1-Methylpiperazine → (3-Iodo-5-methoxy-phenyl)-(4-methyl-piperazin-1-yl)-methanone
反応式
[CH2:1]([NH:8][C:9](=[O:19])[C:10]1[CH:15]=[C:14]([O:16][CH3:17])[CH:13]=[C:12]([I:18])[CH:11]=1)[C:2]1C=CC=CC=1.[CH3:20][N:21]1CCN[CH2:23][CH2:22]1.IC1C=C(C=C(OC)C=1)C(O)=O>>[I:18][C:12]1[CH:11]=[C:10]([C:9]([N:8]2[CH2:1][CH2:2][N:21]([CH3:20])[CH2:22][CH2:23]2)=[O:19])[CH:15]=[C:14]([O:16][CH3:17])[CH:13]=1参加物
4
実験手順
The title compound was prepared by the same method as N-benzyl-3-iodo-5-methoxy-benzamide. 4-Methylpiperazine was used instead of benzylamine. Starting with 3.1 g of 3-iodo-5-methoxybenzoic acid, 3.2 g (80% yield) of the title compound was obtained.
出典と根拠
- ORDレコード
- ord-15541b4598884175b2dd85859314d68d
- 出典データセット
- uspto-grants-2011_08
- 特許番号
- US07989454B2
反応ノート
読み込み中…