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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2270586Generated: October 26, 2026

5-Amino-3,4-dimethylisoxazole → N-(3,4-dimethyl-5-isoxazolyl)-2-(carbomethoxy)thiophene-3-sulfonamide

https://huagongshe.com/reaction/2270586

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Amino-3,4-dimethylisoxazoleHCID 88317—
Reactant2-Thiophenecarboxylic acid, 3-(chlorosulfonyl)-, methyl esterHCID 2736733—
SolventPyridineHCID 1049—
ProductN-(3,4-dimethyl-5-isoxazolyl)-2-(carbomethoxy)thiophene-3-sulfonamideHCID 1061532279.5%

Reaction Steps

2-Methoxycarbonylthiophene-3-sulfonyl chloride (2.50 g, 10.05 mmol) was added to a solution of 5-amino-3,4-dimethylisoxazole(0.98 g, 8.75 mmol) in dry pyridine (5.0 ml). The reaction mixture was stirred at room temperature for 16 h. Pyridine was removed under reduced pressure and the residue was partitioned between water and dichloromethane. The organic layer was washed with 1 N HCl (2×50 ml) and dried over anhydrous magnesium sulfate. Evaporation of the solvents left an oily residue, which, after purification by column chromatography over silica gel (1:1 hexanes/ethyl acetate as eluent), yielded 2.20 g (65%) of a brown solid. Further purification was achieved by recrystallization from ethyl acetate/hexanes, giving the pure product as a white solid, m.p. 113-116° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06331637B1
Source datasetuspto-grants-2001_12
ORD IDord-967c6bc4fb904b1fa53a6dd7913455c9
Source noteuspto-grants-2001_12