HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1487929Generated: October 31, 2026
Potassium Carbonate → Ethyl 5-bromopyrazolo[1,5-a]pyridine-3-carboxylate
https://huagongshe.com/reaction/1487929
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl propiolate | HCID 12182 | — |
| Reactant | HCID 90021550 | HCID 90021550 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Ethyl 5-bromopyrazolo[1,5-a]pyridine-3-carboxylate | HCID 53249841 | 6% |
Reaction Steps
Into a 250-mL three neck round-bottom flask, was placed a solution of 1-amino-4-bromopyridin-1-ium iodide (compound 64.2, 15 g, ˜50% purity, 24.9 mmol) in N,N-dimethylformamide (80 mL). Potassium carbonate (10.6 g, 76.7 mmol) was added portion-wise followed by the addition of ethyl propiolate (11.7 mL, 115 mmol) drop-wise over 10 min. The resulting mixture was stirred overnight at room temperature, then diluted with EtOAc (300 mL) and water (100 mL). The solids were removed by filtration and the organic layer was washed with brine (3×50 mL), dried (Na2SO4), filtered, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography with ethyl acetate/petroleum ether (1:10) as the eluent to yield the title compound as a brown solid (300 mg, 6%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09428502B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-7d34ab7d93534bad8b2594dac3d0925a |
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| Source note | uspto-grants-2016_08 |
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