Citric Acid → HCID 67274950, compound
Reaction equation
[N:1]1([C:5]2[N:14]=[C:13]3[C:8]([C:9](=[O:31])[C:10]([C:26]([O:28]CC)=[O:27])=[CH:11][N:12]3[CH2:15][C:16]3[CH:21]=[CH:20][C:19]([O:22][CH3:23])=[CH:18][C:17]=3[O:24][CH3:25])=[C:7]([CH3:32])[C:6]=2[F:33])[CH2:4][CH2:3][CH2:2]1.[Li+].[OH-].C(O)(=O)CC(CC(O)=O)(C(O)=O)O>C1COCC1>[N:1]1([C:5]2[N:14]=[C:13]3[C:8]([C:9](=[O:31])[C:10]([C:26]([OH:28])=[O:27])=[CH:11][N:12]3[CH2:15][C:16]3[CH:21]=[CH:20][C:19]([O:22][CH3:23])=[CH:18][C:17]=3[O:24][CH3:25])=[C:7]([CH3:32])[C:6]=2[F:33])[CH2:2][CH2:3][CH2:4]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of Example 5A (250 mg) in THF (30 mL) dichloromethane (10 mL) was treated with 1M LiOH (15 mL), stirred for 18 hours, treated with 10% citric acid, and extracted with dichloromethane; and the extract was concentrated.
Workup
- extractionextracted with dichloromethane
- concentrationand the extract was concentrated
Sources & evidence
- ORD record
- ord-2a375b385bf4484baffd0cae669c64ed
- Source dataset
- uspto-grants-2012_04
- Patent number
- US08163769B2
Reaction notes
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