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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 521660Generated: October 30, 2026

Ammonia → 4-Amino-2-(2-ethylsulfanylphenyl)-7-trifluoromethylquinazoline

https://huagongshe.com/reaction/521660

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantAcetonitrileHCID 6342—
ReactantTetrahydrofuranHCID 8028—
Reactant4-Chloro-2-(2-ethylsulfanylphenyl)-7-trifluoromethylquinazolineHCID 118205819—
SolventWaterHCID 962—
Product4-Amino-2-(2-ethylsulfanylphenyl)-7-trifluoromethylquinazolineHCID 118205828—

Reaction Conditions

Temperature50 °C

Reaction Steps

4.5 ml of a 28% aqueous ammonia solution was added to a mixture of 500 mg of 4-chloro-2-(2-ethylsulfanylphenyl)-7-trifluoromethylquinazoline, 8 ml of THF and 5 ml of acetonitrile, and the mixture was stirred at 50° C. for 2 hours. Water was added to the cooled reaction mixture, and the mixture was extracted with t-butyl methyl ether. The organic layer was washed with water and dried over anhydrous magnesium sulfate, and then concentrated under reduced pressure. The resulting residue was applied to a silica gel column chromatography to obtain 396 mg of 4-amino-2-(2-ethylsulfanylphenyl)-7-trifluoromethylquinazoline (Compound of Present Invention 5).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09328121B1
Source datasetuspto-grants-2016_05
ORD IDord-8159266957cd40a3a339e68e78aa5612
Source noteuspto-grants-2016_05