Hydrochloric Acid → HCID 88177406, compound
Reaction equation
[ClH:1].[CH:2]([N:5]([CH:40]([CH3:42])[CH3:41])[CH2:6][CH2:7][NH:8][C:9]([O:11][CH2:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=1[N:19]([CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH3:39])[CH:20]=[O:21])=[O:10])([CH3:4])[CH3:3]>C(OCC)(=O)C>[ClH:1].[CH:40]([N:5]([CH:2]([CH3:3])[CH3:4])[CH2:6][CH2:7][NH:8][C:9]([O:11][CH2:12][C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][C:14]=1[N:19]([CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH2:38][CH3:39])[CH:20]=[O:21])=[O:10])([CH3:41])[CH3:42]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
4N Hydrochloric acid--ethyl acetate solution (0.20 ml) was added to a solution of [2-[[N-[2-(diisopropylamino)ethyl]carbamoyloxy]methyl]phenyl]-N-octadecylformamide (0.44 g) in ethyl acetate (5 ml) at room temperature. After being stirred for 15 minutes, the reaction mixture was concentrated. The residue was recrystallized from ethyl acetate-ethanol mixed solvent, thereby yielding 0.37 g of the aimed compound as white crystals.
Workup
- concentrationthe reaction mixture was concentrated
- customThe residue was recrystallized from ethyl acetate-ethanol mixed solvent
Sources & evidence
- ORD record
- ord-1fe9f78cdba2445995174893c78b1b14
- Source dataset
- uspto-grants-2000_09
- Patent number
- US06114325
Reaction notes
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