Synthesis of 2-[[(4-Fluoroalkoxy-2-pyridyl)methyl]sulfinyl]-lH-benzimidazoles as Antiulcer Agents

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Abstract

Many 2-[[(4-fluoroalkoxy-2-pyridyl)methyl]sulfinyl]-lH-benzimidazoles were synthesized and tested for antisecretory, antiulcer, and cytoprotective activities. Most of these compounds were superior to omeprazole in antisecretory and antiulcer potencies, and especially in protecting the gastric mucosa from ethanol-induced damage. Among these compounds, 2-[[[3-methyl-4-(2,2,2-trifiuoroethoxy)-2-pyridyl]methyl]sulfinyl]-lH-benzimidazole, AG-1749 (lansoprazole) (6f), was selected for further development and clinical evaluation. © 1990, The Pharmaceutical Society of Japan. All rights reserved.

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Kubo, K., Oda, K., Kaneko, T., Satoh, H., & Nohara, A. (1990). Synthesis of 2-[[(4-Fluoroalkoxy-2-pyridyl)methyl]sulfinyl]-lH-benzimidazoles as Antiulcer Agents. Chemical and Pharmaceutical Bulletin, 38(10), 2853–2858. https://doi.org/10.1248/cpb.38.2853

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