Hydrochloric Acid → [2'-(1-Ethyl-3-methyl-ureidomethyl)-5,4'-bis-trifluoromethyl-biphenyl-3-yl]-acetic acid
Reaction equation
C[O:2][C:3](=[O:33])[CH2:4][C:5]1[CH:6]=[C:7]([C:15]2[CH:20]=[CH:19][C:18]([C:21]([F:24])([F:23])[F:22])=[CH:17][C:16]=2[CH2:25][N:26]([CH2:31][CH3:32])[C:27]([NH:29][CH3:30])=[O:28])[CH:8]=[C:9]([C:11]([F:14])([F:13])[F:12])[CH:10]=1.[Li+].[OH-].Cl>O1CCOCC1>[CH2:31]([N:26]([CH2:25][C:16]1[CH:17]=[C:18]([C:21]([F:23])([F:24])[F:22])[CH:19]=[CH:20][C:15]=1[C:7]1[CH:8]=[C:9]([C:11]([F:12])([F:13])[F:14])[CH:10]=[C:5]([CH2:4][C:3]([OH:33])=[O:2])[CH:6]=1)[C:27]([NH:29][CH3:30])=[O:28])[CH3:32]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To [2′-(1-ethyl-3-methyl-ureidomethyl)-5,4′-bis-trifluoromethyl-biphenyl-3-yl]-acetic acid methyl ester (0.18 mmol) was added 1:1 1N aqueous LiOH: 1,4-dioxane (2 mL), and the reaction was stirred at room temperature for 30 minutes. 10% Aqueous HCl was added to acidify the solution to pH 3, and the mixture was extracted with EtOAc. The crude material was purified by silica gel chromatography to give the title compound. M+H is 463.
Workup
- extractionthe mixture was extracted with EtOAc
- customThe crude material was purified by silica gel chromatography
Sources & evidence
- ORD record
- ord-2ff5ab93d8554692b749b4539ffdc43f
- Source dataset
- uspto-grants-2011_11
- Patent number
- US08067445B2
Reaction notes
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