Hydrochloric Acid → HCID 68427067, compound

HRID 1831864Notes

Reaction equation

HRID 1831864 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

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

  1. concentrationThe mixture is then concentrated by evaporation
  2. customthe resulting colorless oil is triturated repeatedly with diethyl ether
  3. filtrationThe resulting crystals are filtered
  4. customdried

Sources & evidence

ORD record
ord-dc478fbbb2004dbeaf5cb5e6cbb78c26
Source dataset
uspto-grants-2006_06
Patent number
US07067694B2

Reaction notes

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