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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1937567Generated: November 1, 2026

Piperidine → HCID 57231128, compound

https://huagongshe.com/reaction/1937567

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant5-Ethyl-1,3-dihydro-2H-indol-2-oneHCID 10154189—
Reactant3-(5-formyl-4-methyl-1H-pyrrol-3-yl)propanoic acidHCID 15160752—
SolventEthanolHCID 702—
ProductHCID 57231128HCID 5723112832.1%

Reaction Steps

4-(2-Carboxyethyl)-2-formyl-3-methylpyrrole (90.6 mg), 80.5 mg 5-ethyl-2-oxindole, and 75 μL of piperidine in 2 mL of ethanol were heated at 95° C. for 5 hours. The reaction mixture was cooled and concentrated. The residue was suspended in 6 N of aqueous hydrochloric acid. The precipitate was filtered, washed with water to pH 6 and dried in a vacuum oven overnight. The crude solid was purified by a chromatography on a silica gel column eluting with ethyl acetate-hexane-acetic acid to give 52 mg (32%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06395734B1
Source datasetuspto-grants-2002_05
ORD IDord-3b7e87159d4248c1ada1d748539470f6
Source noteuspto-grants-2002_05