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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 931244Generated: October 31, 2026

(R)-ethyl 1-(6-amino-5-nitropyridin-2-yl)piperidine-3-carboxylate → (R)-ethyl 1-(5,6-diaminopyridin-2-yl)piperidine-3-carboxylate

https://huagongshe.com/reaction/931244

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-ethyl 1-(6-amino-5-nitropyridin-2-yl)piperidine-3-carboxylateHCID 131735158—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product(R)-ethyl 1-(5,6-diaminopyridin-2-yl)piperidine-3-carboxylateHCID 13173515992.8%

Reaction Steps

To a solution of (R)-ethyl 1-(6-amino-5-nitropyridin-2-yl)piperidine-3-carboxylate (300 mg, 1.019 mmol) in ethanol (15 mL) was added a suspension of 10% palladium-on-carbon (200 mg) in ethanol under nitrogen atmosphere. The mixture was hydrogenated using a hydrogen balloon for 2 h at room temperature then was filtered through a pad of Celite. The filtrate was concentrated to afford (R)-ethyl 1-(5,6-diaminopyridin-2-yl)piperidine-3-carboxylate (250 mg) which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296745B2
Source datasetuspto-grants-2016_03
ORD IDord-2b7ac2ac477e4519be0bc0117ff8f79a
Source noteuspto-grants-2016_03