1-(3,4-Dinitrobenzyl)-4-methylpiperazine → 1-(3,4-Diaminobenzyl)-4-methylpiperazine
反応式
[N+:1]([C:4]1[CH:5]=[C:6]([CH:15]=[CH:16][C:17]=1[N+:18]([O-])=O)[CH2:7][N:8]1[CH2:13][CH2:12][N:11]([CH3:14])[CH2:10][CH2:9]1)([O-])=O>CN(C=O)C.CO.[Pd]>[NH2:1][C:4]1[CH:5]=[C:6]([CH:15]=[CH:16][C:17]=1[NH2:18])[CH2:7][N:8]1[CH2:13][CH2:12][N:11]([CH3:14])[CH2:10][CH2:9]1参加物
4
実験手順
1-(3,4-Dinitrobenzyl)-4-methylpiperazine (2.8 g, 10 mmol), was dissolved in DMF:MeOH (1:1, 20 mL) and agitated with 10% Pd/C (280 mg) under an atmosphere of H2 for 12 hrs. The reaction was monitored by TLC. The mixture was then filtered and evaporated to give a dark solid which was used immediately without any further purification.
後処理
- filtrationThe mixture was then filtered
- customevaporated
- customto give a dark solid which
- customwas used immediately without any further purification
出典と根拠
- ORDレコード
- ord-505c0efd4d0e4ae981e1aed54d9f72a7
- 出典データセット
- uspto-grants-2014_10
- 特許番号
- US08859553B2
反応ノート
読み込み中…