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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1179607Generated: October 23, 2026

Cesium carbonate → 2-Methyl-5-[(3R)-3-methyl-1-piperazinyl]quinoline

https://huagongshe.com/en/reaction/1179607

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantBinap, (A+-)-HCID 634876—
Reactant2-Methylpiperazine, (R)-HCID 7330434—
Reactant2-Methylquinolin-5-yl trifluoromethanesulfonateHCID 49851899—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
Product2-Methyl-5-[(3R)-3-methyl-1-piperazinyl]quinolineHCID 5744433958%

Reaction Steps

(2R)-2-Methylpiperazine (0.550 g; 2 eq), caesium carbonate (1.78 g; 2 eq), palladium acetate (0.123 g; 0.2 eq) and 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (0.513 g; 0.3 eq) were added to a solution of 2-methyl-5-quinolinyl trifluoromethanesulfonate (D1) (0.8 g; 1 eq) in toluene (30 mL) under an inert atmosphere. The reaction mixture was stirred at reflux under nitrogen for 3 hours. The reaction cooled to room temperature, quenched using saturated aqueous ammonium chloride solution (15 mL) and extracted with ethyl acetate (3×20 mL). The organic layers were combined, dried over sodium sulfate and concentrated under reduced pressure. The crude was purified by flash chromatography on silica gel, eluting with dichloromethane-methanol (95:5) affording the title compound in 58% yield (0.383 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07279481B2
Source datasetuspto-grants-2007_10
ORD IDord-ff665965fea64949812a36f84c1c419f
Source noteuspto-grants-2007_10