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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 428129Erstellt: 24. Oktober 2026

Triethylamine → (E)-N-methyl-3-(3-pyridyl)-N-(3,4,5-trimethoxyphenethyl)-2-propenamide

https://huagongshe.com/de/reaction/428129

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktN-MethylmescalineHCID 138365—
EduktSodium BicarbonateHCID 516892—
Edukttrans-3-(3-Pyridyl)acrylic acidHCID 776396—
LösungsmittelDimethylformamideHCID 6228—
Produkt(E)-N-methyl-3-(3-pyridyl)-N-(3,4,5-trimethoxyphenethyl)-2-propenamideHCID 2306729694%

Reaktionsschritte

N-Methyl-3,4,5-trimethoxyphenethylamine (1.60 g, 7.11 mmol) and trans-3-(3-pyridyl)acrylic acid (1.17 g) were dissolved in dimethylformamide (8 ml), and diethylphosphoric cyanide (1.3 ml) and triethylamine (2.2 ml) were sequentially added under ice-cooling and stirring and stirred at room temperature for 1 hour. Saturated aqueous sodium bicarbonate solution was added to the reaction mixture, and the reaction mixture was extracted with dichloromethane, washed with water and dried over potassium carbonate. The solvent was distilled out under reduced pressure and the residue was purified by silica gel column chromatography (ethyl acetate:hexane=10:1) to yield amorphous (E)-N-methyl-3-(3-pyridyl)-N-(3,4,5-trimethoxyphenethyl)-2-propenoic acid amide (2.37 g, 94%). Then, hydrogen chloride-methanol was added to the product (1.80 g) to produce its hydrochloride, which was recrystallized in a mixed solvent of ethyl acetate-methanol to yield the titled compound (1.59 g, 57%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06313153B1
Quelldatensatzuspto-grants-2001_11
ORD IDord-c2f9a2806f274d10848e86d2d0cd1129
Quellennotizuspto-grants-2001_11