Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1713819Generated: October 30, 2026

Methyl [1-(5-nitropyridin-2-yl)piperidin-4-yl]acetate → Methyl [1-(5-aminopyridin-2-yl)piperidine-4-yl]acetate

https://huagongshe.com/reaction/1713819

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl [1-(5-nitropyridin-2-yl)piperidin-4-yl]acetateHCID 47357980—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductMethyl [1-(5-aminopyridin-2-yl)piperidine-4-yl]acetateHCID 5946407885.8%

Reaction Steps

A solution of methyl [1-(5-nitropyridin-2-yl)piperidin-4-yl]acetate (710 mg, 2.60 mmol) in EtOH (26 mL) was treated with 10% Pd on charcoal (71 mg), and stirred vigorously under an atmosphere of hydrogen for 4 h. The reaction mixture was filtered through diatomaceous earth and the filtrate was evaporated to dryness to give the title compound (556 mg, 70%) as an oil; 1H NMR δ 1.12-1.27 (2H, m), 1.67 (2H, d), 1.75-1.89 (1H, m), 2.25 (2H, d), 2.56 (2H, t), 3.33 (2H, s), 3.58 (3H, s), 4.52 (2H, s), 6.61 (1H, d), 6.86-6.93 (1H, m), 7.58 (1H, d); MS m/e MH+ 250.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795283B2
Source datasetuspto-grants-2010_09
ORD IDord-97b9017391684f28993846c1aa9fbcfd
Source noteuspto-grants-2010_09