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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 232737Generated: October 25, 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/232737

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 numberUS05591761
Source datasetuspto-grants-1997_01
ORD IDord-b36f574adcf54b81930a0f8630ee57dc
Source noteuspto-grants-1997_01