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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 595805Generated: October 29, 2026

HCID 68081227, compound → tert-Butyl 4-(6-aminopyridin-3-yl)piperidine-1-carboxylate

https://huagongshe.com/reaction/595805

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 68081227HCID 68081227—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Producttert-Butyl 4-(6-aminopyridin-3-yl)piperidine-1-carboxylateHCID 4983996332%

Reaction Steps

A suspension of tert-butyl 6-amino-5′,6′-dihydro-[3,4′-bipyridine]-1′(2′H)-carboxylate (560 mg, 2.03 mmol), 5% Pd/C (1082 mg, 0.5 mmol) in methanol (30 mL) was purged with nitrogen for 2 min. The reaction mixture was stirred under hydrogen at ambient temperature for 16 h. The reaction mixture was diluted with dichloromethane (50 mL) and was filtered through Celite pad. The filtrate was concentrated and the residue was purified by flash column chromatography on silica gel (ISCO) eluting with 0-90% ethyl acetate in heptane to give tert-butyl 4-(6-aminopyridin-3-yl)piperidine-1-carboxylate (180 mg, 31.9%) as yellow color solid. LCMS (m/z): 278 (MH+), 0.57 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09242996B2
Source datasetuspto-grants-2016_01
ORD IDord-2912efda56224b4a85abd2d332c1b767
Source noteuspto-grants-2016_01