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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 434567Generated: October 30, 2026

Iodoethane → HCID 12770912, compound

https://huagongshe.com/reaction/434567

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantTriethylamineHCID 8471—
ReactantHCID 12770893HCID 12770893—
SolventDimethylformamideHCID 6228—
ProductHCID 12770912HCID 1277091220.5%

Reaction Conditions

Temperature90 °C

Reaction Steps

Triethylamine (0.2 g), 1-ethyl-6,8-difluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)quinoline-3-carboxylic acid hydrochloride (0.3 g), ethyl iodide (0.19 g), and DMF (5 ml) were mixed, heated with stirring at 90° C. for 3 hours, and the solvent was evaporated. The residue was dissolved in 2N sodium hydroxide solution. The alkaline solution was neutralized with aqueous acetic acid and extracted with dichloromethane. The dichloromethane layer was washed with water, dried over anhydrous sodium sulfate, and evaporated. The residue was recrystallized from a mixture of DMF and ethanol to give 1-ethyl-7-(4-ethyl-1-piperazinyl)-6,8-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid (0.06 g), mp 236°-239° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04398029
Source datasetuspto-grants-1983_08
ORD IDord-b56fb3c055eb4d27b6b191baa5617f16
Source noteuspto-grants-1983_08