Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | HCID 87235637 | HCID 87235637 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 67010948 | HCID 67010948 | 56.4% |
Reaction Steps
3.3 g (16 mmol) of (2-(5-methyl-3-isoxazolyl)amino)nicotinaldehyde was dissolved in ethanol (60 mL), and 3.9 g (24 mmol) of diethyl malonate and 0.56 g (6.5 mmol) of piperidine were added thereto. The resulting mixture was stirred overnight at 90° C. The reaction mixture was cooled, and then the solvent was distilled off. The residue was purified by column chromatography (ethyl acetate:n-hexane=1:4 to 7:3), and thus 2.7 g of the title compound was obtained as pale yellow crystals (yield: 55%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08334236B2 |
|---|
| Source dataset | uspto-grants-2012_12 |
|---|
| ORD ID | ord-197eb23dc7cb458f80380d741a620b34 |
|---|
| Source note | uspto-grants-2012_12 |
|---|