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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1067618Generated: November 1, 2026

4-Bromo-3-methylisoxazol-5-amine → N-(4-Bromo-3-methyl-5-isoxazolyl)-5-(4-ethylphenyl)thiophene-2-sulfonamide

https://huagongshe.com/reaction/1067618

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-3-methylisoxazol-5-amineHCID 10487519—
Reactant5-Chlorosulphonyl-2-(4-ethylphenyl)thiopheneHCID 23445565—
SolventChloroform methanolHCID 21584188—
ProductN-(4-Bromo-3-methyl-5-isoxazolyl)-5-(4-ethylphenyl)thiophene-2-sulfonamideHCID 23445288—

Reaction Steps

N-(4-Bromo-3-methyl-5-isoxazolyl)-5-(4-ethylphenyl) thiophene-2-sulfonamide was prepared in the same manner as described in Example 10. Reaction of 5-chlorosulfonyl-2-(4-ethylphenyl) thiophene (47.1 mg, 11.16 mmol) with 5-amino-4-bromo-3-methyl isoxazole (29 mg, 0.16 mmol) yielded, after flash chromatography using 10% MeOH/CHCl3, a pale brown solid (46 mg, 66% yield), m.p. 172-175° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06248767B1
Source datasetuspto-grants-2001_06
ORD IDord-b93c4e0d25954240947b63eab7b038cc
Source noteuspto-grants-2001_06