Sodium Hydroxide → HCID 10481724, compound
Reaction equation
[F:1][C:2]1[CH:3]=[C:4]([CH:37]=[CH:38][C:39]=1[F:40])[O:5][CH:6]([CH2:12][C:13]1[CH:18]=[CH:17][C:16]([O:19][CH2:20][CH2:21][NH:22][C:23](=[O:36])[C:24]2[CH:29]=[CH:28][C:27]([C:30]3[CH:35]=[CH:34][CH:33]=[CH:32][N:31]=3)=[CH:26][CH:25]=2)=[CH:15][CH:14]=1)[C:7]([O:9]CC)=[O:8].[OH-].[Na+]>>[F:1][C:2]1[CH:3]=[C:4]([CH:37]=[CH:38][C:39]=1[F:40])[O:5][CH:6]([CH2:12][C:13]1[CH:14]=[CH:15][C:16]([O:19][CH2:20][CH2:21][NH:22][C:23](=[O:36])[C:24]2[CH:29]=[CH:28][C:27]([C:30]3[CH:35]=[CH:34][CH:33]=[CH:32][N:31]=3)=[CH:26][CH:25]=2)=[CH:17][CH:18]=1)[C:7]([OH:9])=[O:8]Participants
3
Procedure
In a similar manner to that described in Example 2, ethyl 2-(3,4-difluorophenoxy)-3-[4-[2-(4-pyridine-2-ylbenzoylamino)ethoxy]phenyl]propionate (281 mg), which is the product of Example 140, was reacted with aqueous sodium hydroxide solution (1N, 1.02 ml) and the reaction mixture was treated to give the title compound (246 mg) as a white powder.
Workup
- additionthe reaction mixture was treated
Sources & evidence
- ORD record
- ord-c13cfe1dcb00463ca7e690b27c818eaf
- Source dataset
- uspto-grants-2003_03
- Patent number
- US06528525B1
Reaction notes
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