HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
4-Aminophenol → 4-(4-aminophenoxy)-N,N-dimethylpyridine-2-carboxamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 4-Aminophenol | HCID 403 | — |
| Edukt | Dimethylamine | HCID 674 | — |
| Edukt | 4-chloro-N,N-dimethylpyridine-2-carboxamide | HCID 4962252 | — |
| Edukt | 4-chloropyridine-2-carbonyl Chloride | HCID 11095146 | — |
| Produkt | 4-(4-aminophenoxy)-N,N-dimethylpyridine-2-carboxamide | HCID 23614563 | — |
Reaktionsschritte
Entry 24; 4-Chloropyridine-2-carbonyl chloride was reacted with dimethylamine according to Method A2, Step 3b. The resulting 4-chloro-N,N-dimethyl-2-pyridinecarboxamide was reacted with 4-aminophenol according to Method A2, Step 4 to give 4-(2-(N,N-dimethylcarbamoyl)-4-pyridyloxy)aniline. 5-(Trifluoromethyl)-2-methoxyaniline was converted into 5-(trifluoromethyl)-2-methoxyphenyl isocyanate according to Method B1. 5-(Trifluoromethyl)-2-methoxyphenyl isocyanate was reacted with 4-(2-(N,N-dimethylcarbamoyl)-4-pyridyloxy) an line according to Method C1a to afford the urea.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US07897623B2 |
| Quelldatensatz | uspto-grants-2011_03 |
| ORD ID | ord-c2a4d9ae63384325a095aaee73a3f8a9 |
| Quellennotiz | uspto-grants-2011_03 |