HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 872360Generated: October 30, 2026
Potassium Phosphate, Tribasic → HCID 66665431, compound
https://huagongshe.com/reaction/872360
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 1-tert-Butoxycarbonyl-1H-pyrazole-4-boronic acid | HCID 44118675 | — |
| Reactant | HCID 56645032 | HCID 56645032 | — |
| Catalyst | HCID 178418851 | HCID 178418851 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 66665431 | HCID 66665431 | — |
Reaction Steps
A mixture of 1-[4-(6-bromo-8-methoxy-3-phenyl-imidazo[1,2-a]pyridin-2-yl)-phenyl]-cyclobutylamine (120 mg), [1-(tert-butoxycarbonyl)-1H-pyrazol-4-yl]boronic acid (170 mg) and potassium phosphate (170 mg) in toluene (0.9 mL), EtOH (1.86 mL) and water (0.93 mL) was placed under argon and bis(tri-tert-butyl phosphine)palladium(0) (13.7 mg) was added. The mixture was heated at 120° C. under microwave irradiation for 30 minutes. On cooling the mixture was partitioned between DCM and water and the phases separated. The organic portion was concentrated in vacuo to give the crude title compound which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08975265B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-b96be80b46a04402b6052de98ba0c3c7 |
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| Source note | uspto-grants-2015_03 |
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