Division of Pharmaceutical Sciences, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, Okayama University.
Chem Pharm Bull (Tokyo). 2022;70(2):146-154. doi: 10.1248/cpb.c21-00911.
Small-molecular drugs, which are generally inexpensive compared with biopharmaceuticals and can often be taken orally, may contribute to the Sustainable Development Goals (SDGs) adopted by the United Nations. We previously reported the retinoid X receptor (RXR) agonist 4-(ethyl(3-isobutoxy-4-isopropylphenyl)amino)benzoic acid (NEt-3IB, 1) as a small-molecular drug candidate to replace biopharmaceuticals for the treatment of inflammatory bowel disease. The previous synthetic method to 1 required a large amount of organic solvent and extensive purification. In line with the SDGs, we aimed to develop an environmentally friendly, inexpensive method for the large-scale synthesis of 1. The developed method requires only a hydrophobic ether and EtOH as reaction and extraction solvents. The product was purified by recrystallization twice to afford 99% pure 1 at 100 mmol scale in about 30% yield. The optimized process showed a 35-fold improvement of the E-factor (an index of environmental impact) compared to the original method. This work, which changes the solvent used to environmentally preferable ones based on the existing synthetic method for 1, illustrates how synthetic methods for small-molecular drugs can be adapted and improved to contribute to the SDGs.
小分子药物与生物制药相比通常较为廉价,且通常可口服,因此可能有助于实现联合国通过的可持续发展目标 (SDGs)。我们曾报道过视黄醇 X 受体 (RXR) 激动剂 4-(乙基(3-异丁氧基-4-异丙基苯基)氨基)苯甲酸 (NEt-3IB,1) 是一种小分子药物候选物,可替代生物制药来治疗炎症性肠病。之前合成 1 的方法需要大量有机溶剂和广泛的纯化。为了符合 SDGs,我们旨在开发一种环保、廉价的大规模合成 1 的方法。所开发的方法仅需要疏水性醚和 EtOH 作为反应和萃取溶剂。通过两次重结晶对产物进行纯化,以约 30%的收率在 100mmol 规模下得到 99%纯度的 1。与原始方法相比,优化后的工艺使环境影响指数 (E 因子) 提高了 35 倍。这项工作基于 1 的现有合成方法改变了所用溶剂,使之更为环保,说明了如何调整和改进小分子药物的合成方法以助力 SDGs。