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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183810Generated: October 25, 2026

Methyl Acrylate → 2-anilino-6-[(E)-3-methoxy-3-oxo-1-propenyl]-7-methyl-1-phenyl-1,8-naphthyridin-4(1H)-one

https://huagongshe.com/reaction/2183810

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl AcrylateHCID 7294—
ReactantTriphenylphosphineHCID 11776—
Reactant2-anilino-6-bromo-7-methyl-1-phenyl-1,8-naphthyridin-4(1H)-oneHCID 21948208—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
Product2-anilino-6-[(E)-3-methoxy-3-oxo-1-propenyl]-7-methyl-1-phenyl-1,8-naphthyridin-4(1H)-oneHCID 1153881824.3%

Reaction Conditions

Temperature120 °C

Reaction Steps

To a suspension of 2-anilino-6-bromo-7-methyl-1-phenyl-1,8-naphthyridin-4(1H)-one (41 mg, 0.1 mmol) in DMF (2.0 mL) were successively added Pd(OAc)2 (0.70 mg, 0.003 mmol), Ph3P (5.2 mg, 0.02 mmol), TEA (0.03 mL) and methyl acrylate (17.2 mg, 0.2 mmol). The suspension was heated at 120° C. in a sealed tube for 64 h. The residue obtained after concentration in vacuo was washed with water and extracted with EtOAc. The organic layer was dried over MgSO4 and concentrated in vacuo. Purification by prep-HPLC provided methyl (2E)-3-(7-anilino-2-methyl-5-oxo-8-phenyl-5,8-dihydro-1,8-naphthyridin-3-yl)-2-propenoate (10.0 mg, 24%): LCMS RT: 2.61 min, MH+: 412.3, Rf=0.26 (1:1 EtOAc:Hex).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06900205B2
Source datasetuspto-grants-2005_05
ORD IDord-6bfd13c452c34f53b757ac314a819992
Source noteuspto-grants-2005_05