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

HRID 429149
ノート
印刷プレビュー

反応式

HRID 429149 の反応式
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]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 1049PyridineHCID 11178065HCID 11178065、化合物HCID 221860806-Chloro-5-methylindoline

生成物 1

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

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-8e0f5063581d4fe9b011a3ff69a13f43
出典データセット
uspto-grants-2001_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06316450B1

反応ノート

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