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作 者:李龙珠 张玉心 吴成柱 李红梅 马涛 LI Long-zhu;ZHANG Yu-xin;WU Cheng-zhu;LI Hong-mei;MA Tao(School of Pharmacy,Bengbu Medical College,Bengbu Anhui 233030,China;School of Laboratory Medicine,Bengbu Medical College,Bengbu Anhui 233030,China)
机构地区:[1]蚌埠医学院药学院,安徽蚌埠233030 [2]蚌埠医学院检验医学院,安徽蚌埠233030
出 处:《蚌埠医学院学报》2021年第3期391-395,共5页Journal of Bengbu Medical College
基 金:安徽省高校自然科学研究重点项目(KJ2018A1009)。
摘 要:目的:采用三氯乙酰亚胺酯法合成紫草素-1′-O-β-D-吡喃葡萄糖苷。方法:以β-D-吡喃葡萄糖为起始原料制得糖基供体2,3,4,6-四-O-乙酰基-β-D-吡喃半乳糖酰基2,2,2-三氯乙酰亚胺酯,然后与紫草素反应得1-(1-(5,8-二羟基-1,4-萘醌-2-基)-4-甲基-3-戊烯氧基)-2,3,4,6-四-O-乙酰基-β-吡喃葡萄糖苷,最后在甲醇钠/甲醇体系下醇解脱去乙酰基得到目标化合物,采用核磁共振波谱(NMR)和电喷雾-质谱(ESI-MS)表征其结构。结果:NMR和ESI-MS鉴定目标化合物为紫草素-1′-O-β-D-吡喃葡萄糖苷。三氯乙酰亚胺酯法合成紫草素-1′-O-β-D-吡喃葡萄糖苷总收率为38.9%,HPLC测定纯度为96.7%。结论:本方法合成紫草素-1′-O-β-D-吡喃葡萄糖苷具有高立体选择性和高收率的优点,为紫草素糖基化修饰产物的化学合成提供了参考。Objective:To synthesize shikonin-1′-O-β-D-glucopyranoside by the trichloroacetimide ester method.Methods:The glycosyl donor 2,3,4,6-tetra-O-acetyl-β-D-galactopyranoyl-2,2,2-trichloroacetyl was prepared fromβ-D-glucopyranose as starting material.The imine ester was then reacted with shikonin to obtain1-(1-(5,8-dihydroxy-1,4-naphthoquinone-2-yl)-4-methyl-3-pentenoxy)-2,3,4,6-tetra-O-acetyl-β-glucopyranoside,and finally alcoholyzed to remove the acetyl group under the sodium methoxide/methanol system to obtain the target compound.The structure of the target compound was elucidated by nuclear magnetic resonance spectroscopy(NMR)and electrospray ionization mass spectrometry(ESI-MS).Results:The target compound was identified as shikonin-1′-O-β-D-glucopyranoside by NMR and ESI-MS.The total yield of shikonin-1′-O-β-D-glucopyranoside synthesized by the trichloroacetimide ester method was 38.9%,and the purity determined by HPLC was 96.7%.Conclusions:The method has the advantages of high stereoselectivity and high yield.It can be used for the synthesis of shikonin-1'-O-β-D-glucopyranoside,and provide a reference for the chemical synthesis of shikonin glycosylation modified products.
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