Hydrochloric Acid → HCID 178489893, compound

HRID 599543Notes

Reaction equation

HRID 599543 reaction equation
[OH-].[Na+].[F:3][C:4]1[CH:9]=[CH:8][C:7]([C:10]2[NH:14][C:13](/[CH:15]=[CH:16]/[C:17]3[CH:22]=[CH:21][C:20]([N:23]4[CH:27]=[C:26]([CH3:28])[N:25]=[CH:24]4)=[C:19]([O:29][CH3:30])[CH:18]=3)=[N:12][C:11]=2[C:31]([O:33]C)=[O:32])=[CH:6][CH:5]=1.Cl>CO>[F:3][C:4]1[CH:5]=[CH:6][C:7]([C:10]2[NH:14][C:13](/[CH:15]=[CH:16]/[C:17]3[CH:22]=[CH:21][C:20]([N:23]4[CH:27]=[C:26]([CH3:28])[N:25]=[CH:24]4)=[C:19]([O:29][CH3:30])[CH:18]=3)=[N:12][C:11]=2[C:31]([OH:33])=[O:32])=[CH:8][CH:9]=1

Participants

5

Conditions

Temperature
80 °C

Procedure

A 2 N sodium hydroxide solution (1 mL) was added to a solution of methyl 5-(4-fluorophenyl)-2-{(E)-2-[3-methoxy-4-(4-methyl-1H-imidazol-1-yl)phenyl]vinyl}-1H-imidazole-4-carboxylate (143 mg) in methanol (1 mL), and the reaction solution was stirred at room temperature for 1.5 hours and at 80° C. for 17 hours. The reaction solution was left to cool to room temperature. Then, 2 N hydrochloric acid (1 mL) was added to the reaction solution, which was then stirred at room temperature for 30 minutes. The solid precipitated from the reaction solution was collected by filtration to obtain 139 mg of the title compound.

Workup

  1. waitThe reaction solution was left
  2. temperatureto cool to room temperature
  3. stirringwas then stirred at room temperature for 30 minutes
  4. customThe solid precipitated from the reaction solution
  5. filtrationwas collected by filtration

Sources & evidence

ORD record
ord-716e893af8c04ce196c49c6d698c326b
Source dataset
uspto-grants-2011_03
Patent number
US07897632B2

Reaction notes

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