Hydrochloric Acid → HCID 68427067, compound
Reaction equation
[ClH:1].[C:2]([CH2:5][CH2:6][CH2:7][CH2:8][N:9]([CH2:33][C:34]1[CH:42]=[CH:41][C:37]([C:38]([OH:40])=[O:39])=[CH:36][CH:35]=1)[CH2:10][CH2:11][C:12]1[CH:17]=[CH:16][C:15]([F:18])=[CH:14][C:13]=1[O:19][CH2:20][C:21]1[CH:26]=[CH:25][C:24]([CH:27]2[CH2:32][CH2:31][CH2:30][CH2:29][CH2:28]2)=[CH:23][CH:22]=1)([OH:4])=[O:3]>O1CCOCC1>[ClH:1].[C:2]([CH2:5][CH2:6][CH2:7][CH2:8][N:9]([CH2:33][C:34]1[CH:42]=[CH:41][C:37]([C:38]([OH:40])=[O:39])=[CH:36][CH:35]=1)[CH2:10][CH2:11][C:12]1[CH:17]=[CH:16][C:15]([F:18])=[CH:14][C:13]=1[O:19][CH2:20][C:21]1[CH:26]=[CH:25][C:24]([CH:27]2[CH2:32][CH2:31][CH2:30][CH2:29][CH2:28]2)=[CH:23][CH:22]=1)([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 (0.43 mmol) of 4-{[(4-carboxybutyl)(2-{2-[(4-cyclohexylbenzyl)oxy]-4-fluorophenyl}ethyl)amino]methyl}benzoic acid from Ex. 1 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-4a354ec23aca4d488faab5aa5fdeba88
- Source dataset
- uspto-grants-2010_04
- Patent number
- US07700653B2
Reaction notes
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