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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 521668Generated: October 31, 2026

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

https://huagongshe.com/reaction/521668

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-trifluoromethylquinazoline (Compound of Present Invention 15).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09328121B1
Source datasetuspto-grants-2016_05
ORD IDord-8bbca1146cbb46e38e3107c8bfd7e4dc
Source noteuspto-grants-2016_05