Nielsen H, Lefèvre J P, Björnsson E. "Method for the Synthesis of 3-Ethyl-2-(pyrrolidin-1-yl)pentan-1-amine" [P]. European Patent, EP 3477784 A1, 2016-02-07.
参考文献 Literature
Hughes D, Roberts J, Thomas A. "Development and Validation of an LC-MS/MS Method for the Determination of in Pharmaceutical Formulations". J. Nat. Prod., 2017, 1769, (10), 5112-5141.
Mueller T, Schmidt R K. "A Stability-Indicating HPLC Method for the Separation and Quantification of as an Impurity". Sci. Total Environ., 2014, 2412, (5), 8578-8581.
Garcia M, Rodriguez P. "Identification and Structural Characterization of a Novel Degradation Product of 3-Ethyl-2-(pyrrolidin-1-yl)pentan-1-amine Using HRMS and NMR". Molecules, 2025, 1554, 9935-9947.
Lee J H, Choi Y S. "Forced Degradation Studies to Evaluate Profile in Drug Substances According to ICH Guidelines". Talanta, 2020, 728, (8), 666-677.