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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1681646Generated: November 3, 2026

Water → 1-(2-Methylsulfonyloxyethyl)-5-formamidopyrazole

https://huagongshe.com/reaction/1681646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant5-Formamido-1-(2-hydroxyethyl)pyrazoleHCID 15077737—
SolventDichloromethaneHCID 6344—
Product1-(2-Methylsulfonyloxyethyl)-5-formamidopyrazoleHCID 15077738—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 1-(2-hydroxyethyl)-5-formamidopyrazole (10 g) and triethylamine (18 ml) in methylene chloride (100 ml) was added dropwise methanesulfonyl chloride (8.5 ml) under ice-cooling. The mixture was stirred at 0° C. for 1.5 hours. The reaction mixture was poured into water (20 ml) and the methylene chloride layer was separated. The aqueous layer was reextracted with tetrahydrofuran twice. The organic layers were combined and dried over magnesium sulfate. The solvent was evaporated and the residue was subjected to column chromatography on silica gel (200 g) using ethyl acetate as an eluent. Fractions containing the object compound were combined and evaporated in vacuo to give 1-(2-methylsulfonyloxyethyl)-5-formamidopyrazole (3.2 g) as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05173485
Source datasetuspto-grants-1992_12
ORD IDord-520796391dd44fefa81355fdbb215376
Source noteuspto-grants-1992_12