HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1392912Generated: November 1, 2026
Imidazole → 2-chloro-5-(1H-imidazol-1-ylmethyl)pyridine
https://huagongshe.com/reaction/1392912
Participants
| Role | Name | HCID | Charge |
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| Reactant | Imidazole | HCID 795 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Chloro-5-(chloromethyl)pyridine | HCID 155479 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-chloro-5-(1H-imidazol-1-ylmethyl)pyridine | HCID 1473524 | 69% |
Reaction Steps
To a solution of 2-chloro-5-(chloromethyl)pyridine (500 mg, 3.08 mmole) in 4 mL of dry acetonitrile is added 420 mL (6.17 mmol) of imidazole followed by 852 mg (6.17 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 410 mg (69% yield) of 2-Chloro-5-imidazol-1-ylmethyl-pyridine. Diagnostic C13 NMR (100 MHz, CDCl3) 47.7, 119.2, 124.9, 130.6, 131.1, 137.5, 137.8, 148.6, 151.8; MS 194.2 (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-354606aecfae4862a8371380c07ca21f |
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| Source note | uspto-grants-2008_03 |
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