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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 326732Generated: October 30, 2026

2-Pyrrolidin-1-ylmethyl-piperidine → 1-(Indene-1-carbonyl)-2-(pyrrolidin-1-ylmethyl)piperidine

https://huagongshe.com/reaction/326732

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Pyrrolidin-1-ylmethyl-piperidineHCID 2760541—
Reactant1H-Indene-1-carbonyl chlorideHCID 18915077—
SolventTriethylamineHCID 8471—
Product1-(Indene-1-carbonyl)-2-(pyrrolidin-1-ylmethyl)piperidineHCID 1891504632.2%

Reaction Steps

From 2.36 g of 2-(pyrrolidin-1-ylmethyl)piperidine. 2.5 g of indene-1-carbonyl chloride and 4.88 ml of triethylamine. 1.4 g of 1-(indene-1-carbonyl)-2-(pyrrolidin-1-ylmethyl)piperidine was obtained using a procedure similar to that in Example 2. In a mixed solvent to methanol, water and ethanol (2:1:1), this compound was catalytically reduced with 10% palladium on carbon. After completion of the reduction, the catalyst was filtered off. After evaporation of the solvent, the residue was treated with a 4N 1,4-dioxane solution of hydrogen chloride to obtain 1.05 g of the title compound, melting at 218°-221° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05270327
Source datasetuspto-grants-1993_12
ORD IDord-6cd615d1c8364f64afd0f52b3b22aee5
Source noteuspto-grants-1993_12