
This paper reports a novel synthesis of bosutinib starting from 3-methoxy-4-hydroxybenzoic acid. The process starts with esterification of the starting material, followed by alkylation, nitration, reduction, cyclization, chlorination and two successive amination reactions. The intermediates and target molecule were characterized by 1H-NMR, 13C-NMR, MS and the purities of all the compounds were determined by HPLC.
Aniline Compounds, Magnetic Resonance Spectroscopy, 3-methoxy-4-hydroxybenzoic acid, Molecular Structure, bosutinib; protein kinase inhibitors; 3-methoxy-4-hydroxybenzoic acid, Organic chemistry, Parabens, bosutinib, Article, Mass Spectrometry, protein kinase inhibitors, QD241-441, Nitriles, Quinolines, Chromatography, High Pressure Liquid
Aniline Compounds, Magnetic Resonance Spectroscopy, 3-methoxy-4-hydroxybenzoic acid, Molecular Structure, bosutinib; protein kinase inhibitors; 3-methoxy-4-hydroxybenzoic acid, Organic chemistry, Parabens, bosutinib, Article, Mass Spectrometry, protein kinase inhibitors, QD241-441, Nitriles, Quinolines, Chromatography, High Pressure Liquid
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