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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183817Generated: November 1, 2026

HCID 10269984, compound → HCID 10132117, compound

https://huagongshe.com/reaction/2183817

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 numberUS06900205B2
Source datasetuspto-grants-2005_05
ORD IDord-8558199e5deb4b8eacd178690878ba29
Source noteuspto-grants-2005_05