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HRID 522590作成日:2026年10月26日

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

https://huagongshe.com/reaction/522590

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Sodium hydrideHCID 24758—
反応物3-(1H-imidazol-2-yl)-1-(phenylsulfonyl)-1H-indoleHCID 57516836—
溶媒TetrahydrofuranHCID 8028—
生成物1-(phenylsulfonyl)-3-(1-(phenylsulfonyl)-1H-imidazol-2-yl)-1H-indoleHCID 5751683740%

反応手順

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.2 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]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09334242B2
出典データセットuspto-grants-2016_05
ORD IDord-b74a64cc7b8545b2a279571ad39819f8
出典メモuspto-grants-2016_05