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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1251660Generated: October 27, 2026

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

https://huagongshe.com/reaction/1251660

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 1061532265%

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 mg (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 numberUS06342610B2
Source datasetuspto-grants-2002_01
ORD IDord-b3120ad43d844973ad7e8a062000b250
Source noteuspto-grants-2002_01