Acetic Acid → HCID 14390404, compound

HRID 2351693Notes

Reaction equation

HRID 2351693 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[N:16]([CH2:17][C:18]([N:20]([CH3:22])[CH3:21])=[O:19])[C:11]3=[N:12][CH:13]=[CH:14][CH:15]=[C:10]3[N:9]=2)=[CH:4][CH:3]=1.C(O)(=[O:25])C.ClC1C=CC=C(C(OO)=O)C=1>O>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[N:16]([CH2:17][C:18]([N:20]([CH3:22])[CH3:21])=[O:19])[C:11]3=[N+:12]([O-:25])[CH:13]=[CH:14][CH:15]=[C:10]3[N:9]=2)=[CH:4][CH:3]=1

Participants

5

Reactant 3

HCID 176Acetic AcidHCID 70297m-Chloroperbenzoic acidHCID 14390220HCID 14390220, compound

Product 1

HCID 14390404HCID 14390404, compoundYield 88%

Reagents, catalysts & solvents 1

HCID 962WaterSolvent

Conditions

Temperature
60 °C

Procedure

A mixture of 2-(4-chlorophenyl)-N,N-dimethyl-3H-imidazo[4,5-b]pyridine-3-acetamide (0.3 g, 0.00096 mole), glacial acetic acid (2.5 ml), and m-chloroperbenzoic acid (0.66 g, 0.00384 mole) was heated at 60° C. for a total of 4 hrs. The reaction mixture was diluted with water and the organic acid which precipitated was filtered. The aqueous filtrate was neutralized for peroxides with 10% sodium sulfite. The aqueous solution was evaporated to dryness and the residue was dissolved in methylene chloride. The methylene chloride was extracted with a minimum of saturated sodium bicarbonate. The methylene chloride wad dried and evaporated to a residue which crystallized upon standing. The solid was recrystallized from tetrahydrofuran-hexanes with refrigeration overnight. The solid was collected by filtration and dried under high vacuum overnight to give 0.28 g (88%) of the title compound, mp. 200°-201.5° C.

Workup

  1. customthe organic acid which precipitated
  2. filtrationwas filtered
  3. customThe aqueous solution was evaporated to dryness
  4. dissolutionthe residue was dissolved in methylene chloride
  5. extractionThe methylene chloride was extracted with a minimum of saturated sodium bicarbonate
  6. dry with materialThe methylene chloride wad dried
  7. customevaporated to a residue which
  8. customcrystallized
  9. customThe solid was recrystallized from tetrahydrofuran-hexanes with refrigeration overnight
  10. filtrationThe solid was collected by filtration
  11. customdried under high vacuum overnight

Sources & evidence

ORD record
ord-6fc658e6b3d2418a95e87e0144c62b15
Source dataset
uspto-grants-1989_10
Patent number
US04873251

Reaction notes

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