Ethanol → HCID 15617192, compound

HRID 2072946Notes

Reaction equation

HRID 2072946 reaction equation
C([O:3][C:4](=[O:25])[CH2:5][N:6]1[C:10]2=[N:11][CH:12]=[CH:13][CH:14]=[C:9]2[N:8]=[C:7]1[C:15]1[CH:20]=[CH:19][C:18]([C:21]([F:24])([F:23])[F:22])=[CH:17][CH:16]=1)C.[OH-].[K+].C(O)C>O>[F:24][C:21]([F:22])([F:23])[C:18]1[CH:19]=[CH:20][C:15]([C:7]2[N:6]([CH2:5][C:4]([OH:25])=[O:3])[C:10]3=[N:11][CH:12]=[CH:13][CH:14]=[C:9]3[N:8]=2)=[CH:16][CH:17]=1

Participants

5

Procedure

A solution of 2-[4-(trifluoromethyl)phenyl]-3H-imidazo[4,5-b] pyridine-3-acetic acid ethyl ester (17.7 g, 0.051 mole), potassium hydroxide pellets (4.5 g, 0.080 mole), 95% ethanol (150 ml), and water (10 ml) was refluxed for 21/2 hrs. The ethanol was evaporated in vacuo, the residue acidified with glacial acetic acid, and the mixture filtered. The filter cake was suspended in water (300 ml) and filtered. The filter cake was air dried (17 g) and recrystallized from ethanol-water to give 12.21 g (75%) of a white solid, mp 240°-241° C.

Workup

  1. customThe ethanol was evaporated in vacuo
  2. filtrationthe mixture filtered
  3. filtrationfiltered
  4. customdried (17 g)
  5. customrecrystallized from ethanol-water

Sources & evidence

ORD record
ord-cf2b5f3194a745a4a64f90b5939b33bf
Source dataset
uspto-grants-1990_04
Patent number
US04914109

Reaction notes

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