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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1166813Generated: October 29, 2026

4-Bromo-5-chlorothiophene-2-sulfonyl chloride → N-(4-Bromo-3-methyl-5-isoxazolyl)-4-bromo-5-chloro-thiophene-2-sulfonamide

https://huagongshe.com/reaction/1166813

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-5-chlorothiophene-2-sulfonyl chlorideHCID 2797220—
Reactant4-Bromo-3-methylisoxazol-5-amineHCID 10487519—
ProductN-(4-Bromo-3-methyl-5-isoxazolyl)-4-bromo-5-chloro-thiophene-2-sulfonamideHCID 1534206325%

Reaction Steps

N-(4-Bromo-3-methyl-5-isoxazolyl)-4-bromo-5-chloro-thiophene-2-sulfonamide was prepared in the same manner as described in Example 2 from 5-amino-4-bromo-3-methylisoxazole and 4-bromo-5-chlorothiophene-2-sulphonyl chloride in 25% yield. Purification was achieved by recrystallization from ethyl acetate/hexanes to give a crystalline solid, m.p. 143-145° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06613804B2
Source datasetuspto-grants-2003_09
ORD IDord-79a86d8a1e4a494997fa32df1ab41ab3
Source noteuspto-grants-2003_09