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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1775260Generated: November 1, 2026

Acetonitrile → 2-(2-Ethylsulfanylphenyl)-4-propylamino-7-trifluoromethylquinazoline

https://huagongshe.com/reaction/1775260

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantPropylamineHCID 7852—
ReactantTetrahydrofuranHCID 8028—
Reactant4-Chloro-2-(2-ethylsulfanylphenyl)-7-trifluoromethylquinazolineHCID 118205819—
SolventWaterHCID 962—
Product2-(2-Ethylsulfanylphenyl)-4-propylamino-7-trifluoromethylquinazolineHCID 118205827—

Reaction Steps

0.5 ml of n-propylamine was added to a mixture of 450 mg of 4-chloro-2-(2-ethylsulfanylphenyl)-7-trifluoromethylquinazoline, 3 ml of acetonitrile and 3 ml of THF, and the mixture was stirred at room temperature for 30 minutes. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure to obtain 495 mg of 2-(2-ethylsulfanylphenyl)-4-propylamino-7-trifluoromethylquinazoline (Compound of Present Invention 8).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260436B2
Source datasetuspto-grants-2016_02
ORD IDord-2755af5f698341749a87261b0ea646cc
Source noteuspto-grants-2016_02