HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 581953Generated: November 3, 2026
Imidazole → 2-chloro-6-(1H-imidazol-1-yl)pyridine
https://huagongshe.com/reaction/581953
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,6-Dichloropyridine | HCID 16989 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-chloro-6-(1H-imidazol-1-yl)pyridine | HCID 53799988 | — |
Reaction Steps
A mixture of 2,6-dichloropyridine (5 g, 33.78 mmol), imidazole (2.3 g, 33.78 mmol) and potassium carbonate (4.66 g, 33.78 mmol) in DMF (50 ml) is heated to 85° C. over night. The cooled mixture is poured into ice-water and unreacted starting material is filtered off. The filtrate is acidified with diluted hydrochloric acid and is extracted once with ethyl acetate. The aqueous phase is rendered alkaline by addition of aqueous sodium hydroxide (10 M) and extracted with ethyl acetate. The organic extract is dried over sodium sulfate, concentrated under reduced pressure and eluted through silica gel with a mixture of ethyl acetate and methanol (9:1). Evaporation of solvent leaves 15a. Yield: 2.37 g (39%). Mp 71-73° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05922724 |
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| Source dataset | uspto-grants-1999_07 |
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| ORD ID | ord-811f07460ca2475286ff3cc1dd633e62 |
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| Source note | uspto-grants-1999_07 |
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