Hydrochloric Acid → HCID 18770432, compound
Reaction equation
[ClH:1].[CH3:2][O:3][C:4]1[CH:5]=[C:6]([C:14]2[CH:60]=[CH:59][C:17]([C:18]([N:20]3[CH2:25][CH2:24][CH:23]([CH2:26][CH:27]([CH2:55][N:56]([CH3:58])[CH3:57])[CH2:28][CH:29]4[CH2:34][CH2:33][N:32]([C:35](=[O:54])[C:36]5[CH:41]=[CH:40][C:39]([C:42]6[CH:47]=[C:46]([O:48][CH3:49])[C:45]([O:50][CH3:51])=[C:44]([O:52][CH3:53])[CH:43]=6)=[CH:38][CH:37]=5)[CH2:31][CH2:30]4)[CH2:22][CH2:21]3)=[O:19])=[CH:16][CH:15]=2)[CH:7]=[C:8]([O:12][CH3:13])[C:9]=1[O:10][CH3:11]>C(O)C>[ClH:1].[CH3:53][O:52][C:44]1[CH:43]=[C:42]([C:39]2[CH:38]=[CH:37][C:36]([C:35]([N:32]3[CH2:31][CH2:30][CH:29]([CH2:28][CH:27]([CH2:55][N:56]([CH3:57])[CH3:58])[CH2:26][CH:23]4[CH2:22][CH2:21][N:20]([C:18](=[O:19])[C:17]5[CH:16]=[CH:15][C:14]([C:6]6[CH:5]=[C:4]([O:3][CH3:2])[C:9]([O:10][CH3:11])=[C:8]([O:12][CH3:13])[CH:7]=6)=[CH:60][CH:59]=5)[CH2:25][CH2:24]4)[CH2:34][CH2:33]3)=[O:54])=[CH:41][CH:40]=2)[CH:47]=[C:46]([O:48][CH3:49])[C:45]=1[O:50][CH3:51]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Concentrated hydrochloric acid (0.020 ml; 0.24 mmol) was added to a solution of 1,3-bis[1-[4-(3,4,5-trimethoxyphenyl)benzoyl]-4-piperidinyl]-2-[(dimethylamino)methyl]propane (62 mg) in ethanol (5 ml) and the reaction mixture was concentrated under reduced pressure. A process of adding ethanol (10 ml) to the residue and concentrating the mixture under reduced pressure was performed twice to obtain the title compound as a pale yellow amorphous powder.
Workup
- concentrationthe reaction mixture was concentrated under reduced pressure
- concentrationA process of adding ethanol (10 ml) to the residue and concentrating the mixture under reduced pressure
Sources & evidence
- ORD record
- ord-83f21b7d096041f9993e41e6097c0b86
- Source dataset
- uspto-grants-2003_11
- Patent number
- US06645957B2
Reaction notes
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