Brown S R, Mueller T, Davis P L. "Method for the Synthesis of 5-Amino-2,6-dimethylpyrimidin-4(1H)-one" [P]. US Patent, US 10421034 B2, 2025-03-12.
Williams B T, Anderson J P, Stevens L M. "A Process for Preparing High-Purity 5-Amino-2,6-dimethylpyrimidin-4(1H)-one" [P]. US Patent, US 11004352 B2, 2015-02-22.
参考文献 Literature
Kim S H, Park J Y. "Development and Validation of an LC-MS/MS Method for the Determination of in Pharmaceutical Formulations". Molecules, 2015, 312, (1), 3425-3430.
Smith J A, Johnson M B. "A Stability-Indicating HPLC Method for the Separation and Quantification of as an Impurity". Biomed. Chromatogr., 2020, 267, (12), 998-1025.
Jensen P, Larsen A M, Olsen K. "Identification and Structural Characterization of a Novel Degradation Product of 5-Amino-2,6-dimethylpyrimidin-4(1H)-one Using HRMS and NMR". Sci. Total Environ., 2021, 701, (11), 2466-2496.
Kowalski T, Nowak Z. "Forced Degradation Studies to Evaluate Profile in Drug Substances According to ICH Guidelines". Anal. Methods, 2020, 1164, 3005-3012.