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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1168950Generated: October 29, 2026

Water → Methyl(3-(5-(phenylmethoxy)(3-pyridyloxy))propyl)amine Hemigalactarate

https://huagongshe.com/reaction/1168950

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantGalactaric acidHCID 3037582—
ReactantMethyl(3-(5-(phenylmethoxy)(3-pyridyloxy))propyl)amineHCID 9881953—
SolventEthanolHCID 702—
ProductMethyl(3-(5-(phenylmethoxy)(3-pyridyloxy))propyl)amine HemigalactarateHCID 1211222465.2%

Reaction Steps

To a solution of methyl(3-(5-(phenylmethoxy)(3-pyridyloxy))propyl)amine (1.07 g, 3.929 mmol) in ethanol (15 mL) was added galactaric acid (0.413 g, 1.964 mmol). Water (1.5 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) (5 mL). The filtrate was diluted with ethanol (23 mL). The mixture was allowed to cool to ambient temperature; however, no solids precipitated. The solution was concentrated by rotary evaporation and briefly dried under high vacuum. The resulting brown solids were dissolved in a mixture of hot 2-propanol (˜15 mL) and water (0.8 mL); the dark-brown solution was allowed to cool to ambient temperature. After 30 min of precipitation, the batch was diluted with 2-propanol (30 mL) and stored at 5° C. for 16 h. The resulting solids were filtered, washed with cold 2-propanol (3×5 mL) and vacuum dried at 45° C. to give 0.967 g (65.2%) of a beige powder, mp 137-140° C. The compound exhibits a Ki of 2 nM; the effect at muscle sites is 1 percent; and the effect at ganglia sites is 3 percent. The compound exhibits neurotransmitter release of 38 percent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06627648B1
Source datasetuspto-grants-2003_09
ORD IDord-0aadfd4b060f48729ca637f803725b1a
Source noteuspto-grants-2003_09