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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 428139생성일: 2026년 10월 26일

Triethylamine → (E)-N-[2-(3,4-dimethoxyphenyl)-2-oxoethyl]-N-methyl-3-(3-pyridyl)-2-propenamide

https://huagongshe.com/reaction/428139

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Pivaloyl chlorideHCID 62493—
반응물trans-3-(3-Pyridyl)acrylic acidHCID 776396—
반응물1-(3,4-Dimethoxyphenyl)-2-(methylamino)ethanone hydrobromideHCID 18357830—
용매DichloromethaneHCID 6344—
생성물(E)-N-[2-(3,4-dimethoxyphenyl)-2-oxoethyl]-N-methyl-3-(3-pyridyl)-2-propenamideHCID 2070137356.1%

반응 단계

Dichloromethane (50 ml) and triethylamine (2.69 ml, 19.30 mmol) were sequentially added to trans-3-(3-pyridyl)acrylic acid (1.44 g, 9.65 mmol) and stirred for 10 minutes. Then, pivaloyl chloride (1.18 ml, 9.65 mmol) was added and stirred for 13 minutes. 1-(3,4-Dimethoxyphenyl)-2-(methylamino)ethanone hydrobromide (2.79 g, 9.65 mmol) was dissolved in dichloromethane (4 ml) and triethylamine (1.34 ml, 9.65 mmol), added to the reaction mixture and stirred at room temperature for 30 minutes. After the reaction mixture was washed with water and aqueous saturated sodium bicarbonate solution, the organic phase was dried over magnesium sulfate and the solvent was distilled out under reduced pressure. The residue was purified by silica gel column chromatography (dichloromethane:methanol=10:1) to yield a crude product. The crude product was recrystallized to yield the titled compound (1.84 g, 5.41 mmol, 56%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06313153B1
출처 데이터셋uspto-grants-2001_11
ORD IDord-d4cf7afa31954f7aaa77507c51625fd1
출처 메모uspto-grants-2001_11