HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1775344Generated: November 2, 2026
Triethylamine → 1-(4-Methyl-2-pyridinyl)-4-(methylsulfonyl)piperazine
https://huagongshe.com/reaction/1775344
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-(4-Methylpyridin-2-yl)piperazine | HCID 2760058 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-(4-Methyl-2-pyridinyl)-4-(methylsulfonyl)piperazine | HCID 89826010 | 96.3% |
Reaction Steps
To a cooled (0° C.) solution of 1-(4-methyl-2-pyridyl)piperazine (228 mg, 1.286 mmol) in DCM (10 ml) were added triethylamine (360 μl, 2.59 mmol) and methanesulfonyl chloride (105 μl, 2.59 mmol). The mixture was stirred at 0° C. for one hour, then a saturated solution of sodium bicarbonate was added, the layers were separated, the aqueous layer was extracted with DCM (2×), the organic layers were combined, dried (sodium sulfate) and concentrated under reduced pressure to yield 316 mg of a white solid (1.238 mmol, yield 96%) MS (ESI) m/z=256.1 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09260441B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-20af93d2e879493286abf166b7a243bb |
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| Source note | uspto-grants-2016_02 |
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