Hydrochloric Acid → HCID 178430527, compound
Reaction equation
C([NH:3][C:4]1[CH:5]=[C:6]([C:14]([NH2:16])=[O:15])[C:7]2[N:11]=[CH:10][NH:9][C:8]=2[C:12]=1[CH3:13])=O.Cl>CO>[NH2:3][C:4]1[CH:5]=[C:6]([C:14]([NH2:16])=[O:15])[C:7]2[N:11]=[CH:10][NH:9][C:8]=2[C:12]=1[CH3:13]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 6-(Formylamino)-7-methyl-1H-benzimidazole-4-carboxamide (11) (0.35 g, 1.6 mmol), 1M aqueous HCl (10 mL) and methanol (3 mL) is heated to reflux for about 1 hour. The reaction mixture is allowed to cool to ambient temperature and is then concentrated in vacuo to a white solid. The white solid is recrystallized from ethanol/water (3/1 v/v) to provide 6-(Amino)-7-methyl-1H-benzimidazole-4-carboxamide; hydrochloric acid salt (12) as a white solid (0.164 g, 54% Yield).
Workup
- temperatureis heated
- temperatureto reflux for about 1 hour
- concentrationis then concentrated in vacuo to a white solid
- customThe white solid is recrystallized from ethanol/water (3/1 v/v)
Sources & evidence
- ORD record
- ord-0640b0b1cf2a481b80016da5aff05eb7
- Source dataset
- uspto-grants-2007_12
- Patent number
- US07304084B2
Reaction notes
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