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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 520496Generated: October 26, 2026

Methanesulfonyl chloride → Tert-butyl (5-chloromethylpyridin-2-yl)carbamate

https://huagongshe.com/reaction/520496

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-Butyl 5-(hydroxymethyl)pyridin-2-ylcarbamateHCID 3575389—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl (5-chloromethylpyridin-2-yl)carbamateHCID 6799313663%

Reaction Steps

To a solution of tert-butyl 5-(hydroxymethyl)pyridin-2-ylcarbamate 116 (85.0 g, 379 mmol) and diisopropylethylamine (296 g, 2.27 mol) in THF (850 mL) was added methanesulfonyl chloride (130 g, 1.14 mol) over a period of 30 min at 0° C. The mixture was stirred for 12 h at room temperature then washed with H2O (2×100 mL) and dried over Na2SO4. The mixture was concentrated and the crude residue was purified by flash chromatography (petroleum ether: ethyl acetate=10:1) to give 117 (30 g, 63% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09326986B2
Source datasetuspto-grants-2016_05
ORD IDord-47f2c440dc2341f1908de76ccb927349
Source noteuspto-grants-2016_05