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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716560Generated: November 2, 2026

HCID 68509534, compound → 1,1-Dimethylethyl 4-[(2-amino-4-methylphenyl)amino]-1-piperidinecarboxylate

https://huagongshe.com/reaction/1716560

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 68509534HCID 68509534—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product1,1-Dimethylethyl 4-[(2-amino-4-methylphenyl)amino]-1-piperidinecarboxylateHCID 5885228890.3%

Reaction Steps

To a solution of 4-(4-methyl-2-nitro-phenylamino)-piperidine-1-carboxylic acid tert-butyl ester (9.5 g, 28.4 mmol) in ethanol (150 mL) was added 10% Pd/C (125 mg) and the reaction mixture was shaken under H2 (50 psi) at rt for 1 h. The catalyst was then removed by filtration through a pad of Celite® and washed with ethanol. The filtrate was concentrated in vacuo to provide 4-(2-amino-4-methyl-phenylamino)-piperidine-1-carboxylic acid tert-butyl ester (7.83 g) in 90% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803816B2
Source datasetuspto-grants-2010_09
ORD IDord-fc9efd3eb23a46cfb00f0a537f66af38
Source noteuspto-grants-2010_09