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HRID 7028作成日:2026年10月24日

cis-2-(4-Chlorobenzenesulfonylamino)-cyclohexanecarboxylic acid amide → (1S,2S)-2-(4-Chlorobenzenesulfonylamino)-cyclohexanecarboxylic acid amide

https://huagongshe.com/ja/reaction/7028

反応式

関与物質

役割名称HCID仕込み量
反応物cis-2-(4-Chlorobenzenesulfonylamino)-cyclohexanecarboxylic acid amideHCID 69655699—
反応物(1S,2S)-2-(4-chlorobenzenesulfonylamino)-cyclohexanecarboxylic acidHCID 69656119—
生成物(1S,2S)-2-(4-Chlorobenzenesulfonylamino)-cyclohexanecarboxylic acid amideHCID 6965607796%

反応手順

(1S,2S)-2-(4-Chlorobenzenesulfonylamino)-cyclohexanecarboxylic acid amide was synthesized from (1S,2S)-2-(4-chlorobenzenesulfonylamino)-cyclohexanecarboxylic acid (0.76 mmol) according to the method described for the preparation of (1R,2S)-2-(4-chlorobenzenesulfonylamino)-cyclohexanecarboxylic acid amide. The crude product (230 mg) was obtained in 96% yield and carried into the next reaction without purification: 1H NMR (300 Mz, CDCl3) δ 7.72 (d, 2 H, J=8.4), 7.42 (d, 2 H, J=8.8), 3.23 (m, 1 H), 2.13 (m, 1 H), 1.85 (m, 1 H), 1.65 (m,3 H), 1.42 (m, 1 H), 1.13 (m, 3 H); MS m/e 339 (M+Na)+.

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-8edc0774097f4d56800f94b9e74b6e5c
出典メモuspto-grants-2006_08