反応式
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:10]=[CH:11][CH:12]=1)[CH2:6][N:7]=[C:8]=[S:9].Cl.Cl.C[CH:16]1[N:21]([CH2:22][C:23]2[CH:28]=[CH:27][C:26]([Cl:29])=[C:25]([Cl:30])[CH:24]=2)[CH2:20][CH2:19][N:18]([CH2:31][CH:32](NC(=O)C2C=CC(C)=CC=2)[CH:33]([CH3:35])[CH3:34])[CH2:17]1.C([NH:53][C@H](C(O)=O)C(C)C)(OC(C)(C)C)=O>C(Cl)Cl>[Cl:30][C:25]1[CH:24]=[C:23]([CH:28]=[CH:27][C:26]=1[Cl:29])[CH2:22][N:21]1[CH2:20][CH2:19][N:18]([CH2:31][CH:32]([C:5]2([CH:10]=[CH:11][CH:12]=[C:3]([O:2][CH3:1])[CH2:4]2)[CH2:6][NH:7][C:8]([NH2:53])=[S:9])[CH:33]([CH3:35])[CH3:34])[CH2:17][CH2:16]1参加物
5
反応物 3
生成物 1
試薬・触媒・溶媒 1
実験手順
3-Methoxybenzyl isothiocyanate (22 mg, 0.12 mmol) was added to a solution of 1-(RS)-[4-(3,4-dichlorobenzyl)piperazin-1-ylmethyl]-2-methylpropylamine (40 mg, 0.12 mmol) [prepared as described in Example 1 by substituting L-N-BOC-valine with DL-N-BOC-valine] in methylene chloride (1.5 ml). The reaction mixture was stirred for 2 h and then concentrated. Purification by flash chromatography with 20:1 methylene chloride: methanol as the eluant gave 1-{1-(RS)-[4-(3,4-dichlorobenzyl)piperazin-1-ylmethyl]-2-methylpropyl}-3-methoxybenzyl-2-thiourea (18 mg) as a solid.
後処理
- concentrationconcentrated
- customPurification by flash chromatography with 20:1 methylene chloride
出典と根拠
- ORDレコード
- ord-7b4ca1cb5ba84af6992b0116ef6e4208
- 出典データセット
- uspto-grants-2006_01
- 特許番号
- US06984637B2
関連ノート
読み込み中…