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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 897231Generated: October 29, 2026

4-Toluenesulfonyl chloride → 6-Chloro-4-(1-ethoxycarbonyl-piperidin-4-ylamino)2-oxo-1,2-dihydro-quinoline-3-carboxylic acid methyl ester

https://huagongshe.com/reaction/897231

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Toluenesulfonyl chlorideHCID 7397—
ReactantDiisopropylethylamineHCID 81531—
ReactantEthyl 4-amino-1-piperidinecarboxylateHCID 100867—
ReactantMethyl 6-chloro-4-hydroxy-2-oxo-1,2-dihydroquinoline-3-carboxylateHCID 69738561—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
Product6-Chloro-4-(1-ethoxycarbonyl-piperidin-4-ylamino)2-oxo-1,2-dihydro-quinoline-3-carboxylic acid methyl esterHCID 6973695832%

Reaction Steps

To a suspension of 6-Chloro-4-hydroxy-2-oxo-1,2dihydro-quinoline-3-carboxylic acid methyl ester (445 mg, 1.8 mmol) and diisopropylethlyamine (607 uL, 3.5 mmol) in acetonitrile (30 mL) was added p-toluenesulfonyl chloride (400 mg, 2.1 mmol). The reaction was stirred at room temperature and monitored by TLC to completion (2 h). 4-amino-piperidine-1-carboxylic acid ethyl ester was then added to the reaction mixture which was stirred at 50° C. for 8 h. The reaction mixture was then diluted up with CH2Cl2 and washed with water. The organic portion was dried with MgSO4 and evaporated. The residue was purified by flash chromatography through a silica gel column with dichloromethane and methanol (95:5 v/v) to provide a white solid (235 mg, 32%) which was carried onto the next step without characterization.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06921821B2
Source datasetuspto-grants-2005_07
ORD IDord-4ee168613424446aa7450eaf5cec838c
Source noteuspto-grants-2005_07