戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 11723作成日:2026年10月27日

Triethylamine → 2-(4-Chloro-2-cyanato-phenoxy)-1-[4-(4-fluoro-benzyl)-(2R)-2-methyl-piperazin-1-yl]-ethanone

https://huagongshe.com/reaction/11723

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Cyanogen BromideHCID 10476—
反応物2-(4-Chloro-2-hydroxy-phenoxy)-1-[4-(4-fluoro-benzyl)-(2R)-2-methyl-piperazin-1-yl]-ethanoneHCID 69655856—
溶媒DichloromethaneHCID 6344—
生成物2-(4-Chloro-2-cyanato-phenoxy)-1-[4-(4-fluoro-benzyl)-(2R)-2-methyl-piperazin-1-yl]-ethanoneHCID 69655365—

反応条件

温度-5 °C

反応手順

To a solution of 2-(4-chloro-2-hydroxy-phenoxy)-1-[4-(4-fluoro-benzyl)-(2R)-2-methyl-piperazin-1-yl]-ethanone (0.168 g, 0.427 mmol) in methylene chloride (2 mL) was added triethylamine (0.12 mL, 0.86 mmol). The solution was cooled to −5° C. via an acetone/ice bath then cyanogen bromide was added (0.22 mL, 0.66 mmol). The reaction was stirred at −5° C. for 30 minutes then concentrated in vacuo to give the crude title compound which was taken directly on to the next step (0.17 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07098212B2
出典データセットuspto-grants-2006_08
ORD IDord-43200a14bd5d42a5942f72c148bce99b
出典メモuspto-grants-2006_08