A kind of derivative of polyasparagine and its preparation method and application
A technology for polyasparagine and derivatives, which is applied in the field of derivatives of polyasparagine and its preparation, can solve the problems of low biodegradation rate, unsatisfactory physical properties, limited popularization and application, etc., and achieves good inhibition effect, The effect of simple synthesis method and simple raw materials
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Embodiment 1
[0045] Weigh 1.0 g of the above-mentioned intermediate product polysuccinimide in a 250 mL round bottom flask, measure 10 mL of DMF to dissolve, and place it in an ice-water bath (0°C) to cool after completely dissolving. Polysuccinimide-based Slowly add 0.022 mol of n-propylamine dropwise, and react in an oil bath at 60°C for 6 h. After the reaction, pour the solution into 250 mL of anhydrous ether to precipitate, wash it several times, and dry it in a vacuum oven. Formula I is obtained.
Embodiment 2
[0047] Weigh 1.0 g of polysuccinimide and dissolve it in 10 mL of DMF. After completely dissolving, slowly add 0.0042 mol of n-hexylamine dropwise in an ice-water bath, react in an oil bath at 70°C for 6 h, cool down to room temperature and then add Add 0.011 mol of 3-diethylamino-1-propylamine dropwise in an ice-water bath (excess 3-diethylamino-1-propylamine helps the obtained product formula II satisfy x / y = 7 / 3), react at 30°C After 24 hours, after the reaction, the solution was poured into anhydrous ether to precipitate, washed several times, and dried in a vacuum oven to obtain formula II (m=5).
Embodiment 3
[0049] Weigh 1.0 g of polysuccinimide and dissolve it in 10 mL of DMF. After completely dissolving, slowly add 0.0042 mol of n-heptylamine dropwise in an ice-water bath, react in an oil bath at 70°C for 6 h, cool down to room temperature and then Add 0.011 mol 3-diethylamino-1-propylamine dropwise in an ice-water bath (excess 3-diethylamino-1-propylamine helps to obtain product formula II satisfying x / y = 7 / 3), and react at 30°C After 24 hours, after the reaction, the solution was poured into anhydrous ether to precipitate, washed several times, and dried in a vacuum oven to obtain formula II (m=6).
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