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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 63239생성일: 2026년 10월 24일

Benzenesulfonyl chloride → 1-(phenylsulfonyl)-3-(1-(phenylsulfonyl)-1H-imidazol-2-yl)-1H-indole

https://huagongshe.com/ko/reaction/63239

반응식

참여 물질

역할이름HCID투입량
반응물Benzenesulfonyl chlorideHCID 7369—
반응물Sodium hydrideHCID 24758—
반응물3-(1H-imidazol-2-yl)-1-(phenylsulfonyl)-1H-indoleHCID 57516836—
용매TetrahydrofuranHCID 8028—
생성물1-(phenylsulfonyl)-3-(1-(phenylsulfonyl)-1H-imidazol-2-yl)-1H-indoleHCID 5751683740%

반응 단계

To a solution of 3-(1H-imidazol-2-yl)-1-(phenylsulfonyl)-1H-indole (9ya) (20 mmol) in anhydrous THF (300 mL) at 0° C. was added sodium hydride (60% dispersion in mineral oil, 1.2 equiv, 24 mmol) and stirred for 20 min. Benzenesulfonyl chloride (1.2 equiv, 24 mmol) was added and the reaction mixture was stirred overnight. After dilution by 200 mL of saturated NaHCO3 solution (aqueous), the reaction mixture was extracted by ethyl acetate (600 mL). The organic layer was dried over magnesium sulfate and concentrated. The residue was purified by flash column chromatography (hexane:ethyl acetate 5:1) to give a white solid. Yield: 40%. 1H NMR (CDCl3, 300 MHz) δ 8.02-8.08 (m, 4H), 7.72 (d, J=1.5 Hz, 1H), 7.35-7.60 (m, 8H), 7.23 (d, J=1.5 Hz, 1H), 7.10-7.16 (m, 3H). MS (ESI) calcd for C23H17N3O4S2 463.1. found 486.0 [M+Na]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09447049B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-8ff8dc1d75a74b2392126e049a48f1bd
출처 메모uspto-grants-2016_09