Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1744552Generated: October 30, 2026

5-Amino-2-(piperidin-1-yl)benzonitrile → N-(3-Cyano-4-piperidinophenyl)-1,5-dimethylpyrazole-4-carboxamide

https://huagongshe.com/reaction/1744552

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Amino-2-(piperidin-1-yl)benzonitrileHCID 10845751—
Reactant1-Hydroxybenzotriazole 1,5-dimethylpyrazole-4-carboxylateHCID 22228208—
SolventEthanolHCID 702—
ProductN-(3-Cyano-4-piperidinophenyl)-1,5-dimethylpyrazole-4-carboxamideHCID 2222810749.7%

Reaction Conditions

Temperature78 °C

Reaction Steps

1-Hydroxybenzotriazole 1,5-dimethylpyrazole-4-carboxylate (1.2 g) and 5-amino-2-piperidinobenzonitrile (0.9 g) were added to ethanol (20 ml) and the mixture was stirred at 78° C. for 3 h. After evaporation of the solvent, aqueous potassium carbonate solution was added to the residue and the mixture was 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. n-Hexane was added to the residue to allow crystallization. The crystals were recrystallized from hydrous ethanol to give the title compound (0.7 g), melting point: 217–218° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07015218B1
Source datasetuspto-grants-2006_03
ORD IDord-21eeb7599b8c4d37a0462f8b5b9a2398
Source noteuspto-grants-2006_03