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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 720719Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/720719

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt6-Hydrazinylpyridine-3-sulfonamideHCID 12096590—
EduktN-(1-ethoxy-ethylidene)-4-bromo-benzamideHCID 21894671—
LösungsmittelMethanolHCID 887—
LösungsmittelDichloromethaneHCID 6344—
Produkt6-[5-(4-Bromo-phenyl)-3-methyl-[1,2,4]triazole-1-yl]-pyridine-3-sulfonic acid amideHCID 1021606053%

Reaktionsschritte

N-(1-ethoxy-ethylidene)-4-bromo-benzamide 565 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 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, 6-[5-(4-bromo-phenyl)-3-methyl-[1,2,4]triazole-1-yl]-pyridine-3-sulfonic acid amide (437 mg, yield: 53%) was obtained as a solid phase.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07135572B2
Quelldatensatzuspto-grants-2006_11
ORD IDord-df6ddb7336a74d149746110cdd4dff1f
Quellennotizuspto-grants-2006_11