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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 528821생성일: 2026년 10월 24일

1-Acetylindoline-5-sulfonamide → 1-ethyl-2,3-dihydro-1H-indole-5-sulfonamide

https://huagongshe.com/ko/reaction/528821

반응식

참여 물질

역할이름HCID투입량
반응물1-Acetylindoline-5-sulfonamideHCID 804208—
반응물Borane;tetrahydrofuranHCID 2723981—
용매TetrahydrofuranHCID 8028—
생성물1-ethyl-2,3-dihydro-1H-indole-5-sulfonamideHCID 32103726101.6%

반응 단계

To a suspension of 1-acetylindoline-5-sulfonamide (Intermediate 52A, 120 mg, 0.50 mmol) in THF (2.0 mL) was added BH3.THF (5.0 mL, 5.0 mmol, 1.0M solution in THF). The resulting reaction mixture was stirred at room temperature for 1 h, then quenched carefully with MeOH and concentrated in vacuo to give the title compound (115 mg, 100%) as a white solid. 1H NMR (CD3OD) δ 7.56 (dd, J=8.4, 2.0 Hz, 1H), 7.48 (d, J=1.6 Hz, 1H), 6.46-6.44 (m, 1H), 3.51 (t, J=8.6 Hz, 2H), 3.24-3.20 (m, 2H), 2.99 (t, J=8.5 Hz, 2H), 1.17-1.13 (m, 3H); MS(ESI+) m/z 227.2 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09346795B2
출처 데이터셋uspto-grants-2016_05
ORD IDord-a4461fd026ea40dfb4bae997112420eb
출처 메모uspto-grants-2016_05