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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1738539Generated: October 29, 2026

5-Amino-3-methylisoxazole → N-(3-methyl-5-isoxazolyl)-5-bromothiophene-2-sulfonamide

https://huagongshe.com/reaction/1738539

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Amino-3-methylisoxazoleHCID 84590—
Reactant5-Bromothiophene-2-sulfonyl chlorideHCID 2733924—
ProductN-(3-methyl-5-isoxazolyl)-5-bromothiophene-2-sulfonamideHCID 22998516—

Reaction Steps

N-(3-methyl-5-isoxazolyl)-5-bromothiophene-2-sulfonamide was prepared in the same manner as described in Example 14 from 5-bromothiophene-2-sulfonyl chloride and 5-amino-3-methyl isoxazole. Purification was achieved by extraction of the crude sulfonamide into aqueous 2N NaOH, washing of the aqueous layer with ethyl acetate and acidification, using concentrated HCl, to pH ~2. Re-extraction into ethyl acetate was followed by washing of the organic material with water, brine and drying over magnesium sulfate. After evaporation of solvents, a brownish solid remained which was sufficiently pure to use in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05962490
Source datasetuspto-grants-1999_10
ORD IDord-21e32cc69c574b03b21d89132c33e819
Source noteuspto-grants-1999_10