HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 3-Phenyl-2-p-tolylpyrido[2,3-b]pyrazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Tolylboronic acid | HCID 79799 | — |
| Reactant | 2-Chloro-3-phenylpyrido[2,3-b]pyrazine | HCID 86681858 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 3-Phenyl-2-p-tolylpyrido[2,3-b]pyrazine | HCID 59090400 | — |
Reaction Steps
2-Chloro-3-phenylpyrido[2,3-b]pyrazine (step 3) (175 mg, 0.724 mmol) in dry dioxane (4 ml) under nitrogen was treated with p-tolylboronic acid (108 mg, 0.797 mmol), potassium carbonate (200 mg, 1.448 mmol) in water (0.5 ml) and tetrakis(triphenylphosphine)palladium(0) (41.8 mg, 0.036 mmol). The resulting mixture was heated using microwave radiation at 150° C. for 1 hour. After cooling to RT, the mixture was diluted with water (100 ml) and extracted with DCM (×3). The combined organic extracts were washed with brine, dried over MgSO4 and filtered. The solvent was removed in vacuo and the crude product was purified by chromatography on silica eluting with 0-30% EtOAc/iso-hexane to afford the title compound as a yellow solid;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09132127B2 |
| Source dataset | uspto-grants-2015_09 |
| ORD ID | ord-928ef7a329204e63976d94e8f84dbada |
| Source note | uspto-grants-2015_09 |