戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 17854作成日:2026年10月25日

Bromine → 3,7-dibromo-2,3,4,5-tetrahydro-1H-1-benzazepin-2-one

https://huagongshe.com/reaction/17854

反応式

関与物質

役割名称HCID仕込み量
反応物BromineHCID 24408—
反応物2,3,4,5-tetrahydro-1H-1-benzazepineHCID 576503—
反応物3-Bromo-1,3,4,5-tetrahydro-2H-1-benzazepin-2-oneHCID 2757184—
溶媒Acetic AcidHCID 176—
生成物3,7-dibromo-2,3,4,5-tetrahydro-1H-1-benzazepin-2-oneHCID 58857219—

反応手順

Scheme 5 describes an example of bromination of a tetrahydrobenzazepine intermediate. Bromine can be added slowly to commercially available 3-bromo-1,3,4,5-tetrahydro-1-benzazepin-2-one in acetic acid with stirring at room temperature to provide the useful intermediate 3,7-dibromo-1,3,4,5-tetrahydro-1-benzazepin-2-one, which can be used in many transformations described herein. Bromination using similar conditions can be carried out on other amino aryl cores described herein to provide intermediates for transformation to the compounds of the invention described in Schemes 8, 9 and 10.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07741317B2
出典データセットuspto-grants-2010_06
ORD IDord-5dc8d1a4d7a64005aaa34528a13933b9
出典メモuspto-grants-2010_06