Citric Acid → HCID 178440183, compound

HRID 1197602Notes

Reaction equation

HRID 1197602 reaction equation
[CH3:1][C:2]1[N:3]([C:8]2[N:9]=[C:10]([CH2:35][CH2:36][CH3:37])[N:11]([CH2:17][C:18]3[CH:23]=[CH:22][C:21]([C:24]4[CH:29]=[CH:28][CH:27]=[CH:26][C:25]=4[C:30]4[NH:34][N:33]=[N:32][N:31]=4)=[CH:20][CH:19]=3)[C:12]=2[C:13]([O:15]C)=[O:14])[C:4]([CH3:7])=[CH:5][CH:6]=1.[OH-].[Na+].C(O)(=O)CC(CC(O)=O)(C(O)=O)O>CO>[CH3:1][C:2]1[N:3]([C:8]2[N:9]=[C:10]([CH2:35][CH2:36][CH3:37])[N:11]([CH2:17][C:18]3[CH:23]=[CH:22][C:21]([C:24]4[CH:29]=[CH:28][CH:27]=[CH:26][C:25]=4[C:30]4[NH:31][N:32]=[N:33][N:34]=4)=[CH:20][CH:19]=3)[C:12]=2[C:13]([OH:15])=[O:14])[C:4]([CH3:7])=[CH:5][CH:6]=1

Participants

5

Procedure

A mixture of methyl 4-(2,5-dimethyl-1H-pyrrol-1-yl)-2-propyl-1-[(2'-(1H-tetrazol-5-yl)biphen-4-yl)methyl]1H-imidazole-5-carboxylate 9 (Example 70) in methanol (5 mL) containing 5 mL of 2.5N NaOH was heated under reflux for 3 hours. The reaction mixture was cooled, acidified with 10% citric acid to pH 4, and extracted with ethyl acetate. The combined organic layers were dried over anhydrous MgSO4 and the solvent removed under reduced pressure. The acid was further purified by flash chromatography on silica gel eluting with 5% methanol in ethyl acetate to furnish 0.2 g for the title compound 4-(2,5-dimethyl-1H-pyrrol-1-yl)-2-propyl-1-[(2'-(1H-tetrazol-5-yl)biphen-4-yl)methyl]-1H-imidazole-5-carboxylic acid. MS (FAB, thioglycerol) 482 (M+).

Workup

  1. temperaturewas heated
  2. temperatureunder reflux for 3 hours
  3. temperatureThe reaction mixture was cooled
  4. extractionextracted with ethyl acetate
  5. dry with materialThe combined organic layers were dried over anhydrous MgSO4
  6. customthe solvent removed under reduced pressure
  7. customThe acid was further purified by flash chromatography on silica gel eluting with 5% methanol in ethyl acetate

Sources & evidence

ORD record
ord-4c9bcba84dbf4348b1cad4ea87660095
Source dataset
uspto-grants-1994_01
Patent number
US05276048

Reaction notes

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