HuagongsheHuagongshe Chemistry Print Report · For research reference only
P-Anisidine → 3-(4-Methoxybenzoyl)amino-N-(4-methoxyphenyl)-2-indolecarboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | P-Anisidine | HCID 7732 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 3-(4-Methoxybenzoyl)amino-2-indolecarboxylic acid | HCID 12069549 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(4-Methoxybenzoyl)amino-N-(4-methoxyphenyl)-2-indolecarboxamide | HCID 15908565 | 14.2% |
Reaction Steps
To a solution p-anisidine (79 mg, 0.645 mmol) in methylene chloride (5 mL) was added 3-(4-methoxybenzoyl)amino-2-indolecarboxylic acid (200 mg, 0.645 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (247 mg, 1.29 mmol), and 4-dimethylaminopyridine (8.0 mg, 0.065 mmol). The resulting solution was stirred at room temperature for 6 h. The resulting precipitate was collected via vacuum filtration to provide 38 mg (14%) of the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06586459B2 |
| Source dataset | uspto-grants-2003_07 |
| ORD ID | ord-ea68df5daac349e185019f1ba29715da |
| Source note | uspto-grants-2003_07 |