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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,4'-Bipiperidine | HCID 78607 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| Reactant | 4-[3-(4,5,6,7-Tetramethoxyindan-2-yl)propoxy]benzoic acid | HCID 18348551 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 4,5,6,7-Tetramethoxy-2-[3-[4-[(4-piperidinopiperidino)carbonyl]phenoxy]propyl]indan hydrochloride | HCID 18348534 | 98.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06326369B1 |
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| Source dataset | uspto-grants-2001_12 |
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| ORD ID | ord-c62c12c3c1c245c7af11574d0b567a5d |
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| Source note | uspto-grants-2001_12 |
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