Hydrochloric Acid → HCID 22402961, compound
Reaction equation
[CH2:1]([N:3]1[C:7]2=[CH:8][CH:9]=[C:10]([C:16]([O:18]C)=[O:17])[C:11]([C:12]([O:14]C)=[O:13])=[C:6]2[N:5]=[C:4]1[CH3:20])[CH3:2].[OH-].[Na+].Cl>CO>[CH2:1]([N:3]1[C:7]2=[CH:8][CH:9]=[C:10]([C:16]([OH:18])=[O:17])[C:11]([C:12]([OH:14])=[O:13])=[C:6]2[N:5]=[C:4]1[CH3:20])[CH3:2]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 100 °C
Procedure
A mixture of dimethyl 1-ethyl-2-methyl-4,5-benzimidazoledicarboxylate (5.30 g, 19.2 mmol), methanol and 5N sodium hydroxide (30 mL, 150 mmol) is stirred for 4 hours at 100° C., cooled, acidified with hydrochloric acid and filtered to give the title product as a lemon yellow powder (4.07 g, 85.5%), identified by 1HNMR spectral analysis.
Workup
- temperaturecooled
- filtrationfiltered
Sources & evidence
- ORD record
- ord-b456f1208d7342da8a8ed8853145b1e7
- Source dataset
- uspto-grants-1996_05
- Patent number
- US05516751
Reaction notes
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