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HRID 428139作成日:2026年10月26日

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

https://huagongshe.com/reaction/428139

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Pivaloyl chlorideHCID 62493—
反応物trans-3-(3-Pyridyl)acrylic acidHCID 776396—
反応物1-(3,4-Dimethoxyphenyl)-2-(methylamino)ethanone hydrobromideHCID 18357830—
溶媒DichloromethaneHCID 6344—
生成物(E)-N-[2-(3,4-dimethoxyphenyl)-2-oxoethyl]-N-methyl-3-(3-pyridyl)-2-propenamideHCID 2070137356.1%

反応手順

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%).

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-d4cf7afa31954f7aaa77507c51625fd1
出典メモuspto-grants-2001_11