HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 2-{4-[N-(5,6-diphenylpyrazin-2-yl)-N-isopropylamino]butylthio}acetic Acid Methyl Ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl Thioglycolate | HCID 16907 | — |
| Reactant | 1-bromo-4-[N-(5,6-diphenylpyrazin-2-yl)-N-isopropylamino]butane | HCID 18452633 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-{4-[N-(5,6-diphenylpyrazin-2-yl)-N-isopropylamino]butylthio}acetic Acid Methyl Ester | HCID 69354987 | 96.9% |
Reaction Steps
1.17 g of 1-bromo-4-[N-(5,6-diphenylpyrazin-2-yl)-N-isopropylamino]butane, 0.29 g of methyl thioglycolate, 0.46 g of potassium carbonate, a catalytic amount of potassium iodide and 27 ml of acetonitrile were mixed and the mixture was refluxed for 4 hours. The insoluble matter was removed by filtration and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography to obtain 1.19 g of the desired compound as a pale yellow crystal having a melting point of 64 to 67° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07205302B2 |
| Source dataset | uspto-grants-2007_04 |
| ORD ID | ord-c45c2e87adad4e048ee59e42e4f4f7cd |
| Source note | uspto-grants-2007_04 |