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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2120259Generated: October 30, 2026

Piperidine → HCID 69883661, compound

https://huagongshe.com/reaction/2120259

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant3-(5-formyl-2,4-dimethyl-1H-pyrrol-3-yl)propanoic AcidHCID 1512520—
ReactantHCID 9948092HCID 9948092—
SolventEthanolHCID 702—
ProductHCID 69883661HCID 6988366158.2%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 4-[2-(4-isopropyl-phenoxy)-ethyl]-1,3-dihydro-indol-2-one (118 mg, 0.4 mmol), 4-carboxyethyl-3,5-dimethyl-2-formylpyrrole (78 mg, 0.4 mmol) and piperidine (0.3 mL) in 1.0 mL of ethanol was heated in a sealed tube at 90° C. for 18 hours and cooled to room temperature. The reaction mixture was concentrated and the residue was dissolved in methylene chloride followed by the addition of diethyl ether. The precipitate was filtered and washed with ethyl acetate to give 110 mg (58%) of 3-(5-{4-[2-(4-isopropyl-phenoxy)-ethyl]-2-oxo-1,2-dihydro-indol-3-ylidenemethyl}-2,4-dimethyl-1H-pyrrol-3-yl)-propionic acid (piperidine salt).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06689806B1
Source datasetuspto-grants-2004_02
ORD IDord-c4f95d54eb4f4d34aa7fd924648af937
Source noteuspto-grants-2004_02