HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → 3-[N-(3,5-dichlorophenyl)pyrrol-2-yl]-5-acetylaminoindolin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 1-(3,5-dichlorophenyl)-1H-pyrrole-2-carbaldehyde | HCID 2777016 | — |
| Reactant | N-(2-oxoindolin-5-yl)acetamide | HCID 11206280 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-[N-(3,5-dichlorophenyl)pyrrol-2-yl]-5-acetylaminoindolin-2-one | HCID 9865697 | 40% |
Reaction Steps
2.68 g (11 mmol) of 3-[N-(3,5-dichlorophenyl)pyrrole-2-carboxaldehyde are added to a solution of 2.12 g (11 mmol) of 5-acetylaminoindolin-2-one in 220 ml of ethanol containing 0.5 ml of piperidine. The reaction medium is heated under reflux for 3 hours. After cooling, the precipitate formed is drained, washed with twice 5 ml of ice-cold ethanol and dried under reduced pressure. 1.81 g (40%) of 3-[N-(3,5-dichlorophenyl)pyrrol-2-yl]-5-acetylaminoindolin-2-one are thus obtained in the form of a yellow solid whose characteristic is the following: melting point=267° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06930124B2 |
| Source dataset | uspto-grants-2005_08 |
| ORD ID | ord-f118c9603e6248938a577aa879b4df7d |
| Source note | uspto-grants-2005_08 |