Sodium Bicarbonate → HCID 57860018, compound

HRID 1947126Notes

Reaction equation

HRID 1947126 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

  1. extractionthe mixture was extracted with ethyl acetate
  2. washThe extract was washed with brine
  3. dry with materialdried over magnesium sulfate
  4. concentrationconcentrated under reduced pressure
  5. customThe residue was purified by aminosilica gel chromatography (eluate; ethyl acetate/methanol=20/1)
  6. 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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