Lei Huang, Yi Zhang, Xiaohan Shan, Yu Liu, Jian-qi Li
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引用次数: 0
摘要
摘要(3 R,4 S,5 R,6 R)-3,4,5-三(苄基氧基)-6-甲基四氢-2 H -吡喃-2- 1(1)是制备SGLT2抑制剂的关键中间体,目前正在进行糖尿病治疗的临床试验。然而,在工业规模上证明化合物1的制备的报道较少。本文探索了以市售甲基-α- D -葡萄糖吡喃苷为原料,经TBS保护、苄基保护、TBS去除、碘化、还原、去甲基化和氧化7个步骤高效制备工业生产中间体的方法。该批验证工艺为42.82 kg, HPLC纯度为99.31%。该方法的主要优点是总成本低于实验室规模的合成方法,质量可重复性好,过程安全环保。
Industrial-Scale Preparation of a Key Intermediate for the Manufacture of Therapeutic SGLT2 Inhibitors
Abstract (3 R ,4 S ,5 R ,6 R )-3,4,5-tris(benzyloxy)-6-methyltetrahydro-2 H -pyran-2-one ( 1 ) is a key intermediate for the preparation of promising SGLT2 inhibitors currently undergoing clinical tests for diabetes therapy. However, fewer reports have demonstrated the preparation of compound 1 at an industrial scale. In this article, an efficient preparation of the intermediate for the industrial production was explored from commercially available methyl-α- D -glucopyranoside in seven steps, including TBS protection, benzyl protection, TBS removal, iodination, reduction, demethylation, and oxidation. The batch of the validation process was 42.82 kg with a HPLC purity of 99.31%. The main advantages of this approach are that the total cost is lower than the reported laboratory-scale synthetic method, the quality is reproducible, and the process is safe and environmentally friendly.