HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 69872Generated: October 28, 2026
4-Nitro-3-(piperidin-1-yl)pyridine 1-oxide → 3-(Piperidin-1-yl)pyridin-4-amine
https://huagongshe.com/reaction/69872
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Nitro-3-(piperidin-1-yl)pyridine 1-oxide | HCID 14735913 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-(Piperidin-1-yl)pyridin-4-amine | HCID 69047368 | 73% |
Reaction Steps
To a solution of 4-nitro-3-(piperidin-1-yl)pyridine 1-oxide (1.0 equiv.) in ethanol, at a concentration of 0.1 M, was added 10% palladium on carbon (0.1 eq.). The resultant heterogeneous solution was put under an atmosphere of hydrogen and was stirred for 15 hours. At this time LC/MS analysis indicated that the nitro was reduced to the amine, but the N-oxide was remaining. More 10% palladium on carbon (0.2 eq.) was added and the mixture was resubmitted to a balloon atmosphere of hydrogen. After stirring for 24 hours, more 10% palladium on carbon (0.2 eq.) was added and the mixture was resubmitted to a balloon atmosphere of hydrogen. After stirring for an additional 3 days the mixture was filtered through a pad of celite eluting with methanol. The volatiles were removed in vacuo yielding 3-(piperidin-1-yl)pyridin-4-amine (73%). LCMS (m/z): 178.0 (MH+); LC Rt=1.66 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08822497B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-88ea49dceea6479bb3324053034ea6bf |
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| Source note | uspto-grants-2014_09 |
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