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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1417276Erstellt: 25. Oktober 2026

Hydrochloric Acid → N-[4-(2-Fluoro-5-trifluoromethyl-phenyl)-thiazol-2-yl]-4-methyl-benzenesulfonamide

https://huagongshe.com/reaction/1417276

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt4-Toluenesulfonyl chlorideHCID 7397—
Edukt4-(2-Fluoro-5-trifluoromethyl-phenyl)-thiazol-2-ylamine hydrobromideHCID 21845595—
LösungsmittelPyridineHCID 1049—
ProduktN-[4-(2-Fluoro-5-trifluoromethyl-phenyl)-thiazol-2-yl]-4-methyl-benzenesulfonamideHCID 11742624—

Reaktionsschritte

A mixture of 0.5 g of 4-(2-fluoro-5-trifluoromethyl-phenyl)-thiazol-2-ylamine hydrobromide with 0.30 g of p-toluenesulfonyl chloride was stirred for 3 hours with 2 ml of pyridine. The resulting, red colored suspension was poured into 30 ml of 1N hydrochloric acid and the mixture was extracted with ethyl acetate. The organic phase was dried with magnesium sulphate and concentrated. The residue was dissolved in a mixture of 20 ml of ethanol and 20 ml of 2N sodium hydroxide solution. After the addition of 0.3 g of active charcoal the mixture was stirred at room temperature for 30 minutes and subsequently the active charcoal was filtered off. 0.36 g of N-[4-(2-fluoro-5-trifluoromethyl-phenyl)-thiazol-2-yl]-4-methyl-benzenesulfonamide separated as colorless crystals upon neutralization with concentrated hydrochloric acid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05877193
Quelldatensatzuspto-grants-1999_03
ORD IDord-6eeeff84b518420da42ac0de01710a63
Quellennotizuspto-grants-1999_03