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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2061886Generated: October 31, 2026

Potassium Carbonate → HCID 59415816, compound

https://huagongshe.com/reaction/2061886

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-BOC-3-AminopiperidineHCID 545809—
Reactant(Z)-ethyl 3-(dimethylamino)-2-(2-fluoro-5-iodobenzoyl)acrylateHCID 70809441—
SolventWaterHCID 962—
ProductHCID 59415816HCID 59415816312.2%

Reaction Conditions

Temperature50 °C

Reaction Steps

3-Amino-1-N-Boc-piperidine (2.5 g, 12.5 mmol) was added to the solution of (Z)-ethyl 3-(dimethylamino)-2-(3-iodobenzoyl)acrylate (Intermediate 24, 0.34M, 34 mL, 11 3 mmol) and 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 (20 mL) and potassium carbonate powder (2.2 g, 15.8 mmol) was added. The reaction was heated at 70° C. for 3 h then cooled to room temperature. Water (100 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 4.93 g (82% yield) of ethyl 1-(1-(tert-butoxycarbonyl)piperidin-3-yl)-6-iodo-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-a299f2956c904f35aa4aa9034ddb7b1c
Source noteuspto-grants-2012_10