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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 610208Generated: October 31, 2026

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

https://huagongshe.com/reaction/610208

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 3-(3-chloro-2,4,5-trifluorophenyl)-3-oxopropanoateHCID 10934859—
Reactant2-AminoacrylateHCID 22022579—
Reactant3,5-Difluoro-6-methoxypyridin-2-amineHCID 22121264—
ReactantEthyl 3-ethoxy-2-(3-chloro-2,4,5-trifluorobenzoyl)acrylateHCID 54402571—
SolventChloroformHCID 6212—
ProductEthyl 8-chloro-1-(3,5-difluoro-6-methoxypyridin-2-yl)-6,7-difluoro-4-oxo-1,4-dihydroquinoline-3-carboxylateHCID 22121219—

Reaction Conditions

Temperature90 °C

Reaction Steps

To 3 ml chloroform solution of ethyl 3-ethoxy-2-(3-chloro-2,4,5-trifluorobenzoyl)acrylate prepared from 0.78 g of ethyl 3-chloro-2,4,5-trifluorobenzoylacetate by normal process was added 2-amino-3,5-difluoro-6-methoxypyridine until completion of the conversion into the aminoacrylate form was confirmed by monitoring the reaction by TLC. The solution was concentrated under reduced pressure, and to the residue were added 0.80 g of anhydrous potassium carbonate and 2 ml of N,N-dimethylformamide, and the mixture was stirred at 90° C. for 15 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 of distilled water, dried over anhydrous magnesium sulfate, concentrated under reduced pressure, and allowed to stand. The precipitate was collected by filtration, washed with ethanol to obtain 615 mg of the title compound as a pale brown powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05998436
Source datasetuspto-grants-1999_12
ORD IDord-73e323aaf2944eb4acf5f3082ed6fabc
Source noteuspto-grants-1999_12