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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 489831Generated: October 25, 2026

Potassium Phosphate, Tribasic → 5-Amino-1-(4-fluorophenyl)-4-[3-(pyridin-3-yl)benzoyl]pyrazole

https://huagongshe.com/reaction/489831

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant3-Pyridinylboronic acidHCID 2734378—
Reactant3-(1,3,2-Dioxaborinan-2-yl)pyridineHCID 4198005—
Reactant5-Amino4-(3-bromobenzoyl)-1-(4-fluorophenyl)pyrazoleHCID 11451237—
Solvent1,4-DioxaneHCID 31275—
SolventSodium chloride; waterHCID 57417360—
Product5-Amino-1-(4-fluorophenyl)-4-[3-(pyridin-3-yl)benzoyl]pyrazoleHCID 9950664—

Reaction Conditions

Temperature85 °C

Reaction Steps

A mixture of 5-amino-4-(3-bromobenzoyl)-1-(4-fluorophenyl)pyrazole (0.9 g, 2.5 mmol) [prepared as described in Example 1 above], pyridine-3-boronic acid, 1,3-propanediol cyclic ester (0.5 g, 3 mmol), potassium phosphate (0.8 g, 3.73 mmol) and tetrakistriphosphine palladium (0.3 g, 0.25 mmol) in dioxane (20 ml) was heated at 85° C. under argon. After 16 h, the reaction mixture was cooled to room temperature and poured into brine. The product was extracted into ethyl acetate, dried over sodium sulfate and filtered. The organic layer was removed in vacuo and the residue was purified by flash chromatography (elution gradient: 40-80% ethyl acetate/hexane) to give 5-amino-1-(4-fluorophenyl)-4-[3-(pyridin-3-yl)benzoyl]pyrazole (0.50 g) which was recrystallized from ethyl acetate (mpt. 222.2-223.0).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06979693B2
Source datasetuspto-grants-2005_12
ORD IDord-f9e79f097ffd47f197aedf3dcceed4b3
Source noteuspto-grants-2005_12