反応式
[Al+3].[Cl-].[Cl-].[Cl-].[N:5]1[C:14]2[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=2)[CH:8]=[C:7]([C:15](Cl)=[O:16])[CH:6]=1.[CH3:18][N:19]1[CH2:24][CH2:23][CH2:22][CH2:21][CH:20]1[CH2:25][N:26]1[C:34]2[C:29](=[CH:30][CH:31]=[CH:32][CH:33]=2)[CH:28]=[CH:27]1.[OH-].[Na+]>C(Cl)Cl>[CH3:18][N:19]1[CH2:24][CH2:23][CH2:22][CH2:21][CH:20]1[CH2:25][N:26]1[C:34]2[C:29](=[CH:30][CH:31]=[CH:32][CH:33]=2)[C:28]([C:15]([C:7]2[CH:6]=[N:5][C:14]3[C:9]([CH:8]=2)=[CH:10][CH:11]=[CH:12][CH:13]=3)=[O:16])=[CH:27]1参加物
6
実験手順
To the suspension of 200 mg (1.5 mmol) of anhydrous AlCl3 in 8 ml absolute methylene chloride was added 287.4 mg (1.5 mmol) 3-quinolinecarbonyl chloride in 5 ml methylene chloride and the reaction mixture was stirred 30 min at room 22–25° C. The (N-Methyl-2-piperidinyl)methyl-1H-indole 228.3 mg (1.0 mmol) in 5 ml of methylene chloride was added by dropwise during 1.5 h and the mixture stirred 36 h. The reaction was work-up by addition of 20 ml 2M solution of sodium hydroxide and extracted by ethyl acetate (3×20 ml). The combined extract dried by sodium sulfate. After removing of solvents the rest (0.365 g) was purified by chromatography (silica gel, toluene-triethylamine, 10:1).
後処理
- stirringthe mixture stirred 36 h
- extractionextracted by ethyl acetate (3×20 ml)
- extractionThe combined extract
- dry with materialdried by sodium sulfate
- customAfter removing of solvents the rest (0.365 g)
- customwas purified by chromatography (silica gel, toluene-triethylamine, 10:1)
出典と根拠
- ORDレコード
- ord-377f7bc5a6014153902f88cf24e5e304
- 出典データセット
- uspto-grants-2007_02
- 特許番号
- US07173027B2
関連ノート
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