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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 521669Generated: October 30, 2026

Sodium Thiosulfate → 2-(4-Chloro-2-ethylsulfonylphenyl)-4-ethylamino-7-trifluoromethylquinazoline

https://huagongshe.com/reaction/521669

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant2-(4-Chloro-2-ethylsulfanylphenyl)-4-ethylamino-7-trifluoromethylquinazolineHCID 118035083—
SolventChloroformHCID 6212—
Product2-(4-Chloro-2-ethylsulfonylphenyl)-4-ethylamino-7-trifluoromethylquinazolineHCID 118035577—

Reaction Steps

375 mg of 3-chloroperbenzoic acid (purity of 65% or more) was added to a mixture of 306 mg of 2-(4-chloro-2-ethylsulfanylphenyl)-4-ethylamino-7-trifluoromethylquinazoline and 5 ml of chloroform, under ice cooling, and the mixture was stirred at room temperature for 4 hours. A 10% aqueous sodium thiosulfate solution was added to the reaction mixture, and the mixture was extracted with chloroform. The organic layer was washed with a saturated aqueous sodium bicarbonate solution 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 270 mg of 2-(4-chloro-2-ethylsulfonylphenyl)-4-ethylamino-7-trifluoromethylquinazoline (Compound of Present Invention 16).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09328121B1
Source datasetuspto-grants-2016_05
ORD IDord-21e281cad50a41b299b852b691175d44
Source noteuspto-grants-2016_05