HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 335308Generated: October 27, 2026
Sulfuric Acid → Ethyl 7-bromoimidazo[1,2-a]pyridine-3-carboxylate
https://huagongshe.com/reaction/335308
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 2-Amino-4-bromopyridine | HCID 693282 | — |
| Reactant | Potassium (Z)-2-chloro-1-ethoxy-3-oxoprop-1-en-1-olate | HCID 86695681 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 7-bromoimidazo[1,2-a]pyridine-3-carboxylate | HCID 67260906 | — |
Reaction Steps
A solution of 4-bromopyridin-2-amine (10 g, 57.8 mmol) and potassium (Z)-2-chloro-1-ethoxy-3-oxoprop-1-en-1-olate (step 1) (23.4 g, 124 mmol) in ethanol (200 ml) was cooled to 5° C. Sulfuric acid (7.70 ml, 144 mmol) was added dropwise and the reaction heated to reflux at 90° C. for 3 hrs. The mixture was cooled to RT and TEA (20.03 ml, 144 mmol) was slowly added and heating continued at 90° C. for 18 hrs. After cooling to RT, the mixture was filtered and the solid was partitioned between EtOAc and aqueous 2M HCl. The aqueous layer was basified (NaOH, solid pellets) and extracted using EtOAc. The combined organic extracts were dried (MgSO4) and concentrated in vacuo to afford the title compound;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08883819B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-5535a7177e464896b4518d7df2a759c0 |
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| Source note | uspto-grants-2014_11 |
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