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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 544215Generated: November 2, 2026

Ethanol → HCID 12733925, compound

https://huagongshe.com/reaction/544215

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 12733936HCID 12733936—
ProductHCID 12733925HCID 12733925—

Reaction Steps

Thionyl chloride (2.4 g) was added dropwise to a solution of 1-(2-hydroxyethyl)-6-fluoro-7-(4-acetyl-1-piperazinyl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid (0.38 g) in ethanol (20 ml) under cooling with an ice-water bath, and the reaction mixture was refluxed for 5.5 hrs. The reaction mixture was evaporated to dryness, the residue was neutralized with aqueous potassium carbonate solution, and the solution was extracted with chloroform. After removing the chloroform, the residue was recrystallized from a mixture of methylene chloride and ethyl acetate to give 0.36 g of 1-(2-hydroxyethyl)-6-fluoro-7-(4-acetyl-1-piperazinyl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid ethyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04448962
Source datasetuspto-grants-1984_05
ORD IDord-ad8d719118094a589022ce279d0e7cf0
Source noteuspto-grants-1984_05