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Pyridine → 6-Chloro-1-(4-methoxy-3-piperazin-1-ylbenzenesulfonyl)-5-methyl-2,3-dihydro-1H-indole hydrochloride

HRID 429149
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HRID 429149 반응식
N1C=CC=CC=1.[Cl:7][C:8]1[CH:16]=[C:15]2[C:11]([CH2:12][CH2:13][NH:14]2)=[CH:10][C:9]=1[CH3:17].ClC(Cl)(Cl)C([N:22]1[CH2:27][CH2:26][N:25]([C:28]2[CH:29]=[C:30]([S:36](Cl)(=[O:38])=[O:37])[CH:31]=[CH:32][C:33]=2[O:34][CH3:35])[CH2:24][CH2:23]1)=O>ClCCl>[ClH:7].[Cl:7][C:8]1[CH:16]=[C:15]2[C:11]([CH2:12][CH2:13][N:14]2[S:36]([C:30]2[CH:31]=[CH:32][C:33]([O:34][CH3:35])=[C:28]([N:25]3[CH2:26][CH2:27][NH:22][CH2:23][CH2:24]3)[CH:29]=2)(=[O:37])=[O:38])=[CH:10][C:9]=1[CH3:17]
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참가 물질

5

반응물 3

HCID 1049PyridineHCID 11178065HCID 11178065, 화합물HCID 221860806-Chloro-5-methylindoline

생성물 1

HCID 183545496-Chloro-1-(4-methoxy-3-piperazin-1-ylbenzenesulfonyl)-5-methyl-2,3-dihydro-1H-indole hydrochloride수율 110.3%

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

Pyridine (0.28 ml) was added to a stirred solution of 6-chloro-5-methyl-2,3-dihydro-1H-indole (WO-9501976) (0.116 g) and 3-(4-trichloroacetylpiperazin-1-yl)-4-methoxybenzenesulfonyl chloride (D4) (300 mg) in dichioromethane (4 ml) at room temperature. After 18 h the solution was washed with 1M hydrochloric acid (5 ml), water (5 ml), dried (MgSO4) and concentrated to an oil. The oil was dissolved in 1,4-dioxan (13 ml) and a 0.15 M potassium hydroxide solution (6.5 ml) was added. The solution was stirred at room temperature for 4 h then concentrated to remove the organic solvent, diluted with water (10 ml) and the solution extracted with dichloromethane (20 ml). The organic phase was dried (Na2SO4), acidified with 1M ethereal hydrogen chloride (2 ml), concentrated to a solid and stirred with acetone to afford the title compound (0.175 g, 55%). MH+ 422/424.

후처리

  1. washAfter 18 h the solution was washed with 1M hydrochloric acid (5 ml), water (5 ml)
  2. dry with materialdried (MgSO4)
  3. concentrationconcentrated to an oil
  4. dissolutionThe oil was dissolved in 1,4-dioxan (13 ml)
  5. additiona 0.15 M potassium hydroxide solution (6.5 ml) was added
  6. concentrationthen concentrated
  7. customto remove the organic solvent
  8. additiondiluted with water (10 ml)
  9. extractionthe solution extracted with dichloromethane (20 ml)
  10. dry with materialThe organic phase was dried (Na2SO4)
  11. concentrationconcentrated to a solid
  12. stirringstirred with acetone

출처 및 근거

ORD 기록
ord-8e0f5063581d4fe9b011a3ff69a13f43
출처 데이터셋
uspto-grants-2001_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06316450B1

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