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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1899627Generated: November 3, 2026

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

https://huagongshe.com/reaction/1899627

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 2. Reaction of 5-chlorosulphonyl-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 numberUS05571821
Source datasetuspto-grants-1996_11
ORD IDord-b3733b1de3fb4433a45603013309fc4c
Source noteuspto-grants-1996_11