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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2112820Generated: November 2, 2026

Sodium Iodide → 6-Iodo-4-methyl-2-(4-methylpiperidin-1-yl)quinoline

https://huagongshe.com/reaction/2112820

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantN,N'-DimethylethylenediamineHCID 8070—
ReactantEthyl AcetateHCID 8857—
Reactant6-Bromo-4-methyl-2-(4-methylpiperidin-1-yl)quinolineHCID 69063450—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Solvent1,4-DioxaneHCID 31275—
Product6-Iodo-4-methyl-2-(4-methylpiperidin-1-yl)quinolineHCID 69060781—

Reaction Conditions

Temperature110 °C

Reaction Steps

Under an argon atmosphere, 39 mg (0.2 mmol) of CuI, 0.6 g (4.0 mmol) of NaI, and 43 μL N,N′-dimethylethylenediamine are added to a solution of 0.69 g (2.0 mmol) of 6-bromo-4-methyl-2-(4-methylpiperidin-1-yl)quinoline in 2 mL of 1,4-dioxane and the reaction mixture is shaken for 14 hours at 110° C. After cooling, it is combined with 60 mL of EtOAc, and the organic phase is washed twice with 20 mL of 5% NH3 solution and dried over magnesium sulfate. After the desiccant and solvent have been eliminated, the residue is reacted further without purification. Yield: 0.65 g (88% of theoretical); C16H19IN2 (M=366.240); calc.: molpeak (M+H)+: 367; found: molpeak (M+H)+: 367; HPLC-MS: 7.0 min (method A).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07524862B2
Source datasetuspto-grants-2009_04
ORD IDord-413cbaef4ca045f0a9f6fb3e183d45ef
Source noteuspto-grants-2009_04