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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2054387Generated: October 27, 2026

1-Benzyl-4-(ethylamino)piperidine-4-carboxamide → 4-(Ethylamino)piperidine-4-carboxamide

https://huagongshe.com/reaction/2054387

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyl-4-(ethylamino)piperidine-4-carboxamideHCID 70567—
CatalystPalladium hydroxideHCID 9942167—
SolventMethanolHCID 887—
Product4-(Ethylamino)piperidine-4-carboxamideHCID 96573—

Reaction Steps

To a solution of 1-benzyl-4-ethylaminopiperidine-4-carboxylic acid amide (I-1A-1g; 7.39 g, 28.3 mmol) in methanol (100 ml) was added 20% Pd(OH)2 on carbon (50% water; 1.48 g). The mixture was placed on a Parr® shaker and then reduced (50 psi H2) at room temperature overnight. The mixture was filtered through a pad of Celite®, and then concentrated to give a colorless solid I-1A-1 h (4.84 g, quantitative): +APcI MS (M+1) 172.2; 1H NMR (400 MHz, CD2Cl2) δ 2.89 (ddd, J=12.9, 8.7, 3.3 Hz, 2H), 2.75 (ddd, J=12.9, 6.6, 3.7 Hz, 2H), 2.45 (q, J=7.2 Hz, 2H), 1.95 (ddd, J=13.7, 8.3, 3.7 Hz, 2H), 1.55 (ddd, J=13.7, 6.6, 3.3 Hz, 2 h), 1.08 (t, J=7.1 Hz, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07329658B2
Source datasetuspto-grants-2008_02
ORD IDord-ccda71d217094b49bf14ef75fa719904
Source noteuspto-grants-2008_02