Ethyl Acetate → 7-methoxy-N-methyl-1-(2-(4-((naphthalen-2-ylmethyl)amino)piperidin-1-yl)ethyl)-2-oxo-1,2-dihydroquinoline-4-carboxamide hydrochloride

HRID 2193329Notes

Reaction equation

HRID 2193329 reaction equation
C(OCC)(=O)C.[CH3:7][O:8][C:9]1[CH:18]=[C:17]2[C:12]([C:13]([C:40]([NH:42][CH3:43])=[O:41])=[CH:14][C:15](=[O:39])[N:16]2[CH2:19][CH2:20][N:21]2[CH2:26][CH2:25][CH:24]([NH:27][CH2:28][C:29]3[CH:38]=[CH:37][C:36]4[C:31](=[CH:32][CH:33]=[CH:34][CH:35]=4)[CH:30]=3)[CH2:23][CH2:22]2)=[CH:11][CH:10]=1.[ClH:44].C(OCC)(=O)C>CO>[ClH:44].[CH3:7][O:8][C:9]1[CH:18]=[C:17]2[C:12]([C:13]([C:40]([NH:42][CH3:43])=[O:41])=[CH:14][C:15](=[O:39])[N:16]2[CH2:19][CH2:20][N:21]2[CH2:22][CH2:23][CH:24]([NH:27][CH2:28][C:29]3[CH:38]=[CH:37][C:36]4[C:31](=[CH:32][CH:33]=[CH:34][CH:35]=4)[CH:30]=3)[CH2:25][CH2:26]2)=[CH:11][CH:10]=1

Participants

5

Procedure

To a mixed solution of 1 mL ethyl acetate and 2 mL methanol containing 0.20 g of 7-methoxy-N-methyl-1-(2-(4-((naphthalen-2-ylmethyl)amino)piperidin-1-yl)ethyl)-2-oxo-1,2-dihydroquinoline-4-carboxamide, 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 0.16 g of 7-methoxy-N-methyl-1-(2-(4-((naphthalen-2-ylmethyl)amino)piperidin-1-yl)ethyl)-2-oxo-1,2-dihydroquinoline-4-carboxamide hydrochloride as a pale yellow solid.

Workup

  1. customthe solvent was removed under reduced pressure
  2. additionEthyl acetate was added to the residue
  3. customthus obtained
  4. filtrationthe resulting solid was filtered

Sources & evidence

ORD record
ord-114c60b083db4297a26d6ded4baed786
Source dataset
uspto-grants-2012_12
Patent number
US08329694B2

Reaction notes

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