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HRID 1450183作成日:2026年10月25日

Ammonium Hydroxide → 8-Chloro-11-(4-benzyl-1-piperazinyl)-dibenz[b,f][1,4]oxazepine

https://huagongshe.com/reaction/1450183

反応式

関与物質

役割名称HCID仕込み量
反応物Ammonium HydroxideHCID 14923—
反応物1-BenzylpiperazineHCID 75994—
反応物2-Chlorodibenz(b,f)-1,4-oxazepin-11(10H)-oneHCID 76619—
触媒Titanium TetrachlorideHCID 24193—
溶媒TolueneHCID 1140—
生成物8-Chloro-11-(4-benzyl-1-piperazinyl)-dibenz[b,f][1,4]oxazepineHCID 988745195.6%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05602120
出典データセットuspto-grants-1997_02
ORD IDord-5670831b8985425885dfe469db6ea6a7
出典メモuspto-grants-1997_02