Sodium Hydroxide → Sodium 4-(2-fluorophenyl)-2-(5-phenylpyridine-3-carboxamido)-benzoate
Reaction equation
[OH-].[Na+:2].[F:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[C:10]1[CH:18]=[CH:17][C:13]([C:14]([OH:16])=[O:15])=[C:12]([NH:19][C:20]([C:22]2[CH:23]=[N:24][CH:25]=[C:26]([C:28]3[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=3)[CH:27]=2)=[O:21])[CH:11]=1>C(O)C>[F:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=1[C:10]1[CH:18]=[CH:17][C:13]([C:14]([O-:16])=[O:15])=[C:12]([NH:19][C:20]([C:22]2[CH:23]=[N:24][CH:25]=[C:26]([C:28]3[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=3)[CH:27]=2)=[O:21])[CH:11]=1.[Na+:2]Participants
4
Procedure
Ethanol (1.5 mL) and a 1 mol/L aqueous solution of sodium hydroxide (0.087 mL) were sequentially added to the obtained 4-(2-fluorophenyl)-2-(5-phenylpyridine-3-carboxamido)benzoic acid (36 mg), followed by stirring at room temperature for 3 hours. The solid substance was collected by filtration to obtain 22 mg of sodium 4-(2-fluorophenyl)-2-(5-phenylpyridine-3-carboxamido)-benzoate as a white solid.
Workup
- filtrationThe solid substance was collected by filtration
Sources & evidence
- ORD record
- ord-9f892ce130fd41d28e01b5164eb52546
- Source dataset
- uspto-grants-2013_07
- Patent number
- US08492582B2
Reaction notes
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