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A Convergent Approach to the Total Synthesis of Telmisartan via a Suzuki Cross-Coupling Reaction between Two Functionalized Benzimidazoles

机译:通过两个功能化苯并咪唑之间的铃木交叉偶联反应聚合替米沙坦的全合成方法

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摘要

A direct and efficient total synthesis has been developed for telmisartan, a widely prescribed treatment for hypertension. This approach brings together two functionalized benzimidazoles using a high-yielding Suzuki reaction that can be catalyzed by either a homogeneous palladium source or graphene-supported palladium nanoparticles. The ability to perform the cross-coupling reaction was facilitated by the regio-controlled preparation of the 2-bromo-1-methylbenzimidazole precursor. This convergent approach provides telmisartan in an overall yield of 72% while circumventing many issues associated with previously reported processes.
机译:已经开发了一种直接有效的全合成替米沙坦,这是一种广泛使用的高血压治疗药物。该方法使用高产率的Suzuki反应将两种官能化的苯并咪唑聚在一起,该反应可以通过均相钯源或石墨烯负载的钯纳米颗粒进行催化。区域控制的2-溴-1-甲基苯并咪唑前体的制备促进了进行交叉偶联反应的能力。这种收敛方法可提供替米沙坦的总产率为72%,同时避免了与先前报道的工艺相关的许多问题。

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