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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1192599Generated: November 1, 2026

Cesium carbonate → 1-(7-Acetyl-5-chloroquinolin-8-yl)piperidine-4-carbonitrile

https://huagongshe.com/reaction/1192599

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant4-CyanopiperidineHCID 138223—
ReactantBinap, (A+-)-HCID 634876—
ReactantHCID 58368658HCID 58368658—
Catalystpalladium(II) acetateHCID 167845—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product1-(7-Acetyl-5-chloroquinolin-8-yl)piperidine-4-carbonitrileHCID 583685896.6%

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), piperidine-4-carbonitrile (0.045 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 resulting residue was purified on silica gel (eluting with 0 to 5% MeOH in dichloromethane) to give the desired product (7 mg, 6%). LCMS calculated for C17H17ClN3O (M+H)±: m/z=314.1; Found: 314.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680108B2
Source datasetuspto-grants-2014_03
ORD IDord-626f67cc264145c0b08aca27c1f72711
Source noteuspto-grants-2014_03