Preparation of quinoline-based derivative, and applications of quinoline-based derivative in anti-inflammation
A technology of derivatives and quinolines, applied in the field of preparation and application of quinoline derivatives, to achieve good inhibitory activity, strong inhibitory effect, and good correlation effects
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Embodiment 1
[0034] Embodiment 1: the synthesis of compound A2, B2, C2, D2, E2, F2, G2
[0035] 1:1.5 aniline and ethyl acetoacetate were catalyzed by polyphosphoric acid, and reacted at 130°C for 2h. After the reaction, cool to room temperature, add crushed ice, adjust the pH to 8 with sodium hydroxide, precipitate a solid, filter it with suction, dry it by infrared, and put it into the next step without purification.
[0036]
Embodiment 2
[0037] Embodiment 2: the synthesis of compound A3-A17
[0038]
[0039] 1:1 equivalent of benzyl bromide and A2 solution DMF, add 5 equivalents of potassium carbonate, react at room temperature for 8h. After the reaction, it was extracted with ethyl acetate and water, and the organic phase was collected and purified by a silica gel column to obtain a white solid with a yield of 87-93%.
Embodiment 3
[0040] Embodiment 3: the synthesis of compound A18-A32
[0041]
[0042] Dioxane was used as a solvent, 1:1.5 equivalents of A3-A17 were reacted with selenium dioxide at 65°C for 2 hours, filtered after the reaction, the filtrate was collected, purified by a silica gel column, and the yield was 71-85%.
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