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Potassium Hydroxide → 3-Benzyl-6-methyl-6-(3-pyridinyl)-3-azabicyclo[3.1.0]hexane-2,4-dione

HRID 1826463
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HRID 1826463 반응식
[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([C:7](=NN)[CH3:8])[CH:2]=1.[OH-].[K+].[CH2:13]([N:20]1[C:24](=[O:25])[CH:23]=[CH:22][C:21]1=[O:26])[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1>O1CCOCC1.C(O)C.[O-2].[O-2].[Mn+4]>[CH2:13]([N:20]1[C:24](=[O:25])[CH:23]2[CH:22]([C:7]2([CH3:8])[C:3]2[CH:2]=[N:1][CH:6]=[CH:5][CH:4]=2)[C:21]1=[O:26])[C:14]1[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 3

HCID 14797Potassium HydroxideHCID 74204BenzylmaleimideHCID 598980421-(3-Pyridinyl)-1-ethanone hydrazone

생성물 1

HCID 221412363-Benzyl-6-methyl-6-(3-pyridinyl)-3-azabicyclo[3.1.0]hexane-2,4-dione수율 25.7%

시약·촉매·용매 3

HCID 178418406HCID 178418406, 화합물촉매
HCID 702
Ethanol
용매
HCID 312751,4-Dioxane용매

실험 절차

1-(3-Pyridinyl)-1-ethanone hydrazone (Preparation 76, 5.0 g, 40.0 mmol) was dissolved in dioxan (250 ml) and manganese dioxide (6.4 g, 40.0 mmol) was added portionwise followed by a saturated solution of potassium hydroxide in ethanol (2 ml). The reaction mixture was stirred at room temperature for 4 h and then filtered through a pad of Celite®. The filtrate was added to 1-benzyl-1H-pyrrole-2,5-dione (7.5 g, 40.0 mmol) and the reaction mixture was stirred for 16 h at room temperature and was then refluxed for 72 h. The reaction mixture was concentrated in vacuo and the residue was suspended in methanol and filtered to give the title compound as a white solid (3 g, 25%).

후처리

  1. filtrationfiltered through a pad of Celite®
  2. stirringthe reaction mixture was stirred for 16 h at room temperature
  3. temperaturewas then refluxed for 72 h
  4. concentrationThe reaction mixture was concentrated in vacuo
  5. filtrationfiltered

출처 및 근거

ORD 기록
ord-3a12abccfb6b48b28687781654ff89bb
출처 데이터셋
uspto-grants-2006_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07049444B2

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