1-(5-Isoquinolinylsulfonyl)piperazine → HCID 13116936, 화합물

HRID 638375

반응식

HRID 638375 반응식
[CH:1]1[C:10]2[CH:9]=[CH:8][CH:7]=[C:6]([S:11]([N:14]3[CH2:19][CH2:18][NH:17][CH2:16][CH2:15]3)(=[O:13])=[O:12])[C:5]=2[CH:4]=[CH:3][N:2]=1.C(=O)([O-])[O-].[K+].[K+].[CH2:26](Br)[CH3:27].CO.C(Cl)(Cl)Cl>C(O)C.C(Cl)(Cl)Cl>[CH:1]1[C:10]2[CH:9]=[CH:8][CH:7]=[C:6]([S:11]([N:14]3[CH2:19][CH2:18][N:17]([CH2:26][CH3:27])[CH2:16][CH2:15]3)(=[O:12])=[O:13])[C:5]=2[CH:4]=[CH:3][N:2]=1

참가 물질

7

실험 절차

In 100 ml of ethanol were added 2.77 g of 1-(5-isoquinolinesulfonyl)piperazine, i.e., Compound (35), 1.66 g of anhydrous potassium carbonate and 5.45 g of ethyl bromide, and the reaction was carried out at an external temperature of 70° C. for 24 hours. After the reaction solution was filtered, the filtrate was condensed and the residue was dissolved in 50 ml of chloroform, and the solution was extracted twice with a 2N aqueous hydrochloric acid solution. The aqueous hydrochloric acid layer was rendered alkaline, extracted twice with 50 ml of chloroform, and the chloroform layer extracted was washed with water and dried with anhydrous magnesium sulfate. After the chloroform was distilled therefrom, the residue obtained was subjected to a silica gel column chromatography (silica gel: 100 g; solvent: 2% methanol-chloroform) to give 2.26 g of 1-(5-isoquinolinesulfonyl)-4-ethylpiperazine, i.e., Compound (42) in a yield of 74%.

후처리

  1. filtrationAfter the reaction solution was filtered
  2. customcondensed
  3. extractionthe solution was extracted twice with a 2N aqueous hydrochloric acid solution
  4. extractionextracted twice with 50 ml of chloroform
  5. extractionthe chloroform layer extracted
  6. washwas washed with water
  7. dry with materialdried with anhydrous magnesium sulfate
  8. distillationAfter the chloroform was distilled
  9. customthe residue obtained

출처 및 근거

ORD 기록
ord-118dcab10db243cba38965d8a598788b
출처 데이터셋
uspto-grants-1985_12
특허 번호
US04560755

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