Ethyl cyanoacetate → HCID 21934570、化合物
反応式
[H-].[Na+].[C:3]([CH2:5][C:6]([O:8][CH2:9][CH3:10])=[O:7])#[N:4].I[CH2:12][CH2:13][C:14]1[CH:15]=[CH:16][C:17]2[N:22]([CH3:23])[CH2:21][CH2:20][N:19]([C:24]([O:26][C:27]([CH3:30])([CH3:29])[CH3:28])=[O:25])[C:18]=2[N:31]=1>CN(C=O)C>[C:3]([CH:5]([C:6]([O:8][CH2:9][CH3:10])=[O:7])[CH2:12][CH2:13][C:14]1[CH:15]=[CH:16][C:17]2[N:22]([CH3:23])[CH2:21][CH2:20][N:19]([C:24]([O:26][C:27]([CH3:30])([CH3:29])[CH3:28])=[O:25])[C:18]=2[N:31]=1)#[N:4]参加物
反応条件
- 温度
- 0 °C
実験手順
NaH (620 mg, 24.55 mmol) was suspended in DMF (203 mL) at 0° C. under N2. Ethyl cyanoacetate (2.6 mL, 24.55 mmol) was added and the resulting mixture stirred for 30 min at 0° C. Tert-butyl 6-(2-iodoethyl)-1-methyl-2,3-dihydropyrido[2,3-b]pyrazine-4(1H)-carboxylate (6.6 g, 16.37 mmol) in DMF (10 mL) was introduced to the reaction mixture and stirred for 2 hours at room temperature. The mixture was cooled to 0 and quenched with water and extracted with EtOAc (3×). The organic layers were washed with brine, dried over Na2SO4 and concentrated in vacuo. The residue was purified by flash chromatography (silica, 90% EtOAC/Hex) to afford colorless oil (5.78 g, 91% yield). H NMR (CDCl3) δ 1.35 (q, 3H), 1.55 (s, 9H), 2.38 (m, 2H), 2.89 (t, 2H), 2.93 (s, 3H), 3.32 (t, 2H), 3.85 (t, 2H), 3.90(m, 1H), 4.30 (q, 2H), 6.85(d, 2H). LC-MS (M+H) 389.
後処理
- stirringstirred for 2 hours at room temperature
- temperatureThe mixture was cooled to 0
- customquenched with water
- extractionextracted with EtOAc (3×)
- washThe organic layers were washed with brine
- dry with materialdried over Na2SO4
- concentrationconcentrated in vacuo
- customThe residue was purified by flash chromatography (silica, 90% EtOAC/Hex)
出典と根拠
- ORDレコード
- ord-96eacbfe30fc480d988965779e722b1f
- 出典データセット
- uspto-grants-2006_10
- 特許番号
- US07115596B2
反応ノート
読み込み中…