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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 873014Generated: October 29, 2026

4-Chloropyridine-2-carboxamide → 4-(4-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamido)phenoxy)picolinamid

https://huagongshe.com/reaction/873014

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloropyridine-2-carboxamideHCID 303543—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantN-(4-hydroxyphenyl)-1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamideHCID 90032700—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product4-(4-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamido)phenoxy)picolinamidHCID 11784259273%

Reaction Steps

To a solution of N-(4-hydroxyphenyl)-1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamide (1.80 g, 5.57 mmol) in DMF (35 mL) was added potassium tert-butoxide (1.87 g, 16.7 mmol). The solution was stirred at rt for 20 minutes, followed by the addition of 4-chloropicolinamide (1.046 g, 6.68 mmol). The reaction was heated at 120° C. for 3 hours, then cocentrated to 2 mL in vacuo, and diluted with water (60 mL). The precipitate was obtained by filtration, washed with water (5 mL) and dried. The crude product was washed with DCM (20 mL) to give the title compound as a brown solid (1.8 g, 73%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975282B2
Source datasetuspto-grants-2015_03
ORD IDord-dc02544c97ea414283604be9af68c0bd
Source noteuspto-grants-2015_03