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HRID 1450191作成日:2026年10月25日

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/1450191

反応式

関与物質

役割名称HCID仕込み量
反応物1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
反応物1-NonylpiperazineHCID 2737098—
反応物8,11-Dichlorodibenzo[b,f][1,4]oxazepineHCID 18940415—
溶媒AcetonitrileHCID 6342—
生成物8-Chloro-11-(4-nonyl-1-piperazinyl)dibenz[b,f][1,4]oxazepineHCID 9932912—

反応手順

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 title compound was obtained as a white solid (0.15 g, 28%), m.p. 64°-66° C., MS 440 (M+ +1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05602121
出典データセットuspto-grants-1997_02
ORD IDord-2a86a5ccf062426180fdfd456bd589e3
出典メモuspto-grants-1997_02