Water → HCID 59676099, compound

HRID 642759Notes

Reaction equation

HRID 642759 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-39a29d87674d4f4dab6450228a930351
Source dataset
uspto-grants-2010_04
Patent number
US07696239B2

Reaction notes

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