HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Malonate → HCID 135528464, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | HCID 136050723 | HCID 136050723 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 135528464 | HCID 135528464 | 71% |
Reaction Steps
To a suspension of tert-butyl 3-[2-amino-3-formyl-6-(2-hydroxyphenyl)4-pyridinyl]-1-piperidinecarboxylate (0.86 g, 2.16 mmol) in ethanol (25 mL) were added diethyl malonate (6.93 g, 43.27 mmol) and piperidine (2.14 mL, 21.64 mmol) and, and the mixture was heated at reflux overnight. The mixture was allowed to cool to room temperature, and then diluted with ethanol. The resulting precipitate was collected by filtration, washed with ethanol and dried under reduced pressure to give ethyl 5-[1-(tert-butoxycarbonyl)-3-piperidinyl]-7-(2-hydroxyphenyl)-2-oxo-1,2-dihydro-1,8-naphthyridine-3-carboxylate as a yellow solid (0.752 g, yield; 71%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06562811B1 |
| Source dataset | uspto-grants-2003_05 |
| ORD ID | ord-58f5ddc3d6e8415d8bbf29ff57bfe3de |
| Source note | uspto-grants-2003_05 |