HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → HCID 131720169, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | HCID 86751207 | HCID 86751207 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 131720169 | HCID 131720169 | 80% |
Reaction Steps
To a solution of 5-carboxy-3-[(7-azaindol-3-yl)methylen]-2-oxindole (0.305 g, 1 mmol) in ethanol (10 ml) was added piperidine (0.085 g, 1 mmol) and the mixture was concentrated under vacuum to a small volume. To the ice-cooled mixture ether was added, the precipitate filtered off, washed with ice-cooled ether and dried under vacuum. Thus almost pure title compound was obtained in about 80% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05663346 |
| Source dataset | uspto-grants-1997_09 |
| ORD ID | ord-be796687cb2641c69370b214c7753e3b |
| Source note | uspto-grants-1997_09 |