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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1510735Generated: October 27, 2026

Sodium Thiosulfate → 7-Fluoro-1,5-naphthyridine 1-oxide

https://huagongshe.com/reaction/1510735

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium ThiosulfateHCID 24477—
Reactantm-Chloroperbenzoic acidHCID 70297—
Reactant3-Fluoro-1,5-naphthyridineHCID 53416191—
SolventChloroformHCID 6212—
Product7-Fluoro-1,5-naphthyridine 1-oxideHCID 5781521571.3%

Reaction Steps

To a solution of 76 mg of 3-fluoro-1,5-naphthyridine in 3 mL of chloroform, 136 mg of m-chloroperbenzoic acid was added, and the mixture was stirred at room temperature for 2.5 hours. Thereto was added 27 mg of m-chloroperbenzoic acid, and the mixture was stirred at room temperature for 1 hour. To the reaction mixture, a 5% aqueous sodium thiosulfate solution and chloroform were added, the organic layer was separated and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The resultant residue was purified by silica gel column chromatography using silica gel; Silica Gel 60N made by KANTO CHEMICAL CO., INC., and an eluent of chloroform:methanol=50:1 to obtain 60 mg of 7-fluoro-1,5-naphthyridine 1-oxide as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08211908B2
Source datasetuspto-grants-2012_07
ORD IDord-6dbb183ad10443a890132034e828ba9b
Source noteuspto-grants-2012_07