関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Tetrahydrofuran | HCID 8028 | — |
| 反応物 | 2-Chloro-6-methoxyquinoline | HCID 83647 | — |
| 反応物 | Lithium diisopropylamide | HCID 2724682 | — |
| 反応物 | 1-Benzyl-2-piperidone | HCID 5170076 | — |
| 生成物 | 1-Benzyl-4-(2-chloro-6-methoxyquinolin-3-yl)piperidin-4-ol | HCID 58181126 | — |
反応手順
Under an argon atmosphere 5.0 g (25 mmol) 2-chloro-6-methoxyquinoline in a small amount of THF were added dropwise at −78° C. to 14 mL (28 mmol) of a 2 M lithium diisopropylamide solution (in THF) in 50 mL THF. Then the mixture was stirred for 1.5 h at −78° C. and 4.5 mL (25 mmol) N-benzylpiperidone was added dropwise. The mixture was stirred for a further 15 min with cooling before slowly being heated to RT. The reaction mixture was stirred overnight, evaporated down and purified by flash chromatography on aluminium oxide. The product-containing fractions were combined and evaporated down.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08829006B2 |
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| 出典データセット | uspto-grants-2014_09 |
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| ORD ID | ord-9443c894840b43aa8c4008ecd5502c39 |
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| 出典メモ | uspto-grants-2014_09 |
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