反应详情

A mixture consisting of 0.45 g of pyrido-[4,3-d]pyrimidine-4-ol, 0.53 g of 2-[4-(t-butyl)phenyl]ethylamine, about 40 mg of (NH4)2SO4 in 4 mL of hexamethyldisilazane was refluxed for about five hours. The mixture was then cooled and excess disilazane was removed in vacuo. The residue was dissolved in CH2Cl2, and the solution was washed with water and filtered through phase separating paper. Evaporated the CH2Cl2 and adsorbed the residue onto silica gel, which was applied to a thin silica pad and eluted with CH2Cl2 →50% EtOAc/50% CH2Cl2EtOAc. Fractions containing the major product were combined and the product which crystallized was recrystallized from hexane/EtOAc. Yield 0.2 g. M.P. 157-158° C.

1. temperaturewas refluxed for about five hours
2. temperatureThe mixture was then cooled
3. customexcess disilazane was removed in vacuo
4. dissolutionThe residue was dissolved in CH2Cl2
5. washthe solution was washed with water
6. filtrationfiltered through phase
7. customseparating paper
8. customEvaporated the CH2Cl2
9. washeluted with CH2Cl2 →50% EtOAc/50% CH2Cl2EtOAc
10. additionFractions containing the major product
11. customthe product which crystallized
12. customwas recrystallized from hexane/EtOAc