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HRID 7027作成日:2026年10月24日

4-Chlorobenzenesulfonyl chloride → cis-2-(4-Chlorobenzenesulfonylamino)-cyclohexanecarboxylic acid amide

https://huagongshe.com/ja/reaction/7027

反応式

関与物質

役割名称HCID仕込み量
反応物4-Chlorobenzenesulfonyl chlorideHCID 7398—
反応物TriethylamineHCID 8471—
反応物cis-2-AminocyclohexanecarboxamideHCID 2724813—
溶媒DichloromethaneHCID 6344—
生成物cis-2-(4-Chlorobenzenesulfonylamino)-cyclohexanecarboxylic acid amideHCID 6965569945.1%

反応手順

To a solution of cis-2-aminocyclohexanecarboxylic acid amide (2.0 g, 14.0 mmol), and triethylamine (3.9 mL, 28 mmol) in dichloromethane (100 mL) was added 4-chlorobenzenesulfonyl chloride (2.95 g, 14.0 mmol). The resulting solution was stirred at room temperature for 18 h. The reaction was then diluted with dichloromethane (200 mL) and washed with H2O, 1.0 M HCl, brine, and dried over Na2SO4. Further purification by flash chromatography (silica gel, 1% to 10% MeOH/CHCl3) afforded cis-2-(4-chlorobenzenesulfonylamino)-cyclohexanecarboxylic acid amide (2.0 g) as a white solid in 45% yield over three steps: 1H NMR (DMSO-d6) δ 7.82 (m, 2 H), 7.63 (m, 2 H), 7.56 (d, 1 H, J=7.0 Hz), 7.22 (s br, 1 H), 6.80 (s br, 1 H), 3.43 (m, 1 H), 2.37 (m,1 H), 1.72 (m, 2 H), 1.45 (m, 3 H), 1.15 (m, 3 H); MS m/e 317.05 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07084178B2
出典データセットuspto-grants-2006_08
ORD IDord-5401af972bfd4b98b671d0bcf01afd38
出典メモuspto-grants-2006_08