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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Edukt1-NonylpiperazineHCID 2737098—
Edukt8,11-Dichlorodibenzo[b,f][1,4]oxazepineHCID 18940415—
LösungsmittelAcetonitrileHCID 6342—
Produkt8-Chloro-11-(4-nonyl-1-piperazinyl)dibenz[b,f][1,4]oxazepineHCID 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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05834459
Quelldatensatzuspto-grants-1998_11
ORD IDord-b813a62d14e3499daf423c279dcf902a
Quellennotizuspto-grants-1998_11