Chloroform → 7-fluoro-1-(2-(4-((naphthalen-2-yl)methylamino)piperidin-1-yl)ethyl)quinoxalin-2(1H)-one hydrochloride

HRID 2193339Notes

Reaction equation

HRID 2193339 reaction equation
C(Cl)(Cl)[Cl:2].[F:5][C:6]1[CH:15]=[C:14]2[C:9]([N:10]=[CH:11][C:12](=[O:36])[N:13]2[CH2:16][CH2:17][N:18]2[CH2:23][CH2:22][CH:21]([NH:24][CH2:25][C:26]3[CH:35]=[CH:34][C:33]4[C:28](=[CH:29][CH:30]=[CH:31][CH:32]=4)[CH:27]=3)[CH2:20][CH2:19]2)=[CH:8][CH:7]=1.Cl.C(OCC)(=O)C>C(OCC)(=O)C>[ClH:2].[F:5][C:6]1[CH:15]=[C:14]2[C:9]([N:10]=[CH:11][C:12](=[O:36])[N:13]2[CH2:16][CH2:17][N:18]2[CH2:23][CH2:22][CH:21]([NH:24][CH2:25][C:26]3[CH:35]=[CH:34][C:33]4[C:28](=[CH:29][CH:30]=[CH:31][CH:32]=4)[CH:27]=3)[CH2:20][CH2:19]2)=[CH:8][CH:7]=1

Participants

5

Procedure

To a mixed solution of 20 mL chloroform and 10 mL ethyl acetate containing 255 mg of 7-fluoro-1-(2-(4-((naphthalen-2-yl)methylamino)piperidin-1-yl)ethyl)-quinoxalin-2(1H)-one, 1 mL of 4 mol/L hydrogen chloride/ethyl acetate was added, and stirred at room temperature for 10 min. The solvent was removed under reduced pressure, ethyl acetate was added, and the resulting solid was filtered to give 257 mg of 7-fluoro-1-(2-(4-((naphthalen-2-yl)methylamino)piperidin-1-yl)ethyl)quinoxalin-2(1H)-one hydrochloride as a pale brown solid.

Workup

  1. customThe solvent was removed under reduced pressure, ethyl acetate
  2. additionwas added
  3. filtrationthe resulting solid was filtered

Sources & evidence

ORD record
ord-7d65e3d70056471d8013374049c7bdf7
Source dataset
uspto-grants-2012_12
Patent number
US08329694B2

Reaction notes

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