HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2178582Erstellt: 24. Oktober 2026
Methoxyisopropylamine → 7-(3,5-Dimethylisoxazol-4-yl)-6-methoxy-N-(1-methoxypropan-2-yl)-3-nitroquinolin-4-amine
https://huagongshe.com/de/reaction/2178582
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methoxyisopropylamine | HCID 123458 | — |
| Edukt | 4-(4-Chloro-6-methoxy-3-nitroquinolin-7-yl)-3,5-dimethylisoxazole | HCID 57465580 | — |
| Lösungsmittel | 1,4-Dioxane | HCID 31275 | — |
| Produkt | 7-(3,5-Dimethylisoxazol-4-yl)-6-methoxy-N-(1-methoxypropan-2-yl)-3-nitroquinolin-4-amine | HCID 70980504 | 111,5% |
Reaktionsschritte
To a solution of 4-(4-chloro-6-methoxy-3-nitroquinolin-7-yl)-3,5-dimethylisoxazole (Manchester Organics) (20 g, 59.9 mmol) in 1,4-dioxane (200 ml) was added 1-methoxypropan-2-amine (31.6 ml, 300 mmol) and the reaction mixture heated at 70° C. for 1.5 h. The solvent was removed under reduced pressure and the resulting solid partitioned between ethyl acetate (3×750 ml) and water (750 ml). The organic layers were combined, dried (hydrophobic frit) and evaporated under reduced pressure to give 7-(3,5-dimethylisoxazol-4-yl)-6-methoxy-N-(1-methoxypropan-2-yl)-3-nitroq uinolin-4-amine (25.8 g), which was used without further purification in the subsequent step.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US09067936B2 |
|---|
| Quelldatensatz | uspto-grants-2015_06 |
|---|
| ORD ID | ord-aecf6af5387a40b59c6c8c01234ba708 |
|---|
| Quellennotiz | uspto-grants-2015_06 |
|---|