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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1517316Generated: November 3, 2026

Dimethylacetamide → 3-chloro-N-[2-(dimethylamino)ethyl]-N-methyl-2-({4-[(1-methyl-1H-pyrazol-3-yl)amino]quinazolin-6-yl}oxy)isonicotinamide

https://huagongshe.com/reaction/1517316

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylacetamideHCID 31374—
Reactant4-[(1-Methyl-1H-pyrazol-3-yl)amino]quinazolin-6-olHCID 23160382—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant3-Chloro-N-[2-(dimethylamino)ethyl]-2-fluoro-N-methylisonicotinamideHCID 68429843—
SolventWaterHCID 962—
Product3-chloro-N-[2-(dimethylamino)ethyl]-N-methyl-2-({4-[(1-methyl-1H-pyrazol-3-yl)amino]quinazolin-6-yl}oxy)isonicotinamideHCID 5950888784%

Reaction Conditions

Temperature80 °C

Reaction Steps

3-Chloro-N-[2-(dimethylamino)ethyl]-2-fluoro-N-methylisonicotinamide (116 mg, 0.45 mmol) and potassium tert-butoxide (70 mg, 0.62 mmol) were added to an N,N-dimethylacetamide solution (1 ml) of 4-[(1-methyl-1H-pyrazol-3-yl)amino]quinazolin-6-ol (650 mg, 0.25 mmol), and stirred under a nitrogen atmosphere at 80° C. for 2 hours. The reaction solution was cooled to room temperature, water was added, and extracted with chloroform. The organic layer was washed with water, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The obtained residue was purified by amine-type silica gel column chromatography (Biotage NH, hexane:ethyl acetate to chloroform:methanol=1:3 to 100:2) to obtain the entitled compound (101 mg, yield: 84%) as a pale yellow amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08232284B2
Source datasetuspto-grants-2012_07
ORD IDord-8eb94bcbb0314b1493a621f3498c2997
Source noteuspto-grants-2012_07