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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2239362Generated: October 31, 2026

Methanesulfonyl chloride → tert-Butyl 4-[(6-{[(methylsulfonyl)oxy]methyl}pyridin-2-yl)oxy]piperidine-1-carboxylate

https://huagongshe.com/reaction/2239362

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-Butyl 4-((6-(hydroxymethyl)pyridin-2-yl)oxy)piperidine-1-carboxylateHCID 86618690—
SolventDichloromethaneHCID 6344—
Producttert-Butyl 4-[(6-{[(methylsulfonyl)oxy]methyl}pyridin-2-yl)oxy]piperidine-1-carboxylateHCID 86618691—

Reaction Conditions

Temperature0 °C

Reaction Steps

tert-Butyl 4-{[6-(hydroxymethyl)pyridin-2-yl]oxy}piperidine-1-carboxylate (0.34 g, 1.10 mmol) and methanesulfonyl chloride (0.13 mL, 1.64 mmol) were dissolved in DCM (15 mL) and stirred at 0° C. (ice bath). DIPEA (0.57 mL, 3.29 mmol) was added to the reaction mixture and stirred for 2 hours. The resulting mixture washed with water (2×15 mL), dried over a phase separator, concentrated in vacuo and was used directly in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723331B2
Source datasetuspto-grants-2010_05
ORD IDord-dadc3e871b554646a860ff280b47c92b
Source noteuspto-grants-2010_05