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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2256037Generated: November 2, 2026

HCID 178418361, compound → HCID 178469888, compound

https://huagongshe.com/reaction/2256037

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 178418361HCID 178418361—
ReactantHCID 178469889HCID 178469889—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 178469888HCID 17846988899.6%

Reaction Steps

A solution of 1-benzyloxycarbonyl-4-(4-ethoxycarbonylimidazol-2-yl)piperidine (0.82 g) in ethanol (20 mL) was hydrogenated over 10% palladium on carbon (0.10 g) at a hydrogen pressure of 3.45 bar for 1 hour. The mixture was filtered through diatomaceous earth and the filter cake was washed with ethanol. The filtrate was evaporated to leave the piperidine derivative as a white foam (0.510 g); NMR: 7.65 (s, 1), 4.18 (q, 2, J=7.1), 2.99 (broad d, 2, J=12.2 H), 2.75 (m, 1), 2.55 (m, 2), 1.80 (broad d, 2, J=12.6), 1.57 (m, 2), 1.25 (t, 3, J=7.1); MS: m/z=252(M+1+28).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05654299
Source datasetuspto-grants-1997_08
ORD IDord-8e16b1d265794b54a42bfea04044324a
Source noteuspto-grants-1997_08