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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 983140Generated: October 30, 2026

4-(4-Fluoro-phenyl)-1,3-dihydro-indol-2-one → 2-[4-(4-fluoro-phenyl)-2-oxo-1,2-dihydro-indol-3-ylidenemethyl]-5-methyl-1 H-pyrrole-3-carboxylic acid (3-pyrrolidin-1-yl-propyl)-amide

https://huagongshe.com/reaction/983140

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(4-Fluoro-phenyl)-1,3-dihydro-indol-2-oneHCID 22561852—
Reactant2-formyl-5-methyl-1H-pyrrole-3-carboxylic acid (3-pyrrolidin-1-yl-propyl)-amideHCID 86587660—
CatalystPiperidineHCID 8082—
SolventEthanolHCID 702—
Product2-[4-(4-fluoro-phenyl)-2-oxo-1,2-dihydro-indol-3-ylidenemethyl]-5-methyl-1 H-pyrrole-3-carboxylic acid (3-pyrrolidin-1-yl-propyl)-amideHCID 7263766679%

Reaction Steps

To a solution of 4-(4-fluoro-phenyl)-1,3-dihydro-indol-2-one (56.8 mg, 0.25 mmol) and 2-formyl-5-methyl-1H-pyrrole-3-carboxylic acid (3-pyrrolidin-1-yl-propyl)-amide (68.5 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 2-[4-(4-fluoro-phenyl)-2-oxo-1,2-dihydro-indol-3-ylidenemethyl]-5-methyl-1H-pyrrole-3-carboxylic acid (3-pyrrolidin-1-yl-propyl)amide as a yellow solid (93.2 mg, 79%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06861418B2
Source datasetuspto-grants-2005_03
ORD IDord-ce5576d6876d4e7f9959cdb8cdb8f7ce
Source noteuspto-grants-2005_03