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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1984710Generated: November 2, 2026

Water → 2-Acetylamino-4-methanesulfonyloxymethylpyridine

https://huagongshe.com/reaction/1984710

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantN-(4-(hydroxymethyl)pyridin-2-yl)acetamideHCID 23151114—
SolventTetrahydrofuranHCID 8028—
Product2-Acetylamino-4-methanesulfonyloxymethylpyridineHCID 2315103487%

Reaction Steps

A solution of triethylamine (1.7 mL, 12 mmol) and methanesulfonyl chloride (0.70 mL, 9.0 mmol) in anhydrous tetrahydrofuran (3.0 mL) was added to a solution of (2-acetylaminopyridin-4-yl)methanol (Reference compound No. 12-1, 1.0 g, 6.0 mmol) in anhydrous tetrahydrofuran (9.0 mL) under ice-cooling, and the mixture was stirred for 20 minutes. Water (30 mL) was added to the reaction mixture, the whole was extracted with ethyl acetate (40 mL) three times, and then the organic layer was dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the resulting solid was filtered off with hexane. The solid was dried under reduced pressure at 40° C. to give 1.3 g of the title reference compound as a pale yellow solid. (Yield 87%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07544703B2
Source datasetuspto-grants-2009_06
ORD IDord-aadaa508f2b74bc1a956ff5a6c05eb4a
Source noteuspto-grants-2009_06