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HRID 29586作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/29586

反応式

関与物質

役割名称HCID仕込み量
反応物4-Methanesulfonylbenzene-1-sulfonyl chlorideHCID 2735182—
反応物(2-Amino-5-chlorophenyl)(pyridin-3-yl)methanoneHCID 13549723—
生成物N-[4-Chloro-2-(pyridine-3-carbonyl)-phenyl]-4-methanesulfonyl-benzenesulfonamideHCID 11744511—

反応手順

The title compound was prepared according to the general procedure for the synthesis of N-Aryl-benzenesulfonamides previously described using (2-amino-5-chloro-phenyl)-pyridin-3-yl-methanone and 4-Methanesulfonyl-benzenesulfonyl chloride and purified by HPLC. 1H NMR (CDCl3): δ 3.01 (s, 3H), 7.36-7.37 (d, J=2.4 Hz, 1H), 7.43 (m, 1H), 7.54 & 7.57 (dd, J=8.8 Hz, 2.4 Hz, 1H), 7.70-7.73 (m, 1H), 7.77 (d, J=8.8 Hz, 1H), 7.90 (m, 4H), 8.59 (d, J=2.0 Hz, 1H), 8.80 & 8.82 (dd, J=4.8 Hz,1.6 Hz, 1H), 9.98 (s, 1H). MS: M/z 450.9 (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-aa447aa95b854353b49d95e91131fe0c
出典メモuspto-grants-2008_09