An Expedient Synthesis of CMF-019: (S)-5-Methyl-3-{1-(pentan-3-yl)-2-(thiophen-2-ylmethyl)-1H-benzo[d]imida zole-5-carboxamido}hexanoic Acid, a Potent Apelin Receptor (APJ) Agonist

作者：Trifonov Lena; Afri Michal; Palczewski Krzysztof; Korshin Edward E^*; Gruzman Arie^*

来源：Medicinal Chemistry, 2018, 14(7): 688-694.

DOI：10.2174/1573406414666180412154952

• CMF-019
• peptidomimetics
• apelin
• apelin receptor
• expedient synthesis
• benzimidazole scaffold

Background: Apelin receptor (APJ) is a G protein-coupled receptor (GPCR) activated by the endogenous peptide apelin. The apelin-APJ system has emerged as an important regulator of cardiovascular homeostasis. Recently, a potent benzimidazole-derived apelin peptidomimetic, CMF-019, was patented but without a comprehensive description of its synthesis and a complete spectroscopic characterization of the intermediates.
Objective: Here, a detailed preparation of CMF-019 through a modified and improved synthetic pathway is described.
Method: In particular, the benzimidazole ring in 7 was tailored by the condensation of methyl 3-amino-4-(pentan-3-ylamino)benzoate (4) with (thiophene-2-yl)acetimidate salt 6. Saponification of 7 and the subsequent condensation of the free acid 8 with the corresponding enantiopure beta-amino acid methyl ester generated methyl (S)-5-methyl-3-11-(pentan-3-yl)-2-(thiophen-2-ylmethyl)-1H-benzo[d]imidazole-5-carboxamidolhexanoate (9). Hydrolysis of the latter with KOH in THE/water, followed by HPLC-purification, afforded the desired product, CMF-019 (potassium salt) 10.
Results & Conclusion: The approach reported herein enables preparation of 10 at a total yield of 12% over seven linear steps. Additionally, it does not require applying expensive designated microwave reactors and high-pressure hydrogenators. Thus, the elaborate synthesis provides a latent availability of potent agonist 10 for further exploring the physiologically essential apelin-APJ system.

• 出版日期2018