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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2112452생성일: 2026년 10월 27일

Pyridine-3-sulfonyl chloride → 4-(1-Piperazinyl)-1-(3-pyridinylsulfonyl)-1H-indole Hydrochloride

https://huagongshe.com/reaction/2112452

반응식

참여 물질

역할이름HCID투입량
반응물Pyridine-3-sulfonyl chlorideHCID 3164136—
반응물tert-Butyl 4-(1H-indol-4-yl)piperazine-1-carboxylateHCID 22015386—
생성물4-(1-Piperazinyl)-1-(3-pyridinylsulfonyl)-1H-indole HydrochlorideHCID 22015331—

반응 단계

The title compound was prepared from 4-(4-boc-piperazinyl)-indole and 3-pyridinylsulfonyl chloride according to Method 3: 1H NMR (270 MHz, DMSO-d6) δ 9.37 (br, 1H), 9.18 (d, J=3 Hz, 1H), 8.86 (d, J=5 Hz, 1H), 8.39 (d, J=8 Hz, 1H), 7.85 (d, J=3 Hz, 1H), 7.70-7.60 (m, 2H), 7.27 (t, J=8 Hz, 4H), 7.00 (d, J=3 Hz, 1H), 6.82 (d, J=8 Hz, 1H), 3.24 (m, 8H); MS (ESI+) for m/z 343 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07524839B2
출처 데이터셋uspto-grants-2009_04
ORD IDord-a7676c7af9104a90af2e59f7707df19e
출처 메모uspto-grants-2009_04