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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2268488Generated: October 27, 2026

1,4'-Bipiperidine → 4,5,6,7-Tetramethoxy-2-[3-[4-[(4-piperidinopiperidino)carbonyl]phenoxy]propyl]indan hydrochloride

https://huagongshe.com/reaction/2268488

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4'-BipiperidineHCID 78607—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Reactant4-[3-(4,5,6,7-Tetramethoxyindan-2-yl)propoxy]benzoic acidHCID 18348551—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
Product4,5,6,7-Tetramethoxy-2-[3-[4-[(4-piperidinopiperidino)carbonyl]phenoxy]propyl]indan hydrochlorideHCID 1834853498.4%

Reaction Steps

The mixture of 4-[3-(4,5,6,7-tetramethoxyindan-2-yl)propoxy]benzoic acid (2.00 g), 4-piperidinopiperidine (1.62 g), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (1.84 g), 1-hydroxybenzotriazole monohydrate (1.47 g), and triethylamine (2.01 ml) in THF (40 ml) was stirred at room temperature for 12 hr. The reaction mixture was diluted with water and extracted with ethyl acetate. The organic layer was washed with water and saturated aqueous sodium chloride and dried. The solvent was removed in vacuo. The residue was purified by alumina column chromatography (hexane to hexane:ethyl acetate=1:2) and converted into its hydrochloride, which was further recrystallized from ethanol-diisopropylether to yield the entitled compound (2.85 g) as crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06326369B1
Source datasetuspto-grants-2001_12
ORD IDord-c62c12c3c1c245c7af11574d0b567a5d
Source noteuspto-grants-2001_12