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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1517302Generated: October 27, 2026

4-[(1-Methyl-1H-pyrazol-3-yl)amino]quinazolin-6-ol → 6-{[3-chloro-5-(2-methoxyethoxy)pyridin-2-yl]oxy}-N-(1-methyl-1H-pyrazol-3-yl)quinazoline-4-amine

https://huagongshe.com/reaction/1517302

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-[(1-Methyl-1H-pyrazol-3-yl)amino]quinazolin-6-olHCID 23160382—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantSodium chloride; waterHCID 57417360—
Reactant2,3-Dichloro-5-(2-methoxyethoxy)pyridineHCID 86645902—
SolventChloroformHCID 6212—
SolventDimethylacetamideHCID 31374—
Product6-{[3-chloro-5-(2-methoxyethoxy)pyridin-2-yl]oxy}-N-(1-methyl-1H-pyrazol-3-yl)quinazoline-4-amineHCID 5950888828.1%

Reaction Conditions

Temperature180 °C

Reaction Steps

2,3-Dichloro-5-(2-methoxyethoxy)pyridine (127 mg, 0.57 mmol) and potassium tert-butoxide (70 mg, 0.62 mmol) were added to an N,N-dimethylacetamide solution (2 ml) of 4-[(1-methyl-1H-pyrazol-3-yl)amino]quinazolin-6-ol (60 mg, 0.25 mmol), and stirred overnight at 180° C. under a nitrogen atmosphere in a sealed tube. The reaction solution was cooled with ice, then sodium chloride water and chloroform were added, the organic layer was washed with water, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The obtained residue was purified by reversed-phase liquid chromatography (YMC CombiPrep Pro C18 AS-360-CC) to obtain the entitled compound (30 mg, yield: 28%) as a pale orange amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08232284B2
Source datasetuspto-grants-2012_07
ORD IDord-358d157985ed42a99633ba4f3ae65b7d
Source noteuspto-grants-2012_07