反応式
Cl[C:2]1[CH:10]=[CH:9][C:8]2[N:7]([CH3:11])[N:6]=[C:5]3[C:12]4[CH:13]=[CH:14][N:15]=[CH:16][C:17]=4[C:18](=[O:19])[C:3]=1[C:4]=23.[CH3:20][N:21]([CH3:25])[CH2:22][CH2:23][NH2:24]>>[CH3:20][N:21]([CH3:25])[CH2:22][CH2:23][NH:24][C:2]1[CH:10]=[CH:9][C:8]2[N:7]([CH3:11])[N:6]=[C:5]3[C:12]4[CH:13]=[CH:14][N:15]=[CH:16][C:17]=4[C:18](=[O:19])[C:3]=1[C:4]=23参加物
3
実験手順
5-chloro-2-methylisoquino[5,6,7-cd]indazole-6 (2H)-one of Example 7 (0.013 g) is added to 2-(dimethylamino)ethylamine (0.34 mL). The yellow mixture is heated quickly to reflux for 1 hour. The excess diamine is removed from the orange solution by a gentle stream of nitrogen. The orange mixture obtained is purified by silica gel column chromatography with a gradient elution (1% methanol/chloroform (25 mL), 2% methanol/chloroform (25 mL), 4% methanol/chloroform (25 mL), 8% methanol/chloroform (25 mL), 12% methanol/chloroform (25 mL), 16% methanol/chloroform (25 mL), 24% methanol/chloroform (50 mL)) to yield 5-[[2-(dimethylamino)ethyl]amino]-2-methylisoquino[5,6,7-cd]indazole-6(2H)-one (0.010 g) as a reddish orange solid.
後処理
- temperatureThe yellow mixture is heated quickly
- temperatureto reflux for 1 hour
- customThe excess diamine is removed from the orange solution by a gentle stream of nitrogen
- customThe orange mixture obtained
- customis purified by silica gel column chromatography with a gradient elution (1% methanol/chloroform (25 mL), 2% methanol/chloroform (25 mL), 4% methanol/chloroform (25 mL), 8% methanol/chloroform (25 mL), 12% methanol/chloroform (25 mL), 16% methanol/chloroform (25 mL), 24% methanol/chloroform (50 mL))
出典と根拠
- ORDレコード
- ord-1c9dcf740d32406b9c542abbe30ce882
- 出典データセット
- uspto-grants-1997_01
- 特許番号
- US05596097
関連ノート
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