反应详情

(6-Ethynyl-isoquinolin-4-yl)-acetic acid (58 mg, 0.28 mmol) is dissolved in DMF (1 ml) and O-(7-azabenzotriazo-1-yl)-N,N,N′,N′-tetramethyluronium hexafluorophosphatc (0.125 g, 0.33 mmol) and Hunig's base (0.180 ml, 1.03 mmol) are added, followed by a solution of 5,6-diamino-1-isobutyl-3-methyl-1H-pyrimidine-2,4-dione (58 mg, 0.28 mmol) in DMF (0.7 ml). The reaction is stirred at room temperature for 2 hours. The solvent is evaporated and the residue purified by flash column chromatography (30:1 dichloromethane-methanol elution). The intermediate is dissolved in methanol (2 ml) and water (2.75 ml) added, followed by 4M aqueous sodium hydroxide (0.25 ml). The reaction is heated at 40° C. for 2 hours, then stirred for 16 hours at ambient temperature. The solvent is evaporated and the crude product purified by flash column chromatography (30:1 dichloromethane-methanol elution) to afford 8-(6-ethynyl-isoquinolin-4-ylmethyl)-3-isobutyl-methyl-3,7dihydro-purine-2,6-dione, [MH]+ 388.

1. customThe solvent is evaporated
2. customthe residue purified by flash column chromatography (30:1 dichloromethane-methanol elution)
3. dissolutionThe intermediate is dissolved in methanol (2 ml)
4. additionwater (2.75 ml) added
5. temperatureThe reaction is heated at 40° C. for 2 hours
6. stirringstirred for 16 hours at ambient temperature
7. customThe solvent is evaporated
8. customthe crude product purified by flash column chromatography (30:1 dichloromethane-methanol elution)