Sodium Bicarbonate → HCID 57860018, compound
Reaction equation
Cl.[NH2:2][C@@H:3]1[CH2:8][CH2:7][CH2:6][CH2:5][C@H:4]1[NH:9][C:10]([C:12]1[N:24]([CH3:25])[C:23]2[C:22]3[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=3[N:16]([CH2:26][C:27](=[O:34])[C:28]3[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=3)[C:15](=[O:35])[C:14]=2[C:13]=1[O:36][CH3:37])=[O:11].C(=O)([O-])O.[Na+]>>[NH2:2][C@@H:3]1[CH2:8][CH2:7][CH2:6][CH2:5][C@H:4]1[NH:9][C:10]([C:12]1[N:24]([CH3:25])[C:23]2[C:22]3[CH:21]=[CH:20][CH:19]=[CH:18][C:17]=3[N:16]([CH2:26][C:27](=[O:34])[C:28]3[CH:29]=[CH:30][CH:31]=[CH:32][CH:33]=3)[C:15](=[O:35])[C:14]=2[C:13]=1[O:36][CH3:37])=[O:11]Participants
3
Procedure
To the thus-obtained N-[trans-2-aminocyclohexyl]-3-methoxy-1-methyl-4-oxo-5-(2-oxo-2-phenylethyl)-4,5-dihydro-1H-pyrrolo[3,2-c]quinoline-2-carboxamide hydrochloride was added saturated sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The extract was washed with brine, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified by aminosilica gel chromatography (eluate; ethyl acetate/methanol=20/1), and the obtained solid was recrystallized from ethyl acetate-ethanol to give the title compound (80.0 mg, 33%) as white crystals.
Workup
- extractionthe mixture was extracted with ethyl acetate
- washThe extract was washed with brine
- dry with materialdried over magnesium sulfate
- concentrationconcentrated under reduced pressure
- customThe residue was purified by aminosilica gel chromatography (eluate; ethyl acetate/methanol=20/1)
- customthe obtained solid was recrystallized from ethyl acetate-ethanol
Sources & evidence
- ORD record
- ord-b8fc60d2e0994edb8d2d250c801be12e
- Source dataset
- uspto-grants-2013_03
- Patent number
- US08399449B2
Reaction notes
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