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HRID 29537作成日:2026年10月25日

p-Bromobenzenesulfonyl chloride → 4-Bromo-N-[4-chloro-2-(pyridine-3-carbonyl)-phenyl]-benzenesulfonamide

https://huagongshe.com/reaction/29537

反応式

関与物質

役割名称HCID仕込み量
反応物p-Bromobenzenesulfonyl chlorideHCID 7396—
反応物(2-Amino-5-chlorophenyl)(pyridin-3-yl)methanoneHCID 13549723—
溶媒PyridineHCID 1049—
生成物4-Bromo-N-[4-chloro-2-(pyridine-3-carbonyl)-phenyl]-benzenesulfonamideHCID 59788554—

反応手順

The title compound was prepared according to the general procedures for the synthesis of N-Aryl-benzenesulfonamides previously described using (2-amino-5-chloro-phenyl)-pyridin-3-yl-methanone 5 g (21.5 mmol) and 4-bromo-benzenesulfonyl chloride 5.78 g (21.5 mmol), in 150 ml anhydrous pyridine, overnight at 80° C., followed by flash column chromatography on silica gel to yield a salmon color solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07420055B2
出典データセットuspto-grants-2008_09
ORD IDord-f4a97278b0ad4c349f317955274e11f5
出典メモuspto-grants-2008_09