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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Trifluoromethanesulfonic anhydride | HCID 67749 | — |
| Reactant | 2-Amino-3-chloropyrazine | HCID 276224 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | S,S-Dimethyl-N-(3-chloropyrazin-2-yl)sulfilimine | HCID 548433 | 79% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04609659 |
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| Source dataset | uspto-grants-1986_09 |
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| ORD ID | ord-dedf95f0970e4dddaa8178b4001a1a89 |
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| Source note | uspto-grants-1986_09 |
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