Sodium Hydroxide → HCID 18625903, compound
Reaction equation
[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[C:7]1[CH:37]=[CH:36][C:10]([C:11]([NH:13][CH2:14][CH2:15][O:16][C:17]2[CH:22]=[CH:21][C:20]([CH2:23][CH:24]([O:29][C:30]3[CH:31]=[N:32][CH:33]=[CH:34][CH:35]=3)[C:25]([O:27]C)=[O:26])=[CH:19][CH:18]=2)=[O:12])=[CH:9][CH:8]=1.[OH-].[Na+]>>[N:1]1[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[C:7]1[CH:8]=[CH:9][C:10]([C:11]([NH:13][CH2:14][CH2:15][O:16][C:17]2[CH:22]=[CH:21][C:20]([CH2:23][CH:24]([O:29][C:30]3[CH:31]=[N:32][CH:33]=[CH:34][CH:35]=3)[C:25]([OH:27])=[O:26])=[CH:19][CH:18]=2)=[O:12])=[CH:36][CH:37]=1Participants
3
Procedure
In a similar manner to that described in Example 2, methyl 3-[4-[2-(4-pyridine-2-ylbenzoylamino)ethoxy]phenyl]-2-(pyridine-3-yloxy)propionate (248 mg), which is the product of Example 154, was reacted with aqueous sodium hydroxide solution (1N, 1.00 ml) and the reaction mixture was treated to give the title compound (212 mg) as colorless crystals.
Workup
- additionthe reaction mixture was treated
Sources & evidence
- ORD record
- ord-0a9c850c1882497ab46966c3c52a4eba
- Source dataset
- uspto-grants-2003_03
- Patent number
- US06528525B1
Reaction notes
Loading…