HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 2,3-dimethyl-4-(2-morpholinoethylthio)pyridine-N-oxide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(2-Chloroethylthio)-2,3-dimethylpyridine-N-oxide | HCID 19963038 | — |
| Solvent | Dimethylformamide toluene | HCID 21735183 | — |
| Product | 2,3-dimethyl-4-(2-morpholinoethylthio)pyridine-N-oxide | HCID 19963100 | — |
Reaction Steps
4-(2-Chloroethylthio)-2,3-dimethylpyridine-N-oxide (6 g) was dissolved in a mixed solution of dimethylformamide-toluene (1:1) and thereto were added potassium carbonate (4.3 g), potassium iodide (4.4 g) and morpholine (1.9 ml). The mixture was reacted at 50-55° C. for 12 hours. After the completion of the reaction, inorganic matters were filtered off and the solvent was distilled away. Water was added to the residue and the mixture was extracted with chloroform. After drying over anhydrous magnesium sulfate, the chloroform was distilled away and the obtained residue was purified by silica gel column chromatography to give 3.4 g of 2,3-dimethyl-4-(2-morpholinoethylthio)pyridine-N-oxide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05616581 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-d7f66b475d3b4a4dade481eadc6048e4 |
| Source note | uspto-grants-1997_04 |