Potassium Carbonate → 1-(5-Isoquinolinesulfonyl)-4-isobutylpiperazine

HRID 638376

反応式

HRID 638376 の反応式
[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

6

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

  1. temperatureunder cooling with ice
  2. customthe mixed solution thus obtained
  3. washthe reaction solution was washed with 20 ml of a 1N aqueous sodium hydroxide solution
  4. extractionextracted twice with a 5N aqueous hydrochloric acid solution
  5. extractionextracted three time with 30 ml of chloroform
  6. extractionthe chloroform layer extracted
  7. washwas washed with water
  8. dry with materialdried with anhydrous magnesium sulfate
  9. distillationAfter the chloroform was distilled
  10. 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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