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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | N,N'-Dimethylethylenediamine | HCID 8070 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 6-Bromo-4-methyl-2-(4-methylpiperidin-1-yl)quinoline | HCID 69063450 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 6-Iodo-4-methyl-2-(4-methylpiperidin-1-yl)quinoline | HCID 69060781 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07524862B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-413cbaef4ca045f0a9f6fb3e183d45ef |
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| Source note | uspto-grants-2009_04 |
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