反応式
[C:1](OC(N1CCNCC1)=O)(C)(C)C.[Cl:14]CC(Cl)=O.C(NC)(C)C.[ClH:24].Cl.CO[CH2:28][CH:29]([NH:31][C:32](=[O:40])[CH2:33][N:34]1[CH2:39][CH2:38][NH:37][CH2:36][CH2:35]1)[CH3:30]>>[ClH:14].[ClH:24].[CH:29]([N:31]([CH3:1])[C:32](=[O:40])[CH2:33][N:34]1[CH2:39][CH2:38][NH:37][CH2:36][CH2:35]1)([CH3:30])[CH3:28]参加物
5
実験手順
N-Isopropyl-N-methyl-2-piperazin-1-yl-acetamide dihydrochloride was prepared from 1-tert-butyloxycarbonyl-piperazine, chloroacetylchloride and N-isopropyl-N-methylamine in an analogous manner as described for the preparation of N-(2-methoxy-1-methyl-ethyl)-2-piperazin-1-yl-acetamide dihydrochloride (example 40).
出典と根拠
- ORDレコード
- ord-1585f7f5f9694b81a8add5fb1cf3b3a8
- 出典データセット
- uspto-grants-2010_04
- 特許番号
- US07705007B2
関連ノート
読み込み中…