Water → HCID 68939062, compound
Reaction equation
C([O:4][C@H:5]1[CH2:10][CH2:9][C@H:8]([C:11]([N:13]2[CH2:18][CH2:17][C@@H:16]([N:19]([C:21]([C:23]3[CH:28]=[CH:27][C:26]([Cl:29])=[CH:25][CH:24]=3)=[O:22])[CH3:20])[C@H:15]([C:30]3[CH:35]=[CH:34][C:33]([Cl:36])=[C:32]([Cl:37])[CH:31]=3)[CH2:14]2)=[O:12])[CH2:7][CH2:6]1)(=O)C.C(=O)([O-])[O-].[Na+].[Na+].O>CO>[Cl:29][C:26]1[CH:27]=[CH:28][C:23]([C:21]([N:19]([C@@H:16]2[CH2:17][CH2:18][N:13]([C:11]([CH:8]3[CH2:9][CH2:10][CH:5]([OH:4])[CH2:6][CH2:7]3)=[O:12])[CH2:14][C@H:15]2[C:30]2[CH:35]=[CH:34][C:33]([Cl:36])=[C:32]([Cl:37])[CH:31]=2)[CH3:20])=[O:22])=[CH:24][CH:25]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of the compound obtained in Example 518 (0.103 g) in methanol (1.8 mL) was added sodium carbonate (0.067 g) and the mixture was stirred at room temperature. The reaction mixture was poured into water, and the resultant product was extracted with ethyl acetate. The organic layer was washed with brine and dried, and the solvent was evaporated under reduced pressure to give the title compound (0.076 g, 80%) as a white powder.
Workup
- extractionthe resultant product was extracted with ethyl acetate
- washThe organic layer was washed with brine
- customdried
- customthe solvent was evaporated under reduced pressure
Sources & evidence
- ORD record
- ord-d4cb5728589047259fe658f3ef1fa315
- Source dataset
- uspto-grants-2013_06
- Patent number
- US08470816B2
Reaction notes
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