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.[Cl:15][C:16]1[CH:17]=[C:18]([CH:41]=[CH:42][C:43]=1[Cl:44])[CH2:19][N:20]1[CH2:25][CH2:24][N:23]([CH2:26][C@@H:27](NC(=O)C2C=CC(C)=CC=2)[CH:28]([CH3:30])[CH3:29])[CH2:22][CH2:21]1.C([NH:52][C@H](C(O)=O)C(C)C)(OC(C)(C)C)=O>C(Cl)Cl>[Cl:15][C:16]1[CH:17]=[C:18]([CH:41]=[CH:42][C:43]=1[Cl:44])[CH2:19][N:20]1[CH2:25][CH2:24][N:23]([CH2:26][CH:27]([C:5]2([CH:10]=[CH:11][CH:12]=[C:3]([O:2][CH3:1])[CH2:4]2)[CH2:6][NH:7][C:8]([NH2:52])=[S:9])[CH:28]([CH3:30])[CH3:29])[CH2:22][CH2:21]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-2a11af390aa84223a064ad2291c1bb29
- 出典データセット
- uspto-grants-2001_11
- 特許番号
- US06323223B1
関連ノート
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