Cyclohexene → 1-Acetyl-5-carbomethoxy-7-chloro-4-methoxyindole

HRID 2074001ノート

反応式

HRID 2074001 の反応式
[CH2:1]([C:4]1[C:5]([O:19][CH3:20])=[C:6]([CH:11]=[C:12]([Cl:18])[C:13]=1[NH:14][C:15](=[O:17])[CH3:16])[C:7]([O:9][CH3:10])=[O:8])[CH:2]=C.I([O-])(=O)(=O)=O.[Na+].C1CCCCC=1>C(O)CCC.O.O1CCOCC1.O.C(O)(C(F)(F)F)=O.C(Cl)Cl.[Os](=O)(=O)(=O)=O>[C:15]([N:14]1[C:13]2[C:4](=[C:5]([O:19][CH3:20])[C:6]([C:7]([O:9][CH3:10])=[O:8])=[CH:11][C:12]=2[Cl:18])[CH:1]=[CH:2]1)(=[O:17])[CH3:16]

参加物

10

実験手順

A 2.5% solution of osmium tetroxide in butanol (0.25 ml) is added to a stirred solution of the methoxy compound from step 7 above (1.5 g) in H2O-dioxane (15 ml/45 ml) and stirred for 30 minutes. Sodium periodate (2.25 g) is added portionwise over one hour and the reaction mixture stirred for 31/2 hours. Cyclohexene (1 ml) is added, the mixture stirred for one hour, diluted with H2O and extracted with CHCl3. The organic layer is separated, dried (MgSO4) and evaporated affording a gum which is dissolved in TFA and allowed to stand for 15 minutes. The acid solution is diluted to 100 mls with CH2Cl2 and washed with H2O, saturated NaHCO3, dried (MgSO4) and evaporated affording a solid which is chromatographed on silica gel affording a colorless solid which is the indole as confirmed by NMR (270 MHz, CDCl2).

後処理

  1. stirringthe reaction mixture stirred for 31/2 hours
  2. stirringthe mixture stirred for one hour
  3. extractionextracted with CHCl3
  4. customThe organic layer is separated
  5. dry with materialdried (MgSO4)
  6. customevaporated
  7. customaffording a gum which
  8. waitto stand for 15 minutes
  9. washwashed with H2O, saturated NaHCO3
  10. dry with materialdried (MgSO4)
  11. customevaporated
  12. customaffording a solid which
  13. customis chromatographed on silica gel affording a colorless solid which

出典と根拠

ORDレコード
ord-f06df5c50ee24a2c8fa824502159fc97
出典データセット
uspto-grants-1990_04
特許番号
US04920219

反応ノート

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