o-Toluenesulfonyl chloride → 1-{1-[(4-Methylphenyl)sulfonyl]-1H-indol-3-yl}ethanone

HRID 736980ノート

反応式

HRID 736980 の反応式
[CH3:1][C:2]([O-])([CH3:4])[CH3:3].[K+].[C:7]([C:10]1[C:18]2[C:13](=[CH:14][CH:15]=[CH:16][CH:17]=2)[NH:12][CH:11]=1)(=[O:9])[CH3:8].[C:19]1(C)[C:20]([S:25](Cl)(=[O:27])=[O:26])=[CH:21]C=CC=1.C(OC(C)=O)C.O>CN(C=O)C>[C:2]1([CH3:4])[CH:3]=[CH:21][C:20]([S:25]([N:12]2[C:13]3[C:18](=[CH:17][CH:16]=[CH:15][CH:14]=3)[C:10]([C:7](=[O:9])[CH3:8])=[CH:11]2)(=[O:27])=[O:26])=[CH:19][CH:1]=1

参加物

6

反応物 4

HCID 8623o-Toluenesulfonyl chlorideHCID 128023-AcetylindoleHCID 22728543Water ethylacetateHCID 23665647Potassium tert-butoxide

生成物 1

HCID 3577941-{1-[(4-Methylphenyl)sulfonyl]-1H-indol-3-yl}ethanone収率 78%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

Add 1.0 M t-BuOK (3.0 mL, 0.003 mol) to a stirring solution of 3-acetyl indole (0.478 g, 0.0030 mol) in dry DMF (20 mL) under N2 at ambient temperature and stir for 30 min. Add toluenesulfonyl chloride to this solution and stir the resulting mixture overnight. Pour the reaction into EtOAc—H2O, separate the organic layer and extract several times with H2O wash with brine, dry (MgSO4), filter, and evaporate on the rotary evaporator. Chromatograph on the ISCO eluting with a gradient hexane-EtOAc (0-100%) over 30 minutes to give 0.73 g (78%) of the title compound as a solid: 1H (CDCl3). δ 7.8 (d, 1H), 8.2 (s, 1H), 7.9 (d, 1H), 7.7 (d, 2H), 7.4 (m, 2H), 7.3 (d, 2H), 2.6 (s, 3H), 2.4 (s, 3H).

後処理

  1. additionPour
  2. customseparate the organic layer
  3. extractionextract several times with H2O
  4. washwash with brine
  5. dry with materialdry (MgSO4)
  6. filtrationfilter
  7. customevaporate on the rotary evaporator
  8. washChromatograph on the ISCO eluting with a gradient hexane-EtOAc (0-100%) over 30 minutes

出典と根拠

ORDレコード
ord-0dea3151871241489e90aa87c1b82c56
出典データセット
uspto-grants-2009_09
特許番号
US07595339B2

反応ノート

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