HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1398207Generated: October 31, 2026
Potassium Iodide → 6-bromo-2-methoxy-3-(4-methyl-1H-imidazol-1-yl)pyridine
https://huagongshe.com/reaction/1398207
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Chloroacetone | HCID 6571 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | N-(6-bromo-2-methoxypyridin-3-yl)formamide | HCID 71492501 | — |
| Product | 6-bromo-2-methoxy-3-(4-methyl-1H-imidazol-1-yl)pyridine | HCID 57609300 | — |
Reaction Steps
To a mixture of N-(6-bromo-2-methoxypyridin-3-yl)formamide (8.0 g), cesium carbonate (20.1 g) and potassium iodide (580 mg) in DMF (40 mL) was added 1-chloropropan-2-one (4.13 mL), and the mixture was stirred at room temperature for 3 hr. The solvent was evaporated under reduced pressure, water was added, and the mixture was extracted with ethyl acetate. The extract was washed with water and saturated brine, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. Acetic acid (50 mL) and ammonium acetate (26.7 g) were added to the residue, and the mixture was stirred at 130° C. for 3 hr. The reaction mixture was allowed to cool to room temperature, and the solvent was evaporated under reduced pressure. Water was added, and the mixture was neutralized with aqueous sodium hydroxide solution and extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (4.72 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08901309B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-b1b17393ceb34338953c6d73b5f85b74 |
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| Source note | uspto-grants-2014_12 |
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