HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
4-Nitrobenzyl chloride → 4-(4-Chlorobenzoyl)-1-(4-nitrobenzyl)-1,3,4,5-tetrahydrobenzo[e][1,4]diazepin-2-on
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 4-Nitrobenzyl chloride | HCID 7482 | — |
| Edukt | Ethyl Acetate | HCID 8857 | — |
| Edukt | Sodium hydride | HCID 24758 | — |
| Edukt | 4-(4-Chlorobenzoyl)-1,3,4,5-tetrahydrobenzo[e][1,4]diazepin-2-on | HCID 22632554 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 4-(4-Chlorobenzoyl)-1-(4-nitrobenzyl)-1,3,4,5-tetrahydrobenzo[e][1,4]diazepin-2-on | HCID 22632469 | — |
Reaktionsschritte
110 mg (0.37 mmol) of 4-(4-chlorobenzoyl)-1,3,4,5-tetrahydrobenzo[e][1,4]diazepin-2-on was dissolved in 5 ml of DMF. 17 mg (0.44 mmol) of sodium hydride was added to the obtained solution, and they were stirred at room temperature for 30 minutes. 76 mg (0.44 mmol) of 4-nitrobenzyl chloride was added to the obtained mixture and they were stirred at 60° C. overnight. The reaction mixture was treated with ethyl acetate as the extracting solvent by an ordinary method to obtain the crude product. After the purification by the silica gel column chromatography, the title compound was obtained.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06825191B2 |
| Quelldatensatz | uspto-grants-2004_11 |
| ORD ID | ord-01905b1ade1a4255994994f9bea9683c |
| Quellennotiz | uspto-grants-2004_11 |