HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
p-Anisoyl chloride → Ethyl 3-(4-methoxybenzamido)-1H-indole-2-carboxylate
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | p-Anisoyl chloride | HCID 7477 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | Ethyl 3-amino-1H-indole-2-carboxylate | HCID 732887 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Lösungsmittel | Ethyl Acetate | HCID 8857 | — |
| Produkt | Ethyl 3-(4-methoxybenzamido)-1H-indole-2-carboxylate | HCID 751363 | 94,1% |
Reaktionsschritte
To a solution of 3-amino-2-indolecarboxylic acid ethyl ester (500 mg, 2.45 mmol) and triethylamine (272 mg, 2.70 mmol) in methylene chloride (5 mL) was added anisoyl chloride (418 mg, 2.45 mmol). The resulting mixture was stirred for 18 h at room temperature. The reaction mixture was diluted with ethyl acetate and washed with water. The organic phase was washed with 1 N aqueous hydrochloric acid, dried (sodium sulfate), filtered, and concentrated in vacuo to provide a yellow solid. Recrystallization from hexane/ethyl acetate provided 780 mg (94%) of the title compound as a yellow solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06313151B1 |
| Quelldatensatz | uspto-grants-2001_11 |
| ORD ID | ord-733b89533ee64034b26e3ebb33f90f79 |
| Quellennotiz | uspto-grants-2001_11 |