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HRID 8114作成日:2026年10月23日

Dichloromethane → 5,7-Difluoro-3-iodo-1-(phenylsulfonyl)-1H-indole

https://huagongshe.com/ja/reaction/8114

反応式

関与物質

役割名称HCID仕込み量
反応物DichloromethaneHCID 6344—
反応物Benzenesulfonyl chlorideHCID 7369—
反応物Iodine chlorideHCID 24640—
反応物5,7-difluoro-1H-indoleHCID 2778730—
触媒Tetrabutylammonium BromideHCID 74236—
溶媒PyridineHCID 1049—
溶媒TolueneHCID 1140—
溶媒Sodium HydroxideHCID 14798—
生成物5,7-Difluoro-3-iodo-1-(phenylsulfonyl)-1H-indoleHCID 2201478487%

反応手順

The 1.0 M ICl in CH2Cl2 (43 ml, 43 mmol) is added to a solution of 5,7-difluoroindole (6 g, 39 mmol) in 35 ml pyridine under N2 at 0° C. and the resulting mixture is stirred for 30 minutes. The reaction is diluted with toluene and washed with brine, 1N HCl, 1N NaOH, dried (Na2SO4), filtered and concentrated. The crude 3-iodo-5,7-difluoroindole is stirred in toluene (85 ml) and 5 N NaOH (70 ml), tetrabutylammonium bromide (1.25 g, 3.9 mmol), then benzenesulfonyl chloride (6.2 ml, 48 mmol) are added and the resulting mixture is stirred 24 hours. The two phase reaction mixture is diluted with toluene, washed with brine, dried(Na2SO4), filtered, concentrated and the residue is triturated with diethyl ether/petroleum ether. The resulting solid is filtered to give 14.2 g of N-Benzenesulfonyl-3-iodo-5,7-difluoroindole (87%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087635B2
出典データセットuspto-grants-2006_08
ORD IDord-563d6e04fa2144da9e95cdda593c8abd
出典メモuspto-grants-2006_08