HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Aminopyridine → 4-Phenyl-1-(4-pyridyl)-piperidin-2,6-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Aminopyridine | HCID 1727 | — |
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | O-Xylene | HCID 7237 | — |
| Reactant | 4-Phenyloxane-2,6-dione | HCID 297882 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Phenyl-1-(4-pyridyl)-piperidin-2,6-dione | HCID 12822550 | — |
Reaction Steps
The starting material is prepared as follows: The mixture of 19 g of 3-phenylglutaric anhydride, 10.3 g of 4-aminopyridine, 350 ml of xylene and 2.5 g of methane sulfonic acid is refluxed on a water separator while stirring for 2 days. The hot solution is decanted from some insolubles, cooled, filtered an the residue triturated with hot isopropanol, to yield the 4-phenyl-1-(4-pyridyl)-piperidin-2,6-dione meling at 229°-230°; the analogously prepared 4-(p-methoxyphenyl)-1-(4-pyridyl)-piperidine-2,6-dione melts at 168°-169°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04255429 |
| Source dataset | uspto-grants-1981_03 |
| ORD ID | ord-144958cd5ae748fa9675cbce395c87c3 |
| Source note | uspto-grants-1981_03 |