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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 520702Generated: October 25, 2026

4-Chloropyridine-2-carboxamide → 4-((6-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamido)pyridin-3-yl)oxy)picolinamide

https://huagongshe.com/reaction/520702

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloropyridine-2-carboxamideHCID 303543—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 90033479HCID 90033479—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product4-((6-(1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamido)pyridin-3-yl)oxy)picolinamideHCID 7305326645.8%

Reaction Steps

To a solution of N-(5-hydroxypyridin-2-yl)-1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamide (468 mg, 1.4 mmol) in DMF (30 mL) was added potassium tert-butoxide (486 mg, 4.33 mmol). The solution was stirred at rt for 20 minutes, followed by the addition of 4-chloropicolinamide (293 mg, 1.87 mmol). The reaction was heated at 120° C. for 2 hours, then cooled to rt, diluted with water (15 mL) and extracted with EtOAc (20 mL×3). The combined organic phases were washed with brine (20 mL) and concentrated in vacuo. The residue was purified by a silica column chromatography (DCM/MeOH (v/v)=50/1) to give the title compound as an off-white solid (285 mg, 44%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09326975B2
Source datasetuspto-grants-2016_05
ORD IDord-04c22a00f2ca4a76ab1dae17b8afcf67
Source noteuspto-grants-2016_05