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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1977152Generated: October 30, 2026

Water → (4E)-N-Methyl-5-(5-i sopropoxy-3-pyridyl)-4-penten-2-amine Hemigalactarate

https://huagongshe.com/reaction/1977152

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantGalactaric acidHCID 3037582—
Reactant(4E)-N-methyl-5-(5-isopropoxy-3-pyridinyl)-4-penten-2-amineHCID 9881145—
SolventMethanolHCID 887—
Product(4E)-N-Methyl-5-(5-i sopropoxy-3-pyridyl)-4-penten-2-amine HemigalactarateHCID 13172255893.5%

Reaction Steps

(4E)-N-Methyl-5-(5-isopropoxy-3-pyridyl)-4-penten-2-amine (69.3 mg, 0.23 mmol) was dissolved in CH3OH (1.5 mL), assisted by heating. The warm solution was treated with galactaric acid (24.3 mg, 0.12 mmol), followed by water (0.3 mL). The resulting solution was warmed and filtered through glass wool to remove a few insoluble particles, washing the filter plug with 0.4 mL of a CH3OH—H2O (4:1, v/v) solution. The filtrate was diluted with CH3OH (1.5 mL), and the light-yellow solution was stored at 5° C. for 15 h. No precipitate had formed; therefore, the solution was concentrated on a rotary evaporator. The resulting solids were triturated with anhydrous diethyl ether (3×6 mL). The product was dried under a stream of nitrogen, dried under high vacuum, followed by further vacuum drying at 45° C. for 15 h to afford 73.0 mg (93.1%) of an off-white powder, mp 144-146.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06232316B1
Source datasetuspto-grants-2001_05
ORD IDord-e2d2e85e2d27404987e72485ebed033f
Source noteuspto-grants-2001_05