HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
2-(2-Azabicyclo[2.2.2]oct-2-yl)-6-nitroquinoline → 2-(2-Azabicyclo[2.2.2]oct-2-yl)quinolin-6-amine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 2-(2-Azabicyclo[2.2.2]oct-2-yl)-6-nitroquinoline | HCID 22018884 | — |
| Katalysator | Palladium hydroxide | HCID 9942167 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | 2-(2-Azabicyclo[2.2.2]oct-2-yl)quinolin-6-amine | HCID 22018930 | — |
Reaktionsschritte
The product of Step A and palladium hydroxide on carbon (1.3 g, 20% by wt) was suspended in methanol (100 mL) and ethyl acetate (100 mL). The resulting mixture was degassed then stirred under hydrogen atmosphere (balloon) for 6 h. The reaction mixture was filtered through filter aid and the solvent removed under vacuum. The resulting oil was dissolved in ethyl acetate and the solvent removed under vacuum. The resulting oil was suspended in ether and triturated until crystallization occurred. The solids were filtered and washed with ice-cold ether then dried under vacuum to afford the product as a brown solid, MS: m/z 254 (MH+), which was used without further purification
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07084156B2 |
| Quelldatensatz | uspto-grants-2006_08 |
| ORD ID | ord-941df1acbb1249ef9c18b030f6937c2a |
| Quellennotiz | uspto-grants-2006_08 |