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Development and Optimization of a New Chemoenzymatic Approach for the Synthesis of Peracetylated Lactosamine (Intermediate for the Synthesis of Pharmacologically Active Compounds) Monitored by RP- HPLC Method

机译:RP-HPLC法监测过乙酰化乳糖胺(合成药理活性化合物的中间体)化学合成新方法的开发与优化

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Abstract Purpose: To describe a chemoenzymatic approach joining an enzymatic regioselective hydrolysis of peracetylated N-acetyl-α-D-glucosamine (1) with a mild controlled acyl relocation which resulted to 2-acetamido-2 deoxy-1,3,6-tri-O-acetyl-α-D-glucopyranose (1b). Methods: Immobilization of lipase on decaoctyl (Sepabeads ECOD/S) and octyl-agarose (Octyl SepharoseR CL-4B) was carried out as reported by the work of Bastida et al. The newly RP-HPLC method for examining the enzymatic hydrolysis was carried out isocratically utilizing a HPLC system. Results: The new approach resulted to get the target compound (3) in 95% yield after purification utilizing flash column chromatography. Candida rugosa-lipase immobilized ondecaoctyl-sepabeads was the best catalyst in terms of activity and regioselectivity in the hydrolysis of substrate (1), delivering the deacetylation at C-6 position (98% general yield). Also, a reversed-phase high-performance liquid-chromatographic (RP-HPLC) method for controlling the regioselective hydrolysis of peracetylated N-acetyl-α-D-glucosamine (1) with a mild monitored acyl movement which led to 2-acetamido-2-deoxy-1,3,6-tri-O-acetyl-α-D-glucopyranose (1b) has additionally been developed. The developed RP-HPLC method was utilized as fingerprints to follow the hydrolysis of substrate (1) and to decide its purity and additionally yield. Furthermore, the acquired compound (3) was further purified by flash chromatography. Compound (3) was further characterized utilizing 1HNMR and mass spectrometry. Conclusion: An efficient chemoenzymatic procedure to optimize the preparation of peracetylated lactosamine 3 containing acetyl ester as extraordinary protecting group is presented. Compound 3 is a significant intermediate for the synthesis of pharmacologically active compound (e.g. complex oligosaccharides for biochemical, biophysical, or biological examinations). Besides, reaction monitoring utilizing HPLC proposes more exact information than spectroscopic methods.
机译:摘要目的:描述一种化学酶方法,该方法将过乙酰化的N-乙酰基-α-D-葡萄糖胺(1)的酶区域选择性水解与轻度受控的酰基转移结合,产生2-乙酰氨基-2脱氧-1,3,6-tri -O-乙酰基-α-D-吡喃葡萄糖(1b)。方法:如Bastida等人的工作报道的,将脂肪酶固定在十辛基(Sepabeads ECOD / S)和辛基琼脂糖(Octyl SepharoseR CL-4B)上。使用HPLC系统等度地进行了新的RP-HPLC检查酶促水解的方法。结果:采用快速柱色谱法纯化后,新方法得到目标化合物(3),产率为95%。就底物(1)的水解活性和区域选择性而言,固定在十二烷基-sepabeads上的皱纹念珠菌脂肪酶是最好的催化剂,可在C-6位进行脱乙酰化(总收率98%)。此外,还采用反相高效液相色谱(RP-HPLC)方法控制过乙酰化的N-乙酰基-α-D-葡萄糖胺(1)的区域选择性水解,同时监测到轻微的酰基移动,从而导致2-acetamido-另外开发了2-脱氧-1,3,6-三-O-乙酰基-α-D-吡喃葡萄糖(1b)。发达的RP-HPLC方法被用作指纹图谱,以追踪底物(1)的水解并确定其纯度和产量。此外,将获得的化合物(3)通过快速色谱法进一步纯化。利用1 HNMR和质谱进一步表征化合物(3)。结论:提出了一种有效的化学酶法程序,以优化含乙酰酯作为非凡保护基的过乙酰化乳糖胺3的制备。化合物3是用于合成药理活性化合物(例如,用于生化,生物物理或生物学检查的复合寡糖)的重要中间体。此外,利用HPLC进行反应监测比光谱方法能提供更准确的信息。

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