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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 276871Generated: October 25, 2026

4-(3-Bromo-phenylamino)-6-fluoro-[1,7]naphthyridine-3-carbonitrile → 4-(3-Bromo-phenylamino)-6-(2-dimethylamino-ethoxy)-[1,7]naphthyridine-3-carbonitrile

https://huagongshe.com/reaction/276871

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(3-Bromo-phenylamino)-6-fluoro-[1,7]naphthyridine-3-carbonitrileHCID 18548979—
ReactantHCID 23680072HCID 23680072—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product4-(3-Bromo-phenylamino)-6-(2-dimethylamino-ethoxy)-[1,7]naphthyridine-3-carbonitrileHCID 18548938—

Reaction Steps

To 100 mg of 4-(3-bromo-phenylamino)-6-fluoro-[1.7]naphthyridine-3-carbonitrile under an inert atmosphere was added 3 mL of 1 M sodium (2-dimethylamino-ethoxide) in tetrahydrofuran. After refluxing for 3 hours, the reaction was diluted with water and the product extracted five times with chloroform. The crude product was purified by flash chromatography with 1% triethyl amine and 10% methanol/chloroform followed by recrystallized from chloroform/ether to give 100 mg of 4-(3-bromo-phenylamino)-6-(2-dimethylamino-ethoxy)-[1.7]naphthyridine-3-carbonitrile as a yellow solid: melting point 138-139° C.; mass spectrum (m/e): M+H 411.9, 413.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06355636B1
Source datasetuspto-grants-2002_03
ORD IDord-4f1c16c9d8ea461597e2d345c86384f0
Source noteuspto-grants-2002_03