Reaktion #7590

Reaktionsgleichung

5-benzyloxy-2-fluoro-4-methylphenol

4-chloro-6-methoxy-7-(2-methoxyethoxy)cinnoline

→

4-(5-benzyloxy-2-fluoro-4-methylphenoxy)-6-methoxy-7-(2-methoxyethoxy)cinnoline

Ausbeute 53.2%

Lösungsmittel

pyridine

Reaktionsbedingungen

Aufarbeitung

1. 1
   Sonstige(prepared
2. 2
   Temperaturat reflux for 15 hours
3. 3
   SonstigeAfter evaporation of the solvent
4. 4
   Sonstigethe residue was partitioned between ethyl acetate and water
5. 5
   SonstigeThe organic layer was separated
6. 6
   Waschenwashed with water
7. 7
   Trocknenbrine, dried (MgSO4)
8. 8
   Sonstigethe solvent evaporated
9. 9
   SonstigeThe residue was purified by flash chromatography

Vorschrift

The starting material, 4-(5-benzyloxy-2-fluoro-4-methylphenoxy)-6-methoxy-7-(2-methoxyethoxy)cinnoline was obtained by heating a solution of 5-benzyloxy-2-fluoro-4-methylphenol (314 mg, 1.3 mmol) and 4-chloro-6-methoxy-7-(2-methoxyethoxy)cinnoline (280 mg, 1 mmol), (prepared as described for the starting material in Example 2), in pyridine (6 ml), at reflux for 15 hours. After evaporation of the solvent, the residue was partitioned between ethyl acetate and water adjusted to pH7. The organic layer was separated, washed with water and then brine, dried (MgSO4) and the solvent evaporated. The residue was purified by flash chromatography using methylene chloride/ether (4/6 followed by 3/7) as eluent to give 4-(5-benzyloxy-2-fluoro-4-methylphenoxy)-6-methoxy-7-(2-methoxyethoxy)cinnoline as a white solid (247 mg, 53%).

Quelle