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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2187544Generated: October 30, 2026

2,3-Dihydroxybutanedioic Acid → 3-[4-(2-Pyridyl)piperidin-1-yl]propylamine l-tartrate salt

https://huagongshe.com/reaction/2187544

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,3-Dihydroxybutanedioic AcidHCID 875—
ReactantL-Tartaric acidHCID 444305—
Reactant4-(2-pyridinyl)-1-PiperidinepropanamineHCID 10176815—
SolventEthanolHCID 702—
Product3-[4-(2-Pyridyl)piperidin-1-yl]propylamine l-tartrate saltHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06410554B1
Source datasetuspto-grants-2002_06
ORD IDord-65ea34007cdb46c395981b68f87869ca
Source noteuspto-grants-2002_06