戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 597242作成日:2026年10月27日

Pyridine → 3,4,5-Trimethoxybenzeneacetyl-1-[(3,4-dimethoxyphenyl)-methylene]isoquinoline

https://huagongshe.com/reaction/597242

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物DiisopropylethylamineHCID 81531—
反応物2-(3,4,5-trimethoxyphenyl)acetyl ChlorideHCID 11032124—
反応物3,4-Dihydro-6,7-dimethoxy-1-[(3,4-dimethoxyphenyl)methylene]isoquinolineHCID 68123391—
溶媒BenzeneHCID 241—
溶媒ChloroformHCID 6212—
生成物3,4,5-Trimethoxybenzeneacetyl-1-[(3,4-dimethoxyphenyl)-methylene]isoquinolineHCID 86734573—

反応手順

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°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04013666
出典データセットuspto-grants-1977_03
ORD IDord-9277f6817e6345548df65511f3cdca40
出典メモuspto-grants-1977_03