HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,3-Dihydroxybutanedioic Acid → 3-[4-(2-Pyridyl)piperidin-1-yl]propylamine l-tartrate salt
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,3-Dihydroxybutanedioic Acid | HCID 875 | — |
| Reactant | L-Tartaric acid | HCID 444305 | — |
| Reactant | 4-(2-pyridinyl)-1-Piperidinepropanamine | HCID 10176815 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-[4-(2-Pyridyl)piperidin-1-yl]propylamine l-tartrate salt | HCID 70151200 | — |
Reaction Steps
A solution of 3-[4-(2-pyridyl)piperidin-1-yl]propylamine, (6), (637.9 g, 3.86 mol) in ethanol (8.5 L) was warmed to 65° C. A solution of L-tartaric acid (637.9 g, 4.25 mol) in ethanol (2.23 L) was added in portions. Approximately 15% of the tartaric acid solution was added and then reaction mixture was aged for 1 hour to afford a thin slurry of crystalline material. The remaining tartaric acid solution was added dropwise. Heating was discontinued and the solution was slowly cooled to ambient temperature overnight. The solids were filtered, rinsed with ethanol (2×1 L) and dried under a stream of nitrogen to afford 3-[4-(2-pyridyl)piperidin-1-yl]propylamine L-tartrate salt, (7), as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06320049B1 |
| Source dataset | uspto-grants-2001_11 |
| ORD ID | ord-b42109ac54cf43b2b9777bd9c1d495e6 |
| Source note | uspto-grants-2001_11 |