Hydrochloric Acid → HCID 53634676, compound
Reaction equation
C([O:3][C:4](=[O:26])[CH2:5][C@@H:6]([C:19]1[CH:24]=[CH:23][CH:22]=[C:21]([F:25])[CH:20]=1)[NH:7][CH2:8][C:9]1[CH:18]=[CH:17][C:16]2[CH2:15][CH2:14][CH2:13][NH:12][C:11]=2[N:10]=1)C.[OH-].[Na+].Cl>CCO>[F:25][C:21]1[CH:20]=[C:19]([C@@H:6]([NH:7][CH2:8][C:9]2[CH:18]=[CH:17][C:16]3[CH2:15][CH2:14][CH2:13][NH:12][C:11]=3[N:10]=2)[CH2:5][C:4]([OH:26])=[O:3])[CH:24]=[CH:23][CH:22]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of ester 9-2 (450 mg, 1.26 mmol) in EtOH (3 mL) was added 1N NaOH (1.39 ml, 1.39 mmol). After stirring for 1 h, the solvents were evaporated and the residue was dissolved in 1N HCl (1.39 ml, 1.39 mmol). The solution was concentrated and then azeotroped with CH3CN to give the acid 9-3 as a brown solid.
Workup
- customthe solvents were evaporated
- concentrationThe solution was concentrated
- customazeotroped with CH3CN
Sources & evidence
- ORD record
- ord-6aae96892bb54834b9e2be9bd8123e4d
- Source dataset
- uspto-grants-2001_10
- Patent number
- US06297249B1
Reaction notes
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