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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1990776Generated: October 30, 2026

O-Xylene → HCID 23153676, compound

https://huagongshe.com/reaction/1990776

Reaction equation

Participants

RoleNameHCIDCharge
ReactantO-XyleneHCID 7237—
ReactantTriethylamine hydrochlorideHCID 11130—
ReactantHydrazinecarboxaldehydeHCID 12229—
ReactantHCID 10585807HCID 10585807—
SolventWaterHCID 962—
ProductHCID 23153676HCID 2315367621%

Reaction Steps

135 mg (2.25 mmol) of formohydrazide and 310 mg (2.25 mmol) of triethylamine hydrochloride were added to a xylene solution (5 ml) of 352 mg (1.5 mmol) of the obtained 6-chloro-4-(4-methoxyphenyl)-3-methyl-pyridazine, and stirred under reflux for 2 hours. Water was added to the reaction liquid, extracted with ethyl acetate, and the organic layer was washed with saturated saline water. This was dried with anhydrous sodium sulfate, concentrated under reduced pressure, and the resulting residue was purified through silica gel column chromatography (hexane/ethyl acetate=1/2) to obtain 75 mg (yield: 21%) of 7-(4-methoxyphenyl)-6-methyl-[1,2,4]triazolo[4,3-b]pyridazine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07645756B2
Source datasetuspto-grants-2010_01
ORD IDord-02637d4b4dc046919a7fdc028bee6b8d
Source noteuspto-grants-2010_01