Sodium Hydroxide → HCID 18625851, compound
Reaction equation
[CH2:1]([O:8][CH:9]([CH2:14][C:15]1[CH:20]=[CH:19][C:18]([O:21][CH2:22][CH2:23][NH:24][C:25](=[O:38])[C:26]2[CH:31]=[CH:30][C:29]([C:32]3[CH:37]=[CH:36][CH:35]=[CH:34][N:33]=3)=[CH:28][CH:27]=2)=[CH:17][CH:16]=1)[C:10]([O:12]C)=[O:11])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[OH-].[Na+]>>[CH2:1]([O:8][CH:9]([CH2:14][C:15]1[CH:20]=[CH:19][C:18]([O:21][CH2:22][CH2:23][NH:24][C:25](=[O:38])[C:26]2[CH:31]=[CH:30][C:29]([C:32]3[CH:37]=[CH:36][CH:35]=[CH:34][N:33]=3)=[CH:28][CH:27]=2)=[CH:17][CH:16]=1)[C:10]([OH:12])=[O:11])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1Participants
3
Procedure
In a similar manner to that described in Example 2, methyl 2-benzyloxy-3-[4-[2-(4-pyridine-2-ylbenzoylamino)ethoxy]phenyl]propionate (94 mg), which is the product of Example 158, was reacted with aqueous sodium hydroxide solution (1N, 0.36 ml) and the reaction mixture was treated to give the title compound (86 mg) as colorless crystals.
Workup
- additionthe reaction mixture was treated
Sources & evidence
- ORD record
- ord-3f13be4cea5b4d3dba4efbe32a9e222b
- Source dataset
- uspto-grants-2003_03
- Patent number
- US06528525B1
Reaction notes
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