HCID 67275357, compound → HCID 67275055, compound
Reaction equation
[C:1]([O:5][C:6]([NH:8][C@@H:9]1[CH2:13][CH2:12][N:11]([C:14]2[N:23]=[C:22]3[C:17]([C:18](=[O:40])[C:19]([C:35]([O:37]CC)=[O:36])=[CH:20][N:21]3[CH2:24][C:25]3[CH:30]=[CH:29][C:28]([O:31][CH3:32])=[CH:27][C:26]=3[O:33][CH3:34])=[C:16]([CH3:41])[C:15]=2[F:42])[CH2:10]1)=[O:7])([CH3:4])([CH3:3])[CH3:2]>[Li+].[OH-].C1COCC1.ClCCl>[C:1]([O:5][C:6]([NH:8][C@@H:9]1[CH2:13][CH2:12][N:11]([C:14]2[N:23]=[C:22]3[C:17]([C:18](=[O:40])[C:19]([C:35]([OH:37])=[O:36])=[CH:20][N:21]3[CH2:24][C:25]3[CH:30]=[CH:29][C:28]([O:31][CH3:32])=[CH:27][C:26]=3[O:33][CH3:34])=[C:16]([CH3:41])[C:15]=2[F:42])[CH2:10]1)=[O:7])([CH3:4])([CH3:3])[CH3:2]Participants
5
Reactant 1
Product 1
Reagents, catalysts & solvents 3
Procedure
A solution of Example 1E (332 mg) in 1M LiOH (3 mL) and THF (7 mL) was stirred at ambient temperature for 18 hours, diluted with dichloromethane, washed with 1M HCl, and dried (Na2SO4), filtered, and concentrated.
Workup
- washwashed with 1M HCl
- dry with materialdried (Na2SO4)
- filtrationfiltered
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-ce61f28ed72b42a4bfdb5ed8002fb96e
- Source dataset
- uspto-grants-2012_04
- Patent number
- US08163769B2
Reaction notes
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