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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 517954Generated: November 1, 2026

Triethylamine → (1-(4-Methylpyridin-2-yl)piperidin-4-yl)methyl methanesulfonate

https://huagongshe.com/reaction/517954

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant(1-(4-Methylpyridin-2-yl)piperidin-4-yl)methanolHCID 61725157—
SolventDichloromethaneHCID 6344—
Product(1-(4-Methylpyridin-2-yl)piperidin-4-yl)methyl methanesulfonateHCID 86673349—

Reaction Steps

(1-(4-Methylpyridin-2-yl)piperidin-4-yl)methanol (0.970 mmol, 0.2 g) and triethylamine (2.91 mmol, 0.404 mL, 0.294 g) were stirred in DCM at 0° C. Methanesulfonyl chloride (1.454 mmol, 0.113 mL, 0.167 g) was added dropwise and the reaction allowed to warm to room temperature and stirred for 1 hour. The reaction mixture was washed with water, dried over Na2SO4 and concentrated in vacuo to afford (1-(4-methylpyridin-2-yl)piperidin-4-yl)methyl methanesulfonate. (0.234 g)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115126B2
Source datasetuspto-grants-2015_08
ORD IDord-bf002950ef5f45cfb2ee204857de9227
Source noteuspto-grants-2015_08