HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 86628083, compound → 5-(3,4-Dimethoxy-5-nitrophenyl)-3-(2-(trifluoromethyl)pyridin-3-yl)-1,2,4-triazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 86628083 | HCID 86628083 | — |
| Reactant | N'-amino-2-(trifluoromethyl)pyridine-3-carboximidamide | HCID 87543466 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-(3,4-Dimethoxy-5-nitrophenyl)-3-(2-(trifluoromethyl)pyridin-3-yl)-1,2,4-triazine | HCID 68701881 | — |
Reaction Steps
To a stirred solution of (Z)-2-(trifluoromethyl)nicotinohydrazonamide (1.02 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. It was 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 5-(3,4-dimethoxy-5-nitrophenyl)-3-(2-(trifluoromethyl)pyridin-3-yl)-1,2,4-triazine, 1.628 g (80%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08536203B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-69bb41e3d1e54a1b9ebe116feed77f24 |
| Source note | uspto-grants-2013_09 |