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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1272236생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1272236

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl EtherHCID 3283—
반응물2-(Dibenzylamino)propanalHCID 10977975—
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 번호US07208505B2
출처 데이터셋uspto-grants-2007_04
ORD IDord-ae0e393b0402442dbca53732cc0b2566
출처 메모uspto-grants-2007_04