Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Perchloric Acid | HCID 24247 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | 4-Hydroxy-1-phenyl-3-(prop-2-en-1-yl)-1,8-naphthyridin-2(1H)-one | HCID 54686095 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 13669715 | HCID 13669715 | — |
Reaction Steps
To a solution of 4.0 g. (0.014 moles) of 4-hydroxy-1-phenyl-3-(2-propenyl)-1,8-naphthyridin-2(1H)-one in 380 ml. of tetrahydrofuran, there is added, dropwise, with stirring at 3°-5° C., 4.0 g. of 70% perchloric acid in 11.5 ml. of water, followed by the slow addition of 10.2 g. of N-iodo-succinimide over a period of 45 minutes. The reaction is stirred at room temperature for three hours, treated with a saturated solution of sodium sulfite, and extracted with 2×250 ml. of ether. The organic layer is dried over magnesium sulfate, filtered and concentrated to a solid residue. The crude products are separated on a 60G silica gel column with methanol:chloroform (5:95). The desired fraction is recrystallized from ethyl acetate to yield the title compound, m.p. 178°-180° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04596809 |
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| Source dataset | uspto-grants-1986_06 |
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| ORD ID | ord-5ddd0288ac3943a58455eaedaaffb295 |
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| Source note | uspto-grants-1986_06 |
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