Reaktion #463032

Reaktionsgleichung

4-chloro-1-ethyl-1H-pyrazolo[3,4-b]quinoline

trans-4-(aminomethyl)cyclohexane carboxylic acid

DMSO

→

1-ethyl-N-[[4-(methylthiomethoxycarbonyl) cyclohexyl]methyl]-1H-pyrazolo[3,4-b]quinolin-4-amine

Reaktionsbedingungen

Aufarbeitung

1. 1
   SonstigeThe reaction mixture was then partitioned between CH2Cl2 and water
2. 2
   Sonstigethe layers were separated
3. 3
   Extraktionthe aqueous layer was extracted with CH2Cl2
4. 4
   Waschenwashed with water
5. 5
   Trocknendried over Na2SO4
6. 6
   Sonstigeevaporated
7. 7
   SonstigeThe residue was purified by column chromatography on silca gel
8. 8
   Sonstigeto afford an oil which
9. 9
   Sonstigewas crystallized from ether/hexane
10. 10
    Sonstigerecrystallized from ether/hexane

Vorschrift

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.

Quelle