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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2204609Generated: November 1, 2026

HCID 58010221, compound → HCID 58010231, compound

https://huagongshe.com/reaction/2204609

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 58010221HCID 58010221—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 58010231HCID 5801023183.9%

Reaction Steps

A mixture of benzyl 3-(3H-imidazo[1,2-a]pyrrolo[2,3-e]pyrazin-8-yl)-4-methylpiperidine-1-carboxylate (0.55 g, 1.4 mmol) and palladium on carbon (10%, 0.38 g, 0.36 mmol) in EtOH (25 mL) was hydrogenated at room temperature under an atmospheric pressure of hydrogen for about 20 h. The catalyst was removed by filtration through a Celite® pad and the filtrate was concentrated in vacuo to give 8-(4-methylpiperidin-3-yl)-3H-imidazo[1,2-a]pyrrolo[2,3-e]pyrazine (0.30 g, 83%) as a yellow amorphous solid: LC/MS (Table 2, Method a) Rt=0.93 min; MS m/z: 256 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365579B2
Source datasetuspto-grants-2016_06
ORD IDord-08c205b69e774075a4b0ae3a131a32ad
Source noteuspto-grants-2016_06