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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 40362Generated: October 25, 2026

Sodium Hydroxide → 8-Chloro-3-fluoro-1,5-naphthyridine

https://huagongshe.com/reaction/40362

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantDichloromethane methanol ammonium hydroxideHCID 21896990—
Reactant7-Fluoro-1,5-naphthyridin-4-olHCID 67504324—
SolventDichloromethaneHCID 6344—
Product8-Chloro-3-fluoro-1,5-naphthyridineHCID 5769093764.3%

Reaction Conditions

Temperature110 °C

Reaction Steps

A pressure resistant vial was charged with 7-fluoro-1,5-naphthyridin-4(1H)-one (600 mg, 3.66 mmol) and POCl3 (6.8 mL, 73.1 mmol). Vessel sealed and stirred at 110° C. for 16 hrs. Reaction mixture was cooled to room temperature and poured onto ice while stirring vigorously. While keeping reaction mixture at 0° C., it was basified to pH˜8 with 6N NaOH. Product extracted with dichloromethane. Organic layer collected, dried over sodium sulfate and concentrated to afford desired material. This was passed through a silica plug in 1-5% (90:10:1 DCM/MeOH/NH4OH)/DCM to afford 8-chloro-3-fluoro-1,5-naphthyridine (430 mg, 64% yield) as a tan solid. MS [M+H]=182.9. Calc'd for C8H4ClFN2=182.58

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524900B2
Source datasetuspto-grants-2013_09
ORD IDord-d2769fba50d040f2a1f4cc61c0e85a31
Source noteuspto-grants-2013_09