HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → N-(4'-chlorobiphenyl-2-yl)-3-trifluoromethyl-pyrazine-2-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Amino-4'-chlorobiphenyl | HCID 262261 | — |
| Reactant | 2-Pyrazinecarbonyl chloride, 3-(trifluoromethyl)- | HCID 87134781 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(4'-chlorobiphenyl-2-yl)-3-trifluoromethyl-pyrazine-2-carboxamide | HCID 66751032 | 85% |
Reaction Steps
Triethylamine (0.32 g: 1.5 mmole) was added to a solution of 4′-chlorobiphenyl-2-ylamine (0.3 g: 1.5 mmole) and 3-trifluoromethylpyrazine-2-carboxylic acid chloride (0.32 g: 1.5 mmole) in THF (10 mL), followed by stirring at room temperature for 2 hours. Water was added to the reaction mixture to suspend the reaction, followed by extraction with ethyl acetate. The ethyl acetate layer was dried over anhydrous sodium sulfate and concentrated in vacuo, and the residue was purified by silica gel column chromatography to give the subject compound (0.47 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08168638B2 |
| Source dataset | uspto-grants-2012_05 |
| ORD ID | ord-3fc1a1ebd7174e0e81979d453b229a3f |
| Source note | uspto-grants-2012_05 |