HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378394Generated: October 30, 2026
1,4'-Bipiperidine → HCID 70258191, compound
https://huagongshe.com/reaction/378394
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,4'-Bipiperidine | HCID 78607 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 19353940 | HCID 19353940 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 70258191 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06030992 |
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| Source dataset | uspto-grants-2000_02 |
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| ORD ID | ord-6d55f190cf7144ad8b4a27499ae1a528 |
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| Source note | uspto-grants-2000_02 |
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