反应详情

To a solution of 0.63 g (2.08 mmol) of 3-(3,4-dimethoxy-phenyl)-acrylic acid (compound of Example 2; Step 1) in 6 mL of toluene, 0.540 g (3.33 mmol) of 1,1-carbonyldiimidazole was added in portions at 25° C. to 30° C. under inert atmosphere. To the thickened mixture, 5 mL of toluene was added and the resulting mixture was stirred at 25° C. to 30° C. for 60 to 90 min. A solution of N-hydroxy-heptanimidamide (compound of Example 41; 0.9 g, 6.2 mmol) in 5 mL of toluene was added to the above reaction mixture at 25° C. to 30° C. The reaction mixture was stirred at 25° C. to 30° C. under nitrogen for 12-14 h, followed by stirring at 100° C. to 105° C. for 6-8 h. After completion of the reaction, the reaction mixture was cooled to 25° C. to 30° C. and quenched with 10 mL of chilled water under stirring at 25° C. to 30° C. The organic layer was separated, and the aqueous layer was washed with 5 mL of toluene. The organic layers were combined and washed with 10 mL of 1N HCl solution, 10 mL of 5% sodium bicarbonate solution and 10 mL of 10% sodium chloride solution. The organic layer was distilled completely to obtain a crude residue, which was purified using column chromatography (silica gel, chloroform-methanol) to yield the title compound.

1. stirringThe reaction mixture was stirred at 25° C. to 30° C. under nitrogen for 12-14 h
2. stirringby stirring at 100° C. to 105° C. for 6-8 h
3. customAfter completion of the reaction
4. temperaturethe reaction mixture was cooled to 25° C. to 30° C.
5. customquenched with 10 mL of chilled water
6. stirringunder stirring at 25° C. to 30° C
7. customThe organic layer was separated
8. washthe aqueous layer was washed with 5 mL of toluene
9. washwashed with 10 mL of 1N HCl solution, 10 mL of 5% sodium bicarbonate solution and 10 mL of 10% sodium chloride solution
10. distillationThe organic layer was distilled completely
11. customto obtain a crude residue, which
12. customwas purified