Sodium Hydroxide → 2-butyl-1-[[2'-carboxy-(1,1'-biphenyl)-4-yl]-methyl]-4-(2-fluoroethylthio)-1H-imidazole-5-carboxylic acid

HRID 36019Notes

Reaction equation

HRID 36019 reaction equation
[OH-].[Na+].[CH2:3]([C:7]1[N:8]([CH2:21][C:22]2[CH:27]=[CH:26][C:25]([C:28]3[CH:33]=[CH:32][CH:31]=[CH:30][C:29]=3[C:34]([OH:36])=[O:35])=[CH:24][CH:23]=2)[C:9]([C:16]([O:18]CC)=[O:17])=[C:10]([S:12][CH2:13][CH2:14][F:15])[N:11]=1)[CH2:4][CH2:5][CH3:6]>C(O)C>[CH2:3]([C:7]1[N:8]([CH2:21][C:22]2[CH:23]=[CH:24][C:25]([C:28]3[CH:33]=[CH:32][CH:31]=[CH:30][C:29]=3[C:34]([OH:36])=[O:35])=[CH:26][CH:27]=2)[C:9]([C:16]([OH:18])=[O:17])=[C:10]([S:12][CH2:13][CH2:14][F:15])[N:11]=1)[CH2:4][CH2:5][CH3:6]

Participants

4

Procedure

2.25 cm3 of a 2N solution of sodium hydroxide is added at ambient temperature to 450 mg of the product obtained in Example 43 dissolved in 10 cm3 of ethanol, then the mixture is left for 3 days. The solvents are evaporated under reduced pressure, the residue is taken up in water, 2.25 cm3 of hydrochloric acid 2M/l is added. The precipitate formed is filtered, washed with water, dried under reduced pressure and 380 mg of expected product is obtained which is recrystallized from isopropanol. M.p.=185°-186° C.

Workup

  1. customThe solvents are evaporated under reduced pressure
  2. addition2.25 cm3 of hydrochloric acid 2M/l is added
  3. customThe precipitate formed
  4. filtrationis filtered
  5. washwashed with water
  6. customdried under reduced pressure

Sources & evidence

ORD record
ord-4019f723fff54f6dbadc5410d244214a
Source dataset
uspto-grants-1995_05
Patent number
US05412101

Reaction notes

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