Hydrochloric Acid → HCID 46945388, compound
Reaction equation
C[O:2][C:3]([C:5]1[C:13]2[N:12]=[C:11]([C:14]3[CH:19]=[CH:18][C:17]([C:20]4[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=4)=[CH:16][CH:15]=3)[NH:10][C:9]=2[CH:8]=[CH:7][CH:6]=1)=[O:4].[OH-].[Na+].Cl>C1COCC1.O>[C:17]1([C:20]2[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=2)[CH:18]=[CH:19][C:14]([C:11]2[NH:10][C:9]3[CH:8]=[CH:7][CH:6]=[C:5]([C:3]([OH:4])=[O:2])[C:13]=3[N:12]=2)=[CH:15][CH:16]=1Participants
6
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
2-Biphenyl-4-yl-1H-benzoimidazole-4-carboxylic acid methyl ester (180 mg, 0.54 mmol) was taken in THF (20 mL) and was refluxed with 5N NaOH (5 mL) solution for 14 h. It was then cooled to room temperature; THF was removed under reduced pressure to obtain a thick mass. This residue was diluted with water (10 mL) and adjusted pH to 2 with conc. hydrochloric acid. The precipitated solid was filtered, washed with water and dried in a vacuum oven to obtain compound the required compound as a pale yellow solid.
Workup
- customTHF was removed under reduced pressure
- customto obtain a thick mass
- filtrationThe precipitated solid was filtered
- washwashed with water
- customdried in a vacuum oven
Sources & evidence
- ORD record
- ord-1cdd4f8c96ba4669abb1199f9950a64f
- Source dataset
- uspto-grants-2015_04
- Patent number
- US09006454B2
Reaction notes
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