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HRID 355673Erstellt: 25. Oktober 2026
1,8-Diazabicyclo(5.4.0)undec-7-ene → 8-Chloro-11-(4-nonyl-1-piperazinyl)dibenz[b,f][1,4]oxazepine
https://huagongshe.com/reaction/355673
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Edukt | 1-Nonylpiperazine | HCID 2737098 | — |
| Edukt | 8,11-Dichlorodibenzo[b,f][1,4]oxazepine | HCID 18940415 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | 8-Chloro-11-(4-nonyl-1-piperazinyl)dibenz[b,f][1,4]oxazepine | HCID 9932912 | — |
Reaktionsschritte
The mixture of 8,11-dichlorodibenz[b,f][1,4]oxazepine (0.32 g, 1.19 mmol), 1-nonylpiperazine (0.38 g, 1.79 mmol) and 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) (0.72 mL, 0.73 g, 4.77 mmol) in acetonitrile (15 mL) was heated at reflux for 6 h. After the mixture was concentrated, water (20 mL) and ethyl acetate (20 mL) were added. The two phases were separated and the aqueous phase was extracted with ethyl acetate (2×20 mL). The combined ethyl acetate solution was dried over magnesium sulfate and filtered. The filtrate was then concentrated in vacuo to dryness and the residue was subjected to column chromatography using ethyl acetate/hexane (1/2) as the eluent. The compound 8-chloro-11-(4-nonyl-1-piperazinyl)dibenz[b,f][1,4]oxazepine was obtained as a white solid (0.15 g, 28%), m.p. 64°-66° C., MS 440 (M+ +1).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05834459 |
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| Quelldatensatz | uspto-grants-1998_11 |
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| ORD ID | ord-b813a62d14e3499daf423c279dcf902a |
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| Quellennotiz | uspto-grants-1998_11 |
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