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Benzenesulfonyl chloride → 1-(Phenylsulfonyl)-4-pyrazin-2-yl-1H-indole

HRID 1159808
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HRID 1159808 반응식
[N:1]1[CH:6]=[CH:5][N:4]=[CH:3][C:2]=1[C:7]1[CH:15]=[CH:14][CH:13]=[C:12]2[C:8]=1[CH:9]=[CH:10][NH:11]2.[C:16]1([S:22](Cl)(=[O:24])=[O:23])[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1.[OH-].[Na+]>S([O-])(O)(=O)=O.C([N+](CCCC)(CCCC)CCCC)CCC.ClCCl.O>[C:16]1([S:22]([N:11]2[C:12]3[C:8](=[C:7]([C:2]4[CH:3]=[N:4][CH:5]=[CH:6][N:1]=4)[CH:15]=[CH:14][CH:13]=3)[CH:9]=[CH:10]2)(=[O:24])=[O:23])[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 3

HCID 7369Benzenesulfonyl chlorideHCID 14798Sodium HydroxideHCID 687176654-pyrazin-2-yl-1H-indole2회

생성물 1

HCID 687170021-(Phenylsulfonyl)-4-pyrazin-2-yl-1H-indole

시약·촉매·용매 3

HCID 94433Tetrabutylammonium hydrogen sulfate촉매HCID 962Water
용매
2회
HCID 6344Dichloromethane용매2회

실험 절차

4-Pyrazin-2-yl-1H-indole (0.060 g, 0.307 mmol, Intermediate 65), benzensulfonyl chloride (0.071 g, 0.40 mmol) and tetrabutylammonium hydrogen sulfate (0.010 g, 0.031 mmol) were dissolved in dichloromethane (3 mL) and NaOH (0.061 g, 1.5 mmol) in water (1 mL) was added. The mixture was stirred at rt overnight and the mixture was diluted with dichloromethane and water and extracted with dichloromethane (2×). The organic phase was dried (MgSO4) and evaporated. The crude product was purified by flash chromatography using CH2Cl2 to 1% MeOH in CH2Cl2 as the eluent. Yield: 81 mg (79%). White solid. MS (electronspray; [M+H]+) m/z 336.4.

후처리

  1. extractionextracted with dichloromethane (2×)
  2. dry with materialThe organic phase was dried (MgSO4)
  3. customevaporated
  4. customThe crude product was purified by flash chromatography

출처 및 근거

ORD 기록
ord-87b331da22134b10804f6b12ed049ebd
출처 데이터셋
uspto-grants-2010_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07812017B2

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