Sodium Hydroxide → HCID 67671474, compound
Reaction equation
[ClH:1].[C:2]([C:5]1[CH:18]=[CH:17][C:8]2[CH:9]=[C:10]([C:12]([O:14]CC)=[O:13])[O:11][C:7]=2[CH:6]=1)(=[NH:4])[NH2:3].[OH-].[Na+]>>[ClH:1].[C:2]([C:5]1[CH:18]=[CH:17][C:8]2[CH:9]=[C:10]([C:12]([OH:14])=[O:13])[O:11][C:7]=2[CH:6]=1)(=[NH:3])[NH2:4]Participants
3
Procedure
Ethyl 6-amidino-2-benzofurancarboxylate hydrochloride (129 mg, 0.480 mmol) was hydrolyzed with a 1N aqueous sodium hydroxide solution to give 65 mg of 6-amidino-2-benzofurancarboxylic acid hydrochloride as a brown solid (56%).
Sources & evidence
- ORD record
- ord-ef284b87d6914ad7acbedfc6e9197447
- Source dataset
- uspto-grants-1997_06
- Patent number
- US05635527
Reaction notes
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