Citric Acid → HCID 57302818, compound
Reaction equation
C([O:3][C:4](=[O:43])[C@@H:5]([NH:33][S:34]([C:37]1[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=1)(=[O:36])=[O:35])[CH2:6][NH:7][C:8](=[O:32])[CH2:9][CH2:10][NH:11][C:12](=[O:31])[CH2:13][O:14][CH:15]1[CH2:20][CH2:19][N:18]([C:21]([O:23][CH2:24][C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=2)=[O:22])[CH2:17][CH2:16]1)C.[OH-].[Na+].C(O)(=O)CC(CC(O)=O)(C(O)=O)O>CN(C=O)C>[C:37]1([S:34]([NH:33][C@@H:5]([CH2:6][NH:7][C:8](=[O:32])[CH2:9][CH2:10][NH:11][C:12](=[O:31])[CH2:13][O:14][CH:15]2[CH2:20][CH2:19][N:18]([C:21]([O:23][CH2:24][C:25]3[CH:26]=[CH:27][CH:28]=[CH:29][CH:30]=3)=[O:22])[CH2:17][CH2:16]2)[C:4]([OH:43])=[O:3])(=[O:36])=[O:35])[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
The compound (144 mg) obtained in the above (2) is dissolved in DMF (3 ml), and thereto is added 1N aqueous sodium hydroxide solution (698 μl) under ice-cooling, and the mixture is stirred for 1.5 hour. The pH value thereof is adjusted to pH 2 with 10% aqueous citric acid solution, and extracted three times with ethyl acetate. The extract is washed twice with a saturated brine, and dried over anhydrous magnesium sulfate. The desiccant is removed by filtration, and the filtrate is concentrated under reduced pressure to give the title compound (92 mg).
Workup
- temperaturecooling
- extractionextracted three times with ethyl acetate
- washThe extract is washed twice with a saturated brine
- dry with materialdried over anhydrous magnesium sulfate
- customThe desiccant is removed by filtration
- concentrationthe filtrate is concentrated under reduced pressure
Sources & evidence
- ORD record
- ord-af399f1256814ab081caad96d435d6f4
- Source dataset
- uspto-grants-1998_01
- Patent number
- US05707994
Reaction notes
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