HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1943987Generated: November 2, 2026
Potassium Carbonate → 6-Bromo-2,3-dimethylimidazo[1,2-a]pyridine
https://huagongshe.com/reaction/1943987
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Butanone, 3-bromo- | HCID 13142 | — |
| Reactant | 2-Amino-5-bromopyridine | HCID 70622 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-Bromo-2,3-dimethylimidazo[1,2-a]pyridine | HCID 14590367 | 16.9% |
Reaction Steps
13.53 mL (130.06 mmol) of 3-bromobutan-2-one are added to a mixture, stirred at 20° C., of 5 g (28.90 mmol) of 2-amino-5-bromopyridine and 4.85 g (57.80 mmol) of sodium hydrogen carbonate in 100 mL of ethanol. The mixture is refluxed for 12 hours and then concentrated under reduced pressure. The mixture obtained is taken up in 100 mL of water. The pH of the solution is basified by successive additions of potassium carbonate. The mixture is then extracted with 3×50 mL of ethyl acetate. The combined organic phases are washed with water (50 mL), dried over sodium sulfate and then concentrated under reduced pressure. An oil is obtained, which is purified by chromatography on a column of silica, eluting with a mixture of dichloromethane and methanol. 1.1 g of the expected product are thus isolated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08394820B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-45ac94157fe94ece9503285807d874bb |
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| Source note | uspto-grants-2013_03 |
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