Methanol → 3-(Phthalimidomethylthio)pyridine

HRID 2210135Notes

Reaction equation

HRID 2210135 reaction equation
C[N:2]([CH3:12])[C:3]([S:5][C:6]1[CH:7]=[N:8][CH:9]=[CH:10][CH:11]=1)=O.[OH-:13].[Na+].C(N([CH2:20][CH3:21])CC)C.[CH3:22][OH:23]>C(O)C>[C:22]1(=[O:23])[N:2]([CH2:3][S:5][C:6]2[CH:7]=[N:8][CH:9]=[CH:10][CH:11]=2)[C:12](=[O:13])[C:6]2=[CH:11][CH:10]=[CH:20][CH:21]=[C:7]12

Participants

6

Conditions

Temperature
60 °C

Procedure

To a solution of 1.00 g (5.49 mmol) of 3-(dimethylaminocarbonylthio)pyridine in 50 ml of methanol, 5.49 ml (5.49 mmol) of a 1N aqueous solution of sodium hydroxide was added. The mixture was heated at 60° C. for 1 hour with stirring. After cooling, the solvent was distilled off. The residue was dissolved in ethanol and dried. The solvent was distilled off. The residue thus obtained and 1.58 g of (6.59 mmol) of (N-bromomethyl)phthalimide were suspended in 50 ml of ethanol, and 0.92 ml (6.59 mmol) of triethylamine was added. The mixture was stirred at room temperature for 4 hours. The solvent was distilled off, and the residue was dissolved in chloroform, washed with water and dried. Then the solvent was distilled off. The residue was purified by column chromatography (eluent: hexane/ethyl acetate=1:1) to obtain powder. The powder thus obtained was washed with ether and dried to obtain 1.20 g of the desired compound (yield: 80.9% colorless powder)

Workup

  1. temperatureAfter cooling
  2. distillationthe solvent was distilled off
  3. dissolutionThe residue was dissolved in ethanol
  4. customdried
  5. distillationThe solvent was distilled off
  6. customThe residue thus obtained
  7. stirringThe mixture was stirred at room temperature for 4 hours
  8. distillationThe solvent was distilled off
  9. dissolutionthe residue was dissolved in chloroform
  10. washwashed with water
  11. customdried
  12. distillationThen the solvent was distilled off
  13. customThe residue was purified by column chromatography (eluent: hexane/ethyl acetate=1:1)
  14. customto obtain powder
  15. customThe powder thus obtained
  16. washwas washed with ether
  17. customdried

Sources & evidence

ORD record
ord-9a8d20fd0f594c93b42142f4df2fa298
Source dataset
uspto-grants-1995_10
Patent number
US05457106

Reaction notes

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