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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1879826Generated: November 1, 2026

HCID 59332343, compound → tert-Butyl 4-(3-aminopyridin-4-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1879826

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 59332343HCID 59332343—
CatalystPalladiumHCID 23938—
SolventEthylacetate methanolHCID 21584119—
Producttert-Butyl 4-(3-aminopyridin-4-yl)piperazine-1-carboxylateHCID 43462405—

Reaction Steps

The 4-(3-nitro-pyridin-4-yl)-piperazine-1-carboxylic acid tert-butyl ester (633 mg) was then diluted with MeOH/EtOAc (1:1, 10 mL) and to the resulting solution was added Pd on carbon (5% Pd). The resulting reaction mixture was stirred under a hydrogen atmosphere at room temperature for about 15 hours. The reaction mixture was filtered through a pad of celite and the filtrate was concentrated in vacuo to provide 4-(3-amino-pyridin-4-yl)-piperazine-1-carboxylic acid tert-butyl ester as a solid form. HPLC-MS RT=1.10 min, mass calculated for formula C14H22N4O2 278.17, observed LCMS m/z 279.28 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318735B2
Source datasetuspto-grants-2012_11
ORD IDord-b7c8822e214f4c60967948f2989b740b
Source noteuspto-grants-2012_11