Hydrochloric Acid → HCID 88176300, compound
Reaction equation
[ClH:1].[CH2:2]([N:12]([C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=1[CH2:21][O:22][C:23](=[O:31])[NH:24][CH2:25][CH2:26][CH2:27][N:28]([CH3:30])[CH3:29])[CH:13]=[O:14])[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH3:11]>C(OCC)(=O)C>[ClH:1].[CH2:2]([N:12]([C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][C:16]=1[CH2:21][O:22][C:23](=[O:31])[NH:24][CH2:25][CH2:26][CH2:27][N:28]([CH3:30])[CH3:29])[CH:13]=[O:14])[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH3:11]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
4N Hydrochloric acid--ethyl acetate solution (0.14 ml) was added to a solution of N-decyl-[2-[[N-[3-(dimethylamino)propyl]carbamoyloxy]methyl]phenyl]formamide (0.200 g) in ethyl acetate (2 ml) at room temperature. After being stirred for 10 minutes, the reaction mixture was concentrated, thereby yielding 0.209 g of the aimed compound as white syrup.
Workup
- concentrationthe reaction mixture was concentrated
Sources & evidence
- ORD record
- ord-7b324c9ed78d45fcb253c8dfd9eb5a22
- Source dataset
- uspto-grants-2000_09
- Patent number
- US06114325
Reaction notes
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