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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 720706Erstellt: 24. Oktober 2026

Water → 4-[5-(4-Chloro-phenyl)-3-methyl-[1,2,4]triazole-1-yl]-benzenesulfonamide

https://huagongshe.com/de/reaction/720706

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktTriethylamineHCID 8471—
Edukt4-Hydrazinylbenzenesulfonamide hydrochlorideHCID 2794567—
EduktN-(1-ethoxy-ethylidene)-4-chloro-benzamideHCID 21894670—
LösungsmittelMethanolHCID 887—
LösungsmittelDichloromethaneHCID 6344—
Produkt4-[5-(4-Chloro-phenyl)-3-methyl-[1,2,4]triazole-1-yl]-benzenesulfonamideHCID 1017226158%

Reaktionsschritte

N-(1-ethoxy-ethylidene)-4-chloro-benzamide 472 mg (2.09 mmol) was dissolved in a mixed solvent of dichloromethane 20 ml and methanol 10 ml, and 4-hydrazinobenzenesulfonamide hydrochloride 515 mg (2.23 mmol) was added to the solution. Then, triethylamine 0.35 ml (2.51 mmol) was slowly added dropwise at room temperature for 10 minutes and stirred for 8 hours. After completing the reaction, water 20 ml was added to the reacting solution and extracted two times with dichloromethane and then, the collected organic layer was washed with saturated brine. The organic layer was dried with anhydrous magnesium sulfate, filtered and concentrated under reduced pressure, and the resulting product was re-crystallized in acetone and hexane phase. As a result, 4-[5-(4-chloro-phenyl)-3-methyl-[1,2,4]triazole-1-yl]-benzenesulfonamide (423 mg, yield: 58%) was obtained as a solid phase.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07135572B2
Quelldatensatzuspto-grants-2006_11
ORD IDord-2fb89ddae253402da3ae0730db67a8b2
Quellennotizuspto-grants-2006_11