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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 7028생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물cis-2-(4-Chlorobenzenesulfonylamino)-cyclohexanecarboxylic acid amideHCID 69655699—
반응물(1S,2S)-2-(4-chlorobenzenesulfonylamino)-cyclohexanecarboxylic acidHCID 69656119—
생성물(1S,2S)-2-(4-Chlorobenzenesulfonylamino)-cyclohexanecarboxylic acid amideHCID 6965607796%

반응 단계

(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)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07084178B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-8edc0774097f4d56800f94b9e74b6e5c
출처 메모uspto-grants-2006_08