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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1618680Generated: November 1, 2026

2-Piperidone → 1-(4-Bromo-5,7-difluoro-3-methylquinolin-2-yl)piperidin-2-one

https://huagongshe.com/reaction/1618680

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-PiperidoneHCID 12665—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant(1S,2S)-(+)-N,N'-Dimethylcyclohexane-1,2-diamineHCID 13822957—
Reactant2,4-Dibromo-5,7-difluoro-3-methylquinolineHCID 59631114—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product1-(4-Bromo-5,7-difluoro-3-methylquinolin-2-yl)piperidin-2-oneHCID 59631061—

Reaction Steps

2,4-Dibromo-5,7-difluoro-3-methylquinoline (2.00 g, 5.90 mmol), piperidin-2-one (590 mg, 5.90 mmol), copper (I) iodide (57.0 mg, 0.300 mmol), (1S,2S)—N1,N2-dimethylcyclohexane-1,2-diamine (0.094 mL, 0.59 mmol) and potassium phosphate tribasic (2.50 g, 11.9 mmol) were combined in 1,4-dioxane (10 mL) and stirred in a microwave reactor for 3.5 h. The reaction was diluted with water and extracted with EtOAc (2×100 mL). The combined organic layers were washed with brine and dried over MgSO4. The crude product was then purified by column chromatography (silica gel, 0 to 100% EtOAc:hexanes) to give 1-(4-bromo-5,7-difluoro-3-methylquinolin-2-yl)piperidin-2-one. Mass Spectrum (ESI) m/e=355.0 [(M+1) (79Br)] and 357.1 [(M+1) (81Br)].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765940B2
Source datasetuspto-grants-2014_07
ORD IDord-700030f9031640b59346c04c97a4890c
Source noteuspto-grants-2014_07