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Synthesis of Water-soluble Methoxyethoxy-Aminoarlyoxy Cosubstituted Polyphosphazenes as Carrier Molecules for Bioactivc Agents

机译:水溶性甲氧基乙氧基-氨基芳氧基共取代的聚磷腈作为生物活性剂载体分子的合成

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The water-soluble poly(methoxyethoxy-aminoarlyoxy phosphazene) has been synthesized and investigated as a polymeric carrier molecule for the covalent attachment of bioactive agents. The synthetic procedures were developed first through the use of cyclic trimeric model systems. These model systems were utilized for the synthesis of polymeric analogues containing bioactive side groups. The sodium salts of 2-methoxyethanol and 4-acetamidophenol were allowed to react with (NPCl) or (NPCl)n or to yield derivatives of type [NP-(OClCHCHOCH)ヶ(OArNHCOCH)y]or n. The 4-acetamido groups were then hydrolyzed to 4-amino-phenoxy units with potassium tert-butoxide. Coupling reactions between amino group and N-acetylglycine was accomplished with the use of dicyclohexylcarbodiimide. Their properties and structural characterization are discussed.
机译:水溶性聚(甲氧基乙氧基-氨基芳氧基磷腈)已被合成并作为聚合物载体分子用于生物活性剂的共价连接。首先通过使用循环三聚体模型系统开发了合成程序。这些模型系统用于合成含有生物活性侧基的聚合物类似物。使2-甲氧基乙醇和4-乙酰氨基苯酚的钠盐与(NPCl 3)3或(NPCl 3)n反应,或产生[NP-(OClCHCHCHCHCHCHCH)OCHNH3 )y]或n。然后用叔丁醇钾将4-乙酰氨基基团水解成4-氨基-苯氧基单元。氨基和N-乙酰基甘氨酸之间的偶联反应是通过使用二环己基碳二亚胺完成的。讨论了它们的性质和结构表征。

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