HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 586283Generated: October 29, 2026
Potassium Phosphate, Tribasic → HCID 10134791, compound
https://huagongshe.com/reaction/586283
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | HCID 11459593 | HCID 11459593 | — |
| Reactant | 3-(3,5-Difluoro-pyridin-2-yl)-4-fluorophenylboronic acid | HCID 11637419 | — |
| Catalyst | CID 53485975 | HCID 53485975 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 10134791 | HCID 10134791 | — |
Reaction Steps
To 4-fluoro-3-(3,5-difluoropyridin-2-yl)phenylboronic acid (0.08 g) and 7-bromo-3-(1-fluoro-1-methylethyl)imidazo[1,2-b][1,2,4]triazine (0.06 g, 0.23 mmol) was added dry potassium phosphate (0.3 g), dichloro[1,1′-bis(diphenylphosphino)ferrocene]palladium(II) dichloromethane adduct (0.04 g) and dry N,N-dimethylformamide (3 ml). The mixture was degassed, then stirred for 24 h at 80° C. under an atmosphere of dry nitrogen. The reaction was cooled to ambient temperature, and the solvent was stripped at reduced pressure. The residue was boiled with toluene (25 ml), and filtered hot. The filtrate was evaporated and the residue subjected to preparative thin layer chromatography (silica gel; 2.5% MeOH/CH2Cl2). The recovered product was crystallised from hot toluene/isohexane to afford the title compound as a yellow solid: 1H NMR (400 MHz, DMSO-d6) δ 1.80 (6H, d, J 22.1 Hz), 7.60 (1H, dd, J 8.8, 9.8 Hz), 8.18 (1H, m), 8.32 (1H, m), 8.37 (1H, m), 8.59 (1H, s), 8.74 (1H, d, J 2.3 Hz), 9.03 (1H, s); MS (ES+) m/z 388 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06936608B2 |
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| Source dataset | uspto-grants-2005_08 |
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| ORD ID | ord-0516099f8e984059954da8a46b13b9a1 |
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| Source note | uspto-grants-2005_08 |
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