Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1839797Generated: October 26, 2026

4-Phenylindolin-2-one → 3-[3-methyl-4-(4-methyl-piperazine-1-carbonyl)-1H-pyrrol-2-ylmethylene]-4-phenyl-1,3-dihydro-indol-2-one

https://huagongshe.com/reaction/1839797

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Phenylindolin-2-oneHCID 13048601—
Reactant3-methyl-4-(4-methyl-piperazine-carbonyl)-1H-pyrrole-2-carbaldehydeHCID 22390955—
CatalystPiperidineHCID 8082—
SolventEthanolHCID 702—
Product3-[3-methyl-4-(4-methyl-piperazine-1-carbonyl)-1H-pyrrol-2-ylmethylene]-4-phenyl-1,3-dihydro-indol-2-oneHCID 6974105638.1%

Reaction Steps

To a solution of 4-phenyl-1,3-dihydro-indol-2-one (52.3 mg, 0.25 mmol) and 3-methyl-4-(4-methyl-piperazine-1-carbonyl)-1H-pyrrole-2-carbaldehyde (61.2 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-methyl-4-(4-methyl-piperazine-1-carbonyl)-1H-pyrrol-2-ylmethylene]-4-phenyl-1,3-dihydro-indol-2-one as a yellow solid (40.6 mg, 38%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06677368B2
Source datasetuspto-grants-2004_01
ORD IDord-d6c03afb679449e28e4ec1fef596338b
Source noteuspto-grants-2004_01