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HRID 273314作成日:2026年10月26日

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

https://huagongshe.com/reaction/273314

反応式

関与物質

役割名称HCID仕込み量
反応物Benzenesulfonyl chlorideHCID 7369—
反応物4-AzaindoleHCID 9226—
反応物Sodium hydrideHCID 24758—
溶媒Dimethyl SulfoxideHCID 679—
溶媒HexaneHCID 8058—
生成物1-(Phenylsulfonyl)-4-azaindoleHCID 4527076683%

反応手順

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)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07456286B2
出典データセットuspto-grants-2008_11
ORD IDord-7afaea33b9224b6aba0d9aaf3a6888a7
出典メモuspto-grants-2008_11