acrylate prepared from 0.70 g of ethyl 3-chloro-2,4,5-trifluorobenzoylacetate by normal process was added 430 mg of 2-amino-3,5-difluoro-6-(methylamino)pyridine. The solution was concentrated under reduced pressure. To the residue were added 0.3 g of anhydrous potassium carbonate and 2 ml of N,N-dimethylformamide, and the mixture was stirred at 90° C. for 10 minutes and allowed to cool. The solution was separated by adding 30 ml of chloroform and 300 ml of distilled water, and the chloroform layer was washed twice with 300 ml distilled water, dried over anhydrous magnesium sulfate, concentrated under reduced pressure, and allowed to stand. The precipitate was collected by filtration, washed with ethanol and diisopropylether successively to obtain 784 mg of the title compound as a colorless powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05998436
Source datasetuspto-grants-1999_12
ORD IDord-49300006170b4822af86d7a27b59f1c9
Source noteuspto-grants-1999_12