Hydrochloric Acid → HCID 53945355, compound
Reaction equation
Cl.[CH2:2]([NH:4][CH:5]([CH2:11][C:12]1[CH:17]=[CH:16][C:15]([O:18][CH2:19][CH2:20][O:21][N:22]=[C:23]([C:25]2[CH:30]=[CH:29][C:28]([C:31]3[CH:36]=[CH:35][CH:34]=[CH:33][N:32]=3)=[CH:27][CH:26]=2)[CH3:24])=[CH:14][CH:13]=1)[C:6]([O:8]CC)=[O:7])[CH3:3].[OH-].[Na+].Cl>>[CH2:2]([NH:4][CH:5]([CH2:11][C:12]1[CH:13]=[CH:14][C:15]([O:18][CH2:19][CH2:20][O:21][N:22]=[C:23]([C:25]2[CH:26]=[CH:27][C:28]([C:31]3[CH:36]=[CH:35][CH:34]=[CH:33][N:32]=3)=[CH:29][CH:30]=2)[CH3:24])=[CH:16][CH:17]=1)[C:6]([OH:8])=[O:7])[CH3:3]Participants
4
Procedure
Reaction was carried out according to Example 2 using 273 mg of ethyl 2-ethylamino-3-[4-[2-[[1-[4-(2-pyridyl)phenyl]ethylidene]aminoxy]ethoxy]phenyl]propionate obtained in Example 15 and 2.4 ml of a 1N aqueous sodium hydroxide solution. When the pH of the reaction mixture thus obtained was adjusted to a value of 4 with 1N hydrochloric acid, the desired compound was obtained as a precipitate. The precipitate was collected by filtration and washed with water to obtain 186 mg of the desired compound.
Workup
- customReaction
- customWhen the pH of the reaction mixture thus obtained
Sources & evidence
- ORD record
- ord-5b8c6ca5e188448a9e2299453aac0bc8
- Source dataset
- uspto-grants-2000_08
- Patent number
- US06103907
Reaction notes
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