反応式
[CH2:1]([NH:8][C@H:9]([C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)[CH3:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Li]CCCC.[CH3:22][C:23]1[N:28]=[CH:27][C:26](/[CH:29]=[CH:30]/[C:31]([O:33][C:34]([CH3:37])([CH3:36])[CH3:35])=[O:32])=[CH:25][CH:24]=1.[NH4+].[Cl-]>C1COCC1>[CH2:1]([N:8]([C@H:9]([C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)[CH3:10])[C@@H:29]([C:26]1[CH:27]=[N:28][C:23]([CH3:22])=[CH:24][CH:25]=1)[CH2:30][C:31]([O:33][C:34]([CH3:37])([CH3:36])[CH3:35])=[O:32])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1参加物
6
反応物 4
生成物 1
試薬・触媒・溶媒 1
実験手順
To a solution of (S)-N-benzyl-1-phenylethanamine (3.64 g, 17.26 mmol) in THF (40 mL) at −70° C., was added dropwise n-BuLi (1.6 M, 14.7 mmol) over a period of 30 min and stirred further. After 1 h, a solution of (E)-tert-butyl 3-(6-methylpyridin-3-yl)acrylate (2.7 g, 12.3 mmol) in THF was added slowly to the above mixture and stirred further. After 2 h, sat. NH4Cl solution was added to the reaction mixture and extracted with EtOAc (3×). The combined organic phase was dried over anhydrous Na2SO4 and concentrated in vacuo to afford a residue. Purification of the residue by column chromatography (Neutral Al2O3, Et2O/Pet ether 5:95) afforded the title compound. MS: 431.6 [M+H]+;
後処理
- stirringstirred further
- waitAfter 2 h
- extractionextracted with EtOAc (3×)
- dry with materialThe combined organic phase was dried over anhydrous Na2SO4
- concentrationconcentrated in vacuo
- customto afford a residue
- customPurification of the residue by column chromatography (Neutral Al2O3, Et2O/Pet ether 5:95)
出典と根拠
- ORDレコード
- ord-e803088ee0dc40768af33c280c1b42ab
- 出典データセット
- uspto-grants-2014_02
- 特許番号
- US08653091B2
関連ノート
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