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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1775261Generated: October 29, 2026

Sodium Thiosulfate → 2-(2-Ethylsulfinylphenyl)-4-propylamino-7-trifluoromethylquinazoline

https://huagongshe.com/reaction/1775261

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant2-(2-Ethylsulfanylphenyl)-4-propylamino-7-trifluoromethylquinazolineHCID 118205827—
SolventChloroformHCID 6212—
Product2-(2-Ethylsulfinylphenyl)-4-propylamino-7-trifluoromethylquinazolineHCID 118205825—
Product2-(2-Ethylsulfonylphenyl)-4-propylamino-7-trifluoromethylquinazolineHCID 118205836—

Reaction Steps

281 mg of 3-chloroperbenzoic acid (purity of 65% or more) was added to a mixture of 305 mg of 2-(2-ethylsulfanylphenyl)-4-propylamino-7-trifluoromethylquinazoline and 4 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 174 mg of 2-(2-ethylsulfinylphenyl)-4-propylamino-7-trifluoromethylquinazoline (Compound of Present Invention 9) and 100 mg of 2-(2-ethylsulfonylphenyl)-4-propylamino-7-trifluoromethylquinazoline (Compound of Present Invention 10).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260436B2
Source datasetuspto-grants-2016_02
ORD IDord-dc1f60a94aa44345a78b32c1736676e5
Source noteuspto-grants-2016_02