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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 273314생성일: 2026년 10월 26일

Benzenesulfonyl chloride → 1-(Phenylsulfonyl)-4-azaindole

https://huagongshe.com/reaction/273314

반응식

참여 물질

역할이름HCID투입량
반응물Benzenesulfonyl chlorideHCID 7369—
반응물4-AzaindoleHCID 9226—
반응물Sodium hydrideHCID 24758—
용매Dimethyl SulfoxideHCID 679—
용매HexaneHCID 8058—
생성물1-(Phenylsulfonyl)-4-azaindoleHCID 4527076683%

반응 단계

Sodium hydride (60% in mineral oil, 203 mg, 5.08 mmol) was washed twice with hexane, and the residue suspended in DMSO (5 ml). 1H-Pyrrolo[3,2-b]pyridine (500 mg, 4.24 mmol) was added and the reaction stirred for 15 minutes. Benzenesulphonyl chloride (749 mg, 4.42 mmol) was added rapidly and the reaction stirred for 0.5 h. After quenching with water the product was extracted into EtOAc, dried (Na2SO4) and concentrated in vacuo. Chromatography (EtOAc, silica) yielded the title compound as a white crystalline solid (903 mg, 83%). δH (d6-DMSO) 8.48 (1H, dd, J 0.8, 3.8 Hz), 8.31 (1H, m), 8.15 (1H, d, J 3.8 Hz), 8.04 (2H, m), 7.72 (1H, m,), 7.61 (2H, m,), 7.36 (1H, dd, J 4.7, 8.4 Hz), 6.98 (1H, dd, J 0.8, 3.8 Hz). LCMS (ES+) RT 3.056 minutes, 259 (M+H)+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07456286B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-7afaea33b9224b6aba0d9aaf3a6888a7
출처 메모uspto-grants-2008_11