3',4'-Dimethoxycinnamic acid → 5-[2-(3,4-Dimethoxy-phenyl)-vinyl]-3-pentyl-[1,2,4]oxadiazole

関与物質

反応手順

To a solution of 0.70 g (3.39 mmol) of 3-(3,4-dimethoxy-phenyl)-acrylic acid (compound of Example 2; Step 1) in 6 mL of toluene, 0.59 g (3.69 mmol) of 1,1-carbonyldiimidazole was added in portions at 25° C. to 30° C. under an inert atmosphere. To the thickened reaction 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-hexanimidamide (compound of Example 38; 0.9 g, 6.9 mmol) diluted with 5 mL of toluene was added to the above reaction mixture at 25° C. to 30° C. The reaction mass 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 the 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 material, which was purified by column chromatography (silica gel, chloroform-methanol) to yield the title compound.

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