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HRID 1765498作成日:2026年10月25日

Benzenesulfonyl chloride, 3,4-dichloro- → N-(2-benzoyl-4-chloro-phenyl)-3,4-dichloro-benzenesulfonamide

https://huagongshe.com/reaction/1765498

反応式

関与物質

役割名称HCID仕込み量
反応物Benzenesulfonyl chloride, 3,4-dichloro-HCID 7383—
反応物2-Amino-5-chlorobenzophenoneHCID 12870—
生成物N-(2-benzoyl-4-chloro-phenyl)-3,4-dichloro-benzenesulfonamideHCID 11247684—

反応手順

The title compound was prepared according to the general procedure for the synthesis of N-Aryl-benzenesulfonamides previously described using 115 mg of (2-amino-5-chloro-phenyl)-phenyl-methanone and 123 mg of 3,4-Dichloro-benzenesulfonyl chloride. 1H-NMR (400 MHz, CDCl3): δ 7.25 (d, 1H, J=8.8 Hz), 7.36–39 (m, 3H), 7.43–47 (m, 3H), 7.53 (dd, 1H, J=8.8 Hz, 2.4 Hz), 7.61 (m, 1H), 7.65 (m, 1H), 7.73 (d, 1H, J=8.8 Hz), 9.56 (s, 1H). MS: m/z 440.7 (M++1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07227035B2
出典データセットuspto-grants-2007_06
ORD IDord-ed522b25da154a67a54218b6776b6db8
出典メモuspto-grants-2007_06