反応式
[CH2:1]([CH:8]1[C:17]2[C:12](=[CH:13][C:14]([O:20][CH3:21])=[C:15]([O:18][CH3:19])[CH:16]=2)[CH2:11][CH2:10][NH:9]1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH3:22][O:23]C1C=CC(CC(Cl)=O)=CC=1.C1(CC(Cl)=O)C=CC=CC=1>>[CH3:22][O:23][C:5]1[CH:4]=[CH:3][C:2]([CH2:1][CH:8]2[C:17]3[C:12](=[CH:13][C:14]([O:20][CH3:21])=[C:15]([O:18][CH3:19])[CH:16]=3)[CH2:11][CH2:10][NH:9]2)=[CH:7][CH:6]=1参加物
4
実験手順
1,2,3,4-Tetrahydro-1-(4-methoxybenzyl)-6,7-dimethoxyisoquinoline was prepared by a procedure analogous to that described in example 17 for 1,2,3,4-tetrahydro-1-benzyl-6,7-di-methoxyisoquinoline but substituting in the first step (4-methoxyphenyl)acetyl chloride for phenylacetyl chloride.
出典と根拠
- ORDレコード
- ord-8fb7878d5365422c956cfe5e043fa3a3
- 出典データセット
- uspto-grants-1999_11
- 特許番号
- US05981521
関連ノート
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