反应详情

温度

70 °C

N-(4-{[7-(Benzyloxy)-6-methoxy-4-quinolyl]oxy}-2,3-dimethylphenyl)-N′-(2-methoxyphenyl)urea (161 mg) was dissolved in N,N-dimethylformamide (4 ml) and triethylamine (1 ml), and palladium hydroxide (32 mg) was added to the solution. The mixture was stirred in a hydrogen atmosphere at room temperature overnight. The reaction solution was filtered through Celite and was washed with chloroform/methanol. The solvent was removed by distillation under the reduced pressure. A 110 mg portion of the residue (223 mg) was dissolved in N,N-dimethylformamide (1.5 ml), and potassium carbonate (23 mg), tetra-n-butylammonium iodide (5 mg), and 2-bromoethyl methyl ether (23 mg) were added to the solution. The mixture was stirred at 70° C. overnight. A saturated aqueous sodium hydroqencarbonate solution was added to the reaction solution, and the mixture was extracted with chloroform. The chloroform layer was dried over anhydrous magnesium sulfate. The solvent was removed by distillation under the reduced pressure. The residue was purified by thin-layer chromatography on silica gel by development with chloroform/acetone (2/1) to give 89 mg of the title compound.

1. filtrationThe reaction solution was filtered through Celite
2. washwas washed with chloroform/methanol
3. customThe solvent was removed by distillation under the reduced pressure
4. dissolutionA 110 mg portion of the residue (223 mg) was dissolved in N,N-dimethylformamide (1.5 ml)
5. additionpotassium carbonate (23 mg), tetra-n-butylammonium iodide (5 mg), and 2-bromoethyl methyl ether (23 mg) were added to the solution
6. additionA saturated aqueous sodium hydroqencarbonate solution was added to the reaction solution
7. extractionthe mixture was extracted with chloroform
8. dry with materialThe chloroform layer was dried over anhydrous magnesium sulfate
9. customThe solvent was removed by distillation under the reduced pressure
10. customThe residue was purified by thin-layer chromatography on silica gel by development with chloroform/acetone (2/1)