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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Pivaloyl chloride | HCID 62493 | — |
| 반응물 | trans-3-(3-Pyridyl)acrylic acid | HCID 776396 | — |
| 반응물 | 1-(3,4-Dimethoxyphenyl)-2-(methylamino)ethanone hydrobromide | HCID 18357830 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | (E)-N-[2-(3,4-dimethoxyphenyl)-2-oxoethyl]-N-methyl-3-(3-pyridyl)-2-propenamide | HCID 20701373 | 56.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06313153B1 |
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| 출처 데이터셋 | uspto-grants-2001_11 |
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| ORD ID | ord-d4cf7afa31954f7aaa77507c51625fd1 |
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| 출처 메모 | uspto-grants-2001_11 |
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