HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
m-Formylbenzonitrile → [5-(5,6-Difluoro-1H-indol-2yl)-2-methoxy-phenyl]-(3-cyano-benzyl)-amine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | m-Formylbenzonitrile | HCID 90670 | — |
| Edukt | Sodium Bicarbonate | HCID 516892 | — |
| Edukt | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Edukt | 5-(5,6-difluoro1H-indol-2-yl)-2-methoxy-phenylamine | HCID 9943439 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | [5-(5,6-Difluoro-1H-indol-2yl)-2-methoxy-phenyl]-(3-cyano-benzyl)-amine | HCID 10293683 | 64,2% |
Reaktionsschritte
3-Cyanobenzaldehyde (0.262 g, 2.0 mmol) was added to a stirred mixture of 5-(5,6-difluoro-1H-indol-2-yl)-2-methoxy-phenylamine (0.548 g, 2.0 mmol) in methylene chloride (125 mL), followed by acetic acid (0.2 g). The resulting mixture was stirred at room temperature for 1 hour. Sodium triacetoxyborohydride (0.46 g, 2.0 mmol) was added in one portion, and the resulting homogeneous solution stirred at room temperature for 3 days. Saturated aqueous sodium bicarbonate solution (100 mL) was added and the mixture stirred for 2 hours. The mixture was shaken, the organic layer separated and dried over Na2S4. The solvent was evaporated to give a white solid. Recrystallization from methanol gave the product (500 mg), mp 154-155° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06858739B2 |
| Quelldatensatz | uspto-grants-2005_02 |
| ORD ID | ord-f64a7462a3de4a72833949b2f318e2f3 |
| Quellennotiz | uspto-grants-2005_02 |