反应详情

0.5 g (1.16 mmol) of N-[2-(3-cyanophenoxy)ethyl]-4-(3,4-dimethoxybenzoyl)benzamide was dissolved in 10 ml of N,N-dimethylformamide (dehydrated). 0.21 g (2.32 mmol) of sodium hydrogensulfide dihydrate and 0.24 g (1.16 mmol) of magnesium chloride hexahydrate were added to the obtained solution under cooling with ice, and they were stirred at room temperature for 2.5 hours. After the treatment with ethyl acetate as the extraction solvent in an ordinary manner, the solvent was evaporated, and the obtained crude product was dissolved in 20 ml of acetone. 0.56 ml (9.0 mmol) of methyl iodide was added to the solution, and they were refluxed for 3 hours. The solvent was evaporated, and the obtained crude product was washed with ethyl acetate. After the filtration, the obtained crystals were dissolved in 10 ml of methanol. 155 mg (2.0 mmol) of ammonium acetate was added to the obtained solution, and they were stirred for 3 hours. The solvent was evaporated, and the residue was treated in the same manner as that in step 7 in Example 51 to obtain the title compound.

1. temperatureunder cooling with ice, and they
2. customAfter the treatment with ethyl acetate as the extraction solvent in an ordinary manner, the solvent was evaporated
3. customthe obtained crude product
4. temperaturewere refluxed for 3 hours
5. customThe solvent was evaporated
6. customthe obtained crude product
7. washwas washed with ethyl acetate
8. filtrationAfter the filtration
9. dissolutionthe obtained crystals were dissolved in 10 ml of methanol
10. stirringwere stirred for 3 hours
11. customThe solvent was evaporated
12. additionthe residue was treated in the same manner as that in step 7 in Example 51