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HRID 8711作成日:2026年10月25日

Ethyl Acetate → alpha-(5-BRomo-1,3-benzodioxol-4-yl)-5-isoquinolinemethanol

https://huagongshe.com/reaction/8711

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物1-Bromo-3,4-(methylenedioxy)benzeneHCID 75831—
反応物Lithium diisopropylamideHCID 2724682—
反応物Isoquinoline-5-carboxaldehydeHCID 7016853—
溶媒TetrahydrofuranHCID 8028—
生成物alpha-(5-BRomo-1,3-benzodioxol-4-yl)-5-isoquinolinemethanolHCID 1098120065%

反応条件

温度-78 °C

反応手順

To a solution of 4-bromo-1,2-(methylendioxy)benzene (3.01 g, 15 mmol) in THF (20 mL) at −78° C. was added dropwise lithium diisopropylamide (10.6 mL of 1.5 M in cyclohexane, 16 mmol). The reaction mixture was stirred at −78° C. under argon for 20 minutes. A brown solution was formed. A solution of 5-isoquinolinecarboxaldehyde (1.90 g, 12 mmol) in THF (4 mL) was added dropwise. The resulting mixture was stirred at −78° C. for 10 minutes and warmed to room temperature. Stirring was continued for 30 minutes at room temperature, and then the mixture was quenched with saturated NH4Cl solution. The product was extracted with EtOAc and the solvent was removed under reduced pressure. Chromatography (SiO2 Type-H, 35% EtOAc in Hexanes) of the residue yielded the title compound as a yellow solid (2.8 g, 7.8 mmol, 65% yield): mp 173–175° C.;

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07091212B2
出典データセットuspto-grants-2006_08
ORD IDord-d7ba93572fa64fddbb46271e8f729e27
出典メモuspto-grants-2006_08