Water → HCID 59676099, compound

HRID 1880451Notes

Reaction equation

HRID 1880451 reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]2[NH:15][C:14]3[C:13]4[CH:16]=[CH:17][CH:18]=[CH:19][C:12]=4[S:11][CH2:10][CH2:9][C:8]=3[C:7]=2[CH:20]=1.C1OCCOCCOCCOCCOCCOC1.O>CN(C=O)C>[CH3:1][O:2][C:3]1[CH:4]=[CH:5][C:6]2[NH:15][C:14]3[C:13]4[CH:16]=[CH:17][CH:18]=[CH:19][C:12]=4[S:11][CH:10]=[CH:9][C:8]=3[C:7]=2[CH:20]=1

Participants

5

Procedure

9-Methoxy-6,7-dihydro-12H-5-thia-12-aza-dibenzo[a,e]azulene (57 mg, 0.203 mmoL) in DMF (2 mL) was treated with KO2 (58 mg, 0.811 mmoL) and 18-Crown-6 (54 mg, 0.203) and the reaction mixture was stirred at room temperature for 6 hours. Water was added to quench the reaction. The mixture was then partitioned between EtOAc and saturated NH4Cl. The aqueous phase was extracted two times with EtOAc. The organic layer from each extraction was combined, washed with water, brine, dried over anhydrous Na2SO4, filtered and concentrated to yield a brown oil. The crude material (the oil) was then purified by column chromatography (silica gel, 1:1 hexanes:EtOAc as eluent) to yield the title compound as a brown solid.

Workup

  1. customto quench
  2. customthe reaction
  3. customThe mixture was then partitioned between EtOAc and saturated NH4Cl
  4. extractionThe aqueous phase was extracted two times with EtOAc
  5. extractionThe organic layer from each extraction
  6. washwashed with water, brine
  7. dry with materialdried over anhydrous Na2SO4
  8. filtrationfiltered
  9. concentrationconcentrated
  10. customto yield a brown oil
  11. customThe crude material (the oil) was then purified by column chromatography (silica gel, 1:1 hexanes:EtOAc as eluent)

Sources & evidence

ORD record
ord-4c8f5e4aa977498695da718a23bcfc68
Source dataset
uspto-grants-2012_11
Patent number
US08318766B2

Reaction notes

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