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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643677Generated: October 27, 2026

Water → 7-Chloro-3-(2-chlorophenyl)-5-methyl-[1,2,4]triazolo[4,3-a]pyridine

https://huagongshe.com/reaction/643677

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantChloramine trihydrateHCID 18757622—
Reactant4-chloro-N-[(E)-(2-chlorophenyl)methylideneamino]-6-methylpyridin-2-amineHCID 59261367—
SolventEthanolHCID 702—
Product7-Chloro-3-(2-chlorophenyl)-5-methyl-[1,2,4]triazolo[4,3-a]pyridineHCID 59261365—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of (E)-1-(2-chlorobenzylidene)-2-(4-chloro-6-methylpyridin-2-yl)hydrazine (0.247 g, 0.882 mmol) and chloramine trihydrate (0.273 g, 0.970 mmol) in 7 mL of EtOH was heated at 80° C. for 2 h. After cooling to RT, water was added and the mixture was extracted with EtOAc (3×). The combined organic layers were dried over anhydrous sodium sulfate, filtered and concentrated to give 1.05 g of crude material. The crude material was purified by silica gel chromatography (50-75% EtOAc in hexanes) to afford 7-chloro-3-(2-chlorophenyl)-5-methyl-[1,2,4]triazolo[4,3-a]pyridine as an off white solid. MS (ESI, pos. ion) m/z: 278.0 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700593B2
Source datasetuspto-grants-2010_04
ORD IDord-d6089245da524cfbbc597e73c2f74eda
Source noteuspto-grants-2010_04