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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 619064Erstellt: 25. Oktober 2026

Methane → 4-Amino-N-[4-(2-fluoro-5-trifluoromethyl-phenyl)-thiazol-2-yl]-benzenesulfonamide

https://huagongshe.com/reaction/619064

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethaneHCID 297—
EduktHydrochloric AcidHCID 313—
EduktN-Acetylsulfanilyl chlorideHCID 8481—
Edukt4-(2-Fluoro-5-trifluoromethyl-phenyl)-thiazol-2-ylamine hydrobromideHCID 21845595—
LösungsmittelEthanolHCID 702—
LösungsmittelPyridineHCID 1049—
LösungsmittelSodium HydroxideHCID 14798—
Produkt4-Amino-N-[4-(2-fluoro-5-trifluoromethyl-phenyl)-thiazol-2-yl]-benzenesulfonamideHCID 984485034,5%

Reaktionsschritte

A mixture of 0.5 g of 4-(2-fluoro-5-trifluoromethyl-phenyl)-thiazol-2-ylamine hydrobromide with 0.38 g of 4-acetaminobenzenesulfonyl chloride was stirred for 2 hours with 2 ml of pyridine. The resulting, red colored suspension was poured into 30 ml of 1N hydrochloric acid and stirred at room temperature for 30 minutes. The separated solid was dissolved in a mixture of 20 ml of ethanol and 20 ml of 2N sodium hydroxide solution. After the addition of 0.5 g of active charcoal the mixture was stirred at room temperature for 30 minutes and subsequently the active charcoal was filtered off. The 4-acetamino-N-[4-(2-fluoro-5-trifluoromethyl-phenyl)-thiazol-2-yl]-benzenesulfonamide, which separated upon neutralization with concentrated hydrochloric acid, was suspended in 9 ml of 6N hydrochloric acid and boiled for 36 hours. The mixture was cooled, treated with 30 ml of ethanol and neutralized with 2N sodium hydroxide solution. Recrystallization of the product, which thereby separated, from 20 ml of 50% ethanol yielded 0.21 g of 4-amino-N-[4-(2-fluoro-5-trifluoromethyl-phenyl)-thiazol-2-yl]benzenesulfonamide as colorless crystals.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05958910
Quelldatensatzuspto-grants-1999_09
ORD IDord-2129ff4e1e1c484ba6b233a1f4f93fbf
Quellennotizuspto-grants-1999_09