HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminopyridine → (4-Benzyloxy-pyridin-2-yl)-pyridin-2-yl-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminopyridine | HCID 10439 | — |
| Reactant | 4-(Benzyloxy)-2-bromopyridine | HCID 15389199 | — |
| Reactant | HCID 178418922 | HCID 178418922 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (4-Benzyloxy-pyridin-2-yl)-pyridin-2-yl-amine | HCID 58545055 | 73% |
Reaction Steps
Compound I (2.325 mg, 8.80 mmol), 2-aminopyridine (911 mg, 9.68 mmol), tBuOK (1.481 g, 13.20 mmol), (±)-BINAP (219 mg, 0.35 mmol) and Pd2(dba)3 (201 mg, 0.22 mmol) were stirred in toluene (35 mL) at 90° C. under Ar(g) for 17 h. The reaction mixture was then diluted with CH2Cl2 (20 mL) and silica was added followed by the removal of the solvent under reduced pressure. The resulting dry loaded material was purified by silica gel column chromatography eluting with hexane/EtOAc (60:40 then 50:50) to furnish II as a yellow oil (1.773 g, 73%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09340503B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-26ba17396cc246e3af65201915259b2b |
| Source note | uspto-grants-2016_05 |