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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1839752Generated: October 25, 2026

3,5-Dimethyl-1H-pyrrole-2-carbaldehyde → 3-(3,5-Dimethyl-1H-pyrrol-2-ylmethylene)-4-(4-bromo-phenyl)-1,3-dihydro-indol-2-one

https://huagongshe.com/reaction/1839752

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-Dimethyl-1H-pyrrole-2-carbaldehydeHCID 270465—
Reactant4-(4-Bromo-phenyl)1,3-dihydro-indol-2-oneHCID 22561721—
CatalystPiperidineHCID 8082—
SolventEthanolHCID 702—
Product3-(3,5-Dimethyl-1H-pyrrol-2-ylmethylene)-4-(4-bromo-phenyl)-1,3-dihydro-indol-2-oneHCID 6974110751%

Reaction Steps

To a solution of 4-(4-bromo-phenyl)-1,3-dihydro-indol-2-one (72 mg, 0.25 mmol) and 3,5-dimethyl-1H-pyrrole-2-carbaldehyde (32 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-(3,5-Dimethyl-1H-pyrrol-2-ylmethylene)-4-(4-bromo-phenyl)-1,3-dihydro-indol-2-one as a yellow solid (50 mg, 51%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06677368B2
Source datasetuspto-grants-2004_01
ORD IDord-5b6cef1ed25141c7be1f54a6255b4eff
Source noteuspto-grants-2004_01