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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1899615Generated: November 2, 2026

5-(Phenylsulfonyl)-2-thiophenesulfonyl chloride → HCID 22998399, compound

https://huagongshe.com/reaction/1899615

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(Phenylsulfonyl)-2-thiophenesulfonyl chlorideHCID 580877—
Reactant4-Bromo-3-methylisoxazol-5-amineHCID 10487519—
ProductHCID 22998399HCID 2299839959%

Reaction Steps

N-(4-Bromo-3-methyl-5-isoxazolyl)-5-(benzenesulfonyl)thiophene-2-sulfonamide was prepared: in the same manner as described in Example 2 from 5-amino-4-bromo-3-methylisoxazole and 5-benzenesulfonylthiophene-2-sulphonyl chloride in 59% yield. Purification was achieved by recrystallization from ethyl acetate/hexanes to give a crystalline solid, m.p. 139°-142° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05571821
Source datasetuspto-grants-1996_11
ORD IDord-9fe08cc7cef44e02b843d05cfad11f30
Source noteuspto-grants-1996_11