HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Aminopyridine → 3-(4-Pyridyl)-3-azaspiro[5,5]undecan-2,4-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Aminopyridine | HCID 1727 | — |
| Reactant | O-Xylene | HCID 7237 | — |
| Reactant | 1,1-Cyclohexanediacetic Anhydride | HCID 2734289 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(4-Pyridyl)-3-azaspiro[5,5]undecan-2,4-dione | HCID 12822540 | — |
Reaction Steps
The starting material is prepared as follows: The mixture of 25 g of 2,2-cyclohexane diacetic anhydride, 12.92 g of 4-aminopyridine, and 400 ml of xylene is refluxed for 25 hours using a water separator. The hot, supernatant xylene solution is decanted from an oily precipitate (which is discarded), cooled, filtered and the residue recrystallized from ethanol, to yield the 3-(4-pyridyl)-3-azaspiro[5,5]undecan-2,4-dione melting at 213°-215°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04309541 |
| Source dataset | uspto-grants-1982_01 |
| ORD ID | ord-89f65a8d750041a2871301255c516bec |
| Source note | uspto-grants-1982_01 |