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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diethyl Ether | HCID 3283 | — |
| 반응물 | 2-(Dibenzylamino)propanal | HCID 10977975 | — |
| 반응물 | 5,7-Difluoro-3-iodo-1-(phenylsulfonyl)-1H-indole | HCID 22014784 | — |
| 반응물 | HCID 178418443 | HCID 178418443 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2-(N,N-dibenzylamino)-1-(1-benzenesulfonyl-5,7-difluoro-1H-indol-3-yl)-propan-1-ol | HCID 22014816 | 76.8% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07208505B2 |
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| 출처 데이터셋 | uspto-grants-2007_04 |
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| ORD ID | ord-ae0e393b0402442dbca53732cc0b2566 |
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| 출처 메모 | uspto-grants-2007_04 |
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