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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1839411Generated: November 1, 2026

HCID 10269984, compound → HCID 10132117, compound

https://huagongshe.com/reaction/1839411

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 10269984HCID 10269984—
ReactantHCID 178418689HCID 178418689—
CatalystHCID 178418745HCID 178418745—
SolventTetrahydrofuranHCID 8028—
ProductHCID 10132117HCID 1013211741.3%

Reaction Steps

To a solution of 2-anilino-5-chloro-7-methyl-1-phenyl-1,6-naphthyridin-4(1H)-one (80 mg, 0.22 mmol) in THF (3mL) was added Ni(dppp)Cl2 (24 mg, 0.044 mmol) at room temperature. After stirring for a few minutes MeMgBr (3M, 0.59 mL, 1.76 mmol) was added and the mixture was allowed to stir for 24 h. The mixture was quenched with 1N HCl and extracted with EtOAc. The organic layer was washed with brine, dried over MgSO4, and concentrated in vacuo. Purification by reverse-phase preparative HPLC (10% CH3CN in water with 0.1% TFA to 95% CH3CN in water, 10 mL/min, 10 min) provided 2-anilino-5,7-dimethyl-1-phenyl-1,6-naphthyridin-4(1H)-one (31 mg, 40%): LCMS RT: 1.51 min, MH+: 342.4.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06677352B1
Source datasetuspto-grants-2004_01
ORD IDord-e1ccc9ae637c4f2e8f0aa7b2ec8fc3fb
Source noteuspto-grants-2004_01