Reaktion #50131

Reaktionsgleichung

Methyl 5-diphenylacetyl-4,5,6,7-tetrahydroimidazo-[4,5-c]pyridine-4-carboxylate

sodium hydride

[2'-(1-trityl-1H-tetrazol-5-yl)bipheyl-4-yl]methyl bromide

→

methyl 5-diphenylacetyl-3-[2'-(1-trityl-1H-tetrazol-5-yl)biphenyl-4-yl]methyl-4,5,6,7-tetrahydroimidazo[4,5-c]pyridine-4-carboxylate

Ausbeute 11.8%

Lösungsmittel

dimethylformamide

Reaktionsbedingungen

Aufarbeitung

1. 1
   Temperaturcooling
2. 2
   workup.STIRRINGthe mixture is stirred under ice-
3. 3
   Temperaturcooling for one hour
4. 4
   workup.WAITfurther at room temperature for one hour
5. 5
   EinengenThe reaction solution is concentrated under reduced pressure
6. 6
   workup.ADDITIONto the residue are added chloroform and water
7. 7
   SonstigeThe organic layer is dried
8. 8
   Sonstigeevaporated
9. 9
   Sonstigeto remove the solvent
10. 10
    SonstigeThe resulting residue is purified by silica gel column chromatography (solvent; chloroform/methanol=100:1)

Vorschrift

Methyl 5-diphenylacetyl-4,5,6,7-tetrahydroimidazo-[4,5-c]pyridine-4-carboxylate (1.60 g) is dissolved in dimethylformamide (20 ml), and thereto is added sodium hydride (60% oil-dispersion, 176 mg) under ice-cooling. The mixture is stirred at 0° C. for 20 minutes, and thereto is added [2'-(1-trityl-1H-tetrazol-5-yl)bipheyl-4-yl]methyl bromide (2.40 g), and the mixture is stirred under ice-cooling for one hour, and further at room temperature for one hour. The reaction solution is concentrated under reduced pressure, and to the residue are added chloroform and water. The organic layer is dried, and evaporated to remove the solvent. The resulting residue is purified by silica gel column chromatography (solvent; chloroform/methanol=100:1) to give methyl 5-diphenylacetyl-3-[2'-(1-trityl-1H-tetrazol-5-yl)biphenyl-4-yl]methyl-4,5,6,7-tetrahydroimidazo[4,5-c]pyridine-4-carboxylate (430 mg) as a colorless foam.

Quelle