戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 29567作成日:2026年10月25日

4-Ethylbenzene-1-sulfonyl chloride → N-[4-chloro-2-(pyridine-4-carbonyl)-phenyl]-4-ethyl-benzenesulfonamide

https://huagongshe.com/reaction/29567

反応式

関与物質

役割名称HCID仕込み量
反応物4-Ethylbenzene-1-sulfonyl chlorideHCID 570959—
反応物(2-Amino-5-chlorophenyl)-pyridin-4-yl methanoneHCID 10214538—
生成物N-[4-chloro-2-(pyridine-4-carbonyl)-phenyl]-4-ethyl-benzenesulfonamideHCID 10431143—

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 102 mg of 4-ethyl-benzenesulfonyl chloride. 1H-NMR (400 MHz, CDCl3): δ 0.94 (t, 3H, J=7.6 Hz), 2.38 (q, 2H, J=15.2 Hz, 7.6 Hz), 6.94 (d, 2H, J=6.8 Hz), 7.16 (m, 2H), 7.23 (m, 1H), 7.30 (m, 4H), 8.60 (b, 2H), 9.73 (b,1H). MS: m/z 401.1 (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-8931a765bfef41b294b3c2f7459f4865
出典メモuspto-grants-2008_09