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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1192602Generated: October 29, 2026

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

https://huagongshe.com/reaction/1192602

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantBinap, (A+-)-HCID 634876—
Reactant3-FLUOROPIPERIDINE HYDROCHLORIDEHCID 2759156—
ReactantHCID 58368658HCID 58368658—
Catalystpalladium(II) acetateHCID 167845—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product1-[5-Chloro-8-(3-fluoropiperidin-1-yl)quinolin-7-yl]ethanoneHCID 5836848928%

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-fluoropiperidine hydrochloride (0.057 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 to dryness. The residue was purified on silica gel (eluting with 0 to 5% methanol in dichloromethane) to give the desired product (28.7 mg, 28%). LCMS calculated for C16H17ClFN2O (M+H)+: m/z=307.1; Found 307.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680108B2
Source datasetuspto-grants-2014_03
ORD IDord-c6b09a1d716e4510a388d78237fcebc5
Source noteuspto-grants-2014_03