Cesium carbonate → 3-[4-(2-Pyrrolidin-1-ylethyl)phenyl]propynoic acid-biphenyl-4-ylamide
反応式
I[C:2]1[CH:7]=[CH:6][C:5]([CH2:8][CH2:9][N:10]2[CH2:14][CH2:13][CH2:12][CH2:11]2)=[CH:4][CH:3]=1.C(=O)([O-])[O-].[Cs+].[Cs+].[C:21]1([C:32]2[CH:37]=[CH:36][CH:35]=[CH:34][CH:33]=2)[CH:26]=[CH:25][C:24]([NH:27][C:28](=[O:31])[C:29]#[CH:30])=[CH:23][CH:22]=1>[Cu]I>[C:21]1([C:32]2[CH:33]=[CH:34][CH:35]=[CH:36][CH:37]=2)[CH:26]=[CH:25][C:24]([NH:27][C:28](=[O:31])[C:29]#[C:30][C:2]2[CH:7]=[CH:6][C:5]([CH2:8][CH2:9][N:10]3[CH2:14][CH2:13][CH2:12][CH2:11]3)=[CH:4][CH:3]=2)=[CH:23][CH:22]=1参加物
反応物 3
生成物 1
試薬・触媒・溶媒 1
実験手順
25 mL of THF are degassed and combined with 0.25 g (0.83 mmol) of 1-[2-(4-iodophenyl)ethyl]pyrrolidine, 0.81 g (2.49 mmol) of cesium carbonate, 16 mg (0.083 mmol) of copper (I) iodide and 38 mg (0.033 mmol) of tetrakistriphenylphosphine palladium. Then the mixture is again degassed, and 184 mg (0.83 mmol) of propynoic acid-biphenyl-4-ylamide are added. The reaction mixture is stirred for 3 hours at ambient temperature, poured onto water and extracted with ethyl acetate. The organic phase is extracted three times with water and dried over sodium sulfate. The purification is carried out by column chromatography on silica gel (dichloromethane/methanol/ammonia=10:1:0.1)). Yield: 90 mg (27.5% of theory); melting point: 180-189° C.; C27H26N2O (M=394.52); calc.: molecular ion peak (M+H)+: 395; found: molecular ion peak (M+H)+: 395.
後処理
- custom25 mL of THF are degassed
- customThen the mixture is again degassed
- additionpoured onto water
- extractionextracted with ethyl acetate
- extractionThe organic phase is extracted three times with water
- dry with materialdried over sodium sulfate
- customThe purification
出典と根拠
- ORDレコード
- ord-522583451aa741fab7993b1a81b520d2
- 出典データセット
- uspto-grants-2009_09
- 特許番号
- US07592373B2
反応ノート
読み込み中…