Calcium Chloride → 3-Hexyl-6-(3-aminophenyl)-6-(2,2,2-trifluoroethyl)-3-azabicyclo[3.1.0]hexane-2,4-dione

HRID 1826479ノート

反応式

HRID 1826479 の反応式
[CH2:1]([N:7]1[C:12](=[O:13])[CH:11]2[CH:9]([C:10]2([C:19]2[CH:24]=[CH:23][CH:22]=[C:21]([N+:25]([O-])=O)[CH:20]=2)[CH2:14][C:15]([F:18])([F:17])[F:16])[C:8]1=[O:28])[CH2:2][CH2:3][CH2:4][CH2:5][CH3:6].[Cl-].[Ca+2].[Cl-]>C(O)C.O.[Fe]>[CH2:1]([N:7]1[C:8](=[O:28])[CH:9]2[CH:11]([C:10]2([C:19]2[CH:24]=[CH:23][CH:22]=[C:21]([NH2:25])[CH:20]=2)[CH2:14][C:15]([F:16])([F:17])[F:18])[C:12]1=[O:13])[CH2:2][CH2:3][CH2:4][CH2:5][CH3:6]

参加物

6

実験手順

3-Hexyl-6-(3-nitrophenyl)-6-(2,2,2-trifluoroethyl)-3-azabicyclo[3.1.0]hexane-2,4-dione (Preparation 103, 178 mg, 0.45 mmol) was dissolved in ethanol (15 ml). Iron powder (225 mg, 4.0 mmol) was added at room temperature followed by calcium chloride (50 mg, 0.45 mmol), dissolved in water (2 ml). The vigorously stirred mixture was heated under reflux for 2 h then cooled to room temperature and filtered through a pad of silica. The solvent was removed in vacuo and the filtrate was dissolved in dichloromethane and filtered through a Whatman anotop 10 plus™ cartridge. The organic mixture was concentrated in vacuo to give the product as a brown gum (170 mg, 100%).

後処理

  1. temperatureThe vigorously stirred mixture was heated
  2. temperatureunder reflux for 2 h
  3. filtrationfiltered through a pad of silica
  4. customThe solvent was removed in vacuo
  5. dissolutionthe filtrate was dissolved in dichloromethane
  6. filtrationfiltered through a Whatman anotop 10 plus™ cartridge
  7. concentrationThe organic mixture was concentrated in vacuo

出典と根拠

ORDレコード
ord-d9b7218696f141c09391d81a031459b9
出典データセット
uspto-grants-2006_05
特許番号
US07049444B2

反応ノート

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