Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 2-Nitrophenol | HCID 6947 | — |
| Edukt | Quinazoline | HCID 9210 | — |
| Edukt | 4-Chloroquinoline | HCID 69140 | — |
| Edukt | 4-(Nitrophenoxy)quinoline | HCID 21890535 | — |
| Katalysator | HCID 178418390 | HCID 178418390 | — |
| Katalysator | HCID 178502593 | HCID 178502593 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | Quinazoline | HCID 9210 | — |
| Produkt | 4-(Aminophenoxy)quinoline | HCID 21890324 | — |
Reaktionsschritte
Next, a 4-(aminophenoxy)quinoline derivative or a corresponding quinazoline derivative is produced by reacting nitrophenol with the 4-chloroquinoline derivative or corresponding quinazoline derivative in the presence or absence of a suitable solvent to synthesize a 4-(nitrophenoxy)quinoline derivative or a corresponding quinazoline derivative, then conducting stirring in a suitable solvent, for example, N,N-dimethyl formamide, in the presence of a catalyst, for example, palladium hydroxide-carbon or palladium-carbon, under a hydrogen atmosphere. Alternatively, the 4-(aminophenoxy)quinoline derivative or a corresponding quinazoline derivative may also be produced by reacting amino phenol with a 4-chloroquinoline derivative or a corresponding quinazoline derivative in the presence of a base, for example, sodium hydride.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US07598258B2 |
|---|
| Quelldatensatz | uspto-grants-2009_10 |
|---|
| ORD ID | ord-84c2fb696c4a42c8b8fd59fb00e33e09 |
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| Quellennotiz | uspto-grants-2009_10 |
|---|