関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ethylene Oxide | HCID 6354 | — |
| 反応物 | 4-(7-Bromo-3-isoquinolinyl)benzonitrile | HCID 67104258 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 4-[7-(2-Hydroxyethyl)-3-isoquinolinyl]benzonitrile | HCID 67104667 | — |
反応手順
The product from Example 74A (4 mmol) is dissolved in 20 mL THF and is cooled to −60° C. under nitrogen. n-BuLi (4.4 mmol) is added dropwise, and the mixture is stirred at −60° C. for additional 30 minutes. A solution of ethylene oxide (20 mmol) in 10 ml THF is added and the mixture is allowed to warm to 10° C. and is stirred to complete the reaction. The mixture iss cooled back down to 0° C. and is slowly quenched with 2N HCl to pH=3. The solvent is removed under vacuum and the residue is dissolved in 20 mL methylene chloride, is washed with water, and is concentrated under reduced pressure. The residue is chromatographed on silica gel (5:95 MeOH:CHCl3) to provide the title compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07153889B2 |
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| 出典データセット | uspto-grants-2006_12 |
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| ORD ID | ord-c6892702ce77413c9623e8d4f763bff1 |
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| 出典メモ | uspto-grants-2006_12 |
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