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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 528828생성일: 2026년 10월 26일

Benzoyl chloride → 1-Benzoylindoline-5-sulfonamide

https://huagongshe.com/reaction/528828

반응식

참여 물질

역할이름HCID투입량
반응물Benzoyl chlorideHCID 7412—
반응물2,3-dihydro-1H-indole-5-sulfonamideHCID 8027252—
반응물1-(Cyclohexanecarbonyl)indoline-5-sulfonamideHCID 60698742—
생성물1-Benzoylindoline-5-sulfonamideHCID 1768113779%

반응 단계

Following a procedure analogous to that for the synthesis of Intermediate 55, indoline-5-sulfonamide (Intermediate 54A, 100 mg, 0.50 mmol) and benzoyl chloride (64 μL, 0.56 mmol) were converted to the title compound (120 mg, 79%). 1H NMR (DMSO-d6) δ 7.70 (s, 1H), 7.65-7.60 (m, 3H), 7.57-7.49 (m, 4H), 7.24 (s, 2H), 4.07 (t, J=8.5 Hz, 2H), 3.15 (t, J=8.4 Hz, 2H); MS(ESI+) m/z 303.2 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09346795B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-e980f2a76d114151a079ad587acb17b1
출처 메모uspto-grants-2016_05