Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1839735Generated: October 30, 2026

5-formyl-2,4-dimethyl-1H-pyrrole-3-carboxylic acid (2-[1,2,3)triazol-1-yl-ethyl)amide → HCID 24941311, compound

https://huagongshe.com/reaction/1839735

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-formyl-2,4-dimethyl-1H-pyrrole-3-carboxylic acid (2-[1,2,3)triazol-1-yl-ethyl)amideHCID 20761730—
Reactant4-(3-Bromo-phenyl)1,3-dihydro-indol-2-oneHCID 22561849—
CatalystPiperidineHCID 8082—
SolventEthanolHCID 702—
ProductHCID 24941311HCID 2494131135.1%

Reaction Steps

To a solution of 4-(3-bromo-phenyl)-1,3-dihydro-indol-2-one (72 mg, 0.25 mmol) and 5-formyl-2,4-dimethyl-1H-pyrrole-3-carboxylic acid (2-[1,2,3]triazol-1-yl-ethyl)-amide (67.9 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 5-[4-(3-bromo-phenyl)-2-oxo-1,2-dihydro-indol-3-ylidenemethyl]-2,4-dimethyl-1H-pyrrole-3-carboxylic acid (2-[1,2,3]triazol-1-yl-ethyl)-amide as a yellow solid (46.6 mg, 35%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06677368B2
Source datasetuspto-grants-2004_01
ORD IDord-023052e7c2424c04b1b01a2f8b3eacc9
Source noteuspto-grants-2004_01