HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 341159Generated: November 1, 2026
Potassium Carbonate → HCID 59320975, compound
https://huagongshe.com/reaction/341159
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole | HCID 2773987 | — |
| Reactant | HCID 59320890 | HCID 59320890 | — |
| Catalyst | HCID 178418851 | HCID 178418851 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 59320975 | HCID 59320975 | — |
Reaction Steps
A solution of 1-[3-(7-chloro-imidazo[1,2-a]pyridin-3-yl)-phenyl]-3-ethyl urea (200 mg, 0.636 mmol, 1 equivalent, made using procedure F1a), 1-methylpyrazole-4-boronic acid pinacol ester (commercially available, 265 mg, 1.272 mmol, 2 equivalents), potassium carbonate (527 mg, 3.816 mmol, 6 equivalents), and bis(tri-t-butylphosphine)palladium(0) (16 mg, 0.032 mmol, 0.05 equivalents) in ethanol (10 ml), toluene (10 ml) and water (10 ml) was heated at 70° C. for 24 h. The reaction mixture was partitioned between ethyl acetate and water. The organic layer was washed with a saturated brine solution, dried (MgSO4), filtered and the solvent evaporated in vacuo. The residue was purified by column chromatography (Biotage SP4, 25S, flow rate 25 ml/min, gradient 0% to 20% methanol in ethyl acetate) to give 1-ethyl-3-{3-[7-(1-methyl-1H-pyrazol-4-yl)-imidazo[1,2-a]pyridin-3-yl]-phenyl}-urea as a white solid (35 mg). MS: [M+H]+ 361.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08895745B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-f608dc540ae440c9a127d5b7c97d2694 |
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| Source note | uspto-grants-2014_11 |
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