HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1256182Generated: October 27, 2026
m-Chloroperbenzoic acid → HCID 57815209, compound
https://huagongshe.com/reaction/1256182
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | m-Chloroperbenzoic acid | HCID 70297 | — |
| Reactant | 3-Bromo-1,5-naphthyridine | HCID 12878818 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57815209 | HCID 57815209 | — |
| Product | HCID 58310524 | HCID 58310524 | — |
Reaction Steps
4.43 g (21.2 mmol, 1 eq) of 3-bromo-1,5-naphthyridine (W. Czuba, Recueil des Travaux Chimiques des Pays-Bas 1963, 82, 988-996) were introduced in 165 mL of methylene chloride. 5.23 g (21.2 mmol, 1 eq) of meta-chloroperbenzoic acid were then added portionwise at 0° C. The mixture was stirred at rt for 18 h. The mixture was washed with 1M aqueous NaOH solution and water. Organic layer was dried over Na2SO4, filtered and evaporated to dryness. The residue was purified by column chromatography using methylene chloride and then methylene chloride/ethanol: 98/2 as eluent. The solvent was evaporated to dryness to afford 3.08 g of 3-bromo-1,5-naphthyridine-5-oxide (pale yellow powder) with 64% yield and 1.00 g of 3-bromo-1,5-naphthyridine-1-oxide (yellow powder) with 21% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08461178B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-157d1c9e7e6e45b4b3e95202712b7e8c |
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| Source note | uspto-grants-2013_06 |
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