反応式
CO[C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][C:12]=1OC)[C:9](=[CH:15][C:16]1[CH:21]=[CH:20][C:19]([O:22][CH3:23])=[C:18]([O:24][CH3:25])[CH:17]=1)[NH:8][CH2:7][CH2:6]2.N1C=CC=CC=1.C(N(C(C)C)C(C)C)C.[CH3:41][O:42][C:43]1[CH:44]=[C:45]([CH2:53][C:54](Cl)=[O:55])[CH:46]=[C:47]([O:51][CH3:52])[C:48]=1[O:49][CH3:50]>C(Cl)(Cl)Cl.C1C=CC=CC=1>[CH3:52][O:51][C:47]1[CH:46]=[C:45]([CH2:53][C:54]([C:7]2[NH:8][C:9](=[CH:15][C:16]3[CH:21]=[CH:20][C:19]([O:22][CH3:23])=[C:18]([O:24][CH3:25])[CH:17]=3)[C:10]3[C:5]([CH:6]=2)=[CH:4][CH:3]=[CH:12][CH:11]=3)=[O:55])[CH:44]=[C:43]([O:42][CH3:41])[C:48]=1[O:49][CH3:50]参加物
反応物 4
生成物 1
試薬・触媒・溶媒 2
実験手順
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°.
後処理
- temperatureunder reflux for 1 hour
- temperaturecooled
- washThe resultant solution is washed with water
- dry with materialdried over anhydrous sodium sulfate
- distillationstripped of solvent by vacuum distillation
- customThe residue is crystallized from a mixture of ethyl acetate and ether
出典と根拠
- ORDレコード
- ord-9277f6817e6345548df65511f3cdca40
- 出典データセット
- uspto-grants-1977_03
- 特許番号
- US04013666
関連ノート
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