HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Ammonium Hydroxide → 8-Chloro-11-(4-benzyl-1-piperazinyl)-dibenz[b,f][1,4]oxazepine
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Ammonium Hydroxide | HCID 14923 | — |
| Edukt | 1-Benzylpiperazine | HCID 75994 | — |
| Edukt | 2-Chlorodibenz(b,f)-1,4-oxazepin-11(10H)-one | HCID 76619 | — |
| Katalysator | Titanium Tetrachloride | HCID 24193 | — |
| Lösungsmittel | Toluene | HCID 1140 | — |
| Produkt | 8-Chloro-11-(4-benzyl-1-piperazinyl)-dibenz[b,f][1,4]oxazepine | HCID 9887451 | 95,6% |
Reaktionsschritte
To a stirred solution of 8-chloro-10,11-dihydro-dibenz[b,f][1,4]oxazepin-11-one (0.3 g; 1.22 mmol) in dry toluene (10 mL) at room temperature was added 1-benzyl piperazine (1.0 mL; 5.61 mmol; Aldrich) followed by the dropwise addition of TiCl4 (1M in toluene, 1.47 mL; 1.47 mmol). The reaction mixture was refluxed for 2 hours, cooled to room temperature and then poured into an ammonium hydroxide solution (30%, 50 mL). The resulting mixture was extracted with dichloromethane (4×50 mL), and the combined organic phases were then dried (K2CO3) and concentrated. Purification of the product was conducted on silica gel using ethyl acetate:hexane (5:1→4:1) as the eluant to give 0.471 g (95%) of the title compound as a yellow solid; m.p. 50°-52° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05602120 |
| Quelldatensatz | uspto-grants-1997_02 |
| ORD ID | ord-5670831b8985425885dfe469db6ea6a7 |
| Quellennotiz | uspto-grants-1997_02 |