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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1281746Generated: October 25, 2026

Piperidine → 4-[(1-Methyl-4-phenylindol-3-yl)methylene]-3-pyridino[3,4-e]pyridin-2-yl-2-pyrazolin-5-one

https://huagongshe.com/reaction/1281746

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantPyrazoloneHCID 11513733—
Reactant5,6-Methylenedioxy-1-methyl-indole-3-carboxaldehydeHCID 22605371—
SolventEthanolHCID 702—
Product4-[(1-Methyl-4-phenylindol-3-yl)methylene]-3-pyridino[3,4-e]pyridin-2-yl-2-pyrazolin-5-oneHCID 6991947459%

Reaction Conditions

Temperature87.5 °C

Reaction Steps

A mixture of the above pyrazolone, (VIk) (10 mg, 0.047 mmol), 5,6-methylenedioxy-1-methyl-indole-3-carboxaldehyde (11 mg, 0.054 mmol) in 1 mL of absolute ethanol along with a drop of piperidine was kept under stirring at 85-90° C. A solid separated. After 2 h the mixture was cooled to room temperature and the solid was filtered, washed with ethanol and dried to isolate the product (11 mg, 59% yield). MS: 398 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06455525B1
Source datasetuspto-grants-2002_09
ORD IDord-c1b96b907ba44ef68f1cd2c95ace8609
Source noteuspto-grants-2002_09