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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1063567Generated: October 26, 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/1063567

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, Rη=0.26 (1:1 EtOAc:Hex).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06964971B2
Source datasetuspto-grants-2005_11
ORD IDord-5ef1118b010c43cfa3281d6bbc3fa053
Source noteuspto-grants-2005_11