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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64609Generated: October 26, 2026

Dimethyl Sulfoxide → S,S-Dimethyl-N-(3-chloropyrazin-2-yl)sulfilimine

https://huagongshe.com/reaction/64609

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
Reactant2-Amino-3-chloropyrazineHCID 276224—
SolventDichloromethaneHCID 6344—
ProductS,S-Dimethyl-N-(3-chloropyrazin-2-yl)sulfilimineHCID 54843379%

Reaction Steps

To a mechanically stirred solution of 3.9 g (0.05 mol) dimethyl sulfoxide in 30 ml dry methylene chloride at -78° under nitrogen is added 13.1 g (0.046 mol) trifluoromethanesulfonic anhydride dropwise to afford a white precipitate. To this is added a solution of 5.0 g (0.039 mol) 2-amino-3-chloropyrazine (1) in 30 ml methylene chloride/15 ml dimethyl sulfoxide and the resulting solution is stirred at -78° for 2 hours and at -55° for 1 hour. The reaction mixture is then quenched with 50 ml of 5% aqueous sodium bicarbonate solution and stirred at -5° for 5 minutes. The reaction mixture is diluted with 200 ml methylene chloride and the phases are separated. The aqueous phase is extracted with 250 ml methylene chloride and the combined organic phases are washed with 3×75 ml portions of water and dried over anhydrous sodium sulfate. The solvent is removed from the rotary evaporator to give 5.8 g (79%) of 2 as yellow crystals, m.p. 106°-108°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04609659
Source datasetuspto-grants-1986_09
ORD IDord-dedf95f0970e4dddaa8178b4001a1a89
Source noteuspto-grants-1986_09