Sodium Hydroxide → HCID 21459791, compound
Reaction equation
[C:1]([O:5][C:6]([NH:8][CH2:9][CH2:10][CH2:11][NH:12][C:13](=[O:26])[NH:14][C:15]1[CH:16]=[C:17]([CH:23]=[CH:24][CH:25]=1)[C:18]([O:20]CC)=[O:19])=[O:7])([CH3:4])([CH3:3])[CH3:2].[OH-].[Na+]>C(O)C>[C:1]([O:5][C:6]([NH:8][CH2:9][CH2:10][CH2:11][NH:12][C:13](=[O:26])[NH:14][C:15]1[CH:16]=[C:17]([CH:23]=[CH:24][CH:25]=1)[C:18]([OH:20])=[O:19])=[O:7])([CH3:4])([CH3:2])[CH3:3]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
2.50 g (6.84 mmol) of ethyl 3-(3-(3-tert-butyloxycarbonylaminopropyl)ureido)benzoate are dissolved in 80 ml of ethanol and treated with 3.42 ml of 2N NaOH. After 7 d at room temperature, the mixture is concentrated in vacuo. The residue is treated with water, and the mixture is acidified with citric acid and extracted with ethyl acetate. After drying (MgSO4), solid is filtered off and the solvent is removed in vacuo.
Workup
- concentrationthe mixture is concentrated in vacuo
- additionThe residue is treated with water
- extractionextracted with ethyl acetate
- dry with materialAfter drying (MgSO4), solid
- filtrationis filtered off
- customthe solvent is removed in vacuo
Sources & evidence
- ORD record
- ord-254efbe1ea8e46b9a16097f3d8b04eaf
- Source dataset
- uspto-grants-1997_12
- Patent number
- US05703050
Reaction notes
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