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Methyl morpholine oxide → 3-Benzyl-4-chloro-1,3-dihydroimidazo[4,5-c]pyridin-2-one

HRID 2112913
Notes
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Reaction equation

HRID 2112913 reaction equation
C[N+]1([O-])CCOCC1.I([O-])(=O)(=O)=O.[Na+].C([N:18]1[C:26]2[CH:25]=[CH:24][N:23]=[C:22]([Cl:27])[C:21]=2[N:20]([CH2:28][C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=2)[C:19]1=[O:35])C=C>O.O1CCOCC1.O=[Os](=O)(=O)=O>[CH2:28]([N:20]1[C:21]2[C:22]([Cl:27])=[N:23][CH:24]=[CH:25][C:26]=2[NH:18][C:19]1=[O:35])[C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

7

Reactant 3

HCID 82029Methyl morpholine oxideHCID 230705921-Allyl-3-benzyl-4-chloro-1,3-dihydroimidazo[4,5-c]pyridin-2-oneHCID 23667635Sodium periodate

Product 1

HCID 230705823-Benzyl-4-chloro-1,3-dihydroimidazo[4,5-c]pyridin-2-oneYield 58.5%

Reagents, catalysts & solvents 3

HCID 30318Osmium Tetroxide
Catalyst
HCID 962WaterSolvent3×
HCID 312751,4-DioxaneSolvent

Conditions

Temperature
60 °C

Procedure

Water (1.5 mL), 4-methylmorpholin-N-oxide (1.06 g), 2% aqueous osmic acid solution (3 mL), and a solution of sodium periodate (1.94 g) in water (6 mL) were added to a solution of 1-allyl-3-benzyl-4-chloro-1,3-dihydroimidazo[4.5-c]pyridin-2-one (0.75 g) in 1,4-dioxane (15 mL). This was then heated at 60° C. for 18 hours. Water (200 mL) was added, and this was extracted with ethyl acetate (100 mL). The obtained organic layer was washed twice with 50 mL of water and then once with 50 mL of saturated aqueous sodium chloride solution, dried over magnesium sulfate, and then concentrated under reduced pressure. The residue was purified by silica gel column chromatography, and the fraction eluted by ethyl acetate-hexane (1:1) gave the title compound (0.38 g).

Workup

  1. extractionthis was extracted with ethyl acetate (100 mL)
  2. washThe obtained organic layer was washed twice with 50 mL of water
  3. dry with materialonce with 50 mL of saturated aqueous sodium chloride solution, dried over magnesium sulfate
  4. concentrationconcentrated under reduced pressure
  5. customThe residue was purified by silica gel column chromatography
  6. washthe fraction eluted by ethyl acetate-hexane (1:1)

Sources & evidence

ORD record
ord-7b999b6c467b4c469708e750c35aa4c3
Source dataset
uspto-grants-2009_04
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07524847B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes