HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Ethynyl-3-methoxybenzene → HCID 10105613, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Ethynyl-3-methoxybenzene | HCID 640753 | — |
| Reactant | 2-Bromo-6-methylpyridin-3-amine | HCID 14418051 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 10105613 | HCID 10105613 | 46.7% |
Reaction Steps
Following the same procedure as described in Example 1, (2-bromo-6-methyl-pyridin-3-yl)amine (200 mg, 1.07 mmol) reacted with (PPh3)2PdCl2 (37 mg, 0.05 mmol), Cul (10 mg, 0.05 mmol) and 1-ethynyl-3-methoxy-benzene (204 μl, 1.60 mmol) in triethylamine (5 ml) during 1.5 h. The crude residue was purified by flash chromatography (hexane/ethyl acetate 4:1) to yield 118 mg (0.50 mmol, 46%) of (2-(3-methoxy-phenylethynyl)-6-methyl-pyridin-3-yl)amine as a yellow brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07205411B2 |
| Source dataset | uspto-grants-2007_04 |
| ORD ID | ord-1c2ba9a75ebe43b8af57bd2ceb74e28c |
| Source note | uspto-grants-2007_04 |