Hydrochloric Acid → HCID 10168581, compound
Reaction equation
[ClH:1].[C:2]([CH2:5][CH2:6][CH2:7][CH2:8][N:9]([CH2:37][C:38]1[CH:46]=[CH:45][C:41]([C:42]([OH:44])=[O:43])=[CH:40][CH:39]=1)[CH2:10][CH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1[O:18][CH2:19][C:20]1[CH:25]=[CH:24][C:23]([C:26]2[CH:31]=[CH:30][C:29]([C:32]([F:35])([F:34])[F:33])=[CH:28][CH:27]=2)=[CH:22][C:21]=1[F:36])([OH:4])=[O:3]>O1CCOCC1>[ClH:1].[C:2]([CH2:5][CH2:6][CH2:7][CH2:8][N:9]([CH2:37][C:38]1[CH:46]=[CH:45][C:41]([C:42]([OH:44])=[O:43])=[CH:40][CH:39]=1)[CH2:10][CH2:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1[O:18][CH2:19][C:20]1[CH:25]=[CH:24][C:23]([C:26]2[CH:31]=[CH:30][C:29]([C:32]([F:34])([F:35])[F:33])=[CH:28][CH:27]=2)=[CH:22][C:21]=1[F:36])([OH:4])=[O:3]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
0.5 ml (2 mmol) of a 4-molar solution of HCl in dioxane is added to a solution of 220 mg of 4-{[(4-carboxybutyl)(2-{2-[(3-fluoro-4′-trifluoromethyl-1,1′-biphenyl4-yl)methoxy]phenyl}ethyl)amino]methyl}benzoic acid from Ex. 3 in 0.2 ml of dioxane, and the mixture is stirred at 60° C. for 1 h. The mixture is then concentrated by evaporation and the resulting colorless oil is triturated repeatedly with diethyl ether. The resulting crystals are filtered and dried.
Workup
- concentrationThe mixture is then concentrated by evaporation
- customthe resulting colorless oil is triturated repeatedly with diethyl ether
- filtrationThe resulting crystals are filtered
- customdried
Sources & evidence
- ORD record
- ord-19feb318d36a4bbe85261f291c7fd951
- Source dataset
- uspto-grants-2005_09
- Patent number
- US06939989B2
Reaction notes
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