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HRID 597145作成日:2026年10月25日

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

反応式

関与物質

役割名称HCID仕込み量
反応物BenzeneHCID 241—
反応物3-(3,4,5-Trimethoxyphenyl)acrylic acidHCID 7021—
反応物N,N-Diethyl-1-propyn-1-amineHCID 77909—
反応物3,4-Dihydro-6,7-dimethoxy-1-[(3,4,5-trimethoxyphenyl)methylene]isoquinolineHCID 70638952—
溶媒PyridineHCID 1049—
生成物(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—

反応手順

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°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04013644
出典データセットuspto-grants-1977_03
ORD IDord-a65d5414117c49ab875f8c002918072d
出典メモuspto-grants-1977_03