HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Aminopyridine → HCID 12822549, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Aminopyridine | HCID 1727 | — |
| Reactant | Methanesulfonic Acid | HCID 6395 | — |
| Reactant | O-Xylene | HCID 7237 | — |
| Reactant | 4-(4-Chlorophenyl)dihydro-2H-pyran-2,6(3H)-dione | HCID 104639 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 12822549 | HCID 12822549 | — |
Reaction Steps
The starting material is prepared as follows: The mixture of 22.4 g of 3-(p-chlorophenyl)-glutaric anhydride, 10.3 g of 4-aminopyridine, 350 ml of xylene and 1.5 g of methane sulfonic acid is refluxed on a water separator while stirring for 4 days. After the first day an additional 0.5 g of methane sulfonic acid is added and the hot solution is finally decanted from some gummy material. The crystals formed on cooling are filtered off, triturated with hot ethanol, cooled, filtered off again and dried to yield the 4-(p-chlorophenyl)-1-(4-pyridyl)-piperidin-2,6-dione melting at 204°-206°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04309541 |
| Source dataset | uspto-grants-1982_01 |
| ORD ID | ord-dcc7aff39aff4299ad27923d98e09079 |
| Source note | uspto-grants-1982_01 |