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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1166808Generated: November 2, 2026

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

https://huagongshe.com/reaction/1166808

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(2-Pyridyl)thiophene-2-sulfonyl chlorideHCID 2737231—
Reactant4-Bromo-3-methylisoxazol-5-amineHCID 10487519—
ProductN-(4-Bromo-3-methyl-5-isoxazolyl)-5-(2-pyridyl)thiophene-2-sulfonamideHCID 1534205840%

Reaction Steps

N-(4-bromo-3-methyl-5-isoxazolyl)-5-(2-pyridyl)thiophene-2-sulfonamide was prepared in the same manner as described in Example 2 from 5-amino-4-bromo-3-methylisoxazole and 5-(2-pyridyl)thiophene-2-sulphonyl chloride in 40% yield. Purification was achieved by recrystallization from ethyl acetate to give a crystalline solid, m.p. 186-188° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06613804B2
Source datasetuspto-grants-2003_09
ORD IDord-8d91526c867b4c2fbe10c66aefc01720
Source noteuspto-grants-2003_09