HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Sulfite → 8-[1-(Chloromethyl)ethenyl]-3,7-difluoro-2-(methyloxy)-1,5-naphthyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | Cerium trichloride heptahydrate | HCID 21585214 | — |
| Reactant | Sodium Hypochlorite | HCID 23665760 | — |
| Reactant | 3,7-Difluoro-8-(1-methylethenyl)-2-(methyloxy)-1,5-naphthyridine | HCID 67527029 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 8-[1-(Chloromethyl)ethenyl]-3,7-difluoro-2-(methyloxy)-1,5-naphthyridine | HCID 67527151 | — |
Reaction Steps
A solution of 3,7-difluoro-8-(1-methylethenyl)-2-(methyloxy)-1,5-naphthyridine (820 mg, 3.5 mmol) in tert-butanol (50 ml) under argon was treated with cerium(III) chloride heptahydrate (1.29 g, 3.5 mmol) followed by a solution of sodium hypochlorite (12% w/v, 2.6 ml, 4.2 mmol). After 30 minutes stirring, saturated aqueous sodium sulphite solution (20 ml) was added. After 15 minutes stirring the mixture was extracted with ether (3×200 ml). The combined organic extracts were dried over magnesium sulphate and evaporated. The residue was chromatographed on silica eluting a gradient of 0-50% ethyl acetate in hexane affording a white solid (320 mg, 34%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07732460B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-1f05eff2dd94404e9c600e754f9a6940 |
| Source note | uspto-grants-2010_06 |