HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1392913Generated: October 24, 2026
N-Methylcyclohexylamine → (6-Chloro-pyridin-3-ylmethyl)-cyclohexyl-methyl-amine
https://huagongshe.com/en/reaction/1392913
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Methylcyclohexylamine | HCID 7514 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Chloro-5-(chloromethyl)pyridine | HCID 155479 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | (6-Chloro-pyridin-3-ylmethyl)-cyclohexyl-methyl-amine | HCID 20116048 | 95.2% |
Reaction Steps
To a solution of 2-chloro-5-(chloromethyl)pyridine (500 mg, 3.08 mmole) in 8 mL of dry acetonitrile is 384 mg (3.39 mmol) of N-methylcyclohexylamine followed by 468 mg (3.39 mmol) of potassium carbonate. The reaction is heated at 80° C. for 20 h. After cooling, the reaction mixture is quenched with 5 mL of water, extracted three-times with methylene chloride, and dried over sodium sulfate. Concentration of the solvent provided an oil which was purified by silica gel chromatography to provide 700 mg (95% yield) of (6-Chloro-pyridin-3-ylmethyl)-cyclohexyl-methyl-amine. C13 NMR 26.1, 26.6, 28.9, 37.7, 54.5, 62.8, 124.1, 135.1, 139.5, 149.9; MS 239.3 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07345038B2 |
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| Source dataset | uspto-grants-2008_03 |
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| ORD ID | ord-bfdb167232b440dbae80b39d59a87147 |
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| Source note | uspto-grants-2008_03 |
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