Piperazine → 2-Methyl-4-(piperazin-1-yl)pyrimidine
반응식
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]=1참가 물질
4
실험 절차
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.
후처리
- 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
출처 및 근거
- ORD 기록
- ord-1684b2b7aac043178849f16e01f9be81
- 출처 데이터셋
- uspto-grants-1992_08
- 특허 번호
- US05138058
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