1,3-Benzodioxol-5-amine → 4-(3,4-Methylenedioxyphenylamino)-1-[[2-(3,4,5-trimethoxyphenyl) pyridin-4-yl]methyl]piperidine
反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:13]2[CH:18]=[C:17]([CH2:19][N:20]3[CH2:25][CH2:24][C:23](=O)[CH2:22][CH2:21]3)[CH:16]=[CH:15][N:14]=2)[CH:6]=[C:7]([O:11][CH3:12])[C:8]=1[O:9][CH3:10].[CH2:27]1[O:36][C:35]2[CH:34]=[CH:33][C:31]([NH2:32])=[CH:30][C:29]=2[O:28]1>>[CH2:27]1[O:36][C:35]2[CH:34]=[CH:33][C:31]([NH:32][CH:23]3[CH2:22][CH2:21][N:20]([CH2:19][C:17]4[CH:16]=[CH:15][N:14]=[C:13]([C:5]5[CH:6]=[C:7]([O:11][CH3:12])[C:8]([O:9][CH3:10])=[C:3]([O:2][CH3:1])[CH:4]=5)[CH:18]=4)[CH2:25][CH2:24]3)=[CH:30][C:29]=2[O:28]1参加物
3
実験手順
1-[[2-(3,4,5-Trimethoxyphenyl)pyridin-4-yl]methyl-4-piperidone (1.40 g) and 3,4-methylenedioxyaniline (646 mg) were treated in the same manner as described in Preparation Example 29 to give the title compound.
後処理
- customas described in Preparation Example 29
出典と根拠
- ORDレコード
- ord-dc4776670e484afeba9de49d8313a0c9
- 出典データセット
- uspto-grants-2005_03
- 特許番号
- US06867221B2
反応ノート
読み込み中…