戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 29556作成日:2026年10月24日

3-Cyanobenzene-1-sulfonyl chloride → N-[4-Chloro-2-(pyridine-4-carbonyl)-phenyl]-3-cyano-benzenesulfonamide

https://huagongshe.com/ja/reaction/29556

反応式

関与物質

役割名称HCID仕込み量
反応物3-Cyanobenzene-1-sulfonyl chlorideHCID 2801360—
反応物(2-Amino-5-chlorophenyl)-pyridin-4-yl methanoneHCID 10214538—
生成物N-[4-Chloro-2-(pyridine-4-carbonyl)-phenyl]-3-cyano-benzenesulfonamideHCID 10453443—

反応手順

The title compound was prepared according to the general procedure for the synthesis of N-Aryl-benzenesulfonamides previously described using 116 mg of (2-amino-5-chloro-phenyl)-pyridin-4-yl-methanone and 100 mg of 3-cyano-benzenesulfonyl chloride. 1H-NMR (400 MHz, CDCl3): δ 7.36 (d, 1H, J=2.4 Hz), 7.57-7.62 (m, 4H), 7.68 (d,1H, J=8.8 Hz), 7.80 (m,1H), 8.04 (m, 2H), 8.90 (dd, 2H, J=4.8 Hz, 1.6 Hz), 10.3 (b, 1H). MS: m/z 398.8 (M++1).

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-a042c8d051bd4a2781ce364f4ae09560
出典メモuspto-grants-2008_09