Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1401301Generated: November 1, 2026

HCID 67037361, compound → HCID 67036856, compound

https://huagongshe.com/reaction/1401301

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67037361HCID 67037361—
ReactantHCID 178492728HCID 178492728—
ProductHCID 67036856HCID 67036856—

Reaction Steps

To a solution of (E)-N-((dimethylamino)methylene)-3,4-dimethoxy-5-nitrobenzamide (1.12 g, 4 mmol) ethanol (30 mL) was added 3-carbamimidoyl-2-(trifluoromethyl)pyridine 1-oxide (0.82 g, 4 mmol). The reaction mixture was heated to reflux for 5 hours. It was cooled to room temperature and the solvent was removed by evaporation. The residue was then dissolved in dichloromethane/isopropanol mixture (50 mL, 70:30) and the organic phase was washed with water, dried over anhydrous magnesium sulphate, filtered and evaporated. The crude product was recrystallized from ethanol to give 3-(4-(3,4-dimethoxy-5-nitrophenyl)-1,3,5-triazin-2-yl)-2-(trifluoromethyl)pyridine 1-oxide, 1.27 g (75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08907099B2
Source datasetuspto-grants-2014_12
ORD IDord-30a909349a6c43a7927ed5e58976c8df
Source noteuspto-grants-2014_12