3',4'-Dimethoxycinnamic acid → HCID 67398066, 화합물

To a solution of 0.59 g (2.84 mmol) of 3-(3,4-dimethoxy-phenyl)-acrylic acid (compound of Example 2; Step 1) in 6 mL of toluene, 0.503 g (3.1 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-hydroxynonanimidamide (compound of example 47; 1.0 g, 3.8 mmol) diluted with 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 to obtain a crude residue, which was purified by column chromatography (silica gel, chloroform-methanol) to yield the title compound.

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

ORD 기록

ord-9f4b5b65f8c2421eafca406fd3dd39ac

출처 데이터셋

uspto-grants-2014_01

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US08629277B2