Terminal double-substituted triazole Schiff base compound, its preparation method and use
A compound and aspect technology, applied in the field of drugs related to thrombosis diseases, can solve the problems of high bleeding risk and the like
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Embodiment 1
[0031] .
[0032] Reaction raw materials: self-made, conventional method.
[0033] 1.66 g (10 mmol) compound II and 1.16g (10 mmol) of compound III-1 Dissolve in 20 mL of glacial acetic acid and heat to reflux overnight. After the reaction mixture was slightly cooled, it was poured into 200 mL of ice water, stirred, and the solid was collected by suction filtration, recrystallized from absolute ethanol, and vacuum-dried at room temperature to obtain the product IV-1 , white crystals. MS, m / z = 265 ([M+H] + ).
[0034] 1.33 g (5 mmol) compound IV-1 , 1.85 g (5 mmol) compound V and 2.07 g (15 mmol) of solid potassium carbonate were stirred overnight in 15 mL of acetonitrile, and then heated to reflux for 3 hours. The reaction mixture was cooled slightly and poured into 200 mL of ice water, stirred, adjusted to pH = 4 with concentrated hydrochloric acid, extracted with 50 mL × 3 dichloromethane, combined organic phases, washed with brine, dried over an...
Embodiment 2-4
[0036] Referring to the method of Example 1, it is possible to synthesize I of the following compounds:
[0037]
Embodiment 5
[0038] Example 5 In vitro platelet aggregation inhibition test
[0039] compound Inhibition of Platelet Aggregation IC50 (nM) Compound I-1 1.7 Compound I-2 3.9 Compound I-3 5.1 Compound I-4 3.7
[0040] It can be seen from the above table that the compound of the present invention exhibits obvious inhibitory effect in the platelet aggregation test.
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