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

HRID 428952
Notes
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Reaction equation

HRID 428952 reaction equation
[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
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 3

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

Product 1

HCID 221412363-Benzyl-6-methyl-6-(3-pyridinyl)-3-azabicyclo[3.1.0]hexane-2,4-dioneYield 27.7%

Reagents, catalysts & solvents 3

HCID 178418406HCID 178418406, compoundCatalyst
HCID 702
Ethanol
Solvent
HCID 312751,4-DioxaneSolvent

Procedure

1-(3-Pyridinyl)-1-ethanone hydrazone (Preparation 76, 5.0 g, 40.0 inmol) 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%).

Workup

  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

Sources & evidence

ORD record
ord-cef9d76723ad48c0911673f2ceb8c7fd
Source dataset
uspto-grants-2001_11
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US06313312B1

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes