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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 518811Generated: November 1, 2026

2-methylpropan-2-yl 4-[4-nitro-3-(propan-2-yloxy)phenyl]-3,6-dihydropyridine-1(2H)-carboxylate → Tert-butyl 4-(4-amino-3-isopropoxyphenyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/518811

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-methylpropan-2-yl 4-[4-nitro-3-(propan-2-yloxy)phenyl]-3,6-dihydropyridine-1(2H)-carboxylateHCID 86697981—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductTert-butyl 4-(4-amino-3-isopropoxyphenyl)piperidine-1-carboxylateHCID 8669798295.8%

Reaction Steps

A solution of 2.76 g of 2-methylpropan-2-yl 4-[4-nitro-3-(propan-2-yloxy)phenyl]-3,6-dihydropyridine-1(2H)-carboxylate in 60 ml of methanol is hydrogenated on 300 mg of palladium-on-carbon (10%) at a pressure of 10 bar and at ambient temperature for 3 h. The catalyst is removed by filtration on Celite and the filtrate is evaporated to dryness so as to obtain 2.44 g of 2-methylpropan-2-yl 4-[4-amino-3-(propan-2-yloxy)phenyl]piperidine-1-carboxylate in the form of a pink powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09115140B2
Source datasetuspto-grants-2015_08
ORD IDord-aead87a2c643479a9b509530b3b7e199
Source noteuspto-grants-2015_08