HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1502651Generated: November 2, 2026
Water → 1-(6-(1H-pyrazol-1-yl)pyridin-3-yl)ethanone
https://huagongshe.com/reaction/1502651
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Pyrazole | HCID 1048 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-Acetyl-2-bromopyridine | HCID 15668195 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(6-(1H-pyrazol-1-yl)pyridin-3-yl)ethanone | HCID 59161970 | 81.4% |
Reaction Steps
407.9 mg (corresponding to 5.99 mmol) of pyrazole was dissolved in 10 mL of dimethylformamide. Then, 400.0 mg (corresponding to 1.99 mmol) of 5-acetyl-2-bromopyridine and 827.9 mg (corresponding to 5.99 mmol) of potassium carbonate were added thereto. The resulting solution was heated at 100° C. for 5 hours. After the completion of the reaction, the reaction solution was cooled down to room temperature, supplemented with water, and extracted twice with dichloromethane. The combined dichloromethane layer was washed with water and a saturated saline solution, dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The resulting crude product was purified by silica gel column chromatography (elution solvent: dichloromethane/ethyl acetate=50/1), to obtain 304.0 mg (corresponding to 1.62 mmol) of 5-acetyl-2-(pyrazole-1-yl)pyridine (FIG. 5, step 1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09211350B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-cff99f09e2a346b794d243da66f76852 |
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| Source note | uspto-grants-2015_12 |
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