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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1738392Generated: November 2, 2026

4-(Benzenesulfonyl)thiophene-2-sulfonyl chloride → N-(4-Bromo-3-methyl-5-isoxazolyl)-4-benzenesulfonylthiophene-2-sulfonamide

https://huagongshe.com/reaction/1738392

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Benzenesulfonyl)thiophene-2-sulfonyl chlorideHCID 625574—
Reactant4-Bromo-3-methylisoxazol-5-amineHCID 10487519—
ProductN-(4-Bromo-3-methyl-5-isoxazolyl)-4-benzenesulfonylthiophene-2-sulfonamideHCID 1534206226%

Reaction Steps

N-(4-Bromo-3-methyl-5-isoxazolyl)-4-(benzenesulfonyl)thiophene-2-sulfonamide was prepared in the same manner as described in Example 2 from 5-amino-4-bromo-3-methylisoxazole and 4-benzenesulfonylthiophene-2-sulphonyl chloride in 26% yield. Purification was achieved by recrystallization from ethyl acetate/hexanes to give a crystalline solid, m.p. 181-184° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05962490
Source datasetuspto-grants-1999_10
ORD IDord-5276012705704927900b0506fa337db4
Source noteuspto-grants-1999_10