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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 733149Generated: October 30, 2026

Potassium Phosphate, Tribasic → 1-[6-fluoro-2'-(trifluoromethoxy)-1,1'-biphenyl-3-yl]-5-methyl-1H-pyrazole-3-carboxamide

https://huagongshe.com/reaction/733149

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2-(Trifluoromethoxy)phenylboronic Acid (contains varying amounts of Anhydride)HCID 2777204—
Reactant1-(3-Chloro-4-fluorophenyl)-5-methyl-1H-pyrazole-3-carboxamideHCID 57839541—
Solvent1,4-DioxaneHCID 31275—
Product1-[6-fluoro-2'-(trifluoromethoxy)-1,1'-biphenyl-3-yl]-5-methyl-1H-pyrazole-3-carboxamideHCID 4986611911.9%

Reaction Conditions

Temperature95 °C

Reaction Steps

To a solution of the carboxamide (from step 2) (0.063 g, 0.2 mmol) and 2-trifluromethoxyphenyl boronic acid (0.076 g, 0.37 mmol) in dioxane (1 mL) were added NiCl2(dppf)2 (0.002 g, 1 mole %) and potassium phosphate (0.158 g, 0.74 mmol) and the mixture was stirred at 95° C. for 16 hours. After cooling, the reaction was partitioned between EtOAc and water. The organic phase was washed with saturated sodium bicarbonate, brine and then dried over sodium sulfate. The crude product, obtained upon concentration of the organic phase, was purified by reverse phase HPLC (acetonitrile/water system) (gradient: 10% to 90% acetonitrile over 10 minutes) to yield the titled product (0.009 g, 9.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07589116B2
Source datasetuspto-grants-2009_09
ORD IDord-3a43a05f902d4f589d5cd50b77abe14a
Source noteuspto-grants-2009_09