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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 528848생성일: 2026년 10월 26일

1H-Indole-5-sulfonamide → 7-Bromo-1-ethyl-1H-indole-5-sulfonamide

https://huagongshe.com/reaction/528848

반응식

참여 물질

역할이름HCID투입량
반응물1H-Indole-5-sulfonamideHCID 21683100—
반응물7-Bromo-1-ethylindoline-5-sulfonamideHCID 86718885—
생성물7-Bromo-1-ethyl-1H-indole-5-sulfonamideHCID 7106228332.3%

반응 단계

Following a procedure analogous to that for the synthesis of Intermediate 54, 7-bromo-1-ethylindoline-5-sulfonamide (Intermediate 76, 140 mg, 0.46 mmol) was converted to the title compound (45 mg, 31%). 1H NMR (DMSO-d6) δ 8.04 (d, J=1.8 Hz, 1H), 7.77 (d, J=1.5 Hz, 1H), 7.63 (d, J=3.1 Hz, 1H), 7.26 (s, 2H), 6.72 (d, J=3.3 Hz, 1H), 4.60 (q, J=7.1 Hz, 2H), 1.38 (t, J=7.2 Hz, 3H); MS(ESI+) m/z 305.2 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09346795B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-9dfc17c0778a430e938297f9845a9c41
출처 메모uspto-grants-2016_05