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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1801866Generated: November 1, 2026

Water → 4-(3-Chloro-4-(3-fluorobenzyloxy)phenylamino)-6-(1-hydroxyethan-1-yl)quinazoline

https://huagongshe.com/reaction/1801866

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
Reactant4-(3-Chloro-4-(3-fluorobenzyloxy)phenylamino) 6-formylquinazolineHCID 57733656—
ReactantHCID 178418573HCID 178418573—
SolventTetrahydrofuranHCID 8028—
Product4-(3-Chloro-4-(3-fluorobenzyloxy)phenylamino)-6-(1-hydroxyethan-1-yl)quinazolineHCID 57733813—

Reaction Steps

In 30 mL of tetrahydrofuran was dissolved 620 mg of 4-(3-chloro-4-(3-fluorobenzyloxy)phenylamino)-6-formylquinazoline (IV-1), the solution was cooled to 0° C. under the nitrogen atmosphere, and 4.9 mL of methylmagnesium bromide (0.93M tetrahydrofuran solution) was added dropwise. After the reaction at 0° C. for 1 hour under the nitrogen atmosphere, water and ethyl acetate were added to separate the layers. The organic layer was washed sequentially with water and aqueous saturated sodium chloride solution, and dried over magnesium sulfate. After concentration, the resulting crystal was washed with chloroform to obtain 330 mg of 4-(3-chloro-4-(3-fluorobenzyloxy)phenylamino)-6-(1-hydroxyethan-1-yl)quinazoline (VI-1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349857B2
Source datasetuspto-grants-2013_01
ORD IDord-eb8861ae6acc4071aab153d2f70efe0e
Source noteuspto-grants-2013_01