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L-脯氨酰-L-亮氨酰-甘氨酰胺(PLG)三肽合成
Synthesis of tripeptide L-prolyl-L-leucyl-glycinamide
【摘要】 L-脯氨酰-L-亮氨酰-甘氨酰胺三肽,具有重要的生理药理作用,可用于治疗帕金森病。以L-脯氨酸、L-亮氨酸和甘氨酰胺为原料,采用混合酸酐法,以苄氧羰基(cbz)为氨基保护基,以氯甲酸异丁酯为成酸酐试剂,以Pd/C催化氢解脱除cbz基合成了L-脯氨酰-L-亮氨酰-甘氨酰胺三肽,并进一步优化了合成条件:L-cbz-pro的最佳工艺条件为n(cbz)/n(L-pro)=2.6/1,反应温度-5℃,反应时间2h;L-cbz-prolyl-L-leu的最佳工艺条件为,反应温度-10℃。在上述工艺条件下产品总收率38.5%,光学纯度98.7%,熔点120~122℃,[α]D20=-46.3°。
【Abstract】 Tripeptide L-prolyl-L-leucyl-glycinamide(PLG) has important physiological and pharmacological functions,and can be used to treat Parkinson’s disease.PLG was synthesized by using the mixed anhydride method from L-proline,L-leucine and glycinamide.The amino groups of L-proline and L-leucine were protected firstly by the carbobenzoxy group,and then the carbobenzoxy group was removed by Pd/C with H2 from L-cbz-prolyl-L-leulyl-gly-NH2 to produce PLG in the end.Isobutyl chloroformate was used as reagent to form mixed anhydride.The optimum conditions to synthesize L-cbz-pro and L-cbz-prolyl-L-leu,were n(cbz)/n(L-pro)=2.6:1 at-5 ℃ for 2 hours and n(i-C4H9OCOCl)/n(L-cbz-pro)=1:1 at-10 ℃ respectively.Under these conditions,the melting point,optical purity and total yield of PLG were 120~122 ℃,98.7% and 38.5% respectively.The specific rotation [α]D20 was-46.3°。
【Key words】 L-prolyl-L-leucyl-glycinamide; peptide synthesis; mixed anhydride method;
- 【文献出处】 化工进展 ,Chemical Industry and Engineering Progress , 编辑部邮箱 ,2006年08期
- 【分类号】TQ464.7
- 【被引频次】4
- 【下载频次】538