Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 846746Generated: October 30, 2026

Benzylamine → Ethyl cis-(4-amino-3-methoxypiperidino)formate

https://huagongshe.com/reaction/846746

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
ReactantThiopheneHCID 8030—
ReactantEthyl 3-methoxy-4-oxopiperidine-1-carboxylateHCID 2724451—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
ProductEthyl cis-(4-amino-3-methoxypiperidino)formateHCID 13677746—

Reaction Steps

To 2 parts of a solution of 2 parts of thiophene in 40 parts of ethanol were added 126 parts of ethyl 3-methoxy-4-oxo-1-piperidinecarboxylate, 70 parts of benzenemethanamine and 400 parts of methanol. The whole was hydrogenated at normal pressure and at room temperature with 5 parts of palladium-on-charcoal catalyst 10%. After up-take of one equivalent of hydrogen, the catalyst was filtered off and hydrogenation was continued with another 5 parts of palladium-on-charcoal catalyst 10%. After the calculated amount of hydrogen was taken up, the catalyst was filtered off and the filtrate was evaporated. The residue contained some oil drops which were separated, yielding 92.9 parts of ethyl cis-4-amino-3-methoxy-1-piperidinecarboxylate (intermediate 54).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05137896
Source datasetuspto-grants-1992_08
ORD IDord-08b3ba627c6a411cb51998f6ccb4192f
Source noteuspto-grants-1992_08