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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1020352Generated: November 2, 2026

HCID 57461799, compound → HCID 57461798, compound

https://huagongshe.com/reaction/1020352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 57461799HCID 57461799—
CatalystAdams' catalystHCID 345198—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductHCID 57461798HCID 57461798100%

Reaction Steps

The 1-benzyl-4-(5-nitropyridin-2-yl)piperazin-2-one (B-14) (195 mg, 0.63 mmol) was stirred in EtOAc (30 mL) and MeOH (15 mL). The mixture was treated with PtO2 (72 mg) and stirred at RT under 1 atm of H2 for 1 h 10 min. Then, the reaction mixture was filtered over a pad of celite and concentrated to yield 4-(5-aminopyridin-2-yl)-1-benzyl-piperazin-2-one (B-15) (176 mg, 100% yield). MS (M+1): 283.2

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716312B2
Source datasetuspto-grants-2014_05
ORD IDord-2215686094bb4af6a904c902f834a8ba
Source noteuspto-grants-2014_05