戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 2395234作成日:2026年10月26日

Dimethylformamide → HCID 18971342、化合物

https://huagongshe.com/reaction/2395234

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Sodium hydrideHCID 24758—
反応物8-Chloro-11-(4-benzyl-1-piperazinyl)-dibenz[b,f][1,4]oxazepineHCID 9887451—
生成物HCID 18971342HCID 18971342—

反応条件

温度0 °C

反応手順

To a stirred solution of 11-(1-piperazinyl)dibenz[b,f][1,4]oxazepine (2.79 g, 10.0 mmol) (prepared from 10,11-dihydrodebenz[b,f][1,4]oxazepine-11-one, Aldrich and piperazine, as in example 1) in DMF (25 mL) was added sodium hydride (0.56 g, 60% in oil, 14 mmol) at 0° C. under argon. The mixture was stirred at 0° C. for 10 minutes at room temperature for 20 minutes, and then treated with β-bromo-ο-tolunitrile (2.35 g, 12.0 mmol, Aldrich). The resulting mixture was stirred at room temperature overnight and quenched with saturated ammonium chloride solution (25 mL). The mixture was separated and extracted with ethyl acetate (3×50 mL). The combined organic phase was dried over magnesium sulfate and filtered. The filtrate was 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 (2.34 g, 59%), m.p. 136°-138° C.; MS 395 (M+ +1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05814628
出典データセットuspto-grants-1998_09
ORD IDord-84c079150d374caeb084e5422e57e433
出典メモuspto-grants-1998_09