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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1053804Generated: October 30, 2026

HCID 86307969, compound → HCID 131736294, compound

https://huagongshe.com/reaction/1053804

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86307969HCID 86307969—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 131736294HCID 131736294110.6%

Reaction Steps

Trans-1-tert-butyl 4-ethyl 3-(((S)-1-phenylethyl)amino)piperidine-1,4-dicarboxylate 6 (3.7 g, 8.3 mmol, 1.0 equiv) was hydrogenated in the presence of 10% Pd/C (0.37 g) catalyst under H2 at 30 atmospheric pressure in MeOH (100 mL) at 50° C. for 8 h. The catalyst was filtered off and the solvent was removed in vacuo to give (trans)-1-tert-butyl 4-ethyl 3-aminopiperidine-1,4-dicarboxylate 7 as light yellow oil (2.5 g, yield: 92%). ESI-MS (M+H)+: 273.1. 1H NMR (400 MHz, CDCl3) δ: 4.18 (q, 2H), 3.97-3.94 (m, 2H), 3.37 (s, 1H), 3.07-3.02 (m, 1H), 2.89-2.85 (m, 1H), 2.60-2.55 (m, 1H), 2.01-1.91 (m, 1H), 1.70-1.54 (m, 3H), 1.46 (s, 9H), 1.28 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09394277B2
Source datasetuspto-grants-2016_07
ORD IDord-0d027f006907490c9859e1cc71eb0d92
Source noteuspto-grants-2016_07