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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 428129생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물N-MethylmescalineHCID 138365—
반응물Sodium BicarbonateHCID 516892—
반응물trans-3-(3-Pyridyl)acrylic acidHCID 776396—
용매DimethylformamideHCID 6228—
생성물(E)-N-methyl-3-(3-pyridyl)-N-(3,4,5-trimethoxyphenethyl)-2-propenamideHCID 2306729694%

반응 단계

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%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06313153B1
출처 데이터셋uspto-grants-2001_11
ORD IDord-c2f9a2806f274d10848e86d2d0cd1129
출처 메모uspto-grants-2001_11