Potassium Carbonate → HCID 58026816, compound

HRID 909326Notes

Reaction equation

HRID 909326 reaction equation
C([O:4][C:5]1[CH:36]=[CH:35][C:8]([C:9]([O:11][CH2:12][C:13]2[C:22]([C:23]3[CH:28]=[CH:27][C:26]([F:29])=[CH:25][C:24]=3[O:30][CH3:31])=[CH:21][CH:20]=[C:19]3[C:14]=2[C:15]([CH3:34])=[CH:16][C:17]([CH3:33])([CH3:32])[NH:18]3)=[O:10])=[CH:7][CH:6]=1)(=O)C.C(=O)([O-])[O-].[K+].[K+]>CO>[F:29][C:26]1[CH:27]=[CH:28][C:23]([C:22]2[C:13]([CH2:12][O:11][C:9](=[O:10])[C:8]3[CH:7]=[CH:6][C:5]([OH:4])=[CH:36][CH:35]=3)=[C:14]3[C:19](=[CH:20][CH:21]=2)[NH:18][C:17]([CH3:32])([CH3:33])[CH:16]=[C:15]3[CH3:34])=[C:24]([O:30][CH3:31])[CH:25]=1

Participants

4

Procedure

5-(4-Acetoxybenzoyloxymethyl)-6-(4-fluoro-2-methoxyphenyl)-2,2,4-trimethyl -1,2-dihydroquinoline (Compound No. 12-5, 40.9 mg, 0.0835 mmol) and potassium carbonate (24.0 mg, 0.174 mmol) were suspended in anhydrous methanol (1 mL), and the mixture was stirred at room temperature for 1.5 hours. After the unsoluble materials were filtered, the filtrate was concentrated under reduced pressure, and ethyl acetate (50 mL) and water (50 mL) were added thereto, and then separated. The organic layer was washed with water (30 mL) and saturated brine (30 mL) successively, dried over anhydrous magnesium sulfate, and then the solvent was removed under reduced pressure. The obtained residue was filtered with hexane to give the titled compound (28.8 mg) as a colorless solid. (Yield 78%)

Workup

  1. filtrationAfter the unsoluble materials were filtered
  2. concentrationthe filtrate was concentrated under reduced pressure, and ethyl acetate (50 mL) and water (50 mL)
  3. additionwere added
  4. customseparated
  5. washThe organic layer was washed with water (30 mL) and saturated brine (30 mL) successively
  6. dry with materialdried over anhydrous magnesium sulfate
  7. customthe solvent was removed under reduced pressure
  8. filtrationThe obtained residue was filtered with hexane

Sources & evidence

ORD record
ord-79970b759d734d9f83ac6740073b3a63
Source dataset
uspto-grants-2011_09
Patent number
US08017775B2

Reaction notes

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