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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 586283Generated: October 29, 2026

Potassium Phosphate, Tribasic → HCID 10134791, compound

https://huagongshe.com/reaction/586283

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantHCID 11459593HCID 11459593—
Reactant3-(3,5-Difluoro-pyridin-2-yl)-4-fluorophenylboronic acidHCID 11637419—
CatalystCID 53485975HCID 53485975—
SolventDimethylformamideHCID 6228—
ProductHCID 10134791HCID 10134791—

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06936608B2
Source datasetuspto-grants-2005_08
ORD IDord-0516099f8e984059954da8a46b13b9a1
Source noteuspto-grants-2005_08