HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1717276Erstellt: 26. Oktober 2026
Potassium Carbonate → 4-azido-N-[2-(4-methylpiperazin-1-yl)ethyl]benzamide
https://huagongshe.com/reaction/1717276
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Potassium Carbonate | HCID 11430 | — |
| Edukt | 1-Methylpiperazine | HCID 53167 | — |
| Edukt | 4-azido-N-(2-bromoethyl)benzamide | HCID 85775432 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | 4-azido-N-[2-(4-methylpiperazin-1-yl)ethyl]benzamide | HCID 86629801 | 32,2% |
Reaktionsschritte
4-Azido-N-(2-bromoethyl)benzamide (2.0 g) obtained in Example 63a) and potassium carbonate (1.34 g, 9.70 mmol, 1.0 eq.) were suspended in acetonitrile (40 ml), N-methylpiperazine (1.63 ml, 14.6 mmol, 1.5 eq.) was added, and the mixture was stirred at room temperature for 16 hr and at 75° C. for 7 hr. The reaction mixture was concentrated, diluted with water (40 ml) and washed with ethyl acetate-hexane (2:1, 50 ml). The organic layer was extracted twice with water (20 ml). The aqueous layers were combined, concentrated, saturated with sodium chloride and extracted with ethyl acetate (40 ml and 30 ml). The organic layers were combined, dried over anhydrous sodium sulfate and concentrated at 30° C. or below to give the title compound as a pale-yellow solid (0.69 g, 2.39 mmol, 24.7%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US07803822B2 |
|---|
| Quelldatensatz | uspto-grants-2010_09 |
|---|
| ORD ID | ord-f1407eb0a6154940b8bc473978689490 |
|---|
| Quellennotiz | uspto-grants-2010_09 |
|---|