Piperazine → 2-Methyl-4-(piperazin-1-yl)pyrimidine
反応式
Cl[C:2]1[CH:7]=[CH:6][N:5]=[C:4]([CH3:8])[N:3]=1.[NH:9]1[CH2:14][CH2:13][NH:12][CH2:11][CH2:10]1>O1CCCC1>[CH3:8][C:4]1[N:3]=[C:2]([N:9]2[CH2:14][CH2:13][NH:12][CH2:11][CH2:10]2)[CH:7]=[CH:6][N:5]=1参加物
4
実験手順
13 g of 4-chloro-2-methyl-pyrimidine were dissolved in 200 ml of tetrahydrofuran, and 17.5 g of piperazine were added. The reaction mixture was refluxed for 24 h. The precipitated piperazine hydrochloride was filtered off with suction and washed with tetrahydrofuran. Concentration of the solution in vacuo resulted in 19 g of 2-methyl-4-piperazino-pyrimidine, which was reacted without further purification.
後処理
- temperatureThe reaction mixture was refluxed for 24 h
- filtrationThe precipitated piperazine hydrochloride was filtered off with suction
- washwashed with tetrahydrofuran
- customConcentration of the solution in vacuo resulted in 19 g of 2-methyl-4-piperazino-pyrimidine
- customwhich was reacted without further purification
出典と根拠
- ORDレコード
- ord-1684b2b7aac043178849f16e01f9be81
- 出典データセット
- uspto-grants-1992_08
- 特許番号
- US05138058
反応ノート
読み込み中…