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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 931322Generated: November 1, 2026

(R)-(1-(6-amino-5-nitropyridin-2-yl)piperidin-3-yl)(pyrrolidin-1-yl)methanone → (R)-(1-(5,6-diaminopyridin-2-yl)piperidin-3-yl)(pyrrolidin-1-yl)methanone

https://huagongshe.com/reaction/931322

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-(1-(6-amino-5-nitropyridin-2-yl)piperidin-3-yl)(pyrrolidin-1-yl)methanoneHCID 89853768—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product(R)-(1-(5,6-diaminopyridin-2-yl)piperidin-3-yl)(pyrrolidin-1-yl)methanoneHCID 89854052—

Reaction Steps

To a solution of (R)-(1-(6-amino-5-nitropyridin-2-yl)piperidin-3-yl)(pyrrolidin-1-yl)methanone (0.11 g, 0.34 mmol) in ethanol (15 mL) was added 10% palladium-on-carbon (210 mg). The resulting suspension was hydrogenated using a balloon filled with hydrogen gas for 3 h at room temperature. The mixture was filtered through a pad of Celite and the filtrate was used for the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296745B2
Source datasetuspto-grants-2016_03
ORD IDord-d110d2ff6d8d4641985709e82074de01
Source noteuspto-grants-2016_03