HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1093521Generated: October 30, 2026
Water → N-(3-Pyrazolo[1,5-a]pyridin-3-yl-phenyl)-acetamide
https://huagongshe.com/reaction/1093521
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (3-Acetamidophenyl)boronic acid | HCID 157274 | — |
| Reactant | 3-Bromo-pyrazolo[1,5-a]pyridine | HCID 2755786 | — |
| Catalyst | HCID 178418851 | HCID 178418851 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-(3-Pyrazolo[1,5-a]pyridin-3-yl-phenyl)-acetamide | HCID 66592668 | 19.9% |
Reaction Steps
A mixture of 3-bromo-pyrazolo[1,5-a]pyridine (197 mg, 1 mmol), (3-acetylaminophenyl)boronic acid (179 mg), K2CO3 (6 eq) and bis(tri-t-butylphosphine)palladium (0) (5 mg) in PhMe (1 ml), MeOH (1 ml), EtOH (1 ml), and H2O (1.8 ml) was stirred and heated at 155° C. in the microwave for 30 minutes. The mixture was partitioned between EtOAc/H2O. The layers were separated and the organic layer was dried, filtered and evaporated. The residue was crystallised from MeOH to give the title compound (50 mg). MS: [M+H]+ 252
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08131527B1 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-0ed27c2bec9143e0a9c72ae02b6f3221 |
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| Source note | uspto-grants-2012_03 |
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