反应详情

4-Amino-2-ethoxymethyl-1-(2-hydroxy-2-methylpropyl)-1H-imidazo[4,5-c]quinolin-7-ol (100 mg, 0.3 mmol), cesium carbonate (488 mg, 1.5 mmol), 2-chloromethyl-1-methyl-1H-imidazole.HCl (100 mg, 0.6 mmol), tetrabutylammonium bromide (96 mg, 0.3 mmol), triethylamine (0.5 ml), and DMF (10 mL) were combined and stirred at ambient temperature overnight. The reaction was concentrated under reduced pressure and dichloromethane was added to the residue. Undissolved solids were removed by filtration. The filtrate was concentrated under reduced pressure and subsequently purified by flash column chromatography on silica gel, eluting with a gradient of 0-5% methanol in dichloromethane. The clean fractions were combined and concentrated under reduced pressure. The resulting solid was recrystallized from isopropanol/diethylether to yield 40 mg of 1-[4-amino-2-ethoxymethyl-7-(1-methyl-1H-imidazol-2-ylmethoxy)-1H-imidazo[4,5-c]quinolin-1-yl]-2-methylpropan-2-ol as an off white solid, mp 200.0-202.0° C.

1. concentrationThe reaction was concentrated under reduced pressure and dichloromethane
2. additionwas added to the residue
3. customwere removed by filtration
4. concentrationThe filtrate was concentrated under reduced pressure
5. customsubsequently purified by flash column chromatography on silica gel
6. washeluting with a gradient of 0-5% methanol in dichloromethane
7. concentrationconcentrated under reduced pressure
8. customThe resulting solid was recrystallized from isopropanol/diethylether