Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 67010948 | HCID 67010948 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 67009989 | HCID 67009989 | 104.5% |
Reaction Steps
1.8 g (6.0 mmol) of ethyl 1-(5-methyl-3-isoxazolyl)-2-oxo-1,2-dihydro-1,8-naphthyridine-3-carboxylate was dissolved in acetic acid (50 mL), and 6 N hydrochloric acid (10 mL) was added to this solution at room temperature. The resulting mixture was stirred for 5 hours at 60° C. The solvent was distilled off from the reaction mixture, and the residue was dissolved in toluene. The solvent was distilled off under reduced pressure, and thus 1.7 g of the title compound was obtained as colorless crystals (yield: quantitative).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08334236B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-6406aca1e6064ec5a943291a613a9762 |
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| Source note | uspto-grants-2012_12 |
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