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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1691849Generated: 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/1691849

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl [1-(5-nitropyridin-2-yl)piperidin-4-yl]acetateHCID 47357980—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductMethyl [1-(5-aminopyridin-2-yl)piperidine-4-yl]acetateHCID 59464078—

Reaction Steps

To a solution of (5′-nitro-3,4,5,6-tetrahydro-2H-[1,2′]bipyridinyl-4-yl)-acetic acid methyl ester (279 mg, 1 mmol) from above in a mixture of tetrahydrofuran (10 mL) and methanol (50 mL) was added 10% palladium on carbon (50 mg). The mixture was hydrogenated at 50 psi for 1 hr. The mixture was filtered and the solvents were evaporated to give (5′-amino-3,4,5,6-tetrahydro-2H-[1,2′]bipyridinyl-4-yl)-acetic acid methyl ester that was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08153644B2
Source datasetuspto-grants-2012_04
ORD IDord-0e2ad3ef829a4a609c4984200d2dbba2
Source noteuspto-grants-2012_04