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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1072608생성일: 2026년 10월 23일

Diethyl Ether → 2-(N,N-dibenzylamino)-1-(1-benzenesulfonyl-5,7-difluoro-1H-indol-3-yl)-propan-1-ol

https://huagongshe.com/ko/reaction/1072608

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl EtherHCID 3283—
반응물(S)-2-Dibenzylamino-propionaldehydeHCID 11107860—
반응물5,7-Difluoro-3-iodo-1-(phenylsulfonyl)-1H-indoleHCID 22014784—
반응물HCID 178418443HCID 178418443—
용매TetrahydrofuranHCID 8028—
생성물2-(N,N-dibenzylamino)-1-(1-benzenesulfonyl-5,7-difluoro-1H-indol-3-yl)-propan-1-olHCID 2201481676.8%

반응 조건

온도0 °C

반응 단계

A 3.0 M diethyl ether solution of ethylmagnesium bromide (7.3 ml, 21.8 mmol) is added under N2 at 0° C. to a 95 ml tetrahydrofuran solution of N-benzenesulfonyl-3-iodo-5,7-difluoro-indole (8.4 g, 20 mmol). The resulting mixture is stirred for 20 minutes at 0° C., allowed to warm to room temperature over 20 minutes, then recooled to 0° C. A 20 ml tetrahydrofuran solution of (S)N,N dibenzyl-2-aminopropanal (Syn. Lett., 1997,2, 223-224, 5.1 g, 22 mmol) is added to the reaction mixture and the resulting mixture is stirred 1 hour as it warmed to room temp. The reaction is quenched with aqueous NH4Cl, extracted with ethyl acetate, washed with brine, dried (Na2SO4), filtered, concentrated, and the residue is purified by flash chromatography (SiO2, ethyl acetate/hexane gradient) to yield 8.4 g of 2-(N,N-dibenzylamino)-1-(1-benzenesulfonyl-5,7-difluoro-1H-indol-3-yl)-propan-1-ol. (77%)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06911463B2
출처 데이터셋uspto-grants-2005_06
ORD IDord-c12aa04480464d17b08ab4f3f1f27987
출처 메모uspto-grants-2005_06