HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 2-[(N,N-Dimethylamino)methyl]-6-[4-[(4-methoxybenzoyl)amino]benzyloxy]tetralin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | p-Anisoyl chloride | HCID 7477 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 6-(4-Aminobenzyloxy)-2-[(N,N-dimethylamino)methyl]tetralin | HCID 21939722 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-[(N,N-Dimethylamino)methyl]-6-[4-[(4-methoxybenzoyl)amino]benzyloxy]tetralin | HCID 21939788 | — |
Reaction Steps
p-Anisoyl chloride (0.20 ml) was added dropwise to pyridine solution (6 ml) of 6-[(4-aminobenzyl)oxy]-2-[(N,N-dimethylamino)methyl]tetralin (300 mg) under ice-cooling, which was stirred at room temperature for 30 minutes. 10% aqueous potassium carbonate solution was added to the reaction mixture, and extraction was conducted using ethyl acetate. The organic layer was washed with water and saturated aqueous sodium chloride solution, dried, and then concentrated. The residue was purified using alumina column chromatography (development solvent: ethyl acetate), and recrystallized (THF-IPE) to give the titled compound (300 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07115750B1 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-bea50ce190f74682ac34c5133ddb52df |
| Source note | uspto-grants-2006_10 |