Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Quinazoline | HCID 9210 | — |
| Reactant | 4-Chloroquinoline | HCID 69140 | — |
| Reactant | 4-(Nitrophenoxy)quinoline | HCID 21890535 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Catalyst | HCID 178502593 | HCID 178502593 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(Aminophenoxy)quinoline | HCID 21890324 | — |
Reaction Steps
Next, 4-chloroquinoline derivative or a corresponding quinazoline derivative is allowed to act on nitrophenol in the presence of a suitable solvent or in the absence of a solvent to synthesize a 4-(nitrophenoxy)quinoline derivative or a corresponding quinazoline derivative which is then stirred in a suitable solvent, for example, N,N-dimethylformamide, in the presence of a catalyst, for example, palladium hydroxide-carbon or palladium-carbon, in a hydrogen atmosphere to give a 4-(aminophenoxy)quinoline derivative or a corresponding quinazoline derivative. Alternatively, a 4-chloroquinoline derivative or a corresponding quinazoline derivative may be allowed to act on aminophenol in the presence of a base, for example, sodium hydride, to give a 4-(aminophenoxy)quinoline derivative or a corresponding quinazoline derivative.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07169789B2 |
|---|
| Source dataset | uspto-grants-2007_01 |
|---|
| ORD ID | ord-69aa180b947e43e791ca73aaa5feb9f1 |
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| Source note | uspto-grants-2007_01 |
|---|