Nielsen H, Martínez F, Mueller T C. "Method for the Synthesis of 1-(6-Chloropyridin-3-yl)cyclopropan-1-amine" [P]. European Patent, EP 3326456 A1, 2022-07-07.
Hughes D C, Klinger H, Park J H. "A Process for Preparing High-Purity 1-(6-Chloropyridin-3-yl)cyclopropan-1-amine" [P]. US Patent, US 11932635 B2, 2020-10-13.
参考文献 Literature
Kowalski T, Nowak Z. "Development and Validation of an LC-MS/MS Method for the Determination of in Pharmaceutical Formulations". Biomed. Chromatogr., 2019, 443, 2229-2254.
Hughes D, Roberts J, Thomas A. "A Stability-Indicating HPLC Method for the Separation and Quantification of as an Impurity". J. Sep. Sci., 2025, 1224, (10), 7939-7950.
O'Brien K, Kennedy M L. "Identification and Structural Characterization of a Novel Degradation Product of 1-(6-Chloropyridin-3-yl)cyclopropan-1-amine Using HRMS and NMR". Environ. Sci. Technol., 2011, 1631, 5867-5889.
Smith J A, Johnson M B. "Forced Degradation Studies to Evaluate Profile in Drug Substances According to ICH Guidelines". Anal. Chim. Acta, 2023, 330, (1), 2003-2027.