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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1681650Generated: November 3, 2026

Methanesulfonyl chloride → HCID 15077739, compound

https://huagongshe.com/reaction/1681650

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantEthyl 5-amino-1-(2-hydroxyethyl)-1H-pyrazole-4-carboxylateHCID 429881—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductHCID 15077739HCID 15077739—

Reaction Steps

To a solution of 1-(2-hydroxyethyl)-4-ethoxycarbonyl-5-aminopyrazole (200 g) in a mixture of methylene chloride (2 l) and triethylamine (210 ml) was added dropwise methanesulfonyl chloride (85.5 ml) under ice-cooling. The mixture was stirred for 1 hour at 3°-5° C. The reaction mixture was poured into ice-water (700 ml). The separated organic layer was washed with 1N hydrochloric acid and water, and dried over magnesium sulfate. The solvent was evaporated to give 1-(2-methylsulfonyloxyethyl)-4-ethoxycarbonyl-5-aminopyrazole (270.8 g) as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05173485
Source datasetuspto-grants-1992_12
ORD IDord-c60e1c548bb94208aee5401f59d90dc6
Source noteuspto-grants-1992_12