1-(2-(4-(3-fluoro-4-methylbenzylamino)piperidin-1-yl)ethyl)-7-methoxy-N-methyl-2-oxo-1,2-dihydroquinoline-4-carboxamide → 1-(2-(4-(3-fluoro-4-methylbenzylamino)piperidin-1-yl)ethyl)-7-methoxy-N-methyl-2-oxo-1,2-dihydroquinoline-4-carboxamide hydrochloride
Reaction equation
[F:1][C:2]1[CH:3]=[C:4]([CH:32]=[CH:33][C:34]=1[CH3:35])[CH2:5][NH:6][CH:7]1[CH2:12][CH2:11][N:10]([CH2:13][CH2:14][N:15]2[C:24]3[C:19](=[CH:20][CH:21]=[C:22]([O:25][CH3:26])[CH:23]=3)[C:18]([C:27]([NH:29][CH3:30])=[O:28])=[CH:17][C:16]2=[O:31])[CH2:9][CH2:8]1.[ClH:36].C(OCC)(=O)C>CO>[ClH:36].[F:1][C:2]1[CH:3]=[C:4]([CH:32]=[CH:33][C:34]=1[CH3:35])[CH2:5][NH:6][CH:7]1[CH2:8][CH2:9][N:10]([CH2:13][CH2:14][N:15]2[C:24]3[C:19](=[CH:20][CH:21]=[C:22]([O:25][CH3:26])[CH:23]=3)[C:18]([C:27]([NH:29][CH3:30])=[O:28])=[CH:17][C:16]2=[O:31])[CH2:11][CH2:12]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To 2 mL of a methanol solution containing the 1-(2-(4-(3-fluoro-4-methylbenzylamino)piperidin-1-yl)ethyl)-7-methoxy-N-methyl-2-oxo-1,2-dihydroquinoline-4-carboxamide obtained, 1 mL of 4 mol/L hydrogen chloride/ethyl acetate was added at room temperature, and the solvent was removed under reduced pressure. Ethyl acetate was added to the residue thus obtained, and the resulting solid was filtered to give 0.15 g of 1-(2-(4-(3-fluoro-4-methylbenzylamino)piperidin-1-yl)ethyl)-7-methoxy-N-methyl-2-oxo-1,2-dihydroquinoline-4-carboxamide hydrochloride as a pale yellow solid.
Workup
- customobtained
- customthe solvent was removed under reduced pressure
- additionEthyl acetate was added to the residue
- customthus obtained
- filtrationthe resulting solid was filtered
Sources & evidence
- ORD record
- ord-74d4db20a7cb4e8982ab46891bdca29a
- Source dataset
- uspto-grants-2013_09
- Patent number
- US08524738B2
Reaction notes
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