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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1744582Generated: October 30, 2026

Potassium Carbonate → N-[3-Cyano-4-(4-hydroxypiperidin-1-yl)phenyl)-1-(4-fluorophenyl)-3-methylpyrazole-4-carboxamide

https://huagongshe.com/reaction/1744582

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant5-Amino-2-(4-hydroxypiperidin-1-yl)benzonitrileHCID 21942313—
Reactant1-(4-fluorophenyl)-3-methyl-1H-pyrazole-4-carboxylic acidHCID 22228057—
SolventDimethylformamideHCID 6228—
ProductN-[3-Cyano-4-(4-hydroxypiperidin-1-yl)phenyl)-1-(4-fluorophenyl)-3-methylpyrazole-4-carboxamideHCID 2222805536.7%

Reaction Steps

1-(4-Fluorophenyl)-3-methylpyrazole-4-carboxylic acid (1.0 g), 5-amino-2-(4-hydroxypiperidin-1-yl)benzonitrile (1.0 g), 1-hydroxybenzotriazole (0.7 g) and 1-ethyl-3-(3′dimethylaminopropyl)carbodiimide (1.0 g) were added to dimethylformamide (20 ml) and the mixture was stirred at room temperature for 5 h. The reaction mixture was treated with aqueous potassium carbonate solution and extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate, after which the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (mobile phase:chloroform:methanol=100:1). Diisopropyl ether was added to the obtained oily substance to allow crystallization. The crystals were recrystallized from a mixed solvent of ethyl acetate-diisopropyl ether to give the title compound (0.7 g), melting point: 224–225° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07015218B1
Source datasetuspto-grants-2006_03
ORD IDord-b630b0abb22644c6b925551c76e58d32
Source noteuspto-grants-2006_03