化学
胺化
催化作用
反应性(心理学)
铜
组合化学
溶剂
配体(生物化学)
有机化学
生物化学
医学
病理
受体
替代医学
作者
Udaysinh Parmar,Dipesh Somvanshi,Santosh Kori,Aman A. Desai,Rambabu Dandela,Dilip Kumar Maity,Anant R. Kapdi
标识
DOI:10.1021/acs.joc.1c00845
摘要
Buchwald–Hartwig amination of chloroheteroarenes has been a challenging synthetic process, with very few protocols promoting this important transformation at ambient temperature. The current report discusses about an efficient copper-based catalytic system (Cu/PTABS) for the amination of chloroheteroarenes at ambient temperature in water as the sole reaction solvent, a combination that is first to be reported. A wide variety of chloroheteroarenes could be coupled efficiently with primary and secondary amines as well as selected amino acid esters under mild reaction conditions. Catalytic efficiency of the developed protocol also promotes late-stage functionalization of active pharmaceutical ingredients (APIs) such as antibiotics (floxacins) and anticancer drugs. The catalytic system also performs efficiently at a very low concentration of 0.0001 mol % (TON = 980,000) and can be recycled 12 times without any appreciable loss in activity. Theoretical calculations reveal that the π-acceptor ability of the ligand PTABS is the main reason for the appreciably high reactivity of the catalytic system. Preliminary characterization of the catalytic species in the reaction was carried out using UV–VIS and ESR spectroscopy, providing evidence for the Cu(II) oxidation state.
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