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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 901274Generated: October 28, 2026

4-Chloro-6-fluoro-1-(4-methoxybenzyl)-2-oxo-1,2-dihydro-[1,8]-naphthyridine-3-carbonitrile → 4-Chloro-6-fluoro-2-oxo-1,2-dihydro-[1,8]-naphthyridine-3-carbonitrile

https://huagongshe.com/reaction/901274

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-6-fluoro-1-(4-methoxybenzyl)-2-oxo-1,2-dihydro-[1,8]-naphthyridine-3-carbonitrileHCID 69216634—
SolventTrifluoroacetic acidHCID 6422—
Product4-Chloro-6-fluoro-2-oxo-1,2-dihydro-[1,8]-naphthyridine-3-carbonitrileHCID 6921717196%

Reaction Steps

4-Chloro-6-fluoro-1-(4-methoxybenzyl)-2-oxo-1,2-dihydro-1,8-naphthyridine-3-carbonitrile (94) (4.3 g, 12.50 mmol) in neat TFA was refluxed for 24 h. The solution was cooled and excess TFA was distilled off under reduced pressure. The residue was taken in water, basified by solid NaHCO3 and filtered. The solids were washed with excess water and dried to yield 2.6 g (96%) of 4-chloro-6-fluoro-2-oxo-1,2-dihydro-[1,8]-naphthyridine-3-carbonitrile (96) as white solids. MP: 272° C.; 1H-NMR (DMSO-d6): δ 8.26 (dd, J=2.8, 8.2 Hz, 1H), 8.81 (d, J=2.8 Hz, 1H), 13.03 (S, 1H); EIMS: 224 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07361760B2
Source datasetuspto-grants-2008_04
ORD IDord-989d535956fc4ca3aef1b37665bf91e1
Source noteuspto-grants-2008_04