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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1398364Generated: November 3, 2026

Sodium Carbonate → 8-chloro-4,6-dimethyl-9-vinylbenzo[c][2,7]naphthyridin-5(6H)-one

https://huagongshe.com/reaction/1398364

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2,4,6-Trivinylboroxin-Pyridine ComplexHCID 2734806—
Reactant8-chloro-9-iodo-4,6-dimethylbenzo[c][2,7]naphthyridin-5(6H)-oneHCID 86710357—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product8-chloro-4,6-dimethyl-9-vinylbenzo[c][2,7]naphthyridin-5(6H)-oneHCID 8671035868%

Reaction Conditions

Temperature90 °C

Reaction Steps

A solution of 8-chloro-9-iodo-4,6-dimethylbenzo[c][2,7]naphthyridin-5(6H)-one (1.2 g, 2.71 mmol), 2,4,6-trivinylcyclotriboroxane pyridine complex (0.784 g, 3.26 mmol), tetrakis(triphenylphosphine)palladium (0.157 g, 0.136 mmol) and Na2CO3 (0.575 g, 5.43 mmol) in toluene (30 mL) and water (0.5 mL) was purged with nitrogen and heated at 90° C. for 16 h. After cooling to room temperature, the mixture was concentrated under reduced pressure. The residue was taken up in ethyl acetate and filtered through diatomaceous earth (Celite®). The EtOAc layer was washed with brine and water. The combined organic layers were dried over Na2SO4, filtered and concentrated under reduced pressure. The crude material was purified by silica gel flash chromatography using EtOAc-hexane as the eluent to afford 8-chloro-4,6-dimethyl-9-vinylbenzo[c][2,7]naphthyridin-5(6H)-one (0.6 g, 1.43 mmol, 68% yield)) as brown gummy solid. LC/MS (ESI) m/e 285.0 [(M+H)+, calcd for C16H14ClN2O, 285.1]; LC/MS retention time (method B): tR=2.25 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901305B2
Source datasetuspto-grants-2014_12
ORD IDord-56a504162dc14a20b3a05fef7f2251ce
Source noteuspto-grants-2014_12