Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1638336Generated: November 2, 2026

Piperidine → HCID 19842210, compound

https://huagongshe.com/reaction/1638336

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
Reactant[2-(5-Chloropyridin-2-yl)-3-oxo-2,3-dihydro-1H-isoindol-1-yl]acetic acidHCID 19842220—
SolventTetrahydrofuranHCID 8028—
ProductHCID 19842210HCID 1984221026.2%

Reaction Steps

3-Oxo-2-(5-chloro-2-pyridyl)isoindoline-1-acetic acid (1 g) and triethylamine (0.8 g) were dissolved in 20 ml of dry tetrahydrofuran and, under ice-cooling with stirring, 0.39 g of ethoxycarbonyl chloride was added portionwise. The mixture was stirred for 30 minutes, 0.56 g of piperidine was added, and the whole mixture was stirred for an additional 30 minutes. The reaction mixture was poured into 500 ml of ice water, followed by extraction with ethyl acetate. The extract was washed with water and dried. The ethyl acetate was then distilled off and the residue was treated with ether. The resulting crystals thus obtained were collected by filtration and recrystallized from ethyl acetate to give 0.32 g of colorless crystals, melted at 165°-166° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04879293
Source datasetuspto-grants-1989_11
ORD IDord-8535a6df4d834e13bac1648d51dcf267
Source noteuspto-grants-1989_11