تفاعل #1519104

ord-88b0a74555e84873b24100e1678debb4

معادلة التفاعل

Oc1cc(-c2cc(Cl)ccn2)nc(-c2ccccn2)n1
6-(4-chloropyrid-2-yl)-2-pyrid-2-yl-pyrimidin-4-ol
CN1CCNCC1
1-methyl-piperazine
CN1CCN(c2ccnc(-c3cc(O)nc(-c4ccccn4)n3)c2)CC1
6-[4-(4-Methyl-piperazin-1-yl)-pyrid-2-yl]-2-pyrid-2-yl-pyrimidin-4-ol

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةis refluxed for 22 hours
  2. 2
    تركيزconcentrated to dryness
  3. 3
    أخرىa rotary evaporator
  4. 4
    workup.ADDITION50 ml of water are added
  5. 5
    workup.ADDITION3.6 g of EDTA are added
  6. 6
    استخلاصExtraction
  7. 7
    تجفيفdried (sodium sulfate)
  8. 8
    تركيزConcentration
  9. 9
    أخرىa rotary evaporator
  10. 10
    أخرىthe crude product is recrystallised from toluene

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07612010B2uspto-grants-2009_11