HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,3-Difluoro-5-iodobenzene → (2-(3,5-Difluoro-phenylethynyl)-6-methyl-pyridin-3-yl)amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,3-Difluoro-5-iodobenzene | HCID 2778221 | — |
| Reactant | 2-Ethynyl-6-methylpyridin-3-amine | HCID 18454776 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | (2-(3,5-Difluoro-phenylethynyl)-6-methyl-pyridin-3-yl)amine | HCID 10332058 | 58% |
Reaction Steps
To a solution of Cul (4.3 mg, 23 μmol) in triethylamine (5 ml) were added (2-ethynyl-6-methyl-pyridin-3-yl)amine (60 mg, 0.45 mmol), (PPh3)2PdCl2 (16 mg, 23 μmol), and 1,3-difluoro-5-iodobenzene (109 mg, 0.45 mmol). The reaction mixture was stirred at room temperature for 20 h. The solvent was evaporated to afford a brown oil which was taken up in DCM and the solution was washed with water. The aqueous phase was extracted twice with DCM. The organic phases were dried over Na2SO4, filtered and concentrated. The crude residue was purified by flash chromatography (hexane/ethyl acetate 7:3) to yield 64 mg (0.26 mmol, 58%) of (2-(3,5-difluoro-phenylethynyl)-6-methyl-pyridin-3-yl)amine as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07205411B2 |
| Source dataset | uspto-grants-2007_04 |
| ORD ID | ord-99b7ae33a07f4627bf712d9e7b4b48c1 |
| Source note | uspto-grants-2007_04 |