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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1389163Generated: November 2, 2026

2,4-Dimethoxybenzylamine → HCID 20298130, compound

https://huagongshe.com/reaction/1389163

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-DimethoxybenzylamineHCID 597250—
ReactantBenzyl 4-(chlorocarbonyl)piperidine-1-carboxylateHCID 2776270—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 20298130HCID 20298130—

Reaction Steps

1-Benzyloxycarbonyl-4-[N-2,4-dimethoxybenzylcarbamoyl]piperidine was prepared similarly to Preparation C starting from 1-benzyloxycarbonylpiperidine-4-carboxylic acid chloride and 2,4-dimethoxybenzylamine. The product was identified by n.m.r. spectroscopy. This product (7.6 g) in ethanol (150 ml) was hydrogenated over 5% palladium on charcoal at 50°/50 p.s.i. The catalyst was removed by filtration and the filtrate evaporated in vacuo to give 4-[N-(2,4-dimethoxybenzyl)carbamoyl]piperidine (5.0 g) as a solid. A sample in chloroform was converted to the hydrochloride salt by treatment with ethereal hydrogen chloride and recrystallised from isopropanol, m.p. 222°-224°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04243666
Source datasetuspto-grants-1981_01
ORD IDord-6c6801cdce084d99805b31017e7fd459
Source noteuspto-grants-1981_01