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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1401299Generated: October 31, 2026

HCID 86628083, compound → HCID 67037355, compound

https://huagongshe.com/reaction/1401299

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86628083HCID 86628083—
ReactantHCID 87244702HCID 87244702—
SolventEthanolHCID 702—
ProductHCID 67037355HCID 67037355—

Reaction Steps

To a stirred solution of (Z)-3-carbamohydrazonoyl-2-(trifluoromethyl)pyridine 1-oxide (1.10 g, 5 mmol) in ethanol (30 mL) was added 2-(3,4-dimethoxy-5-nitrophenyl)-2-oxoacetaldehyde (1.19 g, 5 mmol). The reaction mixture was heated to reflux for 5 hours, and then cooled to room temperature and the solvent was removed by evaporation. The residue was dissolved in dichloromethane (30 mL) and the organic phase was washed with water and dried over anhydrous magnesium sulphate, filtered and evaporated. The crude product was recrystallized from isopropanol to give 3-(5-(3,4-dimethoxy-5-nitrophenyl)-1,2,4-triazin-3-yl)-2-(trifluoromethyl)pyridine 1-oxide, 1.69 g (80%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08907099B2
Source datasetuspto-grants-2014_12
ORD IDord-9163b9084419494f9b0ad27bcb4a0fad
Source noteuspto-grants-2014_12