Sodium Hydroxide → HCID 10255705, compound
Reaction equation
[C:1]1([CH2:7][CH2:8][CH2:9][CH:10]([CH2:16][C:17]2[CH:22]=[CH:21][C:20]([O:23][CH2:24][CH2:25][NH:26][C:27](=[O:40])[C:28]3[CH:33]=[CH:32][C:31]([C:34]4[CH:39]=[CH:38][CH:37]=[CH:36][N:35]=4)=[CH:30][CH:29]=3)=[CH:19][CH:18]=2)[C:11]([O:13]CC)=[O:12])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[OH-].[Na+]>>[C:1]1([CH2:7][CH2:8][CH2:9][CH:10]([CH2:16][C:17]2[CH:22]=[CH:21][C:20]([O:23][CH2:24][CH2:25][NH:26][C:27](=[O:40])[C:28]3[CH:29]=[CH:30][C:31]([C:34]4[CH:39]=[CH:38][CH:37]=[CH:36][N:35]=4)=[CH:32][CH:33]=3)=[CH:19][CH:18]=2)[C:11]([OH:13])=[O:12])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1Participants
3
Procedure
In a similar manner to that described in Example 2, ethyl 2-(3-phenylpropyl)-3-[4-[2-(4-pyridine-2-ylbenzoylamino)ethoxy]phenyl]propionate (767 mg), which is the product of Example 3, was reacted with an aqueous sodium hydroxide solution (1N, 2.86 ml) and the reaction mixture was treated. The residue was crystallized from a mixture of diisopropyl ether and ethyl acetate to give the title compound (361 mg) as colorless crystals.
Workup
- additionthe reaction mixture was treated
- customThe residue was crystallized from a mixture of diisopropyl ether and ethyl acetate
Sources & evidence
- ORD record
- ord-3347712f580f43cbad2796d3539d9011
- Source dataset
- uspto-grants-2003_03
- Patent number
- US06528525B1
Reaction notes
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