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分别用氯化亚砜(方法1)、草酰氯(方法2)两种方法将布洛芬[2-(4-异丁基苯基)丙酸]活化成2-(4-异丁基苯基)丙酰氯(Ⅰ),再与聚乙二醇(PEG)的端羟基反应生成PEG修饰的布洛芬-聚乙二醇酯,即2-(4-异丁基苯基)丙酸-聚乙二醇酯(Ⅱ)。分别用核磁共振(1H-NMR)、红外光谱(IR)和凝胶渗透色谱(GPC)对其进行了表征,结果表明成功合成了含布洛芬端基的PEG大单体,分子量分布窄,d为1.047。溶解性试验表明Ⅱ的水溶性很好。草酰氯法反应条件温和,产率更高,说明草酰氯法更优。

Ibuprofen-polyethylene glycol ester(Ⅱ),2-(4-isobutylphenyl) propionic acid-polyethylene glycol ester,could be designed and obtained from the reaction of polyethylene glycol(PEG) with 2-(4-isobutylphenyl) propionic acyl chloride(Ⅰ),which was prepared in high yield by the reaction of ibuprofen with thionyl chloride(method 1) or oxalyl chloride(method 2).The structure analysis and characterization of Ⅱ were studied by 1H nuclear magnetic resonance spectrum(1H-NMR),infrared spectrum(IR) and gel permeation in chromatography(GPC) method.The results show that Ⅱ is synthesized successfully,and the molecule distribution of Ⅱ is 1.047.Ⅱ is dissolvable in most organic solvents such as CH2Cl2,CHCl3,THF,DMF and DMSO.The solubility of Ⅱ has been improved in aqueous solutions.Compared with method 1,the method 2 has the advantages of milder reaction condition,higher yield.

参考文献

[1] Greenwald RB;Choe YH;McGuire J;Conover CD .Effective drug delivery by PEGylated drug conjugates.[J].Advanced drug delivery reviews,2003(2):217-250.
[2] 信建峰,马吉海,张树芬,陈韶蕊,李海于.酰氯制备方法综述[J].河北化工,2006(11):16-18,20.
[3] Apurba Bhattacharya;David Murphy .Temperature Selective Diastereo-Recognition (TSD): Enantiomeric Ibuprofen via Environmentally Benign Selective Crystallization[J].Organic process research & development,2003(5):717-722.
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