HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → 5-Cyano-3-[1-(pyrrol-2-yl)ethylidene]indolin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 2-Acetylpyrrole | HCID 14079 | — |
| Reactant | 2-Oxo-2,3-dihydro-1H-indole-5-carbonitrile | HCID 2773346 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-Cyano-3-[1-(pyrrol-2-yl)ethylidene]indolin-2-one | HCID 69545231 | — |
Reaction Steps
To a suspension of 5-cyanoindolin-2-one (158 mg, 1 mmol) in ethanol (15 mL) was added 2-acetylpyrrole (95 mg, 1 mmol) and piperidine (0.1 mL). The reaction mixture was refluxed for 2 hours. A golden-colored product precipitated from the reaction mixture, which was filtered and washed with ethanol to afford 5-cyano-3-[1-(pyrrol-2-yl)ethylidene]indolin-2-one; (160 mg) 1H NMR (400 MHz, DMSO-d6) δ 2.80 (s, 3H), 6.40. (m, 1H), 7.04 (d, 1H), 7.20 (m, 1H), 7.42 (m, 1H), 7.60 (dd, 1H), 8.04 (s, 1H), 11.40 (s, 1H) ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07105563B2 |
| Source dataset | uspto-grants-2006_09 |
| ORD ID | ord-b24a7961fea84a1cbb0f94b2e807fcc6 |
| Source note | uspto-grants-2006_09 |