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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1775268Generated: November 2, 2026

Ethylamine → 2-(4-Chloro-2-ethylsulfanylphenyl)-4-ethylamino-7-trifluoromethylquinazoline

https://huagongshe.com/reaction/1775268

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylamineHCID 6341—
Reactant4-Chloro-2-(4-chloro-2-ethylsulfanylphenyl)-7-trifluoromethylquinazolineHCID 118035576—
SolventTetrahydrofuranHCID 8028—
Product2-(4-Chloro-2-ethylsulfanylphenyl)-4-ethylamino-7-trifluoromethylquinazolineHCID 118035083—

Reaction Steps

1.5 ml of ethylamine (a 70% aqueous solution) was added to a mixture of 600 mg of 4-chloro-2-(4-chloro-2-ethylsulfanylphenyl)-7-trifluoromethylquinazoline and 10 ml of THF, and the mixture was stirred at room temperature for 20 minutes. The reaction mixture was concentrated under reduced pressure, and a saturated aqueous sodium bicarbonate solution was added to the residue, and then the mixture was extracted with ethyl acetate. The organic layer was washed with water and concentrated under reduced pressure to obtain 606 mg of 2-(4-chloro-2-ethylsulfanylphenyl)-4-ethylamino-7-trifluoro methylquinazoline (Compound of Present Invention 15).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260436B2
Source datasetuspto-grants-2016_02
ORD IDord-50e37514985f4047b687cf04f82dbdc8
Source noteuspto-grants-2016_02