HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570301Generated: October 25, 2026
Sulfuric Acid → Ethyl 6-bromoimidazo[1,2-a]pyridine-3-carboxylate
https://huagongshe.com/reaction/570301
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 2-Amino-5-bromopyridine | HCID 70622 | — |
| Reactant | Ethyl 2-chloro-3-hydroxyacrylate potassium salt | HCID 86677443 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 6-bromoimidazo[1,2-a]pyridine-3-carboxylate | HCID 22031055 | — |
Reaction Steps
To a stirring suspension of 5-bromopyridin-2-amine (1.2 g, 7.05 mmol) and ethyl 2-chloro-3-hydroxyacrylate potassium salt (6.6 g, 28.19 mmol) (prepared in a similar manner as 22) in EtOH (100 mL) at room temperature was added sulfuric acid (751 μL, 14.10 mmol) dropwise. The reaction mixture was heated at 78° C. overnight. The reaction was cooled to room temperature and the solvent was concentrated. The residue was taken in water and the pH was adjusted between 6-8 with saturated sodium bicarbonate. The crude product was extracted with ethyl acetate. The organic was washed with brine and dried over anhydrous sodium sulfate. The crude product was purified by silica chromatography to yield ethyl 6-bromoimidazo[1,2-a]pyridine-3-carboxylate (24s). MS m/z 270.2 (M+1)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09023839B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-2ed03d57ff7143dcbd8fa771ce168c49 |
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| Source note | uspto-grants-2015_05 |
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