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Lithium diisopropylamide → 2-(6-Ethoxyquinolin-4-yl)-1-(6-methylpyridin-2-yl)ethanone
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Lithium diisopropylamide | HCID 2724682 | — |
| 反応物 | 6-ethoxy-4-methyl-quinoline | HCID 10965252 | — |
| 反応物 | N-methoxy-N,6-dimethylpyridine-2-carboxamide | HCID 45869585 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 2-(6-Ethoxyquinolin-4-yl)-1-(6-methylpyridin-2-yl)ethanone | HCID 59700616 | 20% |
反応手順
To a solution of 6-ethoxy-4-methyl-quinoline (360 mg, 2.0 mmol) in THF at −78° C. add 1.5M lithium diisopropylamide (4.6 ml, 7.0 mmol) dropwise and stir for 1 hour. 6-Methyl-pyridine-2-carboxylic acid methoxy-methyl-amide (430 mg, 2.4 mmol) is then added, and the mixture stirred for 30 minutes at −78° C. before quenching with 1N HCl (5 ml). Neutralize with saturated aqueous NaHCO3 and extract with EtOAc (3×50 ml). The organic phase is then dried with MgSO4 and concentrated in vacuo. The crude product was chromatographed on silica gel (elute with 50/50 Hexane/EtOAc) to give 120 mg (20%) of the title compound. MS ES+ m/e 307.1 (M+1).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07365066B2 |
| 出典データセット | uspto-grants-2008_04 |
| ORD ID | ord-1e59d094cba2480e8ab00ff219a5a1f6 |
| 出典メモ | uspto-grants-2008_04 |