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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378394Generated: October 30, 2026

1,4'-Bipiperidine → HCID 70258191, compound

https://huagongshe.com/reaction/378394

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4'-BipiperidineHCID 78607—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 19353940HCID 19353940—
CatalystTetrabutylammonium IodideHCID 67553—
SolventAcetonitrileHCID 6342—
ProductHCID 70258191HCID 70258191—

Reaction Steps

The title compound was prepared by reacting the compound of Example 76, supra, (0.45 g, 1.0 mmol) with 4-(piperdin-1-yl)piperidine (2.0 g, 11.9 mmol) in the presence of the base N,N-diisopropylethylamine, tetra-n-butylammonium iodide and acetonitrile at 80° C. After incubating overnight at 80° C. the reaction was washed with water (2×500 ml), followed by a wash with a saturated sodium chloride solution (1×500 ml). The organic phase was then dried over potassium carbonate and the solvents were removed in vacuo to yield a light brown oil. The desired product was purified by chromatography and triturated with diethyl ether to yield a light brown powder, which was removed by filtration and washed with diethyl ether to yield the purified title compound. MS 584, 585, NMR, IR, mp 143° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06030992
Source datasetuspto-grants-2000_02
ORD IDord-6d55f190cf7144ad8b4a27499ae1a528
Source noteuspto-grants-2000_02