Cesium carbonate → 2-{[6-(2-Chloro-4-methoxyphenoxy)hexyl]-thio}-3-pyridinol

HRID 2210517Notes

Reaction equation

HRID 2210517 reaction equation
[Cl:1][C:2]1[CH:21]=[C:20]([O:22][CH3:23])[CH:19]=[CH:18][C:3]=1[O:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][S:11][C:12]1S[CH2:14][C:15](=O)[N:16]=1.SC1[C:30]([OH:31])=[CH:29]C=CN=1.C(=O)([O-])[O-].[Cs+].[Cs+]>C(#N)C>[Cl:1][C:2]1[CH:21]=[C:20]([O:22][CH3:23])[CH:19]=[CH:18][C:3]=1[O:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][S:11][C:12]1[C:30]([OH:31])=[CH:29][CH:14]=[CH:15][N:16]=1

Participants

5

Procedure

Stir 300 mg. of the iodide prepared in Examples 2 or 3, 3 ml. acetonitrile 112 mg. 2-mercapto-3-pyridinol and 201 mg. cesium carbonate in a reaction flask overnight at room temperature. Remove the acetonitrile and add methylene chloride. Wash with sodium carbonate solution, water, then brine and dry over sodium sulfate. Remove the solvent then add methylene chloride, heat to dissolve the mixture, add hexane and cool to precipitate the title compound as white crystals.

Workup

  1. customovernight
  2. customat room temperature
  3. customRemove the acetonitrile
  4. additionadd methylene chloride
  5. washWash with sodium carbonate solution, water
  6. dry with materialbrine and dry over sodium sulfate
  7. customRemove the solvent
  8. temperatureadd methylene chloride, heat
  9. dissolutionto dissolve the mixture
  10. additionadd hexane
  11. temperaturecool
  12. customto precipitate the title compound as white crystals

Sources & evidence

ORD record
ord-8d013e71080949b6a059db7d35480c1d
Source dataset
uspto-grants-1995_10
Patent number
US05459144

Reaction notes

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