تفاعل #463032

ord-b91da9fbc55d42aa85ba9406b896131b

ظروف التفاعل

درجة الحرارة
180°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe reaction mixture was then partitioned between CH2Cl2 and water
  2. 2
    أخرىthe layers were separated
  3. 3
    استخلاصthe aqueous layer was extracted with CH2Cl2
  4. 4
    غسيلwashed with water
  5. 5
    تجفيفdried over Na2SO4
  6. 6
    أخرىevaporated
  7. 7
    أخرىThe residue was purified by column chromatography on silca gel
  8. 8
    أخرىto afford an oil which
  9. 9
    أخرىwas crystallized from ether/hexane
  10. 10
    أخرىrecrystallized from ether/hexane

الإجراء التجريبي

A mixture of 4-chloro-1-ethyl-1H-pyrazolo[3,4-b]quinoline (3 g), DMSO (9 ml) and trans-4-(aminomethyl)cyclohexane carboxylic acid (4.1 g) was heated at 180° C. overnight. The reaction mixture was then partitioned between CH2Cl2 and water, the layers were separated and the aqueous layer was extracted with CH2Cl2. The organic layers were combined, washed with water, dried over Na2SO4, and evaporated. The residue was purified by column chromatography on silca gel to afford an oil which was crystallized from ether/hexane and then recrystallized from ether/hexane to afford 1-ethyl-N-[[4-(methylthiomethoxycarbonyl) cyclohexyl]methyl]-1H-pyrazolo[3,4-b]quinolin-4-amine, m.p. 135°-136° C.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05488055uspto-grants-1996_01