反应详情

To a mixture of 4-(3-pyridyl)-2-pyrimidine-amine (172.2 mg, 1.0 mmol), N-(3-bromo-4-methyl-phenyl)-4-(4-methyl-piperazin-1-ylmethyl)-benzamide (402.4 mg, 1.0 mmol) and sodium tert.-butylate (144.2 mg, 1.5 mmol) is added a mixture of rac-BINAP (31.2 mg, 0.050 mmol) and Pd2(dba)3*CHCl3 (13 mg, 0.013 mmol) under argon. After addition of 3 ml of xylene the suspension is sonicated for 10 minutes then stirred for 5 hours under reflux. After cooling to room temperature, water (10 ml) is added to the dark brown oil and the product extracted 4 times with methylene chloride (10 ml each). The combined organic extracts are dried over MgSO4 and concentrated in vacuo. The brown oil is purified by flash-chromatography (SiO2, methanol). The product, a pale yellow solid is dissolved in methylene chloride, filtered and concentrated in vacuo. Yield: 484.3 mg of the title compound, 72% of theory, (99.9% area by HPLC). The product contains typically roughly 10% of isomers which can be eliminated by preparative reversed phase chromatography.

1. additionis added
2. customis sonicated for 10 minutes
3. temperatureunder reflux
4. extractionthe product extracted 4 times with methylene chloride (10 ml each)
5. dry with materialThe combined organic extracts are dried over MgSO4
6. concentrationconcentrated in vacuo
7. customThe brown oil is purified by flash-chromatography (SiO2, methanol)
8. dissolutionThe product, a pale yellow solid is dissolved in methylene chloride
9. filtrationfiltered
10. concentrationconcentrated in vacuo