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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1839796Generated: October 27, 2026

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

https://huagongshe.com/reaction/1839796

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-methyl-4-(4-methyl-piperazine-carbonyl)-1H-pyrrole-2-carbaldehydeHCID 22390955—
Reactant4-(3-Methoxy-phenyl)-1,3-dihydro indol-2-oneHCID 22561809—
CatalystPiperidineHCID 8082—
SolventEthanolHCID 702—
Product4-(3-methoxy-phenyl)-3-[3-methyl-4-(4-methyl-piperazine-1-carbonyl)-1H-pyrrol-2-ylmethylene]-1,3-dihydro-indol-2-oneHCID 2494264941%

Reaction Steps

To a solution of 4-(3-methoxy-phenyl)-1,3-dihydro-indol-2-one (59.8 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 4-(3-methoxy-phenyl)-3-[3-methyl-4-(4-methyl-piperazine-1-carbonyl)-1H-pyrrol-2-ylmethylene]-1,3-dihydro-indol-2-one as a yellow solid (46.4 mg, 41%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06677368B2
Source datasetuspto-grants-2004_01
ORD IDord-2a5f55b78edb4182875d0739b22541a1
Source noteuspto-grants-2004_01