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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 234305Erstellt: 26. Oktober 2026

2-Thiophenesulfonyl chloride → N-(4-Bromo-5-methyl-3-isoxazolyl)thiophene-2-sulfonamide

https://huagongshe.com/reaction/234305

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-Thiophenesulfonyl chlorideHCID 85518—
Edukt4-Bromo-5-methyl-1,2-oxazol-3-amineHCID 2774464—
LösungsmittelPyridineHCID 1049—
ProduktN-(4-Bromo-5-methyl-3-isoxazolyl)thiophene-2-sulfonamideHCID 2299841151%

Reaktionsschritte

Thiophene-2-sulfonyl chloride (183 mg, 1 mmol) was added to a solution of 3-amino-4-bromo-5-methylisoxazole (177 mg, 1 mmol) in dry pyridine (0.5 ml). The reaction mixture was stirred at room temperature for 3 h. Pyridine was removed under reduced pressure and the residue was partitioned between water and ethyl acetate. The organic layer was washed with 1N HCl (3×10 ml), brine (10 ml) and dried over anhydrous magnesium sulfate. Evaporation of the solvents left an oily residue which was solidified at -20° C. and then purified by recrystallization from ethyl acetate/hexanes, to give the pure product (51% yield) as a tan solid, m.p. 156°-158° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05594021
Quelldatensatzuspto-grants-1997_01
ORD IDord-98c55c648c034017af90ed529e7f7646
Quellennotizuspto-grants-1997_01