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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1251652Generated: November 1, 2026

4-bromo-2,5-dichlorothiophene-3-sulfonyl chloride → N-(4-Bromo-3-methyl-5-isoxazolyl)-2,5-dichloro-4-bromothiophene-3-sulfonamide

https://huagongshe.com/reaction/1251652

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-bromo-2,5-dichlorothiophene-3-sulfonyl chlorideHCID 519295—
Reactant4-Bromo-3-methylisoxazol-5-amineHCID 10487519—
ProductN-(4-Bromo-3-methyl-5-isoxazolyl)-2,5-dichloro-4-bromothiophene-3-sulfonamideHCID 1534206758%

Reaction Steps

N-(4-Bromo-3-methyl-5-isoxazolyl)-2,5-dichloro-4-bromothiophene-3-sulfonamide was prepared in the same manner as described in Example 1 from 5-amino-4-bromo-3-methylisoxazole and 4-bromo-2,5-dichlorothiophene-3-sulfonyl chloride in 58% yield. Purification was achieved by recrystallization from ethyl acetate/hexanes to give a crystalline solid, m.p. 146-149° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06342610B2
Source datasetuspto-grants-2002_01
ORD IDord-32bba765a5fe4e59aaa76f0f5419f204
Source noteuspto-grants-2002_01