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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 3-Fluoro-1,5-naphthyridine | HCID 53416191 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 7-Fluoro-1,5-naphthyridine 1-oxide | HCID 57815215 | 71.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08211908B2 |
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| Source dataset | uspto-grants-2012_07 |
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| ORD ID | ord-6dbb183ad10443a890132034e828ba9b |
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| Source note | uspto-grants-2012_07 |
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