反応式
[N:1]1([C:7]([CH2:9][C:10]2[S:11][C:12]3[CH2:21][C:20]4[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=4[C:13]=3[N:14]=2)=O)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[H-].[Al+3].[Li+].[H-].[H-].[H-].O.O.O.O.O.O.O.O.O.O.S([O-])([O-])(=O)=O.[Na+].[Na+]>O1CCCC1>[N:1]1([CH2:7][CH2:9][C:10]2[S:11][C:12]3[CH2:21][C:20]4[CH:19]=[CH:18][CH:17]=[CH:16][C:15]=4[C:13]=3[N:14]=2)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]1参加物
反応条件
- 温度
- 0 °C
実験手順
A solution of 500 mg of 2-[(piperidinocarbonyl)methyl]-8H-indeno[1,2-d]thiazole in 10 ml of tetrahydrofuran was added to a suspension of 160 mg of lithium aluminum hydride in 10 ml of tetrahydrofuran at 0° C., followed by heating under reflux for 1.5 hours. The reaction mixture was cooled to 0° C. again, and sodium sulfate decahydrate was added. The resulting mixture was stirred at room temperature for 30 minutes. After the insoluble matter was removed by filtration, the solvent was evaporated. The resulting oily substance was purified by silica gel column chromatography (eluent: chloroform:methanol=10:1), whereby 120 mg of 2-(2-piperidinoethyl)-8H-indeno[1,2-d]thiazole was obtained. Fumaric acid was added to the product in ethanol to cause crystallization, and the crystals were recrystallized to give a fumarate.
後処理
- temperatureby heating
- temperatureunder reflux for 1.5 hours
- customAfter the insoluble matter was removed by filtration
- customthe solvent was evaporated
- customThe resulting oily substance was purified by silica gel column chromatography (eluent: chloroform:methanol=10:1)
出典と根拠
- ORDレコード
- ord-5a0bc6916ef741158a495d4306794aa3
- 出典データセット
- uspto-grants-1998_11
- 特許番号
- US05834499
関連ノート
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