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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518787Generated: October 31, 2026

Sodium Thiosulfate → HCID 86697949, compound

https://huagongshe.com/reaction/518787

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantMethyl 2-(methylthio)-7-phenylthieno[3,2-d]pyrimidine-6-carboxylateHCID 86697951—
SolventDichloromethaneHCID 6344—
ProductHCID 86697949HCID 86697949—

Reaction Steps

2.3 g of 3-chloroperoxybenzoic acid (75%) are added slowly, in fractions, to a solution of 1.6 g of methyl 2-(methylsulfanyl)-7-phenylthieno[3,2-d]pyrimidine-6-carboxylate (example 4) in 25 ml of dichloromethane, cooled in an ice bath. The mixture is stirred for 2.5 h while cold, and then left at ambient temperature overnight. The mixture is then diluted with 80 ml of dichloromethane and treated with 60 ml of saturated sodium thiosulfate solution. After stirring and settling out, the aqueous phase is extracted with 60 ml of dichloromethane. The organic phases are washed with 60 ml of a saturated sodium bicarbonate solution, and then with 60 ml of a saturated sodium chloride solution. The organic phases are dried over magnesium sulfate, filtered, and then concentrated under vacuum so as to obtain the crude product, which is purified on 200 g of silica, elution being carried out with dichloromethane, so as to obtain 1.4 g of methyl 2-(methylsulfonyl)-7-phenylthieno[3,2-d]pyrimidine-6-carboxylate in the form of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115140B2
Source datasetuspto-grants-2015_08
ORD IDord-5591afcf077f4108b155ecc4948e397a
Source noteuspto-grants-2015_08