反応 #1519104

反応方程式

6-(4-chloropyrid-2-yl)-2-pyrid-2-yl-pyrimidin-4-ol

1-methyl-piperazine

→

6-[4-(4-Methyl-piperazin-1-yl)-pyrid-2-yl]-2-pyrid-2-yl-pyrimidin-4-ol

溶媒

2-methyl-2-butanol

反応条件

後処理

1. 1
   温度is refluxed for 22 hours
2. 2
   濃縮concentrated to dryness
3. 3
   その他a rotary evaporator
4. 4
   workup.ADDITION50 ml of water are added
5. 5
   workup.ADDITION3.6 g of EDTA are added
6. 6
   抽出Extraction
7. 7
   乾燥dried (sodium sulfate)
8. 8
   濃縮Concentration
9. 9
   その他a rotary evaporator
10. 10
    その他the crude product is recrystallised from toluene

実験手順

A mixture of 3.51 g (12.3 mmol) of 6-(4-chloropyrid-2-yl)-2-pyrid-2-yl-pyrimidin-4-ol, 27.4 ml (303 mmol, 20 equivalents, 30.38 g) of 1-methyl-piperazine and 84 mg (0.05 mmol, 0.05 equivalent) of zinc(II) chloride in 50 ml of 2-methyl-2-butanol is refluxed for 22 hours and concentrated to dryness using a rotary evaporator. 50 ml of water are added, 3.6 g of EDTA are added, and the pH is adjusted to 9 using dilute sodium hydroxide solution. Extraction is carried out three times using 150 ml of chloroform each time, and the organic extracts are combined and dried (sodium sulfate). Concentration is carried out using a rotary evaporator and the crude product is recrystallised from toluene. 6-[4-(4-Methyl-piperazin-1-yl)-pyrid-2-yl]-2-pyrid-2-yl-pyrimidin-4-ol is obtained in the form of a whitish solid.

出典