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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1193338Generated: November 1, 2026

N-Benzyl-N-methyl-2-(1-(pyridin-4-yl)piperidin-4-yl)ethanamine → Methyl((2-(1-(pyridin-4-yl)piperidin-4-yl)ethyl))amine

https://huagongshe.com/reaction/1193338

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-Benzyl-N-methyl-2-(1-(pyridin-4-yl)piperidin-4-yl)ethanamineHCID 66799326—
SolventMethanolHCID 887—
ProductMethyl((2-(1-(pyridin-4-yl)piperidin-4-yl)ethyl))amineHCID 5959777330%

Reaction Steps

N-Benzyl-N-methyl-2-(1-(pyridin-4-yl)piperidin-4-yl)ethanamine (1.4 g, 3.63 mmol, 1 eq) was dissolved in MeOH (20 ml) and degassed for 30 min with nitrogen. 20% Pd—(OH)2 (200 mg) was added and hydrogenation was carried out for 2 h at RT under balloon pressure (H2). After monitoring by thin-layer chromatography, the reaction mixture was filtered off over Celite and washed with MeOH (3×25 ml), and the filtrate was concentrated under reduced pressure. Yield: 30% (240 mg, 1.09 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680159B2
Source datasetuspto-grants-2014_03
ORD IDord-7c42841d50d44e3d9072a2a62eb7f34e
Source noteuspto-grants-2014_03