Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1063545Generated: October 29, 2026

HCID 21948152, compound → HCID 10223719, compound

https://huagongshe.com/reaction/1063545

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 21948152HCID 21948152—
ReactantHCID 178418336HCID 178418336—
CatalystHCID 178418745HCID 178418745—
SolventTetrahydrofuranHCID 8028—
ProductHCID 10223719HCID 1022371941%

Reaction Steps

To a solution of 2-anilino-7-chloro-5-methyl-1-phenyl-1,8-naphthyridin-4(1H)-one (100 mg, 0.277 mmol) in THF was added Ni(dppp)Cl2 (37.0 mg, 0.069 mmol). After stirring for 5 min, benzylmagnesium chloride (2M, 1.45 mL, 2.90 mmol) was added dropwise via syringe and the mixture was allowed to stir for 24 h. The mixture was quenched with 1 N HCl and extracted with EtOAc. The organic layer was washed brine, dried over MgSO4, and concentrated in vacuo. Purification by preparative HPLC (10% MeNC in water with 0.1% TFA to 95% CH3CN in water, 10 mL/min, 10 min) provided 2-anilino-7-benzyl-5-methyl-1-phenyl-1,8-naphthyridin-4(1H)-one (47.3 mg, 41%): LCMS RT: 2.85 min, MH+: 418.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06964971B2
Source datasetuspto-grants-2005_11
ORD IDord-c5578776cdca451ea6af12e1679fbc58
Source noteuspto-grants-2005_11