反応式
[CH2:1]([N:5]1[CH2:10][CH2:9][NH:8][CH2:7][CH2:6]1)[CH:2]([CH3:4])[CH3:3].C(=O)([O-])[O-].[K+].[K+].[CH:17]1[C:26]2[CH:25]=[CH:24][CH:23]=[C:22]([S:27](Cl)(=[O:29])=[O:28])[C:21]=2[CH:20]=[CH:19][N:18]=1.CO.C(Cl)(Cl)Cl>C(Cl)(Cl)Cl>[CH:17]1[C:26]2[CH:25]=[CH:24][CH:23]=[C:22]([S:27]([N:8]3[CH2:9][CH2:10][N:5]([CH2:1][CH:2]([CH3:4])[CH3:3])[CH2:6][CH2:7]3)(=[O:29])=[O:28])[C:21]=2[CH:20]=[CH:19][N:18]=1参加物
実験手順
In 30 ml of chloroform were added 1.42 g of 1-isobutylpiperazine and 2.76 g of potassium carbonate, and to the mixture was added dropwise 50 ml of a chloroform solution containing 2.28 g of 5-isoquinolinesulfonyl chloride under cooling with ice. After the dropwise addition of the chloroform solution, the mixed solution thus obtained was stirred at a temperature of 15° C. to 25° C. for two hours, and then the reaction solution was washed with 20 ml of a 1N aqueous sodium hydroxide solution and extracted twice with a 5N aqueous hydrochloric acid solution. The aqueous hydrochloric acid layer was rendered alkaline, extracted three time with 30 ml of chloroform, and the chloroform layer extracted was washed with water and dried with anhydrous magnesium sulfate. After the chloroform was distilled therefrom under reduced pressure, the residue obtained was subjected to a silica gel column chromatography (silica gel: 100 g; solvent: 2% methanol-chloroform) to give 2.60 g of 1-(5-isoquinolinesulfonyl)-4-isobutylpiperazine, i.e., Compound (47) in a yield of 78%.
後処理
- temperatureunder cooling with ice
- customthe mixed solution thus obtained
- washthe reaction solution was washed with 20 ml of a 1N aqueous sodium hydroxide solution
- extractionextracted twice with a 5N aqueous hydrochloric acid solution
- extractionextracted three time with 30 ml of chloroform
- extractionthe chloroform layer extracted
- washwas washed with water
- dry with materialdried with anhydrous magnesium sulfate
- distillationAfter the chloroform was distilled
- customunder reduced pressure, the residue obtained
出典と根拠
- ORDレコード
- ord-905fe4a462c74f6d94703c688847030e
- 出典データセット
- uspto-grants-1985_12
- 特許番号
- US04560755
関連ノート
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