HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1168959Generated: November 2, 2026
Water → Ethyl(3-(3-pyridyloxy)propyl)amine Hemigalactarate
https://huagongshe.com/reaction/1168959
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Galactaric acid | HCID 3037582 | — |
| Reactant | Ethyl(3-(3-pyridyloxy)propyl)amine | HCID 9877539 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl(3-(3-pyridyloxy)propyl)amine Hemigalactarate | HCID 12112226 | — |
Reaction Steps
To a solution of ethyl(3-(3-pyridyloxy)propyl)amine (400 mg, 2.20 mmol) in ethanol (11 mL) was added galactaric acid (233 mg, 1.10 mmol). Water (3.5 mL) was added drop-wise, while warming the solution to reflux. To remove some white, insoluble solids, the warm solution was filtered through a glass wool plug, washing the filter plug with a warm solution of ethanol-water (4:1, v/v) (3.5 mL). The filtrate was diluted with ethanol (17 mL). The mixture was allowed to cool to ambient temperature and was further cooled at 5° C. Very few solids precipitated. Consequently, the solution was concentrated to a residue that was vacuum dried. The solids were slurried in 2-propanol, and the 2-propanol was evaporated. The resulting solids were slurried in anhydrous ether. The product was filtered, washed with ether, and vacuum dried at 40° C. to give 348 mg (55.0%) of a brown, flaky powder, mp 147-150° C. The compound exhibits a Ki of 66 nM; the effect at muscle sites is 13 percent; and the effect at ganglia sites is 13 percent. The compound exhibits neurotransmitter release of 57 percent.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06627648B1 |
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| Source dataset | uspto-grants-2003_09 |
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| ORD ID | ord-5894e74266f945f992a1ff6ada0b8d3b |
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| Source note | uspto-grants-2003_09 |
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