Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-[[2-(3,4,5-Trimethoxyphenyl)pyridin-4-yl]-methyl]piperazine | HCID 12021155 | — |
| Reactant | HCID 22931918 | HCID 22931918 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 86587246 | HCID 86587246 | — |
Reaction Steps
1-[[2-(3,4,5-Trimethoxyphenyl)pyridin-4-yl]-methyl]piperazine (57 mg) was dissolved in acetonitrile (4 mL), and to the solution 3-(3,4,5-trimethoxyphenyl)propyl methanesulfonate (50 mg), potassium iodide (35 mg) and potassium carbonate (46 mg) were added, and the mixture was stirred at 70° C. for 2 hours. Water was added to the reaction mixture to conduct extraction with chloroform. The resultant organic layer was washed with saturated brine, dried over anhydrous sodium sulfate and then concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (chloroform:methanol=20:1). Maleic acid was added to the resultant oil to produce a salt, thereby obtaining the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06552188B2 |
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| Source dataset | uspto-grants-2003_04 |
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| ORD ID | ord-5ff8aabde0a24a3c9764c90439ef5e96 |
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| Source note | uspto-grants-2003_04 |
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