Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 597242생성일: 2026년 10월 27일
Pyridine → 3,4,5-Trimethoxybenzeneacetyl-1-[(3,4-dimethoxyphenyl)-methylene]isoquinoline
https://huagongshe.com/reaction/597242
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Pyridine | HCID 1049 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | 2-(3,4,5-trimethoxyphenyl)acetyl Chloride | HCID 11032124 | — |
| 반응물 | 3,4-Dihydro-6,7-dimethoxy-1-[(3,4-dimethoxyphenyl)methylene]isoquinoline | HCID 68123391 | — |
| 용매 | Benzene | HCID 241 | — |
| 용매 | Chloroform | HCID 6212 | — |
| 생성물 | 3,4,5-Trimethoxybenzeneacetyl-1-[(3,4-dimethoxyphenyl)-methylene]isoquinoline | HCID 86734573 | — |
반응 단계
To a suspension of 12 parts of 3,4-dihydro-6,7-dimethoxy-1-[(3,4-dimethoxyphenyl)methylene]isoquinoline in 50 parts of pyridine and 5 parts of N-ethyl-N-(1-methylethyl)-2-propanamine is added a solution of 10 parts of 3,4,5-trimethoxybenzeneacetyl chloride in 45 parts of benzene. The resultant mixture is heated at the boiling point under reflux for 1 hour, then cooled and thereupon diluted with 500 parts of chloroform. The resultant solution is washed with water, dried over anhydrous sodium sulfate, and stripped of solvent by vacuum distillation. The residue is crystallized from a mixture of ethyl acetate and ether to give (Z)-1,2,3,4-tetrahydro-6,7-dimethoxy-2-(3,4,5-trimethoxybenzeneacetyl-1-[(3,4-dimethoxyphenyl)-methylene]isoquinoline melting at 164°-170°.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04013666 |
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| 출처 데이터셋 | uspto-grants-1977_03 |
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| ORD ID | ord-9277f6817e6345548df65511f3cdca40 |
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| 출처 메모 | uspto-grants-1977_03 |
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