Sodium Hydroxide → HCID 22916442, compound

HRID 265385Notes

Reaction equation

HRID 265385 reaction equation
C([O:3][C:4]([CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][N:13]1[C:17]([C:18]2[CH:23]=[CH:22][C:21]([O:24][CH3:25])=[CH:20][CH:19]=2)=[C:16]([C:26]2[CH:31]=[CH:30][C:29]([O:32][CH3:33])=[CH:28][CH:27]=2)[N:15]=[C:14]1[C:34]1[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=1)=[O:5])C.[OH-].[Na+]>>[C:4]([CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][N:13]1[C:17]([C:18]2[CH:23]=[CH:22][C:21]([O:24][CH3:25])=[CH:20][CH:19]=2)=[C:16]([C:26]2[CH:27]=[CH:28][C:29]([O:32][CH3:33])=[CH:30][CH:31]=2)[N:15]=[C:14]1[C:34]1[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=1)([OH:5])=[O:3]

Participants

3

Procedure

1-(7-Ethoxycarbonylheptyl)-4,5-bis(4-methoxyphenyl)-2-phenylimidazole (10 g) was reacted with 2N sodium hydroxide in a method similar to Example 10. The aqueous reaction mixture was evaporated to dryness in vacuo and the residue was mixed with ethanol (150 ml) and insoluble material was filtered off. The filtrate was evaporated to dryness and the residue was purified by column chromatography on silica gel eluted with a dichloromethane:methanol gradient. Further purification on Amberlite resin IRA-400 eluted with a methanol:water to methanol:2N HCl gradient and recrystallisation from ethanol gave 1-(7-carboxyheptyl)-4,5-bis(4-methoxy-phenyl)-2-phenylimidazole (2.01 g, 21%) as a white solid, m.p. 149°-150°. Found: C, 74.50; H, 6.75; N, 5.69%; C31H34N2O4 0.5% w/w C2H5OH requires: C, 74.56; H, 6.90; N, 5.59%.

Workup

  1. customThe aqueous reaction mixture was evaporated to dryness in vacuo
  2. additionthe residue was mixed with ethanol (150 ml) and insoluble material
  3. filtrationwas filtered off
  4. customThe filtrate was evaporated to dryness
  5. customthe residue was purified by column chromatography on silica gel
  6. washeluted with a dichloromethane
  7. customFurther purification on Amberlite resin
  8. washeluted with a methanol
  9. customwater to methanol:2N HCl gradient and recrystallisation from ethanol

Sources & evidence

ORD record
ord-69d4efd739194f0ebec7dc792b74ca1c
Source dataset
uspto-grants-1997_07
Patent number
US05648373

Reaction notes

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