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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1192615Generated: November 2, 2026

Cesium carbonate → 1-[5-Chloro-8-(3-methoxypiperidin-1-yl)quinolin-7-yl]ethanone

https://huagongshe.com/reaction/1192615

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant3-MethoxypiperidineHCID 4341744—
ReactantHCID 58368658HCID 58368658—
Catalystpalladium(II) acetateHCID 167845—
CatalystBinap, (A+-)-HCID 634876—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product1-[5-Chloro-8-(3-methoxypiperidin-1-yl)quinolin-7-yl]ethanoneHCID 5836848534.4%

Reaction Conditions

Temperature65 °C

Reaction Steps

A stirred mixture of 7-acetyl-5-chloroquinolin-8-yl trifluoromethanesulfonate (0.12 g, 0.34 mmol, from Example 47, Step 2), 3-methoxypiperidine (0.047 g, 0.41 mmol), palladium acetate (1.5 mg, 0.0068 mmol), (S)-(−)-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (6.3 mg, 0.010 mmol), and cesium carbonate (0.31 g, 0.95 mmol) in tetrahydrofuran (3 mL) was heated at 65° C. overnight. The mixture was cooled, diluted with dichloromethane and filtered. The filtrate was washed with brine, dried over MgSO4 and evaporated under reduced pressure. The residue was purified on silica gel (eluting with 0 to 10% methanol in dichloromethane) to give the desired product (37.3 mg, 34%). LCMS calculated for C17H20ClN2O2 (M+H)+: m/z=319.1; Found: 319.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680108B2
Source datasetuspto-grants-2014_03
ORD IDord-7fd9c1a90b074dc7a3110e778e3669b6
Source noteuspto-grants-2014_03