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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 347348생성일: 2026년 10월 24일

4-acetyl-N,N-dimethylbenzene-1-sulfonamide → HCID 11168050, 화합물

https://huagongshe.com/ko/reaction/347348

반응식

참여 물질

역할이름HCID투입량
반응물4-acetyl-N,N-dimethylbenzene-1-sulfonamideHCID 2064041—
반응물2,4-dimethoxy-5-(1-methyl-1H-indol-2-yl)benzaldehydeHCID 21981006—
생성물HCID 11168050HCID 1116805064%

반응 단계

The title compound was prepared in an analogous manner as Ex-1 using 4-acetyl-N,N-dimethyl-benzenesulfonamide (Ex-31A) and 2,4-dimethoxy-5-(1-methyl-1H-indol-2-yl)benzaldehyde (Ex-15A), 64% yield, yellow solid, mp 120–122° C. 1H-NMR (300 MHz, CDCl3) δ 8.18 (d, J=16 Hz, 1H), 8.12 (d, J=8 Hz, 2H), 7.88 (d, J=8 Hz, 2H), 7.69 (s, 1H), 7.64 (d, J=8 Hz, 1H), 7.48 (d, J=16 Hz, 1H), 7.36 (d, J=8 Hz, 1H), 7.22–7.27 (m, 1H), 7.11–7.16 (m, 1H), 6.59 (s, 1H), 6.50 (s, 1H), 4.11 (s, 3H), 3.90 (s, 3H), 3.59 (s, 3H), 2.74 (s, 6H). HRMS (ESI) Calcd. for C28H28N2O5S: 505.1797 (M+H)+; Found: 505.1797.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07173129B2
출처 데이터셋uspto-grants-2007_02
ORD IDord-3e487494273b4d3d8d17659020a2acf3
출처 메모uspto-grants-2007_02