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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2093801Generated: October 31, 2026

tert-butyl-4-(4-aminonaphthalen-1-yl)-5,6-dihydropyridine-1(2H)-carboxylate → Tert-butyl 4-(4-aminonaphthalen-1-yl)piperidine-1-carboxylate

https://huagongshe.com/reaction/2093801

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl-4-(4-aminonaphthalen-1-yl)-5,6-dihydropyridine-1(2H)-carboxylateHCID 67168077—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductTert-butyl 4-(4-aminonaphthalen-1-yl)piperidine-1-carboxylateHCID 58257106—

Reaction Steps

To a solution of tert-butyl-4-(4-aminonaphthalen-1-yl)-5,6-dihydropyridine-1(2H)-carboxylate in 50 mL of MeOH was added 10 wt % Pd—C (100 mg). The reaction was degassed to remove air and stirred under 1 atm. H2 until the starting material is consumed. The Pd—C was removed by filtration and the resulting solution was concentrated in vacuo to afford tert-butyl-4-(4-aminonaphthalen-1-yl)piperidine-1-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445505B2
Source datasetuspto-grants-2013_05
ORD IDord-86165473068b41f7bc7faf6cc45585ac
Source noteuspto-grants-2013_05