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HRID 18893作成日:2026年10月24日

2-Amino-5-chlorobenzophenone → N-(2-benzoyl-4-chloro-phenyl)-2-fluoro-benzenesulfonamide

https://huagongshe.com/ja/reaction/18893

反応式

関与物質

役割名称HCID仕込み量
反応物2-Amino-5-chlorobenzophenoneHCID 12870—
反応物2-Fluorobenzenesulphonyl chlorideHCID 137761—
生成物N-(2-benzoyl-4-chloro-phenyl)-2-fluoro-benzenesulfonamideHCID 11315279—

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)-phenyl-methanone and 2-fluoro-benzenesulfonyl chloride. 1H NMR (CDCl3): δ (ppm): 6.88-6.93 (m, 1H), 7.16-7.20 (m, 1H), 7.38 (d, J=6.4 Hz, 1H), 7.41-7.46 (m, 4H), 7.52 (m, 2H), 7.58-7.62 (m, 1H), 7.70 (d, J=8.8 Hz, 1H), 7.81-7.85 (m, 1H), 10.10 (s, 1H). MS: m/z 390.0 (M++1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07741519B2
出典データセットuspto-grants-2010_06
ORD IDord-dff730c7ec79477badf56038b8a1d2aa
出典メモuspto-grants-2010_06