HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 874952Generated: October 30, 2026
4-Acetamidopiperidine → HCID 49431041, compound
https://huagongshe.com/reaction/874952
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Acetamidopiperidine | HCID 1445156 | — |
| Reactant | 6-Chloro-3-pyridinecarbonitrile | HCID 5152094 | — |
| Solvent | Isoamyl Alcohol | HCID 31260 | — |
| Product | HCID 49431041 | HCID 49431041 | 58.5% |
Reaction Steps
6-Chloronicotinonitrile (300 mg, 2.1 mmol) and 4-acetylaminopiperidine (610 mg, 4.33 mmol) were taken in isoamyl alcohol (15 mL) and the mixture was heated to 140° C. for 2 h. Reaction mixture was cooled to room temperature and the solvent was evaporated under reduced pressure. The crude product was purified by column chromatography (silica gel 60-120 mesh, eluent 5% MeOH in CHCl3) to afford N-(1-(5-cyanopyridin-2-yl)piperidin-4-yl)acetamide (300 mg, yield 57%) as white solid. 1H NMR (400 MHz, DMSO-d6) δ 8.47 (d, J=2.4 Hz, 1H), 7.83-7.80 (m, 2H), 6.95 (d, J=9.3 Hz, 1H), 4.32-4.28 (m, 2H), 3.89-3.80 (m, 1H), 3.14-3.07 (m, 2H), 1.80 (m, 2H), 1.78 (s, 3H), 1.33-1.24 (m, 2H). MS (ESI) m/z: Calculated for C13H16N4O: 244.13. found: 245.2 (M+H)+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08981084B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-fa6dfe0c5a29444da2abf27a9f3b786b |
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| Source note | uspto-grants-2015_03 |
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