An efficient method for the large-scale synthesis of Atorvastatin calcium

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Abstract

Atorvastatin calcium salt (1) was obtained through the preparation of lactone compound (8) from 2-((4R,6R)-6-(2-(2-(4-fluorophenyl)-5-isopropyl-3- phenyl-4-(phenylcarbamoyl)-1H-pyrrol-1-yl)-ethyl)-2-phenyl-1,3, 2-dioxaborinan-4-yl)acetic acid tert-butyl ester (9) by hydrolysis in basic condition. Efficient hydrolysis of boronate compound 9 aimed at the viable synthesis for commercial production and purification of Atorvastatin calcium is reported. Detail studies of evaluation procedure are also reported.

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Lee, H. W., Kim, Y. M., Yoo, C. L., Kang, S. K., & Ahn, S. K. (2008). An efficient method for the large-scale synthesis of Atorvastatin calcium. Biomolecules and Therapeutics, 16(1), 28–33. https://doi.org/10.4062/biomolther.2008.16.1.028

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