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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376085Generated: October 25, 2026

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

https://huagongshe.com/reaction/1376085

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant6-Hydrazinylpyridine-3-sulfonamideHCID 12096590—
ReactantHCID 21894667HCID 21894667—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product6-[5-(4-Fluoro-phenyl)-3-methyl-[1,2,4]triazole-1-yl]-pyridine-3-sulfonic acid amideHCID 1017208356.1%

Reaction Steps

N-(1-ethoxy-ethylidene)-4-fluoro-benzamide 438 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-fluoro-phenyl)-3-methyl-[1,2,4]triazole-1-yl]-pyridine-3-sulfonic acid amide (391 mg, yield: 56%) was obtained as a solid phase.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07169929B2
Source datasetuspto-grants-2007_01
ORD IDord-b5c1b6ee4ca5474cb5bd5af0628cdee6
Source noteuspto-grants-2007_01