Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1755119Generated: November 3, 2026

Dimethyl Sulfoxide → HCID 66816874, compound

https://huagongshe.com/reaction/1755119

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantHydrogen PeroxideHCID 784—
ReactantSodium HydroxideHCID 14798—
ReactantSodium ThiosulfateHCID 24477—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 66818428HCID 66818428—
SolventMethanolHCID 887—
ProductHCID 66816874HCID 66816874—

Reaction Steps

4-{2-[4-(3-Benzyloxy-5-trifluoromethyl-benzoylamino)-4-cyano-piperidine-1-sulfonyl]-ethyl}-3-methyl-benzoic acid tert-butyl ester (1.40 g, 2.04 mmol) was dissolved in DMSO (0.188 ml, 2.65 mmol) and methanol (7.00 ml). A 1 M aqueous sodium hydroxide solution (0.204 ml, 0.204 mmol) and aqueous hydrogen peroxide (30%, 0.265 ml, 2.65 mmol) were added under ice-cooling. The mixture was warmed to room temperature and stirred as such for two hours. After completion of the reaction, an aqueous sodium thiosulfate solution and an aqueous ammonium chloride solution were added, followed by extraction with ethyl acetate. The organic layer was washed with saline, dried over anhydrous magnesium sulfate and then concentrated under reduced pressure to give 4-{2-[4-(3-benzyloxy-5-trifluoromethyl-benzoylamino)-4-carbamoyl-piperidine-1-sulfonyl]-ethyl}-3-methyl-benzoic acid tert-butyl ester as a pale yellow amorphous (1.48 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169254B2
Source datasetuspto-grants-2015_10
ORD IDord-c246132c23084bfa805250ff2cb5bf76
Source noteuspto-grants-2015_10