HCID 15617183, compound → HCID 15617212, compound

HRID 2073115Notes

Reaction equation

HRID 2073115 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[N:16]([CH2:17][CH:18]([C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=3)[OH:19])[C:11]3=[N:12][CH:13]=[CH:14][CH:15]=[C:10]3[N:9]=2)=[CH:4][CH:3]=1.[Cr](Cl)([O-])(=O)=O.[NH+]1C=CC=CC=1>C(Cl)Cl>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[N:16]([CH2:17][C:18]([C:20]3[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=3)=[O:19])[C:11]3=[N:12][CH:13]=[CH:14][CH:15]=[C:10]3[N:9]=2)=[CH:4][CH:3]=1

Participants

4

Procedure

Under nitrogen atmosphere, a solution of 2-(4-chlorophenyl)-α-phenyl-3H-imidazo[4,5-b]pyridine-3-ethanol (9.44 g, 0.027 mole) in methylene chloride (50 ml) was added to a stirred suspension of pyridinium chlorochromate (8.75 g, 0.041 mole) in methylene chloride (100 ml) and allowed to stir at room temperature overnight. The reaction mixture was filtered. The residue was treated with boiling methylene chloride and filtered. The methylene chloride filtrate was treated with Florisil® and filtered. The filtrate was evaporated to dryness and the residue was recrystallized from isopropyl alcohol. The crystals were collected by filtration, washed with isopropyl alcohol/water, and dried under high vacuum overnight at room temperature to give 5.0 g (54%) of title compound, mp. 211°-212.5° C.

Workup

  1. filtrationThe reaction mixture was filtered
  2. additionThe residue was treated with boiling methylene chloride
  3. filtrationfiltered
  4. additionThe methylene chloride filtrate was treated with Florisil®
  5. filtrationfiltered
  6. customThe filtrate was evaporated to dryness
  7. customthe residue was recrystallized from isopropyl alcohol
  8. filtrationThe crystals were collected by filtration
  9. washwashed with isopropyl alcohol/water
  10. customdried under high vacuum overnight at room temperature

Sources & evidence

ORD record
ord-55759df865184f1685ceab42be9869e4
Source dataset
uspto-grants-1990_04
Patent number
US04914109

Reaction notes

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