Sodium Hydroxide → HCID 9983291, compound
Reaction equation
[CH3:1][C:2]([O:33][C:34]1[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=1)([CH2:8][C:9]1[CH:14]=[CH:13][C:12]([O:15][CH2:16][CH2:17][NH:18][C:19](=[O:32])[C:20]2[CH:25]=[CH:24][C:23]([C:26]3[CH:31]=[CH:30][CH:29]=[CH:28][N:27]=3)=[CH:22][CH:21]=2)=[CH:11][CH:10]=1)[C:3]([O:5]CC)=[O:4].[OH-].[Na+]>>[CH3:1][C:2]([O:33][C:34]1[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=1)([CH2:8][C:9]1[CH:10]=[CH:11][C:12]([O:15][CH2:16][CH2:17][NH:18][C:19](=[O:32])[C:20]2[CH:25]=[CH:24][C:23]([C:26]3[CH:31]=[CH:30][CH:29]=[CH:28][N:27]=3)=[CH:22][CH:21]=2)=[CH:13][CH:14]=1)[C:3]([OH:5])=[O:4]Participants
3
Procedure
In a similar manner to that described in Example 2, ethyl 2-methyl-2-phenoxy-3-[4-[2-(4-pyridine-2-ylbenzoylamino)ethoxy]phenyl]propionate (930 mg), which is the product of Example 15, was reacted with aqueous sodium hydroxide solution (1N, 3.60 ml) at 70° C. and the reaction mixture was treated to give the title compound (545 mg) as a white powder.
Workup
- additionthe reaction mixture was treated
Sources & evidence
- ORD record
- ord-9bf629a970aa4860b295aecee3423993
- Source dataset
- uspto-grants-2003_03
- Patent number
- US06528525B1
Reaction notes
Loading…