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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 10706생성일: 2026년 10월 24일

4-Acetylbenzenesulphonamide → 2-{2,4-Dimethoxy-5-[3-oxo-3-(4-aminosulfonyl-phenyl)-E-propenyl]-phenyl}-indole-1-carboxylic acid tert-butyl ester

https://huagongshe.com/ko/reaction/10706

반응식

참여 물질

역할이름HCID투입량
반응물4-AcetylbenzenesulphonamideHCID 74065—
반응물2-(5-Formyl-2,4-dimethoxyphenyl)indole-1-carboxylic acid tert-butyl esterHCID 16116307—
생성물2-{2,4-Dimethoxy-5-[3-oxo-3-(4-aminosulfonyl-phenyl)-E-propenyl]-phenyl}-indole-1-carboxylic acid tert-butyl esterHCID 1041544440%

반응 단계

The title compound was prepared by condensing 4-acetyl-benzenesulfonamide (Ex-26A) and 2-(5-formyl-2,4-dimethoxy-phenyl)-indole-1-carboxylic acid tert-butyl ester (Ex-36A) in a similar manner as described in Ex-22. Yellow solid, 40% yield, mp 120–122° C. 1H-NMR (CDCl3) δ 8.01–8.19 (m, 6H), 7.68 (s, 1H), 7.56 (d, J=8 Hz, 1H), 7.46 (d, J=16 Hz, 1H), 7.21–7.35 (m, 2H), 6.53 (d, J=14 Hz, 2H), 5.01 (s, 2H), 4.00 (s, 3H), 3.85 (s, 3H), 1.42 (s, 9H), MS m/z=563 ([M+H]+). HRMS (ES+) Calcd. for C30H30N2O7S: 563.1852. Found: 563.1862.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07094801B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-5d7a874c547f4e10bf5fff9813a4f7a7
출처 메모uspto-grants-2006_08