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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1648647Generated: November 1, 2026

Hydrochloric Acid → HCID 15023844, compound

https://huagongshe.com/reaction/1648647

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium hydrideHCID 24758—
Reactantethyl 2-[2-amino-5-(difluoromethoxy)-3,4,6-trifluorobenzoyl]-3-(cyclopropylamino)prop-2-enoateHCID 178471897—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15023844HCID 15023844—

Reaction Steps

The whole of the ethyl 3-cyclopropylamino-2-(6-amino-3-difluoromethoxy-2,4,5-trifluorobenzoyl)acrylate prepared as described above was dissolved in 340 ml of tetrahydrofuran, and 3.82 g (0.096 mole) of a 60% w/w dispersion of sodium hydride in mineral oil were added slowly to the resulting solution, whilst ice-cooling. The mixture was then stirred at the same temperature for 30 minutes, and then at room temperature for a further 1 hour. At the end of this time, the reaction mixture was acidified by the addition of 96 ml of 1N aqueous hydrochloric acid, whilst stirring vigorously. The resulting precipitate was collected by filtration and washed with water and with ethanol, in that order, to give 18.76 g of ethyl 5-amino-1-cyclopropyl-8-difluoromethoxy-6,7-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylate [(XXII) R1 =--OCHF2, R17 =C2H5, X=F] as a colorless powder, melting at 295°-296° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05436367
Source datasetuspto-grants-1995_07
ORD IDord-59541a2c129841438b4102665a739812
Source noteuspto-grants-1995_07