HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454918Generated: October 30, 2026
4-Cyanopiperidine → HCID 58547825, compound
https://huagongshe.com/reaction/454918
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Cyanopiperidine | HCID 138223 | — |
| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Reactant | Sodium t-butoxide | HCID 23676156 | — |
| Reactant | HCID 58547880 | HCID 58547880 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 58547825 | HCID 58547825 | 70% |
Reaction Steps
To a solution of 2-(4-((3-bromopyridin-2-yl)oxy)piperidin-1-yl)quinoline (see PREPARATION P2.2; 383 mg, 1.0 mmol) in toluene (10 mL) were added piperidine-4-carbonitrile (110 mg, 1.0 mmol), Pd2(dba)3 (92 mg, 0.1 mmol), 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (BINAP) (62 mg, 0.1 mmol) and sodium tert-butoxide (t-BuONa) (180 mg, 2.0 mmol). The mixture was stirred and heated at reflux overnight under N2 atmosphere. Then the reaction mixture was filtered, diluted with water (50 mL), and extracted with EtOAc (3×20 mL). The combined organic extracts were washed with water (60 mL) and brine (60 mL), dried over Na2SO4, and filtered. The filtrate was evaporated in vacuo and the residue was purified by flash column chromatography on silica gel (20% to 50% EtOAc in hexanes) to give the title product (290 mg, 0.7 mmol, 70% yield) as white solid. ESI-MS (M+1): 414 calc. for C25H27BrN5O 413.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08497265B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-403dba322a9540879dba432e4f8d1139 |
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| Source note | uspto-grants-2013_07 |
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