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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 69909Generated: October 28, 2026

Nitrogen → Tert-butyl 1-(3-aminopyridin-4-yl)-3-methylpiperidin-3-ylcarbamate

https://huagongshe.com/reaction/69909

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantHCID 69094616HCID 69094616—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductTert-butyl 1-(3-aminopyridin-4-yl)-3-methylpiperidin-3-ylcarbamateHCID 69094721—

Reaction Steps

10% Palladium on carbon (0.1 eq) was added to a N2-flushed solution of tert-butyl 3-methyl-1-(3-nitropyridin-4-yl)piperidin-3-ylcarbamate (1 eq) in MeOH (0.2 M). The reaction was purged with H2 under atmospheric pressure for 16 h at it. The crude solids were filtered through a pad of Celite on a paper lined Buchner funnel, washed with EtOAc and MeOH, then concentrated in vacuo. The crude residue was dissolved in CH2Cl2, loaded onto a SiO2 column, and purified by flash chromatography (1:2 EtOAc in hexanes+5% MeOH) to give tert-butyl 1-(3-aminopyridin-4-yl)-3-methylpiperidin-3-ylcarbamate. LC/MS (m/z): 307.2 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08822497B2
Source datasetuspto-grants-2014_09
ORD IDord-a0b132c82ca64477b0ad508f0a9c667e
Source noteuspto-grants-2014_09