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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1775277Generated: November 1, 2026

Sodium Thiosulfate → 2-(2-Ethylsulfonylphenyl)-7-trifluoromethylpyrido[3,2-d]pyrimidine

https://huagongshe.com/reaction/1775277

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantHCID 118205820HCID 118205820—
SolventChloroformHCID 6212—
Product2-(2-Ethylsulfonylphenyl)-7-trifluoromethylpyrido[3,2-d]pyrimidineHCID 118205815—

Reaction Steps

60 mg of 3-chloroperbenzoic acid (purity of 65% or more) was added to a mixture of 40 mg of 2-(2-ethylsulfanylphenyl)-7-trifluoromethylpyrido[3,2-d]pyrimidine and 3 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 to obtain 44 mg of 2-(2-ethylsulfonylphenyl)-7-trifluoromethylpyrido[3,2-d]pyrimidine (Compound of Present Invention 19).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260436B2
Source datasetuspto-grants-2016_02
ORD IDord-2d64dee1c62c4526b12ed4a39c8a77fc
Source noteuspto-grants-2016_02