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HRID 428129作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物N-MethylmescalineHCID 138365—
反応物Sodium BicarbonateHCID 516892—
反応物trans-3-(3-Pyridyl)acrylic acidHCID 776396—
溶媒DimethylformamideHCID 6228—
生成物(E)-N-methyl-3-(3-pyridyl)-N-(3,4,5-trimethoxyphenethyl)-2-propenamideHCID 2306729694%

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06313153B1
出典データセットuspto-grants-2001_11
ORD IDord-c2f9a2806f274d10848e86d2d0cd1129
出典メモuspto-grants-2001_11