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

HRID 39954Notes

Reaction equation

HRID 39954 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]1

Participants

4

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

  1. customobtained
  2. customthe solvent was removed under reduced pressure
  3. additionEthyl acetate was added to the residue
  4. customthus obtained
  5. 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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