反应详情

温度

80 °C

To a solution of methyl {5-[4-(2-bromo-2-methylpropanoyl)phenyl]bicyclo[3.2.2]non-1-yl}acetate (Intermediate 24; 80 mg, 0.19 mmol) in absolute EtOH (20 mL) was added 5,6-diaminopyrimidin-4-ol (30 mg, 0.21 mmol) followed by 1M HCl (0.21 mL). The suspension was heated under gentle reflux (80° C.) overnight then allowed to cool, the solvent removed and the residue treated with 2M NaOH (2 mL). The aqueous phase was extracted into EtOAc (3×50 mL), the organic extracts were combined, dried (MgSO4) and concentrated to leave a pale yellow gum. This was purified on a 12 g Crawford silicycle cartridge, loading in DCM and eluting with 0-5-10% MeOH-DCM, giving the title compound as a pale yellow gum (55 mg, 0.123 mmol, 65%); 1H NMR (CDCl3) 1.41-1.61 (14H, m), 1.71 (6H, s), 2.07 (2H, s), 3.61 (3H, s), 7.11 (2H, d), 7.51 (2H, d), 8.14 (1H, s); MS m/e MH+ 449.

1. temperatureThe suspension was heated
2. temperatureto cool
3. customthe solvent removed
4. additionthe residue treated with 2M NaOH (2 mL)
5. extractionThe aqueous phase was extracted into EtOAc (3×50 mL)
6. dry with materialdried (MgSO4)
7. concentrationconcentrated
8. customto leave a pale yellow gum
9. customThis was purified on a 12 g Crawford silicycle cartridge, loading in DCM
10. washeluting with 0-5-10% MeOH-DCM