Acetic Acid → 1-[(4-Ethyl-5-{5-[4-(3-fluorophenoxy)phenyl]-1,2,4-oxadiazol-3-yl}-2-thienyl)methyl]azetidine-3-carboxylic acid
Reaction equation
[CH2:1]([C:3]1[CH:4]=[C:5]([CH2:27][N:28]2[CH2:31][CH:30]([C:32]([O:34]C)=[O:33])[CH2:29]2)[S:6][C:7]=1[C:8]1[N:12]=[C:11]([C:13]2[CH:18]=[CH:17][C:16]([O:19][C:20]3[CH:25]=[CH:24][CH:23]=[C:22]([F:26])[CH:21]=3)=[CH:15][CH:14]=2)[O:10][N:9]=1)[CH3:2].O.[OH-].[Li+].C(O)(=O)C>>[CH2:1]([C:3]1[CH:4]=[C:5]([CH2:27][N:28]2[CH2:31][CH:30]([C:32]([OH:34])=[O:33])[CH2:29]2)[S:6][C:7]=1[C:8]1[N:12]=[C:11]([C:13]2[CH:14]=[CH:15][C:16]([O:19][C:20]3[CH:25]=[CH:24][CH:23]=[C:22]([F:26])[CH:21]=3)=[CH:17][CH:18]=2)[O:10][N:9]=1)[CH3:2]Participants
4
Reactant 3
Product 1
Procedure
The title compound (83 mg) was synthesized in a yield of 54% as a white crystalline solid by conducting the reaction similar to that mentioned in Example 2 (2e) using methyl 1-[(4-ethyl-5-{5-[4-(3-fluorophenoxy)phenyl]-1,2,4-oxadiazol-3-yl}-2-thienyl)methyl]azetidine-3-carboxylate (0.16 mg, 0.32 mmol) that was obtained in Example 17 (17c), lithium hydroxide monohydrate (30 mg, 0.71 mmol), and acetic acid (39 μL, 0.71 mmol).
Workup
- customthe reaction similar to
Sources & evidence
- ORD record
- ord-1434ac1ad1de467380b5405bdccd529f
- Source dataset
- uspto-grants-2010_03
- Patent number
- US07687491B2
Reaction notes
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