Acetic Acid → HCID 145723584, compound
Reaction equation
[OH-].[Na+].C([O:5][C:6](=[O:38])[CH2:7][O:8][C:9]1[CH:14]=[CH:13][C:12]([C:15](=[O:37])[CH2:16][N:17]2[CH2:25][C:24]3[C:19](=[CH:20][CH:21]=[C:22]([C:26]([NH:28][C:29]([O:31][C:32]([CH3:35])([CH3:34])[CH3:33])=[O:30])=[NH:27])[CH:23]=3)[C:18]2=[O:36])=[CH:11][CH:10]=1)C.CC(O)=O>CO>[C:32]([O:31][C:29]([NH:28][C:26](=[NH:27])[C:22]1[CH:23]=[C:24]2[C:19](=[CH:20][CH:21]=1)[C:18](=[O:36])[N:17]([CH2:16][C:15]([C:12]1[CH:11]=[CH:10][C:9]([O:8][CH2:7][C:6]([OH:38])=[O:5])=[CH:14][CH:13]=1)=[O:37])[CH2:25]2)=[O:30])([CH3:35])([CH3:33])[CH3:34]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Aqueous 0.1N NaOH (11.4 ml; 1.14 mmol) was added to a solution of the compound of example 17a (0.375 g; 0.756 mmol) in MeOH (10 ml), The reaction mixture was stirred at room temperature for 30 min., acidified with AcOH and concentrated. The crude title compound obtained was filtered, washed with cold water and dried under vacuum. Yield, 140 mg.
Workup
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-566adbc7ff684e81bc679f899296d7f4
- Source dataset
- uspto-grants-2010_07
- Patent number
- US07759387B2
Reaction notes
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