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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1474557Generated: October 30, 2026

Sodium Iodide → 5-Fluoro-3-(4-methoxyphenyl)-4-oxo-8-propoxy-1,4-dihydro-quinoline 2-carboxy-[2-(4-methylpiperazin-1-yl)ethyl]amide

https://huagongshe.com/reaction/1474557

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
Reactant1-MethylpiperazineHCID 53167—
ReactantHCID 86658928HCID 86658928—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product5-Fluoro-3-(4-methoxyphenyl)-4-oxo-8-propoxy-1,4-dihydro-quinoline 2-carboxy-[2-(4-methylpiperazin-1-yl)ethyl]amideHCID 8665893014.1%

Reaction Conditions

Temperature80 °C

Reaction Steps

N-methylpiperazine (276 mg, 2.76 mmol), sodium iodide (440 mg, 2.9 mmol) and potassium carbonate (572 mg, 4.14 mmol) were added to a DMF solution (8 ml) of 5-fluoro-3-(4-methoxyphenyl)-4-oxo-8-propoxy-1,4-dihydroquinoline-2-carboxy-(2-chloroethyl)amide (600 mg, 1.38 mmol) and stirred overnight at 80° C. The mixture was cooled to room temperature, and water was then added thereto, followed by extraction using chloroform. The thus-obtained organic layer was concentrated under reduced pressure, and the residue was then purified using medium pressure liquid chromatography (NH silica gel, dichloromethane:methanol=100:0→10:1). The purified product was concentrated under reduced pressure, giving a white powder of 5-fluoro-3-(4-methoxyphenyl)-4-oxo-8-propoxy-1,4-dihydro-quinoline-2-carboxy-[2-(4-methylpiperazin-1-yl)ethyl]amide (100 mg, yield: 14%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018229B2
Source datasetuspto-grants-2015_04
ORD IDord-11220848adf349538be990151aa1d924
Source noteuspto-grants-2015_04