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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1761149Generated: October 30, 2026

ethyl 5-formyl-2,4-dimethyl-1H-pyrrole-3-carboxylate → ethyl 2,4-dimethyl-5-[(2-oxo-1H-indol-3-ylidene)methyl]-1H-pyrrole-3-carboxylate

https://huagongshe.com/reaction/1761149

Reaction equation

Participants

RoleNameHCIDCharge
Reactantethyl 5-formyl-2,4-dimethyl-1H-pyrrole-3-carboxylateHCID 137485—
ReactantOxindoleHCID 321710—
CatalystPiperidineHCID 8082—
SolventEthanolHCID 702—
Productethyl 2,4-dimethyl-5-[(2-oxo-1H-indol-3-ylidene)methyl]-1H-pyrrole-3-carboxylateHCID 565479%

Reaction Conditions

Temperature90 °C

Reaction Steps

A reaction mixture of 134.0 mg of oxindole, 234.3 mg of the 4-ethoxycarbonyl-3,5-dimethylpyrrole-2-carboxaldehyde, and 3 drops of piperidine in 3 mL of ethanol was stirred at 90° C. for 3 h. After cooling, the precipitate was filtered, washed with cold ethanol, and dried to yield 244.6 mg (79%) of the title compound as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06846839B1
Source datasetuspto-grants-2005_01
ORD IDord-12e4aa3fd42e4be3b57717a966cc3b80
Source noteuspto-grants-2005_01