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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2061894Generated: November 1, 2026

Potassium Carbonate → HCID 59415904, compound

https://huagongshe.com/reaction/2061894

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-(1-Methylpiperidin-3-yl)methanamineHCID 13675353—
Reactant(Z)-ethyl 3-(dimethylamino)-2-(2-fluoro-5-iodobenzoyl)acrylateHCID 70809441—
SolventWaterHCID 962—
ProductHCID 59415904HCID 5941590469%

Reaction Conditions

Temperature50 °C

Reaction Steps

1-(1-Methylpiperidine-3-yl)methanamine (500 mg, 3.9 mmol) was added to the solution of (Z)-ethyl 3-(dimethylamino)-2-(3-iodobenzoyl)acrylate (Intermediate 24, 0.34M, 10.4 mL, 2.25 mmol) and the mixture was heated at 50° C. for 3 h. The solvent was removed in vacuo and the residue was dried in a vacuum oven for 1.5 h. The residue was then dissolved in dimethyl formamide (7 mL) and potassium carbonate powder (695 mg, 5.1 mmol) was added. The reaction was heated at 70° C. for 3 h then cooled to room temperature. Water (30 mL) was added and the suspension was extracted with 1:1 ethyl acetate:methyl tert-butyl ether (3×50 mL). The organic layers were dried over sodium sulfate, and the solvent was removed in vacuo. The residue was suspended in methyl tert-butyl ether (20 mL) and stirred at 40° C. for 1 h. The suspension was filtered and the solid dried to give 1.12 mg (69% yield) of ethyl 6-iodo-1-((1-methylpiperidin-3-yl)methyl)-4-oxo-1,4-dihydroquinoline-3-carboxylate as a yellowish powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08283361B2
Source datasetuspto-grants-2012_10
ORD IDord-1778bb46f4754b9dad91389dbb861305
Source noteuspto-grants-2012_10