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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1072607생성일: 2026년 10월 23일

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

https://huagongshe.com/ko/reaction/1072607

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물Benzenesulfonyl chlorideHCID 7369—
반응물Iodine chlorideHCID 24640—
반응물5,7-difluoro-1H-indoleHCID 2778730—
촉매Tetrabutylammonium BromideHCID 74236—
용매PyridineHCID 1049—
용매TolueneHCID 1140—
용매Sodium HydroxideHCID 14798—
생성물5,7-Difluoro-3-iodo-1-(phenylsulfonyl)-1H-indoleHCID 2201478487%

반응 단계

The 1.0 M ICl in CH2Cl2 (43 ml, 43 mmol) is added to a solution of 5,7-difluoro-indole (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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06911463B2
출처 데이터셋uspto-grants-2005_06
ORD IDord-c496902e20ac473d8baa4a21b4e14b25
출처 메모uspto-grants-2005_06