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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 720718Erstellt: 24. Oktober 2026

Water → 6-[5-(4-Chloro-phenyl)-3-methyl-[1,2,4]triazole-1-yl]-pyridine-3-sulfonic acid amide

https://huagongshe.com/de/reaction/720718

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt6-Hydrazinylpyridine-3-sulfonamideHCID 12096590—
EduktN-(1-ethoxy-ethylidene)-4-chloro-benzamideHCID 21894670—
LösungsmittelMethanolHCID 887—
LösungsmittelDichloromethaneHCID 6344—
Produkt6-[5-(4-Chloro-phenyl)-3-methyl-[1,2,4]triazole-1-yl]-pyridine-3-sulfonic acid amideHCID 1023697261%

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 6-hydrazinopyridine-3-sulfonic acid amide 433 mg (2.23 mmol) was added to the solution 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 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, 6-[5-(4-chloro-phenyl)-3-methyl-[1,2,4]triazole-1-yl]-pyridine-3-sulfonic acid amide (446 mg, yield: 61%) was obtained as a solid phase.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07135572B2
Quelldatensatzuspto-grants-2006_11
ORD IDord-3281ffee418f475f8eebced579758931
Quellennotizuspto-grants-2006_11