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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1812084Generated: November 1, 2026

tert-Butyl (5-nitropyridin-2-yl)carbamate → tert-butyl N-(5-aminopyridin-2-yl)carbamate

https://huagongshe.com/reaction/1812084

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl (5-nitropyridin-2-yl)carbamateHCID 11064480—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Producttert-butyl N-(5-aminopyridin-2-yl)carbamateHCID 2206444098%

Reaction Steps

A mixture of tert-butyl 5-nitropyridin-2-ylcarbamate (3.76 g, 15.7 mmol) and Pd/C (Aldrich) (0.588 g, 5.52 mmol) in EtOH (100 mL) was evacuated under vacuum and refilled with hydrogen (6 times). The mixture was hydrogenated under balloon pressure of hydrogen at rt for 2.5 h. The reaction mixture was filtered through a pad of Celite® (diatomaceous earth) (eluent:EtOH) and concentrated to give tert-butyl 5-aminopyridin-2-ylcarbamate (3.22 g, 98% yield) as a cream color solid. 1H NMR (300 MHz, d6-DMSO) δ 9.06 (s, 1H); 7.62 (d, J=1.75 Hz, 1H); 7.40 (d, J=8.62 Hz, 1H); 6.94 (dd, J=8.70, 2.27 Hz, 1H); 4.93 (s, 2H); 1.44 (s, 9H). m/z (ESI, +ve ion) 210.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362241B2
Source datasetuspto-grants-2013_01
ORD IDord-385ce3d5b67d46a69609a01b3d4eb924
Source noteuspto-grants-2013_01