HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → {6-Methoxy-5-[2-methoxy-4-(trifluoromethoxy)phenyl]pyrazin-2-yl}[(4-methoxyphenyl)methyl]amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | (2-Methoxy-4-(trifluoromethoxy)phenyl)boronic acid | HCID 22490042 | — |
| Reactant | (5-Bromo-6-methoxypyrazin-2-yl)[(4-methoxyphenyl)methyl]amine | HCID 23595037 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | {6-Methoxy-5-[2-methoxy-4-(trifluoromethoxy)phenyl]pyrazin-2-yl}[(4-methoxyphenyl)methyl]amine | HCID 22249073 | 88.8% |
Reaction Steps
Tetrakis(triphenylphosphine)palladium(0) (100 mg) and potassium carbonate (2.0 M, 2.0 mL) are added to a stirred solution of (5-bromo-6-methoxypyrazin-2-yl)[(4-methoxyphenyl)methyl]amine (0.80 g, 2.50 mmol) and 2-methoxy-4-trifluoromethoxy benzeneboronic acid (1.75 g, 7.5 mmol) in toluene (25 mL). The mixture is heated to 85 C for 8 hours, cooled to room temperature, diluted with 2.0 M sodium hydroxide and extracted twice with 1:1 hexane-ethyl ether. The combined extracts are dried (sodium sulfate), filtered and concentrated. The residue is purified by flash chromatography, eluting with 60% hexanes in ether to give {6-methoxy-5-[2-methoxy-4-(trifluoromethoxy)phenyl]pyrazin-2yl}[(4-methoxyphenyl)methyl]amine (967 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07179807B2 |
| Source dataset | uspto-grants-2007_02 |
| ORD ID | ord-7a61a56c157344a2bcfaa2b196cbff3f |
| Source note | uspto-grants-2007_02 |