反应详情

TMPZnCl.LiCl (2) (1.3 M in THF, 0.85 mL, 1.1 mmol) was added to a solution of 1,3,7-trimethyl-1H-purine-2,6(3H,7H)-dione (12) (194 mg, 1.0 mmol) in THF (2 mL) at 25° C. and the reaction mixture was then stirred at this temperature for max. 5 min. Pd(dba)2 (17 mg, 3 mol %) and P(o-furyl)3 (14 mg, 6 mol %) dissolved in THF (2 mL), and mixed with 1-chloro-4-iodobenzene (310 mg, 1.3 mmol, 1.3 equiv) were then transferred via cannula to the reaction mixture. The resulting mixture was stirred for 1 h at 25° C. The reaction mixture was then quenched with a sat. aq. NH4Cl solution (20 mL), extracted with diethyl ether (3×50 mL) and dried over anhydrous Na2SO4. After filtration, the solvent was evaporated in vacuo. Purification by flash-chromatography (CH2Cl2/ether, 1:1) furnished compound 14a (226 mg, 74%) as a colourless solid.

1. custom5 min
2. stirringThe resulting mixture was stirred for 1 h at 25° C
3. customThe reaction mixture was then quenched with a sat. aq. NH4Cl solution (20 mL)
4. extractionextracted with diethyl ether (3×50 mL)
5. dry with materialdried over anhydrous Na2SO4
6. filtrationAfter filtration
7. customthe solvent was evaporated in vacuo
8. customPurification by flash-chromatography (CH2Cl2/ether, 1:1)