関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ethyl Acetate | HCID 8857 | — |
| 反応物 | 1-Bromo-3,4-(methylenedioxy)benzene | HCID 75831 | — |
| 反応物 | Lithium diisopropylamide | HCID 2724682 | — |
| 反応物 | Isoquinoline-5-carboxaldehyde | HCID 7016853 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | alpha-(5-BRomo-1,3-benzodioxol-4-yl)-5-isoquinolinemethanol | HCID 10981200 | 65% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07091212B2 |
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| 出典データセット | uspto-grants-2006_08 |
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| ORD ID | ord-d7ba93572fa64fddbb46271e8f729e27 |
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| 出典メモ | uspto-grants-2006_08 |
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