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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2215039Generated: October 29, 2026

HCID 10269984, compound → HCID 10132117, compound

https://huagongshe.com/reaction/2215039

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 numberUS07109196B2
Source datasetuspto-grants-2006_09
ORD IDord-220b53558df54782bbfd7fa233bae0c8
Source noteuspto-grants-2006_09