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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1839421Generated: October 28, 2026

HCID 10269984, compound → HCID 9923433, compound

https://huagongshe.com/reaction/1839421

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 10269984HCID 10269984—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
ProductHCID 9923433HCID 992343391%

Reaction Steps

To a flask containing 2-anilino-5-chloro-7-methyl-1-phenyl-1,6-naphthyridin-4(1H)-one (10 mg, 0.03 mmol) in EtOAc (2 mL) and EtOH (2 mL) at room temperature was added a drop of TEA, and Pd/C (10 weight % on activated carbon Degussa type E101, 2 mg). The system was purged with H2 and left stirring at room temperature overnight. The reaction mixture was filtered and concentrated in vacuo to provide 2-anilino-7-methyl-1-phenyl-1,6-naphthyridin-4(1H)-one (8 mg, 91%): LCMS RT: 1.22 min, MH+: 328.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06677352B1
Source datasetuspto-grants-2004_01
ORD IDord-9a74ecd5a25d48fa9a3e700104e508b4
Source noteuspto-grants-2004_01