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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1398397Generated: October 30, 2026

Sodium Methoxide → 8-chloro-4-methoxy-6-methylbenzo[c][2,7]naphthyridin-5(6H)-one

https://huagongshe.com/reaction/1398397

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium MethoxideHCID 10942334—
Reactant4,8-dichloro-6-methylbenzo[c][2,7]naphthyridin-5(6H)-oneHCID 86710384—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product8-chloro-4-methoxy-6-methylbenzo[c][2,7]naphthyridin-5(6H)-oneHCID 8671038538.9%

Reaction Steps

To a solution of 4,8-dichloro-6-methylbenzo[c][2,7]naphthyridin-5(6H)-one (1.0 g, 3.58 mmol) in MeOH (1 mL) was added sodium methoxide (0.806 mL, 3.58 mmol). The resultant mixture was heated in a microwave at 80° C. for 25 min. The reaction mixture was then diluted with water (20 mL) and extracted with ethyl acetate (30 mL). The organic layer was separated, dried over sodium sulphate and evaporated to dryness to afford 8-chloro-4-methoxy-6-methylbenzo[c][2,7]naphthyridin-5(6H)-one (0.4 g, 1.391 mmol, 39% crude yield) as a brown solid. The material was carried on without further purification. LC/MS (ESI) m/e 274.8 [(M+H)+, calcd for C14H12ClN2O2, 275.0]; LC/MS retention time (method C): tR=2.06 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901305B2
Source datasetuspto-grants-2014_12
ORD IDord-9ed7a0865bd147eb801fc06a5adcb293
Source noteuspto-grants-2014_12