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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1353109Generated: November 2, 2026

Water → Ethyl 1-(2,4-difluorophenyl)-6,7-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylate

https://huagongshe.com/reaction/1353109

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
ReactantHCID 178471931HCID 178471931—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 1-(2,4-difluorophenyl)-6,7-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylateHCID 1047400282.9%

Reaction Steps

The solution of 3.0 g of ethyl 2-(2-chloro-4,5-difluorobenzoyl)-3-(2,4-difluorophenylamino)acrylate in 30 ml of anhydrous tetrahydrofuran was cooled to 10° C. 0.3 g (1.02 eq.) of 60% sodium hydride was added to the reaction mixture, which was refluxed for 4.5 hours. The reaction mixture was cooled to 5˜10° C. 54.6 ml of water was added to the reaction mixture, which was then stirred for 30 minutes. The organic layer was filtered under a reduced pressure and washed with a mixed solution of n-hexane and ether (1/1). The resulting wet cake was dried under a reduced pressure at 40˜45° C. for 6 hours to give 2.26 g of ethyl 1-(2,4-difluorophenyl)-6,7-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylate (Yield: 82.8%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07220861B2
Source datasetuspto-grants-2007_05
ORD IDord-f082c765f10441e0af7cc11f26b5168f
Source noteuspto-grants-2007_05