反应详情

8-chloro-3,7-dihydro-1H-purine-2,6-dione (100 mg, 0.44 mmol) was stirred with sodium carbonate (52 mg, 0.49 mmol) in dry DMF (3 ml) for 45 min., then 4-bromo-1-butene (66 mg, 0.49 mmol) was added and the mixture was stirred under nitrogen at 40 C for 65 h. After cooling to room temperature, the mixture was thoroughly degassed by evacuating the vessel and refilling with nitrogen several times. Tetrakis(triphenylphosphine)palladium(0) (102 mg, 0.09 mmol) was added, the mixture degassed again and then morpholine (0.385 ml, 4.4 mmol) added and stirring continued for 6.5 h. 2M HCl and EtOAc were added, and the 2-phase system was filtered to remove a yellow precipitated solid. The organic phase of the filtrate was separated and evaporated. The residue was dissolved with warming in THF-MeOH (1:1) and loaded onto an aminopropyl SPE (5 g) which was eluted with THF-MeOH (1:1) followed by MeOH and then 5% AcOH in MeOH-DCM (1:1). The product fraction was further purified by mass-directed autoprep to afford the title compound.

1. customthe mixture was thoroughly degassed
2. customby evacuating the vessel
3. customthe mixture degassed again
4. stirringstirring
5. waitcontinued for 6.5 h
6. filtrationthe 2-phase system was filtered
7. customto remove
8. customa yellow precipitated solid
9. customThe organic phase of the filtrate was separated
10. customevaporated
11. dissolutionThe residue was dissolved
12. temperaturewith warming in THF-MeOH (1:1)
13. washwas eluted with THF-MeOH (1:1)
14. customThe product fraction was further purified by mass-directed autoprep