HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 20611468, compound → HCID 69742090, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 20611468 | HCID 20611468 | — |
| Reactant | 4-(2-Fluorophenyl)-1,3-dihydro-indol-2-one | HCID 22561874 | — |
| Catalyst | Piperidine | HCID 8082 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 69742090 | HCID 69742090 | 90.3% |
Reaction Steps
To a solution of 4-(2-fluoro-phenyl)-1,3-dihydro-indol-2-one (56.8 mg, 025 mmol) and 3-[(cis)-3,5-dimethyl-piperazine-1 carbonyl]-5-methyl-1H-pyrrole-2-carbaldehyde (62.3 mg, 0.26 mmol) in ethanol (2 mL) was added piperidine (3 drops). The reaction mixture was stirred at room temperature for three days. A yellow solid product was precipitated out, filtered, washed by ethanol for three times, and dried under high vacuum to provide pure product 3-{3-((cis)-3,5-dimethyl-piperazine-1-carbonyl]-5-methyl-1H-pyrrol-2-ylmethylene}-4-(2-fluoro-phenyl)-1,3-dihydro-indol-2-one as a yellow solid (103.5 mg, 90%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06861418B2 |
| Source dataset | uspto-grants-2005_03 |
| ORD ID | ord-b6a4af2a8ada43df8b47594e8fe1f7b6 |
| Source note | uspto-grants-2005_03 |