反応式
[N:1]1[CH:2]=[CH:3][N:4]2[C:13]=1[CH2:12][C:11]1[CH:10]=[C:9](O)[C:8]([OH:15])=[CH:7][C:6]=1[CH2:5]2.[C:16]([O-:19])([O-])=O.[K+].[K+].O.[CH3:23]N(C=O)C>[Cl-].C1([N+](C)(C)C)C=CC=CC=1>[CH3:23][O:15][C:8]1[C:9]([O:19][CH3:16])=[CH:10][C:11]2[CH2:12][C:13]3[N:4]([CH:3]=[CH:2][N:1]=3)[CH2:5][C:6]=2[CH:7]=1参加物
6
実験手順
A mixture of 5,10-dihydro-imidazo[1,2-b]-isoquinoline-7,8-diol, obtained according to the procedure described in Ex.No. A8 c, (0.155 mol), phenyltrimethylammonium chloride (0.31 mol) and K2CO3 (0.68 mol) in DMF (400 ml) was stirred at 90° C. for 20 hours, cooled, poured out into H2O and filtered over dicalite. The filtrate was separated into its layers. The organic layer was washed with H2O, dried (MgSO4), filtered and the solvent was evaporated. The residue was purified over silica gel on a glass filter (eluent: CH2Cl2/CH3OH 100/0 to 97/3). The pure fractions were collected and the solvent was evaporated, yielding 3 g of 5,10-dihydro-7,8-dimethoxyimidazo[1,2-b]isoquinoline (8.4%) (interm. 22).
後処理
- customobtained
- temperaturecooled
- filtrationfiltered over dicalite
- customThe filtrate was separated into its layers
- washThe organic layer was washed with H2O
- dry with materialdried (MgSO4)
- filtrationfiltered
- customthe solvent was evaporated
- customThe residue was purified over silica gel on a glass
- filtrationfilter (eluent: CH2Cl2/CH3OH 100/0 to 97/3)
- customThe pure fractions were collected
- customthe solvent was evaporated
出典と根拠
- ORDレコード
- ord-ebdb6c09cb774332a0a1cecc00fe64cd
- 出典データセット
- uspto-grants-2006_08
- 特許番号
- US07087595B2
関連ノート
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