Methanol → HCID 57860410, compound
Reaction equation
C([O:4][CH2:5][C:6]([NH:8][CH2:9][CH2:10][N:11]([C:13]([C:15]1[S:27][C:26]2[C:25]3[CH:24]=[CH:23][CH:22]=[CH:21][C:20]=3[N:19]([CH2:28][C:29](=[O:36])[C:30]3[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=3)[C:18](=[O:37])[C:17]=2[C:16]=1[O:38][CH3:39])=[O:14])[CH3:12])=[O:7])(=O)C.[OH-].[Na+].CO>C1COCC1.C(=O)([O-])O.[Na+]>[OH:4][CH2:5][C:6]([NH:8][CH2:9][CH2:10][N:11]([CH3:12])[C:13]([C:15]1[S:27][C:26]2[C:25]3[CH:24]=[CH:23][CH:22]=[CH:21][C:20]=3[N:19]([CH2:28][C:29](=[O:36])[C:30]3[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=3)[C:18](=[O:37])[C:17]=2[C:16]=1[O:38][CH3:39])=[O:14])=[O:7]Participants
6
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
A mixed solution of the compound of Example 504 (120 mg, 0.22 mmol) and 4N aqueous sodium hydroxide solution (2 mL) in THF (4 mL)-methanol (4 mL) was stirred at room temperature for 2 hr, the reaction mixture was diluted with saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, dried over magnesium sulfate, and concentrated under reduced pressure. Recrystallization of the crude solid from ethyl acetate-hexane gave the title compound (65 mg, 58%) as white crystals.
Workup
- extractionthe mixture was extracted with ethyl acetate
- washThe extract was washed with saturated brine
- dry with materialdried over magnesium sulfate
- concentrationconcentrated under reduced pressure
- customRecrystallization of the crude solid from ethyl acetate-hexane
Sources & evidence
- ORD record
- ord-47706c4e32304405b88dfbce854b5ab4
- Source dataset
- uspto-grants-2013_03
- Patent number
- US08399449B2
Reaction notes
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