HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
N-(2-Aminophenyl)-4-methoxybenzamide → N1-(4-Methoxybenzoyl)-N2-(5-chlorobenzofuran-2-ylcarbonyl)-1,2-benzenediamine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | N-(2-Aminophenyl)-4-methoxybenzamide | HCID 785232 | — |
| Edukt | 5-Chloro-1-benzofuran-2-carboxylic acid | HCID 937838 | — |
| Edukt | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Katalysator | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | N1-(4-Methoxybenzoyl)-N2-(5-chlorobenzofuran-2-ylcarbonyl)-1,2-benzenediamine | HCID 21352766 | 60,1% |
Reaktionsschritte
To a solution of N1-(4-methoxybenzoyl)-1,2-benzenediamine (200 mg, 0.826 mmol) in methylene chloride (5 mL) was added 5-chlorobenzofuran-2-carboxylic acid (162 mg, 0.826 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (316 mg, 1.65 mmol), and 4-dimethylaminopyridine (10 mg, 0.083 mmol), The resulting solution was stirred at room temperature for 6 h. The resulting precipitate was collected via vacuum filtration to provide 209 mg (60%) of the title compound as an amorphous off-white solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06605626B2 |
| Quelldatensatz | uspto-grants-2003_08 |
| ORD ID | ord-7d9cc5b1f30945c98294dd9775630341 |
| Quellennotiz | uspto-grants-2003_08 |