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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013622Generated: November 1, 2026

Diphenyl Ether → Ethyl 7-bromo-4-oxo-1,4-dihydro-1,5-naphthyridine-3-carboxylate

https://huagongshe.com/reaction/1013622

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiphenyl EtherHCID 7583—
ReactantDiethyl 2-((5-bromopyridin-3-ylamino)methylene)malonateHCID 67318826—
SolventAcetonitrileHCID 6342—
ProductEthyl 7-bromo-4-oxo-1,4-dihydro-1,5-naphthyridine-3-carboxylateHCID 13459134—

Reaction Steps

In a RBF fitted with a reflux condenser a mixture of diethyl 2-((5-bromopyridin-3-ylamino)methylene)malonate (1 g, 3 mmol) and 1-phenoxybenzene (10 mL, 63 mmol) was heated to reflux for 1 h. The reaction mixture was allowed to cool to RT and CH3CN was added. The resulting solids were filtered and dried to provide the desired product as a light brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981891B2
Source datasetuspto-grants-2011_07
ORD IDord-0aef46e3251f4e13a794bf0434f5c1f2
Source noteuspto-grants-2011_07