HuagongsheHuagongshe Chemistry Print Report · For research reference only
Citric Acid → HCID 178492037, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Citric Acid | HCID 311 | — |
| Reactant | Acetone Cyanohydrin | HCID 6406 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 67010384 | HCID 67010384 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178492037 | HCID 178492037 | 21% |
Reaction Steps
1.78 g (4.5 mmol) of 3-oxo-1-cyclohexenyl 1-(6-methoxy-3-pyridyl)-2-oxo-1,2-dihydro-1,8-naphthyridine-3-carboxylate was dissolved in dichloromethane (50 mL), and 0.77 mL (5.5 mmol) of triethylamine and 0.43 g (5.0 mmol) of acetone cyanohydrin were added to the above solution. The resulting mixture was stirred overnight at room temperature. The reaction mixture was poured into an aqueous solution of citric acid, and the mixture was extracted with dichloromethane. The organic phase was washed with water, dried, and concentrated. The residue was purified by column chromatography (ethyl acetate:n-hexane=1:1 to 7:3), and thus 0.37 g (yield: 21%) of the title compound was obtained as orange-colored crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08334236B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-ce2373898b414b3a9fec1ad0dc72564c |
| Source note | uspto-grants-2012_12 |