Hydrochloric Acid → HCID 46945388, compound

HRID 1470580Notes

Reaction equation

HRID 1470580 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]=1

Participants

6

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

  1. customTHF was removed under reduced pressure
  2. customto obtain a thick mass
  3. filtrationThe precipitated solid was filtered
  4. washwashed with water
  5. 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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