Cesium carbonate → 1-(7-Acetyl-5-chloroquinolin-8-yl)piperidine-4-carbonitrile
反応式
FC(F)(F)S(O[C:7]1[C:8]([C:18](=[O:20])[CH3:19])=[CH:9][C:10]([Cl:17])=[C:11]2[C:16]=1[N:15]=[CH:14][CH:13]=[CH:12]2)(=O)=O.[NH:23]1[CH2:28][CH2:27][CH:26]([C:29]#[N:30])[CH2:25][CH2:24]1.C1C=CC(P(C2C=CC3C(=CC=CC=3)C=2C2C3C(=CC=CC=3)C=CC=2P(C2C=CC=CC=2)C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.C(=O)([O-])[O-].[Cs+].[Cs+]>O1CCCC1.ClCCl.C([O-])(=O)C.[Pd+2].C([O-])(=O)C>[C:18]([C:8]1[C:7]([N:23]2[CH2:28][CH2:27][CH:26]([C:29]#[N:30])[CH2:25][CH2:24]2)=[C:16]2[C:11]([CH:12]=[CH:13][CH:14]=[N:15]2)=[C:10]([Cl:17])[CH:9]=1)(=[O:20])[CH3:19]参加物
8
反応条件
- 温度
- 65 °C
実験手順
A stirred mixture of 7-acetyl-5-chloroquinolin-8-yl trifluoromethanesulfonate (0.12 g, 0.34 mmol, from Example 47, Step 2), piperidine-4-carbonitrile (0.045 g, 0.41 mmol), palladium acetate (1.5 mg, 0.0068 mmol), (S)-(−)-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (6.3 mg, 0.010 mmol), and cesium carbonate (0.31 g, 0.95 mmol) in tetrahydrofuran (3 mL) was heated at 65° C. overnight. The mixture was cooled, diluted with dichloromethane and filtered. The filtrate was washed with brine, dried over MgSO4 and evaporated to dryness. The resulting residue was purified on silica gel (eluting with 0 to 5% MeOH in dichloromethane) to give the desired product (7 mg, 6%). LCMS calculated for C17H17ClN3O (M+H)±: m/z=314.1; Found: 314.0.
後処理
- temperatureThe mixture was cooled
- filtrationfiltered
- washThe filtrate was washed with brine
- dry with materialdried over MgSO4
- customevaporated to dryness
- customThe resulting residue was purified on silica gel (eluting with 0 to 5% MeOH in dichloromethane)
出典と根拠
- ORDレコード
- ord-626f67cc264145c0b08aca27c1f72711
- 出典データセット
- uspto-grants-2014_03
- 特許番号
- US08680108B2
反応ノート
読み込み中…