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

HRID 232097Notes

Reaction equation

HRID 232097 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 and 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-e0ad56bf1074433a91d73b8e2c3a289a
Source dataset
uspto-grants-1989_07
Patent number
US04851423

Reaction notes

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