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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

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물DiisopropylethylamineHCID 81531—
반응물2-(3,4,5-trimethoxyphenyl)acetyl ChlorideHCID 11032124—
반응물3,4-Dihydro-6,7-dimethoxy-1-[(3,4-dimethoxyphenyl)methylene]isoquinolineHCID 68123391—
용매BenzeneHCID 241—
용매ChloroformHCID 6212—
생성물3,4,5-Trimethoxybenzeneacetyl-1-[(3,4-dimethoxyphenyl)-methylene]isoquinolineHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04013666
출처 데이터셋uspto-grants-1977_03
ORD IDord-9277f6817e6345548df65511f3cdca40
출처 메모uspto-grants-1977_03