反応式
[NH2:1][CH2:2][C:3]1[CH:4]=[C:5]2[C:9](=[C:10]([CH3:12])[CH:11]=1)[C:8](=[O:13])[N:7]([CH2:14][C:15]1[CH:20]=[CH:19][C:18]([O:21][C:22]([F:25])([F:24])[F:23])=[CH:17][CH:16]=1)[CH2:6]2.Cl[CH2:27][CH2:28][N:29]([CH2:31][CH2:32]Cl)[CH3:30].C([O-])([O-])=O.[K+].[K+]>CN(C=O)C>[CH3:12][C:10]1[CH:11]=[C:3]([CH2:2][N:1]2[CH2:32][CH2:31][N:29]([CH3:30])[CH2:28][CH2:27]2)[CH:4]=[C:5]2[C:9]=1[C:8](=[O:13])[N:7]([CH2:14][C:15]1[CH:20]=[CH:19][C:18]([O:21][C:22]([F:25])([F:23])[F:24])=[CH:17][CH:16]=1)[CH2:6]2参加物
反応物 3
生成物 1
試薬・触媒・溶媒 1
反応条件
- 温度
- 110 °C
実験手順
In sealed vial, a mixture of 5-aminomethyl-7-methyl-2-(4-trifluoromethoxy-benzyl)-2,3-dihydro-isoindol-1-one (0.104 g, 0.3 mmol), bis(2-chloro-ethyl)-methyl-amine (0.077 g, 0.4 mmol), and K2CO3 (0.083 g, 0.6 mmol) in DMF (3 mL) was stirred at 110° C. for 16 h. After this time, the GC-MS of the reaction mixture indicated the completion of reaction. The reaction was cooled to ambient temperature and the solids removed by filtration. The filtrate was concentrated. Silica gel column chromatography of the resulting material using 5:1 CHCl3-MeOH afforded 7-methyl-5-(4-methyl-piperazin-1-ylmethyl)-2-(4-trifluoromethoxy-benzyl)-2,3-dihydro-isoindol-1-one (0.040 g, 31%). 1H NMR (300 MHz, CDCl3): δ (ppm) 2.24 (s, 3H), 2.34-2.52 (m, 8H), 2.74 (s, 3H), 3.49 (s, 2H), 4.20 (s, 2H), 4.76 (s, 2H), 7.15-7.37 (m, 6H). GC-MS: m/z 433 (M)+.
後処理
- customthe completion of reaction
- temperatureThe reaction was cooled to ambient temperature
- customthe solids removed by filtration
- concentrationThe filtrate was concentrated
出典と根拠
- ORDレコード
- ord-d6fdfeea6ef14a189a92dc3c871e7335
- 出典データセット
- uspto-grants-2011_06
- 特許番号
- US07968570B2
関連ノート
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