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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 657128Generated: October 29, 2026

HCID 86635363, compound → 4-{2-[(3S)-3-(Aminomethyl)-1-piperidinyl]ethyl}-6-(methyloxy)pyrido[2,3-b]pyrazin-3(4H)-one

https://huagongshe.com/reaction/657128

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 86635363HCID 86635363—
CatalystManganese dioxideHCID 14801—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product4-{2-[(3S)-3-(Aminomethyl)-1-piperidinyl]ethyl}-6-(methyloxy)pyrido[2,3-b]pyrazin-3(4H)-oneHCID 68991127—

Reaction Steps

To a solution of phenylmethyl [((3S)-1-{2-[6-(methyloxy)-3-oxopyrido[2,3-b]pyrazin-4(3H)-yl]ethyl}-3-piperidinyl)methyl]carbamate (0.37 g, 0.83 mmol) in MeOH (20 mL) was added 10% Pd/C (0.10 g). The solution was hydrogenated on a Parr apparatus at 50 PSI for 3 h. The Pd/C catalyst was filtered off, MnO2 (0.22 g, 2.48 mmol) was added, and the solution stirred at ambient temperature for 16 h. The MnO2 was filtered off and the crude material (yellowish oil) was used without further purification (0.26 g, 97% over 2 steps).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08071592B2
Source datasetuspto-grants-2011_12
ORD IDord-4c832c8898ae4161905c57600b3a2079
Source noteuspto-grants-2011_12