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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantSodium BicarbonateHCID 516892—
Reactant1-(4-Methylpyridin-2-yl)piperazineHCID 2760058—
SolventDichloromethaneHCID 6344—
Product1-(4-Methyl-2-pyridinyl)-4-(methylsulfonyl)piperazineHCID 8982601096.3%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260441B2
Source datasetuspto-grants-2016_02
ORD IDord-20af93d2e879493286abf166b7a243bb
Source noteuspto-grants-2016_02