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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 597145생성일: 2026년 10월 26일

Benzene → (1Z,2E)-1,2,3,4-tetrahydro-6,7-dimethoxy-1-[(3,4,5-trimethoxyphenyl)methylene]-2-[3-(3,4,5-trimethoxyphenyl)-1-oxo-2-propenyl]isoquinoline

https://huagongshe.com/reaction/597145

반응식

참여 물질

역할이름HCID투입량
반응물BenzeneHCID 241—
반응물3-(3,4,5-Trimethoxyphenyl)acrylic acidHCID 7021—
반응물N,N-Diethyl-1-propyn-1-amineHCID 77909—
반응물3,4-Dihydro-6,7-dimethoxy-1-[(3,4,5-trimethoxyphenyl)methylene]isoquinolineHCID 70638952—
용매PyridineHCID 1049—
생성물(1Z,2E)-1,2,3,4-tetrahydro-6,7-dimethoxy-1-[(3,4,5-trimethoxyphenyl)methylene]-2-[3-(3,4,5-trimethoxyphenyl)-1-oxo-2-propenyl]isoquinolineHCID 21446881—

반응 단계

To a solution of 100 parts of 3-(3,4,5-trimethoxyphenyl)-2-propenoic acid in 1125 parts of benzene is added 22 parts of N,N-diethyl-1-propyne-1-amine. The resultant mixture is stirred for 2 hours, whereupon a solution of 75 parts of 3,4-dihydro-6,7-dimethoxy-1-[(3,4,5-trimethoxyphenyl)methylene]isoquinoline [Ber. deut. chem. Ges., 55, 2889 (1922)] in 200 parts of pyridine is introduced. The mixture thus obtained is stirred and heated at 65° for 3 hours, then cooled, consecutively washed with water and aqueous 5% sodium bicarbonate, 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 (1Z,2E)-1,2,3,4-tetrahydro-6,7-dimethoxy-1-[(3,4,5-trimethoxyphenyl)methylene]-2-[3-(3,4,5-trimethoxyphenyl)-1-oxo-2-propenyl]isoquinoline melting at 180°-183°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04013644
출처 데이터셋uspto-grants-1977_03
ORD IDord-a65d5414117c49ab875f8c002918072d
출처 메모uspto-grants-1977_03