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HRID 1072608作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl EtherHCID 3283—
反応物(S)-2-Dibenzylamino-propionaldehydeHCID 11107860—
反応物5,7-Difluoro-3-iodo-1-(phenylsulfonyl)-1H-indoleHCID 22014784—
反応物HCID 178418443HCID 178418443—
溶媒TetrahydrofuranHCID 8028—
生成物2-(N,N-dibenzylamino)-1-(1-benzenesulfonyl-5,7-difluoro-1H-indol-3-yl)-propan-1-olHCID 2201481676.8%

反応条件

温度0 °C

反応手順

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%)

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06911463B2
出典データセットuspto-grants-2005_06
ORD IDord-c12aa04480464d17b08ab4f3f1f27987
出典メモuspto-grants-2005_06